CA1070615A - Veterinary compositions of semi-synthetic penicillin - Google Patents
Veterinary compositions of semi-synthetic penicillinInfo
- Publication number
- CA1070615A CA1070615A CA257,895A CA257895A CA1070615A CA 1070615 A CA1070615 A CA 1070615A CA 257895 A CA257895 A CA 257895A CA 1070615 A CA1070615 A CA 1070615A
- Authority
- CA
- Canada
- Prior art keywords
- oily vehicle
- esters
- semi
- cloxacillin
- tri
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 43
- 229930182555 Penicillin Natural products 0.000 title claims abstract description 36
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 title claims abstract description 29
- 229940049954 penicillin Drugs 0.000 title claims abstract description 27
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims abstract description 24
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 19
- 239000000194 fatty acid Substances 0.000 claims abstract description 19
- 229930195729 fatty acid Natural products 0.000 claims abstract description 19
- -1 propylene glycol di-esters Chemical class 0.000 claims abstract description 19
- 239000000725 suspension Substances 0.000 claims abstract description 14
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 13
- 150000003626 triacylglycerols Chemical class 0.000 claims abstract description 13
- 241001465754 Metazoa Species 0.000 claims abstract description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 6
- 229960003326 cloxacillin Drugs 0.000 claims description 12
- LQOLIRLGBULYKD-JKIFEVAISA-N cloxacillin Chemical compound N([C@@H]1C(N2[C@H](C(C)(C)S[C@@H]21)C(O)=O)=O)C(=O)C1=C(C)ON=C1C1=CC=CC=C1Cl LQOLIRLGBULYKD-JKIFEVAISA-N 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- 229960000723 ampicillin Drugs 0.000 claims description 9
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 claims description 9
- 239000004094 surface-active agent Substances 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 150000007513 acids Chemical class 0.000 claims description 7
- UIOFUWFRIANQPC-JKIFEVAISA-N Floxacillin Chemical compound N([C@@H]1C(N2[C@H](C(C)(C)S[C@@H]21)C(O)=O)=O)C(=O)C1=C(C)ON=C1C1=C(F)C=CC=C1Cl UIOFUWFRIANQPC-JKIFEVAISA-N 0.000 claims description 6
- 229960003022 amoxicillin Drugs 0.000 claims description 6
- LSQZJLSUYDQPKJ-NJBDSQKTSA-N amoxicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=C(O)C=C1 LSQZJLSUYDQPKJ-NJBDSQKTSA-N 0.000 claims description 6
- 229960004273 floxacillin Drugs 0.000 claims description 6
- LSQZJLSUYDQPKJ-UHFFFAOYSA-N p-Hydroxyampicillin Natural products O=C1N2C(C(O)=O)C(C)(C)SC2C1NC(=O)C(N)C1=CC=C(O)C=C1 LSQZJLSUYDQPKJ-UHFFFAOYSA-N 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 3
- 229960004659 ticarcillin Drugs 0.000 claims description 3
- OHKOGUYZJXTSFX-KZFFXBSXSA-N ticarcillin Chemical compound C=1([C@@H](C(O)=O)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)C=CSC=1 OHKOGUYZJXTSFX-KZFFXBSXSA-N 0.000 claims description 3
- RJQXTJLFIWVMTO-TYNCELHUSA-N Methicillin Chemical compound COC1=CC=CC(OC)=C1C(=O)N[C@@H]1C(=O)N2[C@@H](C(O)=O)C(C)(C)S[C@@H]21 RJQXTJLFIWVMTO-TYNCELHUSA-N 0.000 claims description 2
- 229960003669 carbenicillin Drugs 0.000 claims description 2
- FPPNZSSZRUTDAP-UWFZAAFLSA-N carbenicillin Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)C(C(O)=O)C1=CC=CC=C1 FPPNZSSZRUTDAP-UWFZAAFLSA-N 0.000 claims description 2
- 229960002543 carfecillin Drugs 0.000 claims description 2
- NZDASSHFKWDBBU-KVMCETHSSA-N carfecillin Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)C(C=1C=CC=CC=1)C(=O)OC1=CC=CC=C1 NZDASSHFKWDBBU-KVMCETHSSA-N 0.000 claims description 2
- 229960001585 dicloxacillin Drugs 0.000 claims description 2
- YFAGHNZHGGCZAX-JKIFEVAISA-N dicloxacillin Chemical compound N([C@@H]1C(N2[C@H](C(C)(C)S[C@@H]21)C(O)=O)=O)C(=O)C1=C(C)ON=C1C1=C(Cl)C=CC=C1Cl YFAGHNZHGGCZAX-JKIFEVAISA-N 0.000 claims description 2
- 229960003085 meticillin Drugs 0.000 claims description 2
- 229960000515 nafcillin Drugs 0.000 claims description 2
- GPXLMGHLHQJAGZ-JTDSTZFVSA-N nafcillin Chemical compound C1=CC=CC2=C(C(=O)N[C@@H]3C(N4[C@H](C(C)(C)S[C@@H]43)C(O)=O)=O)C(OCC)=CC=C21 GPXLMGHLHQJAGZ-JTDSTZFVSA-N 0.000 claims description 2
- 229960001019 oxacillin Drugs 0.000 claims description 2
- UWYHMGVUTGAWSP-JKIFEVAISA-N oxacillin Chemical compound N([C@@H]1C(N2[C@H](C(C)(C)S[C@@H]21)C(O)=O)=O)C(=O)C1=C(C)ON=C1C1=CC=CC=C1 UWYHMGVUTGAWSP-JKIFEVAISA-N 0.000 claims description 2
- 229960002780 talampicillin Drugs 0.000 claims description 2
- SOROUYSPFADXSN-SUWVAFIASA-N talampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(=O)OC2C3=CC=CC=C3C(=O)O2)(C)C)=CC=CC=C1 SOROUYSPFADXSN-SUWVAFIASA-N 0.000 claims description 2
- 235000013336 milk Nutrition 0.000 abstract description 7
- 239000008267 milk Substances 0.000 abstract description 7
- 210000004080 milk Anatomy 0.000 abstract description 7
- 239000003981 vehicle Substances 0.000 description 22
- 239000003921 oil Substances 0.000 description 10
- 235000019198 oils Nutrition 0.000 description 9
- 150000002960 penicillins Chemical class 0.000 description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 7
- 229920000136 polysorbate Polymers 0.000 description 5
- 239000003242 anti bacterial agent Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 4
- 244000105624 Arachis hypogaea Species 0.000 description 3
- 208000031462 Bovine Mastitis Diseases 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 3
- 229920000053 polysorbate 80 Polymers 0.000 description 3
- 235000003911 Arachis Nutrition 0.000 description 2
- 241000283690 Bos taurus Species 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 2
- 229940093905 ampicillin / cloxacillin Drugs 0.000 description 2
- SCLZRKVZRBKZCR-SLINCCQESA-M cloxacillin sodium Chemical compound [Na+].N([C@@H]1C(N2[C@H](C(C)(C)S[C@@H]21)C([O-])=O)=O)C(=O)C1=C(C)ON=C1C1=CC=CC=C1Cl SCLZRKVZRBKZCR-SLINCCQESA-M 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 230000006651 lactation Effects 0.000 description 2
- 210000005075 mammary gland Anatomy 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical class CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- NGHVIOIJCVXTGV-ALEPSDHESA-N 6-aminopenicillanic acid Chemical compound [O-]C(=O)[C@H]1C(C)(C)S[C@@H]2[C@H]([NH3+])C(=O)N21 NGHVIOIJCVXTGV-ALEPSDHESA-N 0.000 description 1
- NGHVIOIJCVXTGV-UHFFFAOYSA-N 6beta-amino-penicillanic acid Natural products OC(=O)C1C(C)(C)SC2C(N)C(=O)N21 NGHVIOIJCVXTGV-UHFFFAOYSA-N 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 229930195708 Penicillin V Natural products 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- KLOHDWPABZXLGI-YWUHCJSESA-M ampicillin sodium Chemical compound [Na+].C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C([O-])=O)(C)C)=CC=CC=C1 KLOHDWPABZXLGI-YWUHCJSESA-M 0.000 description 1
- 239000008135 aqueous vehicle Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- PWEOPMBMTXREGV-UHFFFAOYSA-N decanoic acid;octanoic acid;propane-1,2-diol Chemical compound CC(O)CO.CCCCCCCC(O)=O.CCCCCCCC(O)=O.CCCCCCCCCC(O)=O.CCCCCCCCCC(O)=O PWEOPMBMTXREGV-UHFFFAOYSA-N 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000005374 membrane filtration Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 229940056360 penicillin g Drugs 0.000 description 1
- 229940056367 penicillin v Drugs 0.000 description 1
- BPLBGHOLXOTWMN-MBNYWOFBSA-N phenoxymethylpenicillin Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)COC1=CC=CC=C1 BPLBGHOLXOTWMN-MBNYWOFBSA-N 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
- A61K31/43—Compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula, e.g. penicillins, penems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0041—Mammary glands, e.g. breasts, udder; Intramammary administration
-
- 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
- A61P15/14—Drugs for genital or sexual disorders; Contraceptives for lactation disorders, e.g. galactorrhoea
Abstract
ABSTRACT OF THE DISCLOSURE
A veterinary composition for intramammary administration to animals comprising a suspension of semi-synthetic penicillin in an oily vehicle, the said oily vehicle comprising tri-glycerides, or propylene glycol di-esters, of fatty acids containing 8-10 carbon atoms, has a short milk out time, good stability and shelf-life.
A veterinary composition for intramammary administration to animals comprising a suspension of semi-synthetic penicillin in an oily vehicle, the said oily vehicle comprising tri-glycerides, or propylene glycol di-esters, of fatty acids containing 8-10 carbon atoms, has a short milk out time, good stability and shelf-life.
Description
This invention relates to veterinary compositions containing semi-synthetic penicillin suspensions for use in the treatment of mammary disorders in animals, especially bovine mastitis.
Mammary disorders in animals are conventionally treated by the intramammary administration of suspensions or solutions of an antibacterial agent in a suitable vehicle.
It has been found that often such antibacterial agents (such as penicillins3 are unstable in aqueous vehicles and thus it lo is necessary to formulate them for intramammary administration in an oily vehicle to produce a product that has an acceptable shelf-life. The oily vehicles used are usually paraffin oils or vegetable oils such as arachis (peanut) oil. ~-When such products are used during lactation it is important that the antibacterial agent is eliminated as quickly as possible after the treatment has been effected.
In this way a minimum of milk is wasted before the level of antibacterial agent in the milk has been reduced to a level acceptable to the health organisations for human consumption.
We have now discovered that semi-synthetic penicillins suspended in a particular class of oily vehicles on intramammary administration to animals give effective treatment of mammary disorders coupled both with a fast milk out rate and also good stability and shelf-life.
Accordingly the present invention provides a veterinary composition for intramammary administration to animals comprising a suspension of a semi-synthetic penicillin in an oily vehicle, the said oily vehicle comprising tri-glycerides, or propylene glycol di-esters, of fatty acids containing 8-10 carbon atoms.
~ ~, ... : . ,. .. : . -.
" ~ ~ ' ~.. ' . ..
.
. , :.
107~6~5 It will be realised by the skilled man that a semi-synthetic penicillin is a penicillin that is normally prepared by the chemical acylation of 6-aminopenicillanic acid, or by an equivalent chemical process. When used herein semi-synthetic penicillin includes a pharmaceutically acceptable salt or ester thereof. Penicillins such as penicillin G and penicillin V which are normally prepared by fermentation are not ofcourse regarded as semi-synthetic penicillins.
' The oily vehicle for the semi-synthetic penicillin may comprise a mixture of both tri-glycerides and propylene glycol di-esters of C8 10 fatty acids. However, it is normally the case that the oily vehicle will comprise either tri-glycerides of the C fatty acids, or p~ropyle~le glycol di-esters -of the ~8-1 fatty acids but not both. Preferably these C8 10 fa~tyacids are fully saturated, such as _-caprylic and n-capric acids. Tri-glyceride esters are in general to be ; preferred to propylene glycol di-esters.
' ' The oily vehicle is conveniently prepared by the commercial fractionating of naturally occuring coconut oil to give mainly C8 10 fatty acids followed by esterification of these acids with the chosen alcohol. It will be realised that an oil prepared,in this way will contain impurities -oils that do not fall within the class defined above for example - which have not been removed by the fractionating process.
- We have found that such impurities may be tolerated up to a level of 20~ by weight of the total oily vehicle. Thus the oily vehicle will often comprise 80 - 100% of tri-glycerides, or propylene glycol di-esters f C8 10 fatty acids and 0-20% of such esters of other fatty acids.
'''' ' ' . '' .
,.~.
Additives may also be present in the oily vehicle in minor proportions. Examples of such additives include con-ventional thickening agents such as 12-hydroxy stearin, aluminium stearate and colloidal silica, and conventional surfactants such as those sold under the Trade Marks "SPAN"
and "TWEEN". "SPANS" are sorbitan fatty acid esters, such ;~
as the oleate esters; "TWEENS" are polyoxyalkylene sorbitan fatty acid esters, such as the oleate esters. When the compositions contain additives then they are normally present as up to 10% by weight of the composition. It has been found - that the compositions suitably contain 0.1 to 8% by weight, for example 1 to 5% by weight, surfactants. In-particular -a surfactant mixture of a TWEEN and a SPAN has been found particularly advantageous, with a TWEEN:SPA~N ration range of 80:20 to 40:60, preferably 70:30 to 50:50.
; Fractionated coconut oil having the desired composition is commercially available. Examples of such oils are the following: `
Miglyols, such as Miglyol*812 and Miglyol*810, sold by Dynamit-Nobel;
Neobees, such as Neobee*M5 and Neobee*O, sold by PVO International Inc.;
Syndermin7Myritol, such as Syndermin*GTC and Myritol*
318, sold by Henkel;
Alembicols, such as Alembicol D, sold by Lovelock; and MCT Oil, sold by Cow and Gate.
* Trade Mark .
. . . :. , :: : .
. : ' - . . ,: , ; ' ~
All these oils consist essentially of varying proportions of tri-glycerides of _-capryIic and n-capric acids.
Miglyol 840 and Neobee M20 are examples of such oils which consist essentially of varying proportions of propylene glycol di-esters of n-caprylic and n-capric acids.
These commercially available oils are very suitable oily vehicles for use in t~e composition according to the invention. We have found the following to be especially suitable:
Miglyol 812, Syndermin GTC and Neobee M20.
The penicillin used in the composition will be any semi-synthetic penicillin that is known to be effective in the treatment of mammary disorders and that it is compatible with and insoluble in the oily vehicle so that the necessary suspension may be prepared. The composition is particularly useful for the treatment of bovine mastitis and so a penicillin active against this infection will often be used.
Suitable penicillins include the following:
Ampicillin Talampicillin Amoxycillin Nafcillin Carbenicillin Dicloxacillin Cloxacillin Oxacillin Flucloxacillin Methicillin `25 Ticarcillin Carfecillin and mixtures of two penicillins such as:
Ampicillin/Cloxacillin Amoxycillin/Cloxacillin Ampicillin/Flucloxacillin Amoxycillin/Flucloxacillin Ticarci]lin/Flucloxacillin ~07061S
~~ The term "semi-synthetic penicillin" when used herein includes pharmaceutically acceptable salts and esters thereof, and thus for example the sodium or potassium salt of a penicillin may often be used in the place of the free penicillin itself. ~ ~
The most useful penicillins are normally ampicillin, cloxacillin, and penicillin mixtures such as ampicillin/
cloxacillin, amoxycillin/cloxacillin; and sodium and potassium salts thereof.
The present invention also provides a process for the preparation of the said veterinary composition, which process comprising suspending a penicillin in an oily vehicle, the said oily vehicle comprising tri-glycerides, or propylene glycol di-esters, of fatty acids containing 8-10 carbon atoms.
This process will be carried out in the usual manner for suspending penicillins in oily vehicles. For example, in a preferred process,- the oily vehicle is first sterilised and then a thickening agent added to it with appropriate heating and mixing. Then the chosen semi-synthetic penicillin in sterile form is added to the oily vehicle with appropriate mixing and milling operations, to give the desired suspension.
Lastly, the invention provides a method of treatment of mammary disorders in animals, which method comprises the intramammary administration of an effective amount of a penicillin suspended in an oily vehicle as hereinbefore defined.
For such administration, the chosen suspension will be filled into the tubes or syringe packs of the conventional . . .
type for intramammary administration, i.e. provided with a canilula nozzle for insertion into the teat to allow extrusion directly into the mammary gland via the streak canal.
_G-, . :
~, . . . .
.
- ~ A single dose of the composition will normally contain 1 to 10 gm., preferably 3 to 8 gm., of the suspension. The weight of penicillin in such a unit dose will of course depend on the nature of the disorder to be treated, its 5- severity and the penicillin that is chosen. However, we have found that effective treatment during lactation can usually ke obtained with a weight of penicillin in the range 50 ~o 500 mg. per unit dose. For example, a dose containing about 75 mg. of ampicillin and about 200 mg. of cloxacillin 10. has been found to be particularly effective in the treatment of bovine mastitis.
Often a single dose of the composition of the invention will provide effective treatment of the mammary disorder.
However, it is usual practice to repeat the dose at least 15. once (preferably three doses are given), each dosing taking place after milking.
The ~ollowing Examples illustrate the invention.
.
.
107~615 1 kg. of veterinary composition, A, of ~he following composition was prepared: -% by wt.
Sodium ampicillin 2.5 Sodium cloxacillin 6.7 - 12-Hydroxystearin 1.0 Miglyol 812 to 100 [Miglyol 812 has the approximate composition:
lo Triglyceride of caproic acid: 3% max.
Triglyceride of caprylic acid: 50-65%
Triglyceride of capric acid: 30-~5%
Triglyceride of lauric acid: 5% max.]
The Miglyol was sterilised by membrane filtration, and to this sterilised Miglyol was added the 12-hydroxystearin at 50C with high shear mixing. The resultant mixture was allowed to cool, and the semi-synthetic penicillins, in sterile form and finely milled, incorporated therein with ~.
mixing to give a suspension of the penicillins in the Miglyol.
The suspension was then passed through a colloid mill to produce a fine, homogeneous dispersion.
Packs of syringes suitable for intramammary administration were filled with 5 gm. per syringe of the dispersion.
., , 1 . .
, .
, .
- . . .
:. , . - ~ ~ - .: .: . :
. . : '' ~, . .. . .
- , - .: . .. . .
'', " ~ . '' ~ .
1~70615 In order to compare the milk out time and stability of composition A prepared in Example 1 with a standard preparation, a composition B was prepared in an identical manner to A, but the Miglyol 812 was replaced by arachis Oil .
3 gm. of A were administered to the mammary gland of a cow, and it was found that the time taken for the penicillin level in the milk to drop below 0.01 micrograms per ml. was lo 84 hours. In contrast, this time was 120 hours using an identical procedure but replacing composition A with - composition B.
These results show that a substantial fall in the ; milk out time can be obtained by replacing a conventional oily vehicle with an oily vehicle according to the invention.
The stability of composition A was then compared with ; ~- the stability of composition B over a period of 12 months at 6 37C. Again, a worthwhile improvement was found with composition A:
/0 Penicillin Remaining Ampicillin Cloxacillin Composition A 99 98 Composition B B9 94 ` ' ' '.
_g_ .. . . .
!
' , : '.
`~ 1070615 EXAMPLE ~
' ~' .
1 kg. of veterinary composition C, o~ the following composition,was prepared by the method of Example 1. (The surfactant were mixed into the Miglyol at the same time as the 12-hydroxystearin).
% by wt.
Sodium Cloxacillin 6.7 12-hydroxystearin 1.0 -~
Tween 80~ 58:42 Tween Span 80 ) to Span ratio 3.0 Miglyol 812 to lO0 [Span 80 is sorbitan monooleate Tween 80 is polyoxyethylene (20) sorbitan monooleate]
Packs of syringes suitable ~or intramammary administration were filled with 3 gm. per syringe of the dispersion.
, : .
: : : : :
., ~ - . .. .
~ : , :
.
Mammary disorders in animals are conventionally treated by the intramammary administration of suspensions or solutions of an antibacterial agent in a suitable vehicle.
It has been found that often such antibacterial agents (such as penicillins3 are unstable in aqueous vehicles and thus it lo is necessary to formulate them for intramammary administration in an oily vehicle to produce a product that has an acceptable shelf-life. The oily vehicles used are usually paraffin oils or vegetable oils such as arachis (peanut) oil. ~-When such products are used during lactation it is important that the antibacterial agent is eliminated as quickly as possible after the treatment has been effected.
In this way a minimum of milk is wasted before the level of antibacterial agent in the milk has been reduced to a level acceptable to the health organisations for human consumption.
We have now discovered that semi-synthetic penicillins suspended in a particular class of oily vehicles on intramammary administration to animals give effective treatment of mammary disorders coupled both with a fast milk out rate and also good stability and shelf-life.
Accordingly the present invention provides a veterinary composition for intramammary administration to animals comprising a suspension of a semi-synthetic penicillin in an oily vehicle, the said oily vehicle comprising tri-glycerides, or propylene glycol di-esters, of fatty acids containing 8-10 carbon atoms.
~ ~, ... : . ,. .. : . -.
" ~ ~ ' ~.. ' . ..
.
. , :.
107~6~5 It will be realised by the skilled man that a semi-synthetic penicillin is a penicillin that is normally prepared by the chemical acylation of 6-aminopenicillanic acid, or by an equivalent chemical process. When used herein semi-synthetic penicillin includes a pharmaceutically acceptable salt or ester thereof. Penicillins such as penicillin G and penicillin V which are normally prepared by fermentation are not ofcourse regarded as semi-synthetic penicillins.
' The oily vehicle for the semi-synthetic penicillin may comprise a mixture of both tri-glycerides and propylene glycol di-esters of C8 10 fatty acids. However, it is normally the case that the oily vehicle will comprise either tri-glycerides of the C fatty acids, or p~ropyle~le glycol di-esters -of the ~8-1 fatty acids but not both. Preferably these C8 10 fa~tyacids are fully saturated, such as _-caprylic and n-capric acids. Tri-glyceride esters are in general to be ; preferred to propylene glycol di-esters.
' ' The oily vehicle is conveniently prepared by the commercial fractionating of naturally occuring coconut oil to give mainly C8 10 fatty acids followed by esterification of these acids with the chosen alcohol. It will be realised that an oil prepared,in this way will contain impurities -oils that do not fall within the class defined above for example - which have not been removed by the fractionating process.
- We have found that such impurities may be tolerated up to a level of 20~ by weight of the total oily vehicle. Thus the oily vehicle will often comprise 80 - 100% of tri-glycerides, or propylene glycol di-esters f C8 10 fatty acids and 0-20% of such esters of other fatty acids.
'''' ' ' . '' .
,.~.
Additives may also be present in the oily vehicle in minor proportions. Examples of such additives include con-ventional thickening agents such as 12-hydroxy stearin, aluminium stearate and colloidal silica, and conventional surfactants such as those sold under the Trade Marks "SPAN"
and "TWEEN". "SPANS" are sorbitan fatty acid esters, such ;~
as the oleate esters; "TWEENS" are polyoxyalkylene sorbitan fatty acid esters, such as the oleate esters. When the compositions contain additives then they are normally present as up to 10% by weight of the composition. It has been found - that the compositions suitably contain 0.1 to 8% by weight, for example 1 to 5% by weight, surfactants. In-particular -a surfactant mixture of a TWEEN and a SPAN has been found particularly advantageous, with a TWEEN:SPA~N ration range of 80:20 to 40:60, preferably 70:30 to 50:50.
; Fractionated coconut oil having the desired composition is commercially available. Examples of such oils are the following: `
Miglyols, such as Miglyol*812 and Miglyol*810, sold by Dynamit-Nobel;
Neobees, such as Neobee*M5 and Neobee*O, sold by PVO International Inc.;
Syndermin7Myritol, such as Syndermin*GTC and Myritol*
318, sold by Henkel;
Alembicols, such as Alembicol D, sold by Lovelock; and MCT Oil, sold by Cow and Gate.
* Trade Mark .
. . . :. , :: : .
. : ' - . . ,: , ; ' ~
All these oils consist essentially of varying proportions of tri-glycerides of _-capryIic and n-capric acids.
Miglyol 840 and Neobee M20 are examples of such oils which consist essentially of varying proportions of propylene glycol di-esters of n-caprylic and n-capric acids.
These commercially available oils are very suitable oily vehicles for use in t~e composition according to the invention. We have found the following to be especially suitable:
Miglyol 812, Syndermin GTC and Neobee M20.
The penicillin used in the composition will be any semi-synthetic penicillin that is known to be effective in the treatment of mammary disorders and that it is compatible with and insoluble in the oily vehicle so that the necessary suspension may be prepared. The composition is particularly useful for the treatment of bovine mastitis and so a penicillin active against this infection will often be used.
Suitable penicillins include the following:
Ampicillin Talampicillin Amoxycillin Nafcillin Carbenicillin Dicloxacillin Cloxacillin Oxacillin Flucloxacillin Methicillin `25 Ticarcillin Carfecillin and mixtures of two penicillins such as:
Ampicillin/Cloxacillin Amoxycillin/Cloxacillin Ampicillin/Flucloxacillin Amoxycillin/Flucloxacillin Ticarci]lin/Flucloxacillin ~07061S
~~ The term "semi-synthetic penicillin" when used herein includes pharmaceutically acceptable salts and esters thereof, and thus for example the sodium or potassium salt of a penicillin may often be used in the place of the free penicillin itself. ~ ~
The most useful penicillins are normally ampicillin, cloxacillin, and penicillin mixtures such as ampicillin/
cloxacillin, amoxycillin/cloxacillin; and sodium and potassium salts thereof.
The present invention also provides a process for the preparation of the said veterinary composition, which process comprising suspending a penicillin in an oily vehicle, the said oily vehicle comprising tri-glycerides, or propylene glycol di-esters, of fatty acids containing 8-10 carbon atoms.
This process will be carried out in the usual manner for suspending penicillins in oily vehicles. For example, in a preferred process,- the oily vehicle is first sterilised and then a thickening agent added to it with appropriate heating and mixing. Then the chosen semi-synthetic penicillin in sterile form is added to the oily vehicle with appropriate mixing and milling operations, to give the desired suspension.
Lastly, the invention provides a method of treatment of mammary disorders in animals, which method comprises the intramammary administration of an effective amount of a penicillin suspended in an oily vehicle as hereinbefore defined.
For such administration, the chosen suspension will be filled into the tubes or syringe packs of the conventional . . .
type for intramammary administration, i.e. provided with a canilula nozzle for insertion into the teat to allow extrusion directly into the mammary gland via the streak canal.
_G-, . :
~, . . . .
.
- ~ A single dose of the composition will normally contain 1 to 10 gm., preferably 3 to 8 gm., of the suspension. The weight of penicillin in such a unit dose will of course depend on the nature of the disorder to be treated, its 5- severity and the penicillin that is chosen. However, we have found that effective treatment during lactation can usually ke obtained with a weight of penicillin in the range 50 ~o 500 mg. per unit dose. For example, a dose containing about 75 mg. of ampicillin and about 200 mg. of cloxacillin 10. has been found to be particularly effective in the treatment of bovine mastitis.
Often a single dose of the composition of the invention will provide effective treatment of the mammary disorder.
However, it is usual practice to repeat the dose at least 15. once (preferably three doses are given), each dosing taking place after milking.
The ~ollowing Examples illustrate the invention.
.
.
107~615 1 kg. of veterinary composition, A, of ~he following composition was prepared: -% by wt.
Sodium ampicillin 2.5 Sodium cloxacillin 6.7 - 12-Hydroxystearin 1.0 Miglyol 812 to 100 [Miglyol 812 has the approximate composition:
lo Triglyceride of caproic acid: 3% max.
Triglyceride of caprylic acid: 50-65%
Triglyceride of capric acid: 30-~5%
Triglyceride of lauric acid: 5% max.]
The Miglyol was sterilised by membrane filtration, and to this sterilised Miglyol was added the 12-hydroxystearin at 50C with high shear mixing. The resultant mixture was allowed to cool, and the semi-synthetic penicillins, in sterile form and finely milled, incorporated therein with ~.
mixing to give a suspension of the penicillins in the Miglyol.
The suspension was then passed through a colloid mill to produce a fine, homogeneous dispersion.
Packs of syringes suitable for intramammary administration were filled with 5 gm. per syringe of the dispersion.
., , 1 . .
, .
, .
- . . .
:. , . - ~ ~ - .: .: . :
. . : '' ~, . .. . .
- , - .: . .. . .
'', " ~ . '' ~ .
1~70615 In order to compare the milk out time and stability of composition A prepared in Example 1 with a standard preparation, a composition B was prepared in an identical manner to A, but the Miglyol 812 was replaced by arachis Oil .
3 gm. of A were administered to the mammary gland of a cow, and it was found that the time taken for the penicillin level in the milk to drop below 0.01 micrograms per ml. was lo 84 hours. In contrast, this time was 120 hours using an identical procedure but replacing composition A with - composition B.
These results show that a substantial fall in the ; milk out time can be obtained by replacing a conventional oily vehicle with an oily vehicle according to the invention.
The stability of composition A was then compared with ; ~- the stability of composition B over a period of 12 months at 6 37C. Again, a worthwhile improvement was found with composition A:
/0 Penicillin Remaining Ampicillin Cloxacillin Composition A 99 98 Composition B B9 94 ` ' ' '.
_g_ .. . . .
!
' , : '.
`~ 1070615 EXAMPLE ~
' ~' .
1 kg. of veterinary composition C, o~ the following composition,was prepared by the method of Example 1. (The surfactant were mixed into the Miglyol at the same time as the 12-hydroxystearin).
% by wt.
Sodium Cloxacillin 6.7 12-hydroxystearin 1.0 -~
Tween 80~ 58:42 Tween Span 80 ) to Span ratio 3.0 Miglyol 812 to lO0 [Span 80 is sorbitan monooleate Tween 80 is polyoxyethylene (20) sorbitan monooleate]
Packs of syringes suitable ~or intramammary administration were filled with 3 gm. per syringe of the dispersion.
, : .
: : : : :
., ~ - . .. .
~ : , :
.
Claims (11)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A verterinary composition for intramammary administration to animals comprising a suspension of a semi-synthetic penicillin in an oily vehicle, the said oily vehicle comprising tri-glycerides, or propylene glycol di-esters, of fatty acids containing 8-10 carbon atoms.
2. A composition according to claim 1, wherein the semi-synthetic penicillin is ampicillin, amoxycillin, carbenicillin, ticarcillin, cloxacillin, flucloxacillin, dicloxacillin, oxacillin, talampicillin, nafcillin, methicillin, or carfecillin.
3. A composition according to claim 1, wherein the semi-synthetic penicillin is a mixture of ampicillin and cloxacillin, amoxycillin and cloxacillin, or ticarcillin and flucloxacillin.
4. A composotion according to claims 1, 2 or 3, wherein the oily vehicle comprises tri-glycerides or propylene glycol di-esters of n-caprylic and n-capric acids.
5. A veterinary composition for intramammary administration to animals comprising a suspension of ampicillin, cloxacillin or a salt thereof in an oily vehicle, the said oily vehicle comprising tri-glycerides or propylene glycol di-esters, of fatty acids containing 8 to 10 carbon atoms.
6. A composition according to claim 5, comprising a suspension of cloxacillin or a salt thereof in an oily vehicle, the said oily vehicle comprising tri-glycerides, or propylene glycol di-esters, of n-caprylic and n-capric acids.
7. A composition according to claim 5 or 6, containing 0.1 to 8% of a surfactant, which surfactant comprises polyoxyalkylene sorbitan fatty acid esters and sorbitan fatty acid esters in a weight ratio of 80:20 to 40:60.
8. A veterinary composition for intramammary administration to animals comprising a suspension of ampicillin and cloxacillin, or salts thereof, in an oily vehicle, the said oily vehicle comprising tri-glycerides, or propylene glycol di-esters, of fatty acids containing 8 to 10 carbon atoms.
9. A composition according to claim 8, wherein the fatty acids are n-caprylic and n-capric acids.
10. A composition according to claim 8 or 9, containing 0.1 to 8% of a surfactant, which surfactant comprises polyoxyalkylene sorbitan fatty acid esters and sorbitan fatty acid esters in a weight ratio of 80:20 to 40:60.
11. A process for the preparation of veterinary composition according to claim 1, which process comprises suspending the semi-synthetic penicillin in the oily vehicle.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB33847/75A GB1547164A (en) | 1975-08-14 | 1975-08-14 | Veterinary compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1070615A true CA1070615A (en) | 1980-01-29 |
Family
ID=10358231
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA257,895A Expired CA1070615A (en) | 1975-08-14 | 1976-07-27 | Veterinary compositions of semi-synthetic penicillin |
Country Status (16)
Country | Link |
---|---|
US (1) | US4073920A (en) |
JP (1) | JPS5225036A (en) |
AU (1) | AU508341B2 (en) |
BE (1) | BE844989A (en) |
CA (1) | CA1070615A (en) |
CY (1) | CY1063A (en) |
DE (1) | DE2635476A1 (en) |
DK (1) | DK151933C (en) |
FR (1) | FR2320749A1 (en) |
GB (1) | GB1547164A (en) |
HK (1) | HK39180A (en) |
IE (1) | IE43494B1 (en) |
KE (1) | KE3060A (en) |
NL (1) | NL185823C (en) |
SE (1) | SE418246B (en) |
ZA (1) | ZA764463B (en) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2907460A1 (en) * | 1978-03-07 | 1979-09-13 | Sandoz Ag | NEW RESORBABLE GALENIC COMPOSITIONS |
IL58461A0 (en) * | 1978-10-27 | 1980-01-31 | Beecham Group Ltd | Intramammary compositions comprising a clavulanic acid salt |
IL58462A0 (en) * | 1978-10-27 | 1980-01-31 | Beecham Group Ltd | Intramammary compositions comprising a penicillin |
JPS5568350A (en) * | 1978-11-20 | 1980-05-23 | Olympus Optical Co | Connector for endoscope |
JPS57171912A (en) * | 1981-04-14 | 1982-10-22 | Sumitomo Chem Co Ltd | Cream |
GB2119649B (en) * | 1982-05-12 | 1986-02-12 | Beecham Group Plc | Ophthalmic cloxacillin compositions |
US4525339A (en) * | 1982-10-15 | 1985-06-25 | Hoffmann-La Roche Inc. | Enteric coated oral dosage form |
US5639724A (en) * | 1984-07-24 | 1997-06-17 | Sandoz Ltd. | Cyclosporin galenic forms |
GB8813670D0 (en) * | 1988-06-09 | 1988-07-13 | Beecham Group Plc | Veterinary composition |
US4980175A (en) * | 1989-01-03 | 1990-12-25 | Leonard Chavkin | Liquid orally administrable compositions based on edible oils |
US4988679A (en) * | 1989-01-03 | 1991-01-29 | Leonard Chavkin | Liquid sustained release composition |
US7081445B2 (en) * | 1989-02-20 | 2006-07-25 | Novartis Ag | Cyclosporin galenic forms |
IE970892A1 (en) | 1996-12-18 | 2000-02-09 | Bimeda Res And Dev Ltd | A veterinary composition |
US7842791B2 (en) * | 2002-12-19 | 2010-11-30 | Nancy Jean Britten | Dispersible pharmaceutical compositions |
US20040197422A1 (en) * | 2002-12-20 | 2004-10-07 | Pfizer Inc | Veterinary compositions for treating mastitis |
GB0229642D0 (en) † | 2002-12-20 | 2003-01-22 | Pfizer Ltd | Veterinary compositions for treating mastitis |
CA2944753A1 (en) * | 2004-02-02 | 2005-08-11 | Bimeda Research & Development Limited | Sequential delivery injector device |
KR102100271B1 (en) * | 2012-02-27 | 2020-04-14 | 바이엘 뉴질랜드 리미티드 | Controlled release compositions and their methods of use |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1110875A (en) * | 1964-12-11 | 1968-04-24 | Glaxo Lab Ltd | Compositions containing procaine penicillins |
GB1152644A (en) * | 1966-07-01 | 1969-05-21 | Abbott Lab | Stable Solutions of Erythromycin Free Base |
IE32979B1 (en) * | 1968-03-07 | 1974-02-06 | Unilever Ltd | Spreadable fats |
US3826845A (en) * | 1969-02-08 | 1974-07-30 | Sankyo Co | Ointment base |
JPS4891218A (en) * | 1972-03-06 | 1973-11-28 | ||
GB1455296A (en) * | 1973-05-24 | 1976-11-10 | Beecham Group Ltd | Veterinary treatment |
CA1052697A (en) * | 1974-03-29 | 1979-04-17 | Upjohn Company (The) | Composition for treating mastitis in animals |
-
1975
- 1975-08-14 GB GB33847/75A patent/GB1547164A/en not_active Expired
-
1976
- 1976-07-19 IE IE1594/76A patent/IE43494B1/en unknown
- 1976-07-21 CY CY1063A patent/CY1063A/en unknown
- 1976-07-26 ZA ZA764463A patent/ZA764463B/en unknown
- 1976-07-27 CA CA257,895A patent/CA1070615A/en not_active Expired
- 1976-08-06 DE DE19762635476 patent/DE2635476A1/en active Granted
- 1976-08-06 BE BE169647A patent/BE844989A/en not_active IP Right Cessation
- 1976-08-09 US US05/712,890 patent/US4073920A/en not_active Expired - Lifetime
- 1976-08-11 FR FR7624498A patent/FR2320749A1/en active Granted
- 1976-08-12 SE SE7609055A patent/SE418246B/en not_active IP Right Cessation
- 1976-08-13 DK DK368276A patent/DK151933C/en not_active IP Right Cessation
- 1976-08-13 NL NLAANVRAGE7609013,A patent/NL185823C/en not_active IP Right Cessation
- 1976-08-14 JP JP51097409A patent/JPS5225036A/en active Pending
- 1976-08-16 AU AU16880/76A patent/AU508341B2/en not_active Expired
-
1980
- 1980-06-26 KE KE3060A patent/KE3060A/en unknown
- 1980-07-31 HK HK391/80A patent/HK39180A/en unknown
Also Published As
Publication number | Publication date |
---|---|
ZA764463B (en) | 1977-07-27 |
IE43494B1 (en) | 1981-03-11 |
FR2320749A1 (en) | 1977-03-11 |
AU508341B2 (en) | 1980-03-20 |
AU1688076A (en) | 1978-02-23 |
BE844989A (en) | 1977-02-07 |
HK39180A (en) | 1980-08-08 |
NL185823C (en) | 1990-08-01 |
NL185823B (en) | 1990-03-01 |
SE418246B (en) | 1981-05-18 |
DE2635476A1 (en) | 1977-02-24 |
NL7609013A (en) | 1977-02-16 |
CY1063A (en) | 1980-10-24 |
FR2320749B1 (en) | 1979-01-12 |
DE2635476C2 (en) | 1992-08-27 |
US4073920A (en) | 1978-02-14 |
GB1547164A (en) | 1979-06-06 |
DK151933C (en) | 1988-06-20 |
KE3060A (en) | 1980-07-11 |
DK368276A (en) | 1977-02-15 |
IE43494L (en) | 1977-02-14 |
JPS5225036A (en) | 1977-02-24 |
SE7609055L (en) | 1977-02-15 |
DK151933B (en) | 1988-01-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1070615A (en) | Veterinary compositions of semi-synthetic penicillin | |
US4282202A (en) | Intramammary compositions | |
DE3017829C2 (en) | ||
JP2002527465A (en) | Propofol composition containing pentetate | |
US4401674A (en) | Intramammary compositions | |
US5747069A (en) | Percutaneously absorbable preparation | |
US3639560A (en) | Veterinary treatment | |
US3882243A (en) | Aqueous suspensions of stable non-beta type crystals of higher fatty acid esters of chloramphenicol | |
KR960001369B1 (en) | Veterinary composition | |
EP0252004A1 (en) | Pharmaceutical compositions for parenteral application | |
IE51846B1 (en) | Pharmaceutical preparation for veterinary use and an appliance containing it | |
KR102100271B1 (en) | Controlled release compositions and their methods of use | |
US3049473A (en) | Udder-dispersible antibiotic mastitis creams | |
US20020068065A1 (en) | Pharmaceutical composition having specific water activity | |
KR0169711B1 (en) | Veterinary composition | |
JP6189437B2 (en) | Injectable antibiotic preparation and method of use thereof | |
WO2017015690A1 (en) | Concentrate containing alprostadil | |
EP0211434A2 (en) | Rectal dosage forms for ceftriaxone | |
WO1988009665A1 (en) | Preservative free ophthalmic ointments | |
EP0193283A1 (en) | Thiazoloquinoline derivatives, process for their preparation and compositions containing them | |
IE64620B1 (en) | A veterinary preparation |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MKEX | Expiry |