WO2006007337A1 - Vaginal health products - Google Patents
Vaginal health products Download PDFInfo
- Publication number
- WO2006007337A1 WO2006007337A1 PCT/US2005/020286 US2005020286W WO2006007337A1 WO 2006007337 A1 WO2006007337 A1 WO 2006007337A1 US 2005020286 W US2005020286 W US 2005020286W WO 2006007337 A1 WO2006007337 A1 WO 2006007337A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- mucin
- vitamin
- acid
- vaginal
- Prior art date
Links
- 0 *CNC1CCC1 Chemical compound *CNC1CCC1 0.000 description 3
- RSQSQJNRHICNNH-NFMPGMCNSA-N C[C@]([C@@H]([C@@H]([C@](C1)(C2)[C@H]3CC[C@H]1C2=C)C(O)=O)[C@]3(CC1)O2)([C@H]1O)C2=O Chemical compound C[C@]([C@@H]([C@@H]([C@](C1)(C2)[C@H]3CC[C@H]1C2=C)C(O)=O)[C@]3(CC1)O2)([C@H]1O)C2=O RSQSQJNRHICNNH-NFMPGMCNSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
- A61K31/353—3,4-Dihydrobenzopyrans, e.g. chroman, catechin
- A61K31/355—Tocopherols, e.g. vitamin E
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/02—Drugs for genital or sexual disorders; Contraceptives for disorders of the vagina
Definitions
- the present invention relates to the use of vitamin E and various plant hormones for increasing the growth, renewal and mucus production of vaginal epithelial cells and improving the health of the female genital tract.
- estrogen dependent tissue will start to involute and take on the characteristic appearance of estrogen deprivation. Cervical mucus levels dimmish and vaginal mucosa regresses during menopause. With aging, the vagina becomes shortened, ruggae disappear, and elasticity is lost. Vaginal secretion becomes scanty. When estrogen is provided, some of these effects are reversed: the cervix may secrete more mucus and the vaginal mucosa may regain lost layers. However, the symptoms often do not disappear completely, in part because the amount of estrogen provided for hormone replacement is lower than circulating estrogen levels during a normal menstrual cycle.
- vaginal dryness Approximately 40% of postmenopausal women experience atrophic vaginitis or vaginal dryness. During vaginal atrophy, the vaginal epithelium decreases in thickness, hydration, rugae (folds), and blood flow.
- causes of atrophic vaginitis include a decrease in the amount of estrogen present both locally and systemically as well as environmental factors such as chemotherapy, antihistamines, smoking cigarettes, excessive exercise, and perineal products (i.e. douches, deodorants, and perfumes).
- Estrogens or hormone replacement therapies (HRTs) are effective in reducing vaginal dryness.
- possible dangerous side effects include a higher incidence of breast cancer, endometrial cancer, blood clots, nausea, breast tenderness, and headache.
- Products that are available over-the-counter include lubricants such as Astroglide and KY Lubricating Jelly as well as moisturizers such as Replens and KY Long Lasting Moisturizer. These products, which are mostly water in composition, provide only temporary relief (1 -2 days) for symptoms and provide virtually no long-term benefits to the vaginal tissue. Therefore, vaginal dryness and regression of vaginal mucosa are problematic, particularly after menopause. Stimulation of cervical mucus production can help alleviate vaginal dryness, and can also augment the action of exogenously administered estrogen to alleviate vaginal dryness. Moreover compositions and methods for counteracting the regression of vaginal mucosa are also needed.
- the invention provides non-hormonal therapies for treating certain reproductive and vaginal problems, including atrophic vaginitis.
- these therapies have minimal side effects, stimulate natural and non-hormonal mechanisms of action, promote vaginal cell growth and renewal, increase mucus secretion, stimulate gene expression, replace aging tissues with new tissues and maintain or restore healthy tissue function.
- the present invention is directed to a variety of compositions and methods for treating or preventing vaginal and/or reproductive problems in a female mammal.
- the compositions involve an effective amount of a composition that includes vitamin E and/or a plant hormone such as jasmonic acid or gibberellic acid.
- the compositions of the invention can also include a retinoid or carotenoid (e.g. vitamin A) and/or one or more nucleotide(s) or nucleoside(s). In general, these compositions can be administered topically or intravaginally.
- the compositions and methods of the invention can inter alia increase vaginal cell growth, stimulate renewal or turnover of vaginal cell layers, and/or to alleviate or diminish vaginal dryness in a female mammal.
- the compositions and methods of the invention can also stimulate the production of collagen and fibronectin.
- the invention provides a method to increase growth of vaginal or cervical epithelial cells by administering to the female mammal an effective amount of vitamin E and/or a plant hormone such as jasmonic acid or gibberellic acid.
- the compositions of the invention can also include a retinoid or carotenoid (e.g. vitamin A) and/or one or more nucleotide(s) or nucleoside(s).
- the invention provides a method to increase expression of mucin, for example, mucin-4, in vaginal or cervical epithelial cells by administering to the female mammal a composition having an effective amount of vitamin E and/or a plant hormone such as jasmonic acid or gibberellic acid.
- the compositions of the invention can also include a retinoid or carotenoid (e.g. vitamin A) and/or one or more nucleotide(s) or nucleoside(s).
- the method involves increasing the expression of
- compositions of the invention can also include a retinoid or carotenoid (e.g. vitamin A) and/or one or more nucleotide(s) or nucleoside(s).
- Such methods can facilitate renewal of regressing vaginal mucosa, prevent or treat vaginal dryness in a mammal, or maintain or enhance the normal protective function of vaginal mucus in a mammal, hi general, the vitamin E, a plant hormone (e.g. jasmonic acid or gibberellic acid) and other compounds are administered intravaginally.
- the vitamin E, a plant hormone e.g. jasmonic acid or gibberellic acid
- Figure 1 illustrates that 1 ⁇ M vitamin E for 24 hours increases mucin-4 expression.
- An ethidium stained 2.0% agarose gel is shown with separated ⁇ - actin (350 bp positive control) and mucin-4 (800 bp) PCR products.
- Lane 1 contains a DNA marker.
- Lanes 2-5 contain PCR products using cervical cDNA, placenta cDNA, ME-180 cDNA (no treatment), and ME-180 cDNA (1 ⁇ M vitamin E), respectively, as templates.
- Figure 2A-2C illustrates the effects of three concentrations of trans- retinoic acid (circles), 9-cz-f-retinoic acid (square symbols), and 13-cw-retinoic acid (diamonds) on ME-180 cell growth over a period of two days.
- Figure 2A graphically illustrates the effects of 10 ⁇ M tra/w-retinoic acid (circles), 9-cw-retinoic acid (squares), and 13-cz.s-retinoic acid (diamonds) on ME-180 cell growth over a period of two days.
- Figure 2B graphically illustrates the effects of 1 ⁇ M tr ⁇ /w-retinoic acid (circles), 9-cis- retinoic acid (squares), and 13-cw-retinoic acid (diamonds) on ME-180 cell growth over a period of two days.
- Figure 2C graphically illustrates the effects of 100 nM trans-re ⁇ noic acid (circles), 9-cw-retinoic acid (squares), and 13-cis- retinoic acid (diamonds) on ME-180 cell growth over a period of two days. The number of ME-180 cells is provided on the y-axes.
- Figure 3 provides a copy of photograph of an ethidium bromide-stained
- Lanes 1 and 12 are DNA size markers.
- the P2Y 2 product can barely be seen in lanes 2, 3, and 7 where the template cDNA was from cervical cells (lane 2), ME-180 cells without vitamin A (lane 3), and ME-180 cells without vitamin A or serum (lane 7), respectively.
- the addition of 100 nM vitamin A to ME-180 cells caused an increase in P2Y 2 expression in the presence of serum (lanes 4-6) and in the absence of serum (lanes 8-11).
- Figure 4 provides a copy of a photograph of an ethidium bromide-stained 2% agarose gel of PCR products using cDNA derived from ME-180 cervical epithelial cells as template.
- Lane 1 provides DNA size markers.
- Two sets of primers were used to generate the PCR products in lanes 2-10: ER- ⁇ -specific primers (upper band) and ⁇ -actin-specific primers (lower band), hi Lane 2 the template was cDNA from ME- 180 cells cultured in the presence of serum, hi Lanes 3 and 7, the template was cDNA from ME- 180 cells cultured in the absence of serum.
- the templates were cDNAs from ME-180 cells cultured without serum and treated with 100 nM vitamin A for 4, 8 and 16 hours, respectively. Addition of 100 nM vitamin A to ME-180 cells caused an increase in ER- ⁇ expression.
- Figure 5 provides a copy of a photograph of an ethidium bromide-stained 2% agarose gel of PCR products using RNA from various cell types as template. Lanes 1 and 7 provide DNA size markers. Two sets of primers were used to generate the PCR products in lanes 2 - 6: vascular endothelial growth factor
- Lanes 2 and 6 provide the PCR products from cDNA derived from untreated ME-180 cells. Lanes 3-5 provide the PCR products from cDNA derived from ME-180 cells treated with 100 nM vitamin A for 4, 8, and 16 hours, respectively.
- Figure 6 provides a copy of a photograph of an ethidium bromide-stained 2% agarose gel of PCR products using RNA from various cell types as template. Lane 1 of the gel depicted in Figure 6 contains DNA size markers, in particular a lOObp ladder of size markers (the brightest band is 600bp).
- Lane 2 contains the products of a RT-PCR reaction using template cDNA derived from cervical RNA and mucin-4 primers (800bp product) with ⁇ -actin primers (300 bp product).
- Lane 3 contains the products of a similar PCR reaction using template cDNA from ME-180 cells.
- Lane 4 contains the products of a similar PCR reaction using template cDNA from ME- 180 cells treated with 100 nM vitamin A for 24 hours.
- Figure 7 graphically illustrates the effect of jasmonic acid and gibberellic acid on cell renewal time in healthy human volunteers, as compared to human volunteers that received no jasmonic acid or gibberellic acid (control). As shown, cell renewal was slower in volunteers that received no jasmonic acid and no gibberellic acid. Jasmonic acid increased the time required for cell renewal in human skin by about 28%, whereas gibberellic acid increased the cell renewal time by about 20%.
- Figure 8 graphically illustrates the effect of jasmonic acid on cell growth over time as measured by hemocytometer counting. Control cells (open circles) receiving no jasmonic acid had the least cell growth.
- Figure 9 graphically illustrates the effect of jasmonic acid on cell growth over time as measured by direct cell counting.
- Control cells open circles
- plant hormones such as jasmonic acid can increase cell growth in epidermal cells and may be useful in treating vaginal atrophy.
- the invention provides compositions and methods for increasing the secretion of mucus, and stimulating cell growth and renewal of epidermal layers within the reproductive system of a female mammal.
- the compositions of the invention include vitamin E and/or a plant hormone such as jasmonic acid or gibberellic acid. Administration of such compositions can increase mucus production, stimulate cell growth and promote the renewal of vaginal and cervical cells in the female reproductive system.
- the compositions of the invention can facilitate replacement of older cells with new cells, thereby rejuvenating the lining of the female reproductive tract.
- This invention utilizes inexpensive, readily available active compounds that effectively enhance the natural ability of vaginal and cervical tissues to renew themselves and to produce moisture.
- the methods and compositions of the invention therefore avoid strong chemicals and unnatural substances whose effects on the health and reproduction of the user are unknown.
- the methods of the invention may improve the quantity and quality of the secretions of the reproductive organs, repair and replace aging tissues and influence expression of genes within reproductive, epithelial and mucosal cells.
- Genes whose expression may be influenced by the methods of the invention include mucin genes.
- Mucins refer to a family of glycoproteins of high molecular weight, secreted or expressed by goblet and nongoblet epithelial cells of mucosal tissues. Mucins can form mucus, a highly hydrated gel of particular structure and function. Mucins from diverse species have similar structural features, particularly with regard to the mucin protein backbone. Nine distinct mucin genes have been identified (MUCl, 2, 3, 4, MUC5AC, MUC5B, MUC6, 7 and 8). Mucins are glycoproteins containing from fifty to eighty percent carbohydrate.
- oligosaccharide side chains or bristles
- oligosaccharide side chains can be highly variable in their make-up, indicating that the more basic functions of the molecule derive from the protein core.
- These molecules can be crosslinked through disulfide bridges to form very high molecular weight gels.
- Different tissues may produce different types of mucins.
- vitamin E can increase the expression of mucins and thereby provide increased secretion and formation of mucus within the reproductive tracts of female mammals.
- Influences on mucus secretion include, but not limited to, the quantity and type of mucin (e.g. sulfo and/or sialomucin), changes in viscosity, hydrogen ion retardation, hydrophobicity, changes in phospholipid content, glycosylation and sulfation, macromolecular assembly, surface tension, adhesivity, transport properties, elastic modulus, tensile properties, rigidity factors, recoil factors, spinnhus, sperm penetration qualities, consistency, cellularity, ferning, and the like.
- mucin e.g. sulfo and/or sialomucin
- the methods of the invention can change the constitutive and stimulated secretions of the local reproductive system, including those of the vagina, cervix, uterus, fallopian tube, Bartholin or vestibular glands and urethral secretions.
- the methods and compositions of the invention can influence the function of the mucus genes found in the reproductive system, including, but not limited to genes that control mucus production in the cervix, uterus, and Bartholin's glands and other parts of the reproductive system with mucus secreting cells.
- the squamous epithelium of the lower genital tract (vagina; for example) and epithelial cells of the cervix can be treated by the methods of the invention. Included are methods to influence or change the secretary effects of the mucus genes, mucus secreting cells and cells that influence the properties of secretory and cell surface mucins of all the above mentioned glands of the reproductive system.
- Mucus can be defined by its chemical, physical and biological properties.
- Rheological or flow properties of mucus include viscosity, rate of flow, shear index, spinnhus or stretch of mucus due to increased visco elasticity and ferning (crystallization) parameters.
- Changing or stimulating the hydration, viscosity, quantity or other properties of vaginal secretions can influence a variety of conditions and disorders, including, but not limited to contraception, infertility, menopause, dyspareunia, infections, and others related and unrelated conditions. Description of the function and anatomy of these organs can be found in Novak's Gynecology, 12.sup.th edition, eds. Berek, Adashi and Hillard, Williams and Wilkins, Baltimore, Md., 1996.
- the methods and compositions of the invention can also increase the growth of cells lining the female reproductive tract, for example, vaginal and cervical cells.
- Such increased cell growth may occur very quickly, or after only a few days of treatment. For example, after only two or three days of treatment the number of newly formed cells can be almost twice or almost three times or four times or five times that of untreated individuals. As treatment progresses the number of newly formed cells can increase further. For example, treated individuals may have about 2 to about 20 times the number of young, newly formed cells compared to untreated individuals. Other individuals may have about 2 to about 10 times the number of young, newly formed cells as untreated individuals.
- Such increased cell growth can repair and replace aging cells and tissue, rejuvenate the lining of the female reproductive tract and provide greater resilience and improved health to tissues involved in reproduction.
- the invention therefore has at least two general utilities.
- the invention may increase the amount of mucus and/or the water content of secretions of the reproductive organs to improve the health and to increase lubrication of the female reproductive system.
- the invention may be used to rejuvenate aging tissues and enhance the health and resiliency of those tissues, for example, by stimulating cellular growth, gene expression and mucus secretion.
- the tocopherol group (Compounds Ia-d) has a saturated side chain, while the tocotrienol group (Compounds Ila-d) has an unsaturated side chain.
- the tocopherol group comprises compounds of formula I:
- the compound ⁇ -tocopherol (Ia) is a compound of formula I, wherein R 1 , R 2 and R 3 are all methyl.
- the compound /3-tocopherol (Ib) is a compound of formula I, wherein Ri and R 3 are methyl and R 2 is hydrogen.
- the compound ⁇ - tocopherol (Ic) is a compound of formula I, wherein Ri is hydrogen, while R 2 and R 3 are methyl.
- the compound ⁇ -tocopherol (Id) is a compound of formula I, wherein Ri and R 2 are hydrogen, while R 3 is methyl.
- the tocotrienol group comprises compounds of formula II:
- Ri, R 2 and R 3 are all separately hydrogen (H), methyl (CH 3 ) or hydroxyl (OH).
- the compound ⁇ -tocotrienol (Ha) is a compound of formula II, wherein Ri, R 2 and R 3 are all methyl.
- the compound /3-tocotrienol (lib) is a compound of formula II, wherein Ri and R 3 are methyl and R 2 is hydrogen.
- the compound ⁇ -tocotrienol (lie) is a compound of formula II, wherein R 1 is hydrogen, while R 2 and R 3 are methyl.
- the compound ⁇ -tocotrienol (Hd) is a compound of formula II, wherein Ri and R 2 are hydrogen, while R 3 is methyl.
- vitamin E is understood to include all of the above mentioned tocopherols and tocotrienols with vitamin E activity.
- vitamin E compounds can be used in an amount of about 0.0001% to about 50%, or from about 0.001% to about 20%, or from about 0.001% to about 10%, or from about 0.01% to about 5%, or from about 0.05% to about 2% of the composition.
- in situ concentrations of an active gibberellic acid ranging from about 10 "5 M to about 10 "7 M are effective for increasing epithelial cell proliferation and mucin-4 expression.
- Gibberellic acid comprises a class of compounds that is also referred to as gibberellins.
- Gibberellins are plant hormones that affect a wide variety of processes throughout the life cycle of plants, including seed germination, stem elongation, flower induction, anther development, and seed and pericarp growth.
- Gibberellins are tetracyclic diterpenoid acids that can isolated from fungi and higher plants and that have the ent-gibberellane ring system shown in the following structure (III).
- Gibberellins were first isolated by Japanese researchers in the 1930s from cultures of the fungus Gibberella fujikuroi (Fusarium moniliforme). Gibberellins are secondary metabolites that have since been shown to be present in other fungal species, in some ferns, and in many gymnosperms and angiosperms. Of the 121 known gibberellins, 96 have been identified only in higher plants, 12 are present only in Gibberella, and 12 are present in both. As observed in Gibberella, many different gibberellins can be present in individual angiosperms.
- gibberellins Two main types exist: the C 20 -gibberellins, which have 20 carbon atoms (structure IV, below), and the C 19 -gibberellins, in which the twentieth carbon atom has been lost due to metabolism (structure V, below).
- the ent-gibberellane ring system can contain many structural modifications, accounting for the large number of known gibberellins.
- Naturally occurring gibberellins with identified structures are allocated an "A number" (MacMillan et al. (1968) Nature 217: 170-171).
- 126 naturally occurring gibberellins of plant and fungal origin are known.
- Current structural information on gibberellins can be found at the website plant- hormones.bbsrc.ac.uk/gibberellm_information2.htm.
- Variations in gibberellin structure arise in several ways.
- Carbon-20 can exist in different oxidative states, for example, methyl (--CH 3 ), hydroxymethyl (- -CH 2 OH), aldehyde (--CHO), or carboxylic acid (--COOH).
- Substituent groups positioned above the ring plane are said to be in the /3-configuration; their bonding to the ring is designated by a solid, elongated triangle.
- Substituent groups positioned below the ring plane are said to be in the ⁇ -configuration; their bonding to the ring is designated by a dashed, elongated triangle.
- the attachment of substituent groups in the plane of the ring system is indicated by a straight line.
- Gibberellins can exist as conjugates, for example, with a hexose or pentose molecule such as glucose.
- An ether or an ester linkage may link such a glucose molecule to the gibberellin.
- Such conjugation may temporarily or permanently inactivate the activity of a gibberellin within a plant.
- gibberellins The biological activity of different gibberellins varies, and various gibberellins within a plant can be precursors, biosynthetic intermediates, or deactivation products of active gibberellins.
- Three structural features are commonly associated with gibberellin biological activity: a 3-hydroxyl group, a 7-carboxyl group, and a lactone ring.
- a compound possessing the ent-gibberellane ring system but lacking one or more of these structural features can be considered a gibberellin precursor, an intermediate, or a derivative.
- compositions and methods of the invention generally employ active forms of gibberellic acids, gibberellic acid precursors, gibberellic acid intermediates or gibberellic acid derivatives, for example, those having structures related to formulae IV and V as described above.
- the gibberellins employed can also have double bonds within the ring structure at different positions.
- the gibberellic acids can have any of formulae VI, Via, or VIb.
- Gibberellin having formula VI is often referred to as Gibberellin A 3 .
- Gibberellin having formula Via is often referred to as Gibberellin A 4 .
- Gibberellin having formula VIb is often referred to as Gibberellin A 7 .
- gibberellic acids or their derivatives can be used in an amount of about 0.001% to about 50%, or from about 0.01% to about 20%, or from about 0.01% to about 10%, or from about 0.05% to about 5%, or from about 0.05% to about 2% of the composition.
- in situ concentrations of an active gibberellic acid ranging from about 10 "4 M to about 10 "6 M are effective for increasing epidermal cell proliferation.
- Compositions having about 0.5 % gibberellic acid are shown herein to promote skin turnover.
- Jasmonic acid compounds employed in the invention include jasmonic acid and jasmonic acid derivatives available to one of skill in the art. Such compounds include jasmonic acid, methyl jasmonate and their isomers. In the present invention jasmonic acid and jasmonic acid derivatives used also include synthetic and natural stereoisomers of jasmonic acid, dihydrojasmonic acid, hydroxy jasmonic acid and dihydro-hydroxy jasmonic acid. Further examples of jasmonic acid derivatives that may be used in the invention include compounds having any one of formulae VII, VIII, IX or X. wherein:
- R 4 is alkyl
- R 5 is COOR, or -(CH 2 )n-0X, where n is an integer of from 1 to 20;
- R is H, or alkyl
- X is H, or 1 to 6 sugar residues (e.g., hexoses or pentoses).
- the alkyl groups employed in these jasmonic acid compounds have about one to twenty carbon atoms, although in some embodiments lower alkyl groups are used, for example, alkyl groups with about one to eight carbon atoms. Alkyl groups with even lower numbers of carbon atoms can also be used, for example, alkyl groups with one to six, or one to three carbon atoms.
- jasmonic acid is employed in the compositions of the invention.
- Jasmonic acid is a compound of formula VII wherein R 4 is C 2 H 5 and R 5 is COOH.
- Another jasmonic acid compound employed in the invention is a compound of formula VIII.
- R 4 is alkyl
- R 5 is COOR, or -(CH 2 )n-OX, where n is an integer of from 1 to 20;
- R is H, or alkyl
- X is H, or 1 to 6 sugar residues (e.g., hexoses or pentoses).
- dihydrojasmonic acid is employed in the compositions of the invention.
- Dihydrojasmonic acid is a compound of formula VIII wherein R 4 is C 2 H 5 and R 5 is COOH.
- Another jasmonic acid compound employed in the invention is a compound of formula IX
- R 4 is alkyl
- R 5 is COOR, or -(CH 2 )n-0X, where n is an integer of from 1 to 20;
- R is H, or alkyl
- X is H, or 1 to 6 sugar residues (e.g., hexoses or pentoses);
- Y is H, alkyl, or 1 to 6 sugar residues (e.g., hexoses or pentoses).
- hydroxyjasmonic acid is employed in the compositions of the invention.
- Hydroxyjasmonic acid is a compound of formula IX wherein R 4 is C 2 H 5 and R 5 is COOH.
- Another jasmonic acid compound employed in the invention is a compound of formula X.
- R 4 is alkyl
- R 5 is COOR, or -(CH 2 )n-0X, where n is an integer of from 1 to 20; R is H, or alkyl;
- X is H, or 1 to 6 sugar residues (e.g., hexoses or pentoses);
- Y is H, alkyl, or 1 to 6 sugar residues (e.g., hexoses or pentoses).
- dihydro-hydroxyjasmonic acid is employed in the compositions of the invention.
- Dihydro-hydroxyjasmonic acid is a compound of formula X wherein R 4 is C 2 H 5 and R 5 is COOH.
- jasmonic acids or jasmonic acid derivatives can be used in an amount of from about 0.001% to about 50%, or from about 0.01% to about 20%, or from about 0.01% to about 10%, or from about 0.05% to about 5%, or from about 0.05% to about 2% of the composition.
- in situ concentrations of jasmonic acid ranging from about 10 "4 M to about 10 "6 M are effective for increasing cell proliferation in epidermal tissues.
- solutions of about 0.025% jasmonic acid are effective for promoting skin turnover and renewal.
- compositions and methods of the invention include administering to the female mammal an effective amount of retinoid or carotenoid and/or one or more nucleotide(s) or nucleoside(s). These compositions and methods can increase the expression of P2Y 2 receptors or estrogen receptors or vascular endothelial growth factor in vaginal or cervical epithelial cells.
- the compositions of the invention can include one or more retinoids or carotenoids.
- retinoids are a class of compounds consisting of four isoprenoid units joined in a head to tail manner. All retinoids may be formally derived from a monocyclic parent compound containing five carbon-carbon double bonds and a functional group at the terminus of the acyclic portion.
- the basic retinoid structure can be subdivided into three segments, namely the polar terminal end, the conjugated side chain, and the cyclohexenyl ring.
- the basic structures of the most common natural retinoids are called retinol, retinaldehyde, and retinoic acid.
- retinoids of this invention are not limited to just retinol, retinaldehyde, and retinoic acid. Instead, the retinoids and carotenoids of the invention also include compounds falling within Formula XIA or XIB:
- Z is CH, or N
- R is H or alkyl of 1 to 6 carbons; m is an integer having the value of 0-5; n is an integer having the value of 0-2; r is an integer having the value 0-2;
- Q is a phenyl, naphthyl, pyridyl, thienyl, furyl, pyridazinyl, pyrimidinyl, pyrazinyl, thiazolyl, oxazolyl, imidazolyl or pyrrazolyl, wherein the phenyl, naphthyl pyridyl, thienyl, furyl, pyridazinyl, pyrimidinyl, pyrazinyl, thiazolyl, oxazolyl, imidazolyl or pyrrazolyl group can be substituted with one or two R 1 groups;
- W is F, Br, Cl, I, C 1-6 alkyl, fluoro-substituted C 1-6 alkyl, NO 2 , N 3 , OH, OCH 2 OCH 3 , OC 1-10 alkyl, tetrazol, CN, SO 2 C 1-6 -alkyl, SO 2 C 1-6 -fluoro- substituted alkyl, SO-C 1-6 alkyl, CO-Ci -6 alkyl, COOR 8 , phenyl, phenyl itself substituted with a W group other than with phenyl or substituted phenyl, with the proviso that when X is CH and r is 0 then n is not 0 and at least one W group is not alkyl;
- A is (CH 2 ) q where q is 0-5, lower branched chain alkyl having 3-6 carbons, cycloalkyl having 3-6 carbons, alkenyl having 2-6 carbons and 1 or 2 double bonds, alkynyl
- B is COOH or a pharmaceutically acceptable salt thereof, COOR 8 , CONR 9 R 10 , CH 2 OH, CH 2 OR 11 , CH 2 OCOR 11 , CHO, CH(OR 12 ) 2 , CHOR 13 O, COR 7 , CR 7 (OR 12 ) 2 , CR 7 OR 13 O, where R 7 is an alkyl, cycloalkyl or alkenyl group containing 1 to 5 carbons, R 8 is an alkyl group of 1 to 10 carbons or trimethylsilylalkyl where the alkyl group has 1 to 10 carbons, or a cycloalkyl group of 5 to 10 carbons, or R 8 is phenyl or lower alkylphenyl, R 9 and R 10 independently are hydrogen, an alkyl group of 1 to 10 carbons, or a cycloalkyl group of 5-10 carbons, or phenyl or lower alkylphenyl, R 11 is lower alkyl, cycloalkyl, lower alkyl substitute
- the retinoid or carotenoid is a compound defined by Formula XII:
- R 20 , R 21 and R 22 are each independently C 1-6 alkyl, fluoro-substituted C 1-6 alkyl, hydroxy-substituted C 1-6 alkyl, CH 2 OH, CH 2 OR 11 , CH 2 OCOR 11 , CHO,
- alkyl refers to and covers any and all groups that are known as normal alkyl, branched-chain alkyl and cycloalkyl.
- alkenyl refers to and covers normal alkenyl, branch chain alkenyl and cycloalkenyl groups having one or more sites of unsaturation.
- alkynyl refers to and covers normal alkynyl, and branch chain alkynyl groups having one or more triple bonds.
- Lower alkyl means alkyl groups having 1 to 6 carbons, and 3 to 6 carbons for lower branch chained and cycloalkyl groups.
- Lower alkenyl is defined similarly having 2 to 6 carbons for normal lower alkenyl groups, and 3 to 6 carbons for branch chained and cyclo-lower alkenyl groups.
- Lower alkynyl is also defined similarly, having 2 to 6 carbons for normal lower alkynyl groups, and 4 to 6 carbons for branch chained lower alkynyl groups.
- a pharmaceutically acceptable salt may be prepared for any compounds in this invention having a functionality capable of forming such a salt, for example, an acid or amine functionality.
- a pharmaceutically acceptable salt is any salt that retains the activity of the parent compound and does not impart any deleterious or untoward effect on the subject to which it is administered and in the context in which it is administered.
- Pharmaceutically acceptable salts may be derived from organic or inorganic bases. The salt may be a mono or polyvalent ion.
- Organic salts may by be made with amines, particularly ammonium salts such as mono-, di- and trialkyl amines or ethanolamines. Salts may also be formed with caffeine, tromethamine and similar molecules. Where there is a nitrogen sufficiently basic as to be capable of forming acid addition salts, such may be formed with any inorganic or organic acids or alkylating agent such as methyl iodide. Preferred salts are those formed with inorganic acids such as hydrochloric acid, sulfuric acid or phosphoric acid. Any of a number of simple organic acids such as mono-, di- or tri-acid may also be used.
- compositions of the invention can include one or more nucleosides or nucleotides.
- nucleotide or nucleosides can include, for example, dATP, dGTP, dCTP, dTTP, dUTP, ATP, GTP, CTP, TTP, UTP, and any derivative of such nucleotide(s) or nucleoside(s) that is available to one of skill in the art.
- the nucleotide or nucleoside is a compound defined by Formula XIII:
- X 1 , X 2 and X 3 are each independently either O “ or S " . hi some embodiments, X 2 and X 3 are each O " ;
- R 31 is O, imido, methylene, or dihalomethylene (e.g., dichloromethylene, diflouromethylene). hi some embodiments, R 31 is oxygen or difluoromethylene.
- R 32 is H or Br. hi some embodiments, R 32 is H.
- Examples of compounds of Formula XIII are uridine 5'-triphosphate (UTP) and uridine 5'-O-(3- thiotriphosphate) (UTP ⁇ S).
- the nucleotide or nucleoside is a compound defined by Formula XIV:
- V is uracil or adenine.
- the nucleotide or nucleoside is a compound defined by Formula XV:
- X 1 , X 2 , X 3 and R 31 are as defined above;
- nucleotide or nucleoside is a compound defined by Formula XVI:
- X 1 , X 2 , X 3 and R 31 are as defined above;
- compositions of the invention can contain one or more compounds of Formula XIII, XIV, XV or XVI in an amount effective to stimulate mucous secretions in the vagina or reproductive passages of a female.
- Compounds illustrative of the compounds of Formula XIV include P 1 , P 4 -di(adenosine-5') tetraphosphate or P 1 , P 4 -di(uridine-5') tetraphosphate. These compounds can be made in accordance with known procedures, or variations thereof which will be described by: P. Zamecnik, et al., Proc. Natl. Acad. Sci. USA 89, 838-42 (1981); and K. Ng and L. E. Orgel, Nucleic Acids Res. 15 (8), 3572-80 (1987). P 1 , P 4 -di(uridine-5') tetraphosphate can be prepared by methods similar to that described in C. Vallejo, et al, Biochem. Biophys. Acta 438, 304- 09 (1976). Compounds illustrative of the compounds of Formula XV above include
- the present invention is directed to a variety of methods of treating or preventing vaginal and/or reproductive problems in a female mammal. These methods involve administering to the female mammal an effective amount of vitamin E and/or a plant hormone such as gibberellic acid or jasmonic acid. In general, administration is topical or intravaginal.
- Treatment of, or treating, vaginal and/or reproductive problems in a female mammal is intended to include modulation of mucus levels to enhance or diminish fertility in a female mammal, or to alleviate or dimmish vaginal dryness in a female mammal.
- the treatment therefore can include alleviation or diminishment of more than one vaginal and/or reproductive problem in a female mammal.
- the method increases growth of vaginal or cervical epidermal cells.
- the method involves increasing the expression of mucin genes, for example, mucin- 1, mucin-2, mucin-3A, mucin- 3B, mucin-4, mucin-5B, mucin-5AC, mucin-6, mucin-7, mucin- 11, mucin- 13, mucin-15, mucin- 17, mucin- 19, mucin-20 and similar mucin genes.
- mucin genes for example, mucin- 1, mucin-2, mucin-3A, mucin- 3B, mucin-4, mucin-5B, mucin-5AC, mucin-6, mucin-7, mucin- 11, mucin- 13, mucin-15, mucin- 17, mucin- 19, mucin-20 and similar mucin genes.
- mammal refers to an animal, in general, a warm-blooded animal. Mammals include cattle, buffalo, sheep, goats, pigs, horses, dogs, cats, rats, rabbits, mice, and humans. Also included are other livestock, domesticated animals and captive animals.
- Treatment involves administering an effective amount of vitamin E and/or a plant hormone.
- the vitamin E, gibberellic acid and/or jasmonic acid may be administered as a composition that contains other ingredients, for example, one or more nucleotide(s) or nucleoside(s), other vitamins (e.g., a retinoid or carotenoid such as vitamin A), aloe vera and the like.
- compositions containing vitamin E, gibberellic acid or jasmonic acid with or without other com ⁇ ound(s) are administered intravaginally.
- compositions of the invention are administered to improve the health of the female reproductive system, to stimulate secretion of lubricating fluids (mucus), promote cell growth, treat regression of vaginal mucosa and rejuvenate the female reproductive system.
- the composition may be administered as single or divided dosages, for example, of at least about 0.001 ⁇ g/kg to about 100 to 200 mg/kg, of about 0.01 ⁇ g/kg to about 30 to 50 mg/kg, about 0.1 ⁇ g/kg to about 10 to 20 mg/kg or about 1.0 ⁇ g/kg to about 1.0 to about 10 mg/kg of body weight of one or more retinoid or carotenoid or nucleotide or nucleoside, although other dosages may provide beneficial results.
- the amount administered will vary depending on various factors including, but not limited to, the disease, the weight, the physical condition, the health, the age of the mammal, and whether prevention of reproduction or treatment of vaginal dryness is to be achieved.
- Administration of the therapeutic agents in accordance with the present invention may be in a single dose, in multiple doses, in a continuous or intermittent manner, depending, for example, upon the recipient's physiological condition, whether the purpose of the administration is therapeutic or prophylactic, and other factors known to skilled practitioners.
- the administration of the compositions of the invention may be essentially continuous over a pre-selected period of time or may be in a series of spaced doses. Local administration is generally contemplated.
- compositions are prepared by combining the active ingredients in the appropriate concentrations.
- Other active or inactive agents selected by one of skill in the art can optionally be added.
- the absolute weight of a given active agent included in a unit dose can vary widely. For example, about 0.001 ⁇ g to about 50 mg, or about 0.01 ⁇ g to about 10 mg, or about 0.1 ⁇ g to about 1 mg, of at least one vitamin E, gibberellic acid or jasmonic acid, or of a plurality of vitamin E compounds or gibberellic acid compounds or jasmonic acid compounds can be administered.
- the unit dosage can vary from about 0.001 ⁇ g to about 1000 ⁇ g, from about 0.01 ⁇ g to about 750 ⁇ g, from about 0.1 ⁇ g to about 1 mg, from about 1.0 ⁇ g to about 750 ⁇ g, from about 2.5 ⁇ g to about 600 ⁇ g, from about 5.0 ⁇ g to about 500 ⁇ g, or from about 7.5 ⁇ g to about 400 ⁇ g.
- Daily doses of the compositions of the invention can vary as well. Such daily doses can range, for example, from about 0.001 mg/day to about 50 mg/day, from about 0.01 mg/day to about 25 mg/day, from about 0.1 mg/day to about 12 mg/day, from about 0.1 mg/day to about 8 mg/day, from about 0.1 mg/day to about 4 mg/day, and from about 0.1 mg/day to about 2 mg/day of one or more vitamin E, gibberellic acid or jasmonic acid compounds.
- the concentration of vitamin E, gibberellic acid or jasmonic acid within a composition can also vary.
- the concentration can vary from about 0.1 ⁇ M to about 1000 ⁇ M, or from about 0.5 ⁇ M to about 500 ⁇ M, or from about 1 ⁇ M to about 300 ⁇ M, or from about 5 ⁇ M to about 200 ⁇ M, or from about 10 ⁇ M to about 100 ⁇ M.
- one or more suitable unit dosage forms comprising the therapeutic compositions of the invention can be administered by a variety of routes including oral, parenteral (including subcutaneous, intravenous, intramuscular and intraperitoneal), rectal, dermal, transdermal, intrathoracic, intrapulmonary intravaginal and intranasal (respiratory) routes.
- the therapeutic compositions may also be formulated for sustained release (for example, using microencapsulation, see WO 94/ 07529, and U.S. Patent No.4,962,091).
- the formulations may, where appropriate, be conveniently presented in discrete unit dosage forms and may be prepared by any of the methods well known to the pharmaceutical arts.
- Such methods may include the step of mixing the therapeutic agent with liquid carriers, solid matrices, semi-solid carriers, finely divided solid carriers or combinations thereof, and then, if necessary, introducing or shaping the product into the desired delivery system.
- the therapeutic compositions of the invention are prepared for intravaginal administration, they are generally combined with a pharmaceutically acceptable carrier, diluent or excipient to form a pharmaceutical formulation, or unit dosage form.
- the compositions may be present as a solution, a suspension, an emulsion, a powder, a granular formulation, or in a natural or synthetic polymer or resin.
- the active compositions may also be presented as a bolus or paste.
- Intra vaginally administered therapeutic compositions of the invention can also be formulated for sustained release, e.g., the compositions can be coated, micro-encapsulated, or otherwise placed within a sustained delivery device.
- the total active ingredients in such formulations comprise from 0.1 to 99.9% by weight of the formulation.
- pharmaceutically acceptable it is meant a carrier, diluent, excipient, and/or salt that is compatible with the other ingredients of the formulation, and not deleterious to the recipient thereof.
- compositions containing the therapeutic compositions of the invention can be prepared by procedures known in the art using well-known and readily available ingredients.
- the composition can be formulated with common excipients, diluents, or carriers, and formed into tablets, capsules, solutions, suspensions, powders, aerosols and the like.
- excipients, diluents, and carriers that are suitable for such formulations include buffers, as well as fillers and extenders such as starch, cellulose, sugars, mannitol, and silicic derivatives.
- Binding agents can also be included such as carboxymethyl cellulose, hydroxymethylcellulose, hydroxypropyl methylcellulose and other cellulose derivatives, alginates, gelatin, and polyvinyl-pyrrolidone.
- Moisturizing agents can be included such as glycerol, disintegrating agents such as calcium carbonate and sodium bicarbonate.
- Agents for retarding dissolution can also be included such as paraffin.
- Resorption accelerators such as quaternary ammonium compounds can also be included.
- Surface active agents such as cetyl alcohol and glycerol monostearate can be included.
- Adsorptive carriers such as kaolin and bentonite can be added.
- compositions of the invention can also contain thickening agents such as cellulose and/or cellulose derivatives. They may also contain gums such as xanthan, guar or carbo gum or gum arabic, or alternatively polyethylene glycols, bentones and montmorillonites, and the like.
- the compositions of the invention can also contain other vitamins such as vitamin A, vitamin B, vitamin C or vitamin D. In one embodiment, the compositions of the invention can also contain aloe vera.
- the therapeutic compositions of the invention can also be formulated as emulsions, suspensions, aqueous or anhydrous solutions or dispersions, or alternatively the form of an emulsion or suspension or salve for convenient intravaginal administration.
- the active compositions and other ingredients may form suspensions, solutions, or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents.
- the active compositions and other ingredients may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilization from solution, for constitution with a suitable vehicle, e.g., sterile, pyrogen-free water, before use.
- formulations can contain pharmaceutically acceptable carriers, vehicles and adjuvants that are well known in the art. It is possible, for example, to prepare solutions using one or more organic solvent(s) that is/are acceptable from the physiological standpoint, chosen, in addition to water, from solvents such as acetone, ethanol, isopropyl alcohol, glycol ethers such as the products sold under the name "Dowanol,” polyglycols and polyethylene glycols, C1-C4 alkyl esters of short-chain acids, ethyl or isopropyl lactate, fatty acid triglycerides such as the products marketed under the name "Miglyol,” isopropyl myristate, animal, mineral and vegetable oils and polysiloxanes.
- organic solvent(s) that is/are acceptable from the physiological standpoint, chosen, in addition to water, from solvents such as acetone, ethanol, isopropyl alcohol, glycol ethers such as the products sold under the name "Dowanol,” polygly
- an adjuvant chosen from antioxidants, surfactants, other preservatives, film-forming, keratolytic or comedolytic agents, perfumes, flavorings and colorings.
- Antioxidants such as t-butylhydroquinone, butylated hydroxyanisole, butylated hydroxytoluene and ⁇ -tocopherol and its derivatives can be added.
- the compositions are well suited to formulation as sustained release dosage forms and the like. The formulations can be so constituted that they release the active composition within the female reproductive system over a period of time.
- Coatings, envelopes, and protective matrices may be made, for example, from polymeric substances, such as polylactide-glycolates, liposomes, microemulsions, microparticles, nanoparticles, or waxes.
- the therapeutic agents may be formulated as is known in the art for direct application to the vaginal area.
- Forms chiefly conditioned for vaginal application take the form, for example, of creams, milks, gels, dispersion or microemulsions, lotions thickened to a greater or lesser extent, impregnated pads, ointments, aerosol formulations (e.g., sprays or foams), creams, lotions, pastes, jellies, sprays, and aerosols.
- the composition can be formulated to be part of an adhesive polymer, such as polyacrylate or acrylate/vinyl acetate copolymer.
- Ointments and creams may, for example, be formulated with an aqueous or oily base with the addition of suitable thickening and/or gelling agents.
- Lotions may be formulated with an aqueous or oily base and will in general also contain one or more emulsifying agents, stabilizing agents, dispersing agents, suspending agents, thickening agents, or coloring agents.
- Liquid sprays are conveniently delivered from pressurized packs, for example, via a specially shaped closure.
- the active compositions can also be delivered via iontophoresis, e.g., as disclosed in U.S. Patent Nos. 4,140,122; 4,383,529; or 4,051,842.
- the percent by weight of a therapeutic agent of the invention present in a vaginal formulation will depend on various factors, but generally will be from 0.01% to 95% of the total weight of the formulation, and typically 0.1-85% by weight.
- the pharmaceutical formulations of the present invention may include, as optional ingredients, pharmaceutically acceptable carriers, diluents, solubilizing or emulsifying agents, and salts of the type that are available in the art.
- pharmaceutically acceptable carriers such as physiologically buffered saline solutions and water.
- physiologically acceptable buffered saline solutions such as phosphate buffered saline solutions with apH of about 4.5 to about 5.5.
- the active ingredients may also be used in combination with other therapeutic agents, for example, anti-microbial agents, pain relievers, anti-inflammatory agents, vitamins (e.g., vitamin A, B, C or D), aloe vera and the like, whether for the conditions described or some other condition.
- other therapeutic agents for example, anti-microbial agents, pain relievers, anti-inflammatory agents, vitamins (e.g., vitamin A, B, C or D), aloe vera and the like, whether for the conditions described or some other condition.
- the present invention further pertains to a packaged pharmaceutical composition for controlling reproduction and/or vaginal dryness such as a kit or other container.
- the kit or container holds a therapeutically effective amount of a pharmaceutical composition for controlling reproduction and/or vaginal dryness and instructions for using the pharmaceutical composition for control of reproduction and/or vaginal dryness.
- the pharmaceutical composition includes a composition of the present invention, in a therapeutically effective amount such that vaginal dryness is controlled.
- the invention provides a vaginal insert that can release the vitamin E, gibberellic acid or jasmonic acid in a controlled fashion.
- Such a vaginal insert can be biodegradable or non-biodegradable.
- the vaginal insert provides sustained release of the active ingredients at an appropriate rate for achieving the desired level of mucus secretion, gene expression and cellular proliferation.
- the active ingredients can be formulated with oleaginous bases or ointments to form the vaginal insert.
- This class of formulations comprises the active ingredients and hydrocarbon-based semisolids containing dissolved and/or suspended bacteriostats/preservatives and a buffer system.
- the petrolatum component in these bases can be any paraffin ranging in viscosity from mineral oil employing incorporated isobutylene, colloidal silica, or stearate salts to paraffin waxes. White and yellow petrolatum are examples of such systems.
- Bases of this class can be made by incorporating high-melting waxes into a fluid mineral oil via fusion or by incorporation of polyethylene into mineral oil at elevated temperature.
- Polysiloxanes are suitable for use in these bases and typically have a viscosity in the range of about 0.5 to l ⁇ .sup.6 centistokes.
- the organic entities attached to the polysiloxane are preferably lower molecular weight hydrocarbon moieties having from 1 to 8 carbons each, such as lower alkyl, lower alkenyl, phenyl and alkyl substituted phenyl, and phenyl(lower)alkyl, such as benzyl.
- each lower alkyl or alkenyl group preferably has 1 to 3 carbons inclusive, such as in a dimethylsiloxane polymer.
- Absorption bases can be used with such an oleaginous system.
- additional ingredients with the capacity to emulsify a significant quantity of water are employed.
- Water-in-oil (w/o) emulsions can be formed wherein the external phase is oleaginous in character.
- Preservatives/bacteriostats, such as the parabens, buffer systems, etc. can be incorporated into these bases as emulsified aqueous solutions together with the active ingredient.
- emulsifiers include, but are not limited to, cholesterol, lanolin (which contains cholesterol and cholesterol esters and other emulsifiers), lanolin derivatives, beeswax, fatty alcohols, wool wax alcohols, low HLB (hydrophobe/lipophobe balance) emulsifiers, and assorted ionic and nonionic surfactants, singularly or in combination.
- Water-In-Oil (W/O) emulsion bases can be employed in the vaginal inserts of the invention. These formulations can be an expansion of the general class of absorption bases that includes liquids or creams. They can be prepared by taking a mixture of the active ingredients with oil phase ingredients, bacteriostats/preservatives and buffer salts which are dissolved or suspended therein and to which water has been added to form a water-in-oil emulsion.
- Oil-In- Water (O/W) emulsion bases can also be utilized in the vaginal inserts of the invention. These systems are semisolid emulsions, microemulsions, or foam emulsion systems containing metronidazole. Usually such a system has a "creamy white" appearance.
- the internal oil phase is in the range in percentage composition of about 10% to about 40% oil by weight and the external phase may contain 80% or more water.
- the oleaginous phase may contain, but is not limited to, long-chain alcohols (cetyl, stearyl), long-chain esters (myristates, palmitates, stearates), long-chain acids (palmitic, stearic), vegetable and animal oils and assorted waxes.
- Vaginal inserts and suppositories containing the active ingredients can be, for example, oleaginous in nature that melt at body temperature, or polyethylene glycol-based compositions that dissolve in the vaginal fluids. Additional bases for suppositories are glycerin and glycerinated gelatin.
- the active ingredients can also be formulated into vaginal inserts using buffered gels made with gelling agents. Some examples of these gelling agents are: cellulosics, cationic polymers, polyoxyalkylenes, and carboxyvinyl polymers.
- Cellulosics useful in the formulations of the invention include, for example, methyl cellulose, carboxymethyl cellulose, hydroxyethyl cellulose, and hydroxypropyl cellulose.
- Cationic Polymers useful in the formulations of the invention include "Polyquaternium-10", a polymeric quaternary ammonium salt of hydroxyethyl cellulose reacted with a trimethyl ammonium-substituted epoxide, and the like.
- Polyoxyalkylenes useful in the invention include olyoxyethylene-polyoxypropylene esters of lanolin and derivatives thereof.
- Carboxyvinyl polymers useful for the formulations of the invention include cross-linked acrylic acid polymers, e.g., those commercially available from B. F. Goodrich Co., Akron, Ohio, under the designation CARBOPOLTM.
- the vaginal insert can comprise a mixture or coating of polymers that provide release of the active agents at a constant rate over a prolonged period of time, hi some embodiments, the vaginal insert comprises water-soluble pore forming agents, such as polyethylene glycol (PEG) that can be mixed with water insoluble polymers to increase the durability of the insert and to prolong the release of the active ingredients.
- PEG polyethylene glycol
- Such a water-soluble pore forming agent can be polyethylene glycol, polypropylene glycol, a mixture or polymer of sugars (lactose, sucrose, dextrose, etc.), salts, poloxamers, polyvinyl alcohol and other water soluble food grade and other excipients.
- the molecular weight of PEG is in the range from about 200 to about 20,000, alternatively, from about 400 to about 8,000.
- PEG having a molecular weight of about 540 to about 8,000 is used.
- the PEG has a molecular weight of about or above 1,000 to about 8,000.
- the molecular weight of PEG used for the coating with the formulation of the invention will depend on the ability of PEG to form a coating film that is non-sticky, having enough strength and creating adequate pore size for controlling the release of active ingredients over the desired time period both in vitro and in vivo.
- the pore-forming agent is used in the formulation of the invention in the amount effective to regulate the release of a biologically active compound at a desired rate.
- the effective amount of the pore-forming agent provides long term delivery of the active agent thus increasing the useful life of a sustained-release drug implant.
- the effective amount of the pore forming agent will depend on the desired rate and duration of the release and the ability to form a continuous microporous film during the coating process.
- PEG with higher molecular weights is used.
- PEG 8000 can provide release over a period of time that is longer than 100 days, when used in a concentration from 10 to 50%, preferably from 20 to 45% and most preferably from 30 to 45%.
- the concentration of PEG is expressed herein in % weight per dry basis and represents the concentration of PEG in the coating film after drying.
- the thickness of the coating film is from 5 to 50 ⁇ m, preferably 30 from 10 to 30 ⁇ m and most preferably from 15 to 25 ⁇ m.
- the PEG concentration ranges can be adjusted as needed. For example, in vivo duration of a coated insert may be predicted simply from the in vitro dissolution rate of the active agent at the 120-hour time point.
- the vaginal insert of the invention may also comprise a water insoluble polymer.
- a water insoluble polymer examples include ethylcellulose, acrylic resins, co- polymer of methacrylic acid and acylic acid ethyl ester, polylactic acid, PLGA, polyurethane, polyethylene vinyl acetate copolymer, polystyrene-butadiene copolymer and silicone rubber, or mixtures thereof.
- polymers sold under trade names Aquacoat ECD 30 and Eudragit RS 30 and NE 30D registered trademarks of Rliom Tech, Inc.
- a polymer suitable for use in this invention is a polymer that is capable of forming a continuous coating film during the process of spraying and drying with a pore-forming agent.
- the rate controlling film prepared with such a polymer is very stable during implantation.
- the film should have enough strength to withstand tear and inner osmotic pressure, and have the stability not to swell or hydrate during the implantation life.
- the coating formulation of the invention is used to coat pellets comprising the active ingredients that are compressed to form a solid, biodegradable insert and then administered for stimulating mucus secretion, gene expression and/or cellular proliferation.
- ME- 180 Human cervical epithelial cells (ME- 180, ATCC) were propagated in culture at 37°C using 5% CO 2 in McCoy's 5A media (Invitrogen) with 10% heat-inactivated fetal bovine serum (Invitrogen). Vitamin E was purchased from ICN Biomedicals. Vitamin E stock solutions were made up in absolute ethanol. RNA Extraction from ME-180 cells. ME-180 cells were plated at 2 x 10 5 cells per T75 flask (15 mL total volume) and were allowed to propagate for four days. On day four, the media was removed. Fifteen mL of McCoy's 5 A media with or without 10% FBS containing 0 or 1 ⁇ M vitamin E were added to ME- 180 cells in duplicate.
- ME- 180 cells were incubated with these solutions for 24 hours. The media was removed, and 1500 ⁇ L of lysis buffer was added to the flasks. The cells were scraped off of the flask with a cell scraper.
- the RNA was isolated using the Ambion RN Aqueous kit according to the manufacturer's instructions. Precipitated RNA was resuspended in DEPC-treated water with 1 ⁇ L of RNase inhibitor.
- RNA Reverse Transcription of RNA.
- RNA was incubated with 3 ⁇ L of primer at 80 °C for 10 minutes then immediately placed on ice.
- Ten ⁇ L of master mix was added to the RNA/primer solution and placed at 42 0 C for 2 hours.
- the resulting cDNA was incubated with 3.5 ⁇ L of NaOH solution at 70 0 C for 10 minutes to hydrolyze the remaining RNA.
- Five ⁇ L of 0.5M Tris/EDTA was added to neutralize the solution.
- cDNA was resuspended in 10-12 ⁇ L of PCR grade water.
- PCR Polymerase Chain Reaction
- a master mix using the Advantage 2 PCR kit (Ambion) was made for the PCR reactions containing 37-38 ⁇ L of PCR grade water, 5 ⁇ L of 10x PCR buffer, 1 ⁇ L of dNTPs, 1 ⁇ L of /3-actin primers (10 ⁇ M, optional control), and 2 ⁇ L of test primers (10 ⁇ M, P2Y 2 , or Mucin-4 (MUC-4)).
- Two microliters of cDNA and 1 mL of DNA polymerase were added. Cycling conditions were as follows: 5 min at 95 0 C; 25-30 cycles (30 sec at 95 °C, 1 min at 65 0 C, 3 min at 68 0 C); 5 min at 68 0 C.
- the PCR primers employed were as follows:
- P2Y 2 -specific primers yielding a PCR product of 650 bp: coding strand: 5'-TGTCTTCGCCCTCTGCTTCC-S' (SEQ ID NQ: 1) noncoding strand: 5'-GTCAGGCCAGGGGTGTCATT-S' (SEQ ID NO:2)
- jS-actin-specific primers (PCR product 300 bp): coding strand: 5'-AGTCGGTTGGAGCGAGCATC-S' (SEQ ID NO: 0
- noncoding strand 5'-GGGCACGAAGGCTCATCATT-S' (SEQ ID NO:4)
- Mucin-4 (MUC-4) specific primers (PCR product 800 bp) : coding strand: 5 ' -AGCCC AGGACTGTGGTCTGC-3 ' (SEQ ID NO: 0
- ME- 180 cells were incubated with vitamin E at various concentrations for three days. At 10 ⁇ M vitamin E, ME- 180 cell growth was inhibited (data not shown). However, this may be due to the presence of a larger concentration of ethanol (used as a solvent for vitamin E) in the media. The negative control with the same amount of ethanol (no vitamin E) also showed no ME-180 cell growth. At 1 ⁇ M vitamin E, ME-180 cell growth was enhanced more than the corresponding negative control. At 100 nM vitamin E, cell growth was not effected in comparison to the negative control. Therefore, a concentration of 1 ⁇ M vitamin E was used to measure changes in RNA expression over a 24 hour period.
- ME-180 cells were treated with 0 or 1 ⁇ M vitamin E in the presence and absence of fetal bovine serum. Previous results by the inventors had shown that few changes in RNA expression occur in the presence of serum. However, when the serum was removed, ME-180 cell growth slowed down, an effect that is observed in vaginal atrophy. Therefore, ME-180 cells maintained without serum was used as a model of atrophic vaginitis.
- vitamin E can enhance human cervical epithelial cell growth as well as increase the expression of mucin-4 in an atrophic vaginitis model. Therefore, vitamin E may be useful in the treatment of atrophic vaginitis.
- trans- retinoic acid enhances ME- 180 cell growth in culture.
- cells treated with 13-czs-retinoic acid did not grow as well as the negative control, indicating that 13-cw-retinoic acid is toxic to ME-180 cells at micromolar concentrations.
- VEGF vascular endothelial growth factor
- vitamin A traHs-retinoic acid
- Vitamin A increases cervical cell growth at micromolar concentrations, which could help to strengthen vaginal tissue.
- the presence of vitamin A increases the expression of estrogen receptor alpha, vascular endothelial growth factor and the P2Y 2 receptor gene in cervical epithelial cells. Such increases in expression may help to treat the symptoms of atrophic vaginitis.
- This Example provides data showing the cell proliferating effect of jasmonic acid and gibberellic acid on human skin keratinocytes.
- a human skin keratinocyte cell line from Clonetics (Walkersville, MD, normal human epidermal keratinocytes, neonatal, catalog number cc-2503) was exposed to the jasmonic acid and gibberellic acid (from Sigma Chemical Co.) to determine their effect on proliferation of keratinocytes.
- the gibberellic acid used had the following structure (Gibberellin A 3 ).
- Table 1 illustrates the cell proliferating effect of jasmonic acid on human keratinocytes, where the concentration of jasmonic acid varied between 1 x lO '4 M (designated JA4), 1 x 10 "5 M (designated JA5) and 1 x 10 '6 M (designated JA6).
- Table 2 illustrates the cell proliferating effect of gibberellic acid on human keratinocytes, where the concentration of gibberellic acid varied between
- EXAMPLE 5 Stimulation of Collagen Production This example provides data showing that jasmonic acid and gibberellic acid stimulate collagen production.
- the stimulation response of jasmonic acid and gibberellic acid (Gibberellin A 3 , formula V) on collagen production in the human skin fibroblast cell line was measured using Takara Biomedicals EIA assay kit (TAK MKlOl) sold by Panvera (Madison, WI).
- TAK MKlOl Takara Biomedicals EIA assay kit
- the cells were first grown in a 96-well assay system using Dulbecco's Modified Eagle's Medium (DMEM) with 10% fetal bovine serum (FBS) both purchased from Sigma Chemical Co, St. Louis, MO. Serum- free DMEM was used as a control.
- DMEM Dulbecco's Modified Eagle's Medium
- FBS fetal bovine serum
- 100 ⁇ l of vehicle (serum-free DMEM) was added to 4 wells as control. The plate was incubated for 48 hours at 37°C in a humidified, 5% CO 2 atmosphere.
- the assay was done by using the recommended 20ul of the supernatant from each well of the 96-well plate. Standard buffer and stop solutions were freshly prepared before running the assay. lOOul of antibody-POD conjugate solution (supplied with the kit) was added into the wells using pre antibody coated 96 well plate (supplied with the kit). 20ul of standard and test solutions (from the other 96-well plate containing fibroblasts) were added to appropriate wells. Plate was mixed gently, sealed and incubated for three hrs. at 37°C.
- Table 3 illustrates the collagen production of human fibroblast cells exposed to varying concentrations of jasmonic acid and gibberellic acid.
- the concentration of jasmonic acid varied between 1 x 10 "4 M (designated JA4), 1 x 10 "5 M (designated JA5) and 1 x 10 "6 M (designated JA6).
- the concentration of gibberellic acid varied between 1 x 10 "4 M (designated GA4), 1 x 10 "5 M (designated GA5) and 1 x 10 '6 M (designated GA6).
- Table 3 Effect of Jasmonic Acid or Gibberellic Acid on Collagen Production by Human Fibroblasts
- This example provides data showing the effect of jasmonic acid and gibberellic acid on fibronectin production.
- the stimulation response of jasmonic acid and gibberellic acid (Gibberellin A 3 , formula V) on fibronectin production in the human skin fibroblast cell line was measured using Takara Biomedicals EIA assay kit (TAK MKl 15) sold by Panvera (Madison, WI).
- TAK MKl 15 Takara Biomedicals EIA assay kit
- the cells were first grown in a 96-well assay system using Dulbecco's Modified Eagle's Medium (DMEM) with 10% fetal bovine serum (FBS) both purchased from Sigma Chemical Co, St. Louis, MO. Serum-free DMEM was used as a control.
- DMEM Dulbecco's Modified Eagle's Medium
- FBS fetal bovine serum
- the compounds were tested in three concentrations IxIO "4 M, IxIO "5 M and 1x10 ⁇ 6 M in duplicate.
- Cells were seeded into a 96 well plate at a concentration of 1x10 4 cells in 100 ⁇ l of DMEM containing 10% fetal bovine serum (FBS, Sigma Chemical Co., St. Louis, MO). The plate was incubated for 48 hours at 37° C in a humidified 5% CO 2 atmosphere. After incubation, the medium was aspirated and the wells were rinsed twice with 100 ⁇ l of serum-free DMEM.
- FBS fetal bovine serum
- the plate was incubated for 48 hours at 37 0 C in a humidified, 5% CO 2 atmosphere.
- the fibronectin assay was performed using the recommended 100 ⁇ l of the supernatant from each well of the 96-well plate. Standard buffer and stop solutions were freshly prepared before running the assay.
- a pre-antibody-coated 96 well plate (provided with the kit) was used to transfer the test samples and control.
- the plate was mixed, sealed and incubated for 1 hour at 37 0 C. All the wells were washed after removing sample solutions, 3 times (300 ⁇ l) with washing buffer. lOOul of antibody-POD conjugate solution was added into the wells. Plate was mixed, sealed and incubated for one hour at 37 0 C. Solutions were removed and the wells were washed 3 times with washing buffer. All the wells were completely emptied at the end of washing from any liquid.
- substrate solution hydrogen peroxide and tetramethylbenzidine in a buffered solution
- stop solution freshly prepared IN H 2 SO 4
- Table 4 illustrates the fibronectin production of human fibroblast cells exposed to varying concentrations of jasmonic acid or gibberellic acid.
- the concentration of jasmonic acid varied between 1 x 10 "4 M (designated JA4), 1 x 10 "5 M (designated JA5) and 1 x 10 "6 M (designated JA6).
- the concentration of gibberellic acid varied between 1 x 10 ⁇ 4 M (designated GA4), 1 x 10 '5 M (designated GA5) and 1 x 10 "6 M (designated GA6).
- the example provides data showing that the rate of skin renewal is increased by compositions containing jasmonic acid or gibberellic acid in healthy female volunteers.
- the stratum corneum renewal time is the time taken for the whole thickness of the stratum corneum to be exfoliated and replaced by new cells from the dividing epidermis. This renewal time is a fundamental indicator of skin health. Previous work has demonstrated that the turnover time of the stratum corneum can be measured non-intrusively by impregnating the skin with a fluorescent marker dye that binds avidly to the nonviable epidermal cells.
- a dansyl chloride cell renewal study was conducted in healthy female volunteers ranging from 43-64 years of age. The study consisted of a two-week treatment period during which time the products were applied topically twice daily, including on weekend days, to the test sites. The area of application was designated, approximately 5cm x 10cm on the upper inner arm. The other arm served as a control with no product application. Two compounds, jasmonic acid (JA) and gibberellic acid (GA, Gibberellin A 3 , formula V) were separately tested at a concentration of 0.25% in hyaluronic acid (0.5% aqueous solution). Eight females received jasmonic acid and seven females received gibberellic acid.
- jasmonic acid JA
- gibberellic acid Gibberellin A 3 , formula V
- alpha hydroxy acids e.g. glycolic acid
- the compositions of the invention may satisfy an ongoing need for skin cell renewal anti-aging compositions that do not cause unwanted side effects and that are gentle to the skin.
- This Example illustrates that jasmonic acid can increase cell proliferation in a cervical epithelial cells.
- ME-180 Human cervical epithelial cells (ME-180, ATCC) were propagated in culture at 37 0 C using 5%CO 2 in McCoy's 5A media (Invitrogen) with 10% heat- inactivated fetal bovine serum (Invitrogen). Jasmonic acid (Sigma) was diluted in the ME- 180 media to 100, 10, and 1 microgram/mL. At higher concentrations, the jasmonic acid turned the media yellow in color, indicating that the pH was too low to accomidate normal cell growth.
- ME-180 cells were plated in 12-well plates at a concentration of 5 x 10 4 cells per well in 2 mL of media. The cells were allowed to grow for 1 day. Cells in three wells were counted by trypsinizing and using a hemocytometer to determine cell number on day zero. The media was removed from all other wells and was replaced with fresh media, 100, 10, or 1 ⁇ g/mL jasmonic acid- containing media (2 mL) in triplicate. Cells were counted on days 1 and 2 to determine the effect of the jasmonic acid on cell growth.
- jasmonic acid increased epithelial cell growth after two days of incubation. Therefore, jasmonic acid, as well as other plant hormones, may be useful in the treatment of atrophic vaginitis.
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2005800192547A CN1980650B (en) | 2004-06-17 | 2005-06-09 | Vaginal health products |
MXPA06014457A MXPA06014457A (en) | 2004-06-17 | 2005-06-09 | Vaginal health products. |
EP05760201.3A EP1776101B1 (en) | 2004-06-17 | 2005-06-09 | Vaginal health products |
KR1020067026478A KR101275457B1 (en) | 2004-06-17 | 2005-06-09 | Vaginal Health Products |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/872,194 | 2004-06-17 | ||
US10/872,194 US7485666B2 (en) | 2004-06-17 | 2004-06-17 | Vaginal health products |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006007337A1 true WO2006007337A1 (en) | 2006-01-19 |
Family
ID=34972469
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2005/020286 WO2006007337A1 (en) | 2004-06-17 | 2005-06-09 | Vaginal health products |
Country Status (6)
Country | Link |
---|---|
US (2) | US7485666B2 (en) |
EP (1) | EP1776101B1 (en) |
KR (1) | KR101275457B1 (en) |
CN (2) | CN1980650B (en) |
MX (1) | MXPA06014457A (en) |
WO (1) | WO2006007337A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7485666B2 (en) | 2004-06-17 | 2009-02-03 | Kimberly-Clark Worldwide, Inc. | Vaginal health products |
US7608642B2 (en) | 2002-12-16 | 2009-10-27 | Kimberly-Clark Worldwide, Inc. | Wound and skin care compositions |
CN105524840A (en) * | 2015-09-29 | 2016-04-27 | 浙江钱江生物化学股份有限公司 | Novel fusarium fujikuroi and method for producing gibberellins A4 through fermenting fusarium fujikuroi |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0222522D0 (en) | 2002-09-27 | 2002-11-06 | Controlled Therapeutics Sct | Water-swellable polymers |
GB0417401D0 (en) | 2004-08-05 | 2004-09-08 | Controlled Therapeutics Sct | Stabilised prostaglandin composition |
US7563464B1 (en) * | 2005-04-22 | 2009-07-21 | Bruce Eric Hudkins | Treatment of mucosal membranes utilizing phytoestrogen |
US20070156504A1 (en) * | 2005-12-30 | 2007-07-05 | Kimberly-Clark Worldwide, Inc. | Providing feminine care product recommendations tailored to the composition and rheological properties of vaginal discharge |
GB0613333D0 (en) * | 2006-07-05 | 2006-08-16 | Controlled Therapeutics Sct | Hydrophilic polyurethane compositions |
GB0613638D0 (en) | 2006-07-08 | 2006-08-16 | Controlled Therapeutics Sct | Polyurethane elastomers |
US20080160065A1 (en) * | 2006-07-12 | 2008-07-03 | Janet Anne Halliday | Drug delivery polymer with hydrochloride salt of clindamycin |
GB0620685D0 (en) * | 2006-10-18 | 2006-11-29 | Controlled Therapeutics Sct | Bioresorbable polymers |
JP6010120B2 (en) * | 2011-07-15 | 2016-10-19 | ウニベルシテイト ヘント | Intravaginal delivery system |
US9301920B2 (en) | 2012-06-18 | 2016-04-05 | Therapeuticsmd, Inc. | Natural combination hormone replacement formulations and therapies |
CA2856520C (en) | 2011-11-23 | 2021-04-06 | Therapeuticsmd, Inc. | Natural combination hormone replacement formulations and therapies |
US20150196640A1 (en) | 2012-06-18 | 2015-07-16 | Therapeuticsmd, Inc. | Progesterone formulations having a desirable pk profile |
US20130338122A1 (en) | 2012-06-18 | 2013-12-19 | Therapeuticsmd, Inc. | Transdermal hormone replacement therapies |
US10806740B2 (en) | 2012-06-18 | 2020-10-20 | Therapeuticsmd, Inc. | Natural combination hormone replacement formulations and therapies |
US10806697B2 (en) | 2012-12-21 | 2020-10-20 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
US9180091B2 (en) | 2012-12-21 | 2015-11-10 | Therapeuticsmd, Inc. | Soluble estradiol capsule for vaginal insertion |
US10537581B2 (en) | 2012-12-21 | 2020-01-21 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
US11266661B2 (en) | 2012-12-21 | 2022-03-08 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
US11246875B2 (en) | 2012-12-21 | 2022-02-15 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
US10568891B2 (en) | 2012-12-21 | 2020-02-25 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
US10471072B2 (en) | 2012-12-21 | 2019-11-12 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
MX2016014281A (en) | 2014-05-22 | 2017-02-22 | Therapeuticsmd Inc | Natural combination hormone replacement formulations and therapies. |
US20160175139A1 (en) * | 2014-12-23 | 2016-06-23 | Miguel Angel Fermin | Semen neutralizing condom insert |
US10328087B2 (en) | 2015-07-23 | 2019-06-25 | Therapeuticsmd, Inc. | Formulations for solubilizing hormones |
KR101665261B1 (en) | 2015-08-06 | 2016-10-12 | 순천향대학교 산학협력단 | Compositions for treating or detecting atrophic vaginitis |
WO2017173044A1 (en) | 2016-04-01 | 2017-10-05 | Therapeuticsmd Inc. | Steroid hormone compositions in medium chain oils |
WO2017173071A1 (en) | 2016-04-01 | 2017-10-05 | Therapeuticsmd, Inc. | Steroid hormone pharmaceutical composition |
EP3743150A1 (en) * | 2018-01-26 | 2020-12-02 | The Procter & Gamble Company | Applicators for treating vaginal dryness |
WO2019213464A1 (en) * | 2018-05-04 | 2019-11-07 | The Procter & Gamble Company | Compositions and methods for treating vaginal atrophy |
US11633405B2 (en) | 2020-02-07 | 2023-04-25 | Therapeuticsmd, Inc. | Steroid hormone pharmaceutical formulations |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996020703A1 (en) * | 1995-01-06 | 1996-07-11 | Australian Biomedical Company Pty. Ltd. | Compounds for veterinary and medicinal applications |
WO2003094907A1 (en) * | 2002-05-06 | 2003-11-20 | Kimberly-Clark Worldwide, Inc. | Cell proliferating agents |
WO2004058151A2 (en) * | 2002-12-16 | 2004-07-15 | Kimberly-Clark Worldwide, Inc. | Wound and skin care compositions |
WO2004060394A1 (en) * | 2002-12-16 | 2004-07-22 | Kimberly-Clark Worldwide, Inc. | Wound and skin care products |
Family Cites Families (83)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2798053A (en) | 1952-09-03 | 1957-07-02 | Goodrich Co B F | Carboxylic polymers |
US2798055A (en) | 1954-12-14 | 1957-07-02 | American Cyanamid Co | Rubber compositions containing triazine blowing agents and process for producing cellular rubber therefrom |
US2831854A (en) | 1955-05-24 | 1958-04-22 | Procter & Gamble | Method for preparing fatty esters of non-reducing oligosaccharides in the presence of an amide |
US3963699A (en) | 1974-01-10 | 1976-06-15 | The Procter & Gamble Company | Synthesis of higher polyol fatty acid polyesters |
US4051842A (en) | 1975-09-15 | 1977-10-04 | International Medical Corporation | Electrode and interfacing pad for electrical physiological systems |
US4005195A (en) | 1976-02-12 | 1977-01-25 | The Procter & Gamble Company | Compositions for treating hypercholesterolemia |
US4005196A (en) | 1976-02-12 | 1977-01-25 | The Procter & Gamble Company | Vitaminized compositions for treating hypercholesterolemia |
DE2626348C3 (en) | 1976-06-11 | 1980-01-31 | Siemens Ag, 1000 Berlin Und 8000 Muenchen | Implantable dosing device |
US4383529A (en) | 1980-11-03 | 1983-05-17 | Wescor, Inc. | Iontophoretic electrode device, method and gel insert |
US4603146A (en) * | 1984-05-16 | 1986-07-29 | Kligman Albert M | Methods for retarding the effects of aging of the skin |
JPS58103307A (en) | 1981-12-10 | 1983-06-20 | Taizo Ayukawa | Cream composition |
US4518614A (en) * | 1982-11-04 | 1985-05-21 | Redken Laboratories, Inc. | Cosmetic preparation |
US4509949A (en) | 1983-06-13 | 1985-04-09 | The B. F. Goodrich Company | Water thickening agents consisting of copolymers of crosslinked acrylic acids and esters |
US4517360A (en) | 1983-06-23 | 1985-05-14 | The Procter & Gamble Company | Synthesis of higher polyol fatty acid polyesters using carbonate catalysts |
US4518772A (en) | 1983-06-23 | 1985-05-21 | The Proctor & Gamble Company | Synthesis of higher polyol fatty acid polyesters using high soap:polyol ratios |
FR2557452B1 (en) * | 1983-12-28 | 1986-08-14 | Roussel Uclaf | NOVEL COMPOSITIONS FOR SKIN CARE CONTAINING PRIMER OIL AND RATE TISSUE TRAITS |
GB8401206D0 (en) | 1984-01-17 | 1984-02-22 | Allied Colloids Ltd | Polymers and aqueous solutions |
US5541220A (en) * | 1984-03-07 | 1996-07-30 | Ismail; Roshdy | Agents for the treatment and protection of the skin |
GB8414950D0 (en) | 1984-06-12 | 1984-07-18 | Allied Colloids Ltd | Cationic polyelectrolytes |
US4677120A (en) | 1985-07-31 | 1987-06-30 | Molecular Design International | Topical prodrugs for treatment of acne and skin diseases |
GB8531118D0 (en) | 1985-12-18 | 1986-01-29 | Allied Colloids Ltd | Copolymers |
US4962091A (en) | 1986-05-23 | 1990-10-09 | Syntex (U.S.A.) Inc. | Controlled release of macromolecular polypeptides |
US4937370A (en) | 1987-06-02 | 1990-06-26 | The Procter & Gamble Company | Novel chromophores, sunscreen compositions and methods for preventing sunburn |
US4999186A (en) | 1986-06-27 | 1991-03-12 | The Procter & Gamble Company | Novel sunscreen agents, sunscreen compositions and methods for preventing sunburn |
GB8622797D0 (en) | 1986-09-22 | 1986-10-29 | Allied Colloids Ltd | Polymeric particles |
CA1329283C (en) | 1986-10-01 | 1994-05-03 | David Farrar | Water soluble polymeric compositions |
US4976953A (en) | 1987-03-06 | 1990-12-11 | The Procter & Gamble Company | Skin conditioning/cleansing compositions containing propoxylated glycerol derivatives |
US4797300A (en) | 1987-04-10 | 1989-01-10 | The Procter & Gamble Company | Compositions containing novel solid, nondigestible, fat-like compounds |
USRE34075E (en) | 1987-06-29 | 1992-09-22 | Molecular Design International, Inc. | Dermal uses of trans-retinoids for the treatment of cancer |
US5124356A (en) | 1987-06-29 | 1992-06-23 | Molecular Design International, Inc. | Dermal uses of trans-retinoids for the treatment of photoaging |
US4885311A (en) | 1987-06-29 | 1989-12-05 | Molecular Design International | Topical transretinoids for treatment of acne and skin diseases |
US4847071A (en) | 1987-10-22 | 1989-07-11 | The Procter & Gamble Company | Photoprotection compositions comprising tocopherol sorbate and an anti-inflammatory agent |
EP0496433B1 (en) | 1987-10-22 | 1999-03-24 | The Procter & Gamble Company | Photoprotection compositions comprising chelating agents |
US5049584A (en) | 1988-12-14 | 1991-09-17 | Molecular Design International | Dermal uses of cis-retinoids for the treatment of cancer |
GB8909095D0 (en) | 1989-04-21 | 1989-06-07 | Allied Colloids Ltd | Thickened aqueous compositions |
US5087445A (en) | 1989-09-08 | 1992-02-11 | Richardson-Vicks, Inc. | Photoprotection compositions having reduced dermal irritation |
DK627289D0 (en) | 1989-12-12 | 1989-12-12 | Per C Oden | USE OF BICYCLONONANDER DERIVATIVES |
US5306516A (en) | 1990-04-26 | 1994-04-26 | The Procter & Gamble Company | Shortening compositions containing polyol fatty acid polyesters |
EP0611301B1 (en) | 1990-04-26 | 2003-06-11 | The Procter & Gamble Company | Chelator compositions comprising oxime compounds |
US5306515A (en) | 1990-04-26 | 1994-04-26 | The Procter & Gamble Company | Reduced calorie pourable shortening, cooking oils, salad oils or like compositions |
ATE195247T1 (en) | 1990-04-26 | 2000-08-15 | Procter & Gamble | CHELATE PREPARATION CONTAINING ALPHA-DIAMINE COMPOUNDS |
US5151425A (en) | 1991-06-20 | 1992-09-29 | Clark Lealand L | Method of and composition for treating inflammation and the immunological response thereto |
WO1993006792A1 (en) | 1991-10-04 | 1993-04-15 | Scimed Life Systems, Inc. | Biodegradable drug delivery vascular stent |
EP0752885B1 (en) | 1992-09-25 | 2003-07-09 | Neorx Corporation | Therapeutic inhibitor of vascular smooth muscle cells |
FR2699818B1 (en) | 1992-12-24 | 1995-02-03 | Oreal | Cosmetic or pharmaceutical composition containing in combination a polyphenol and an extract of gingko. |
CA2153778C (en) | 1993-01-13 | 2004-07-06 | Arsinur Burcoglu | Method for using polynucleotides, oligonucleotides and derivatives thereof to treat various disease states |
US5681852A (en) | 1993-11-12 | 1997-10-28 | The Procter & Gamble Company | Desquamation compositions |
CN1039087C (en) * | 1993-12-29 | 1998-07-15 | 昆明宏达实业有限总公司 | External-use medicine for gynecopathy |
US5487899A (en) | 1994-01-31 | 1996-01-30 | Jess Clarke & Sons, Inc. | Wound healing |
US6068834A (en) | 1994-03-04 | 2000-05-30 | The Procter & Gamble Company | Skin lightening compositions |
JPH10501817A (en) | 1994-06-15 | 1998-02-17 | ザ、プロクター、エンド、ギャンブル、カンパニー | Lightening method for hyperpigmented sites in mammalian skin |
JPH08217536A (en) | 1995-02-14 | 1996-08-27 | Tdk Corp | Semiconductor porcelain composition having positive temperature coefficient of resistance and production thereof |
US5607980A (en) | 1995-07-24 | 1997-03-04 | The Procter & Gamble Company | Topical compositions having improved skin feel |
US5663357A (en) | 1995-11-22 | 1997-09-02 | Allergan | Substituted heteroarylamides having retinoid-like biological activity |
US5821250A (en) | 1996-02-01 | 1998-10-13 | The Procter & Gamble Company | Dihydrobenzofuran and related compounds useful as anti-inflammatory agents |
US5837861A (en) | 1997-02-10 | 1998-11-17 | Inspire Pharmaceuticals, Inc. | Dinucleotides and their use as modulators of mucociliary clearance and ciliary beat frequency |
US5789391A (en) | 1996-07-03 | 1998-08-04 | Inspire Pharmaceuticals, Inc. | Method of treating sinusitis with uridine triphosphates and related compounds |
SE9701219D0 (en) | 1997-04-04 | 1997-04-04 | Astra Pharma Prod | New compounds |
SE9702651D0 (en) | 1997-07-09 | 1997-07-09 | Astra Pharma Prod | Novel compounds |
SE9702794D0 (en) | 1997-07-24 | 1997-07-24 | Astra Pharma Prod | New compounds |
US6437003B1 (en) | 1997-10-31 | 2002-08-20 | Jean-Baptiste Roullet | Use of retinoids to treat high blood pressure and other cardiovascular disease |
US5997887A (en) | 1997-11-10 | 1999-12-07 | The Procter & Gamble Company | Skin care compositions and method of improving skin appearance |
US6322978B1 (en) | 1998-04-20 | 2001-11-27 | Joslin Diabetes Center, Inc. | Repeat polymorphism in the frataxin gene and uses therefore |
ITMI981586A1 (en) * | 1998-07-10 | 2000-01-10 | Giorgio Panin | VITAMIN AND ITS ESTERS FOR USE IN TOPICAL TREATMENT OF MUCOSA DISORDERS |
ATE347880T1 (en) | 1998-10-20 | 2007-01-15 | Univ North Carolina | METHODS FOR MOISTURIZING THE NASAL MUCOSA |
US6107091A (en) | 1998-12-03 | 2000-08-22 | Isis Pharmaceuticals Inc. | Antisense inhibition of G-alpha-16 expression |
AU2037700A (en) | 1998-12-03 | 2000-06-19 | E.I. Du Pont De Nemours And Company | Plant vitamin e biosynthetic enzymes |
AU5620600A (en) | 1999-06-16 | 2001-01-02 | University Of Cincinnati, The | Agent and process for isolation of extra-chromosomal nucleic acids |
US6242491B1 (en) * | 1999-06-25 | 2001-06-05 | Rima Kaddurah-Daouk | Use of creatine or creatine compounds for skin preservation |
AU5781800A (en) | 1999-07-06 | 2001-01-22 | General Atomics | Methods and compositions for assaying analytes |
US6221668B1 (en) | 1999-08-20 | 2001-04-24 | Streck Laboratories, Inc. | Hematology control and system for multi-parameter hematology measurements |
US6277855B1 (en) | 2000-04-21 | 2001-08-21 | Inspire Pharmaceuticals, Inc. | Method of treating dry eye disease with nicotinic acetylcholine receptor agonists |
US8252044B1 (en) | 2000-11-17 | 2012-08-28 | Advanced Bio Prosthestic Surfaces, Ltd. | Device for in vivo delivery of bioactive agents and method of manufacture thereof |
AU2002223877A1 (en) | 2000-11-25 | 2002-06-03 | University Of Leeds | Regulation of plant growth by modifying the expression of a putative trna-isope ntenyl transferase |
CA2327962A1 (en) * | 2000-12-11 | 2002-06-11 | Powerdisc Development Corp. Ltd. | Fuel cell stack |
US6469061B1 (en) | 2001-04-04 | 2002-10-22 | Ramot University Authority For Applied Research And Industrial Development Limited | Jasmonate pharmaceutical composition for treatment of cancer |
US20040198829A1 (en) | 2001-04-23 | 2004-10-07 | Sponsel William Eric | Prostanoids augment ocular drug penetration |
US8603502B2 (en) | 2002-02-04 | 2013-12-10 | L'oreal S.A. | Compositions comprising jasmonic acid derivatives and use of these derivatives |
FR2835525B1 (en) | 2002-02-04 | 2006-02-10 | Oreal | NOVEL COMPOUNDS, COMPOSITIONS COMPRISING SAME, AND USE THEREOF FOR PROMOTING DESQUACATION |
US7179481B2 (en) * | 2002-09-19 | 2007-02-20 | Kimberly-Clark Worldwide, Inc. | Vaginal health products |
US7557115B2 (en) * | 2002-09-30 | 2009-07-07 | Cytokinetics, Inc. | Compounds, compositions, and methods |
US7485666B2 (en) | 2004-06-17 | 2009-02-03 | Kimberly-Clark Worldwide, Inc. | Vaginal health products |
US7258878B2 (en) | 2004-12-20 | 2007-08-21 | Kimberly-Clark Worldwide, Inc. | Anti-microbial composition and methods of use thereof |
-
2004
- 2004-06-17 US US10/872,194 patent/US7485666B2/en not_active Expired - Fee Related
-
2005
- 2005-06-09 KR KR1020067026478A patent/KR101275457B1/en active IP Right Grant
- 2005-06-09 MX MXPA06014457A patent/MXPA06014457A/en active IP Right Grant
- 2005-06-09 EP EP05760201.3A patent/EP1776101B1/en not_active Expired - Fee Related
- 2005-06-09 CN CN2005800192547A patent/CN1980650B/en not_active Expired - Fee Related
- 2005-06-09 WO PCT/US2005/020286 patent/WO2006007337A1/en not_active Application Discontinuation
- 2005-06-09 CN CN201010112091XA patent/CN101849936B/en not_active Expired - Fee Related
-
2009
- 2009-02-03 US US12/364,673 patent/US8344022B2/en not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996020703A1 (en) * | 1995-01-06 | 1996-07-11 | Australian Biomedical Company Pty. Ltd. | Compounds for veterinary and medicinal applications |
WO2003094907A1 (en) * | 2002-05-06 | 2003-11-20 | Kimberly-Clark Worldwide, Inc. | Cell proliferating agents |
WO2004058151A2 (en) * | 2002-12-16 | 2004-07-15 | Kimberly-Clark Worldwide, Inc. | Wound and skin care compositions |
WO2004060394A1 (en) * | 2002-12-16 | 2004-07-22 | Kimberly-Clark Worldwide, Inc. | Wound and skin care products |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7608642B2 (en) | 2002-12-16 | 2009-10-27 | Kimberly-Clark Worldwide, Inc. | Wound and skin care compositions |
US7485666B2 (en) | 2004-06-17 | 2009-02-03 | Kimberly-Clark Worldwide, Inc. | Vaginal health products |
US8344022B2 (en) | 2004-06-17 | 2013-01-01 | Kimberly-Clark Worldwide, Inc. | Vaginal health products |
CN105524840A (en) * | 2015-09-29 | 2016-04-27 | 浙江钱江生物化学股份有限公司 | Novel fusarium fujikuroi and method for producing gibberellins A4 through fermenting fusarium fujikuroi |
CN105524840B (en) * | 2015-09-29 | 2018-06-22 | 浙江钱江生物化学股份有限公司 | One plant of new rattan storehouse sickle-like bacteria and its fermentation production of gibberellin A4Method |
Also Published As
Publication number | Publication date |
---|---|
US20090203772A1 (en) | 2009-08-13 |
CN1980650A (en) | 2007-06-13 |
US20050282835A1 (en) | 2005-12-22 |
US8344022B2 (en) | 2013-01-01 |
KR20070018121A (en) | 2007-02-13 |
US7485666B2 (en) | 2009-02-03 |
CN101849936A (en) | 2010-10-06 |
EP1776101B1 (en) | 2016-11-16 |
MXPA06014457A (en) | 2007-03-01 |
KR101275457B1 (en) | 2013-06-14 |
EP1776101A1 (en) | 2007-04-25 |
CN1980650B (en) | 2010-05-26 |
CN101849936B (en) | 2013-02-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US8344022B2 (en) | Vaginal health products | |
CA2497921C (en) | Vaginal health products | |
AU764452B2 (en) | Method of promoting cervical and vaginal secretions | |
US7432252B1 (en) | Method of promoting cervical and vaginal secretions | |
US6436910B1 (en) | Method of promoting mucosal hydration with certain uridine, adenine and cytidine diphosphates and analogs thereof | |
US20110301105A1 (en) | Compositions for proliferation of cells and related methods | |
MXPA05005840A (en) | Compounds that bind p2y2. | |
EP1750725B1 (en) | Compositions comprising mannose phosphate for vaginal treatment | |
JP6993987B2 (en) | Compositions for the treatment of chronic vulvar and perineal pain and associated symptoms and conditions | |
De Vries et al. | Effect of forskolin on beta-adrenergic hyporesponsiveness in skin | |
Burstein | Prostaglandins and Cannabis—IV: A Biochemical Basis for Therapeutic Applications | |
MXPA06010529A (en) | Compositions comprising mannose phosphate for vaginal treatment |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
REEP | Request for entry into the european phase |
Ref document number: 2005760201 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2005760201 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: PA/a/2006/014457 Country of ref document: MX |
|
WWE | Wipo information: entry into national phase |
Ref document number: 200580019254.7 Country of ref document: CN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020067026478 Country of ref document: KR |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWW | Wipo information: withdrawn in national office |
Ref document number: DE |
|
WWP | Wipo information: published in national office |
Ref document number: 1020067026478 Country of ref document: KR |
|
WWP | Wipo information: published in national office |
Ref document number: 2005760201 Country of ref document: EP |