US3850160A - Diagnostic tampon and the use thereof for collecting cellular material - Google Patents

Diagnostic tampon and the use thereof for collecting cellular material Download PDF

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US3850160A
US3850160A US00440166A US44016674A US3850160A US 3850160 A US3850160 A US 3850160A US 00440166 A US00440166 A US 00440166A US 44016674 A US44016674 A US 44016674A US 3850160 A US3850160 A US 3850160A
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film
tampon
cellular material
polycarbonate
supporting body
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J Denson
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B10/00Other methods or instruments for diagnosis, e.g. instruments for taking a cell sample, for biopsy, for vaccination diagnosis; Sex determination; Ovulation-period determination; Throat striking implements
    • A61B10/02Instruments for taking cell samples or for biopsy
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/20Tampons, e.g. catamenial tampons; Accessories therefor
    • A61F13/2051Tampons, e.g. catamenial tampons; Accessories therefor characterised by the material or the structure of the inner absorbing core
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/52Use of compounds or compositions for colorimetric, spectrophotometric or fluorometric investigation, e.g. use of reagent paper and including single- and multilayer analytical elements
    • G01N33/528Atypical element structures, e.g. gloves, rods, tampons, toilet paper

Definitions

  • a diagnostic tampon comprising a supporting body, the surface of which is covered with a film of polycarbonate or a porous sheet composed of pure, biologically inert mixed esters of cellulose.
  • the tampon is particularly adapted for collecting cellular material including bacterial, fungal and parasitic elements, from body cavities, in particular the vaginal cavity, for subsequent examination.
  • the present invention relates to a diagnostic tampon for collecting cellular material, including bacterial, fungal and parasitic elements, from body cavities, in particular the vaginal cavity, wherein the tampon surface is covered with a film of polycarbonate or a porous sheet composed of pure, biologically inert mixed esters of cellulose.
  • the tampon of the present invention is particularly adapted for the mass screening and detection of cancer of the pelvic region, in particular the female genital tract. It is of further use in detecting bacterial, fungal or parasitic elements in the female genital tract.
  • the invention also relates to a method for collecting cellular material from the vaginal cavity.
  • acotton fiber tampon is covered by ajacket made out of a closely woven sheercloth manufactured from a non-absorbent continuous filament yarn such as nylon.
  • This jacket holds whatever cells are collected from the body cavity on its surface and because the cloth of the jacket is not absorbent the cells are not dehydrated. The collected cells are evenly smeared onto a microscopic slide by rotating the tampon is contact with the slide.
  • the other prior art method involves the use of a tampon manufactured from a nylon or other synthetic sponge, which softens and swells as it adsorbs the bodily secretions.
  • the prior art devices suffer from various disadvantages, particularly when the collected cells are to be examined a considerable time after they are collected. There is thus a particular need for a device whereby the cellular materials can be collected unassistedly by the patient and thereafter forwarded, either directly or by mail or parcel post, .to the examining laboratory or treating physician. Such a procedure is particularly suitable for geographical areas having a shortage of physicians and cytopathological laboratories, and such a device would be extremely suitable for large scale examinations where a considerable number of such specimens could be examined at one time.
  • the present invention now provides a suitable diagnostic tampon which can be used directly by the patient to collect cellular material from various body cavities, in particular the vaginal cavity.
  • the diagnostic tampon. of this invention can be given to the patient directly by the personal physician or mailed to her by a cytopathological laboratory at his request. It is also particularly adapted for dispensation by pharmacies upon a doctors prescription.
  • the present invention provides a diagnostic tampon for obtaining cell specimens, including bacterial and fungal microorganisms and the like, for diagnosis comprising a supporting body which is flexible and stiff enough to be inserted into a body cavity wherein the surface of the supporting body is covered with either a film of polycarbonate or a porous sheet composed of pure, biologically inert mixedesters of cellulose.
  • the present invention also describes a vaginal diagnostic tampon for obtaining cell specimens from the vaginal cavity comprising a cylindrical shaped supporting body having a film of polycarbonate secured to the surface of the supporting body.
  • the film is dissolved with an inert solvent, thereby leaving only the cellular material on the slide.
  • FIG. 1 is a perspective view of the herein described tampon, the surface of which is substantially completely covered with polycarbonate film.
  • FIG. 2 is a perspective view ofa modified form of the tampon on FIG. 1 showing only a portion of the tampon covered by the film.
  • the tampon of this invention is of a conventional type exemplified by the catamenial'devices that are widely used.
  • a tampon 10 which comprises a supporting body 13 similar in size and shape to the type generally used for catamenial tampons.
  • This body is of a size and of a material sufficiently flexible and stiff enough to be inserted into a body cavity.
  • the tamon is preferably about 2% inches long with a circumference of about 2 inches.
  • the supporting body can be prepared from various materials, such as cotton, cellulose, nylon and the like.
  • Covering the supporting body 13 is a polycarbonate film or a porous sheet composed of pure, biologically inert mixed esters of cellulose 12. There is also attached at the end of the supporting body a removal string 11. Both the string and the film can be attached to the supporting body by conventional fastenings, such as stitching and the like.
  • FIG. 2 is a modified form of the preferred tampon shown in HO. 1, having only part of the supporting body 13 covered by the film.
  • FlG. 2 thus shows a tampon 14 comprising a supporting body 13 partially covered by a polycarbonate or a porous sheet composed of pure, biologically inert mixed esters of cellulose 16. Attached to the end of supporting body 13 is a removal string 11. While the film is shown in the figures as having a smooth surface, the diagnostic tampon can also be manufactured so that the outer film covering has a cor- 'rugated surface, thereby presenting a larger film surface area to the body cavity.
  • the polycarbonate film is especially preferred.
  • the polycarbonate used to prepare such films are the conventional. thermoplastic, linear polyesters of carbonic acid derived from the polymeric condensation of bisphenols with one or more phosgenes, such as phosgene or its derivatives.
  • a particularly preferred polycarbonate film is that commercially available under the Trademark Nucleopore". a membrane filter available from the Nucleopore Corporation, Pleasanton, California 94566.
  • This particular plycarbonate film contains a large number of straight-through pores, and it is understood that this film is prepared by treating conventional polycarbonate films according to the method disclosed in US. Pat. No. 3,303,085.
  • the commercially available material is available in pore sizes of 20A to 8 microns and can contain ll pores/cm of film. A pore size of 5. 0-8. Op. (microns) is especially preferred. Nevertheless, other polycarbonate films can be used as well, even the conventional polycarbonate films that lack such pores. While the thickness of the film is not critical, a thickness of 8-13 microns is preferred, with a film thickness of 10mg. being especially preferred.
  • Another preferred tampon covering is a porous sheet composed of pure, biologically inert mixed esters of cellulose.
  • Typical mixed esters include cellulose acetate propionate and cellulose acetate butyrate.
  • Other mixed cellulose esters can be prepared containing other combinations of lower alkanoate groups, especially low alkanoate groups containing less than 5 carbon atoms.
  • the porous sheet of mixed es ters of cellulose can be derived from the mixture of the pure, simple cellulose lower alkanoate esters, such as mixtures of cellulose acetate, cellulose propionate, cellulose butyrate and the like. Cellulose nitrate can also be added to such mixtures.
  • US. Pat. No. 2,926,104 discloses a convenient method of preparing microporous cellulose ester films.
  • An especially preferred series of membranes derived from the mixed esters of cellulose are the commercially available MF-Millipore filters available from the Millipore Corporation, Bedford, Massachusetts 01730. These filters come in about 12 distinct sizes containing pores ranging from 8 microns to 25 millimicrons and are microporous screens containing millions of pores/cm of surface area.
  • the tampon of the invention can be inserted into the desired body cavity by means of typical tampon applicators, such as for example those disclosed in U.S. Pat. No. 1,926,900 and US. Pat. No. 3,101,713.
  • the diagnostic tampon of this invention can be used to collect exfoliated cells originating in the epithelial, mesothelial and endothelial tissue and also foreign elements such as bacterial or fungal microorganisms and the like. Accordingly, as used herein the expression cellular material should be understood to include all of such elements.
  • the tampon of this invention is particularly adapted for a wide variety of diagnostic purposes. First and foremost it is especially suitable foruse in obtaining a cervical vaginal smear for diagnosis in the Pap test. In addition, it can be used to collect pathological bacteria such as Neisseria gonorr/weae, the causative organism of gonorrhea, as well as pathogenic fungal parasites, such as Candida albicans, the causative agent of Moniliasis, which can be particularly troublesome in the vaginal tract. Other bacterial infections that can be diagnosed include Trichbmonas vagina/is and Hemoplzilus vaginalis, as well as various gonococsal, spirochetal, staphylococcal and streptococcal infections.
  • pathological bacteria such as Neisseria gonorr/weae, the causative organism of gonorrhea
  • pathogenic fungal parasites such as Candida albicans
  • Moniliasis the caus
  • the tampon is inserted into the vagina to the point of contact with the cervix.
  • the diagnostic tampon shown in FIG. 1 is preferred since the end of the tampon is covered with the film thereby facilitating collection of cells from the external cervical os.
  • the tampon is left in place several minutes while the patient is in an erect or semi-erect position.
  • the tampon is then withdrawn, utilizing the attached removal string and immediately thereafter placed in a fixative.
  • fixatives for use in the Pap smear which are well-known to those skilled in the art.
  • the tampon is inserted into an appropriate mailer which releases the fixative upon enclosing.
  • the patients identification and history generally accompany the specimen to the laboratory.
  • the polycarbonate film covering the tampon is removed and divided into two portions, each of which is placed on a glass slide.
  • the film can easily be removed from the supporting body of the tampon by placing the tampon in an upright position, such as on a spindle, and then with a surgical scapel bisecting the film lengthwise, i.e. vertically, and then cutting the bottom of the film. which remains attached to the supporting body, thereby providing two film sections having rounded edges at one end.
  • the slides are then stained with the conventional Pap smear staining reagents.
  • the fixing and staining techniques used in preparing the cells for examination are conventional and can be found in most laboratory handbooks describing methods for carrying out the Pap test.
  • Typical texts include Diagnostic Cytology And Its Histopathologic Basis, Leopold G. Koss, Second Ed., 1968. Since the polycarbonate film is transparent, it has the advantage of being able to be viewed directly in the microscope without causing any objectionable background. Nevertheless, if desired, the polycarbonate film can be dissolved in a suitable inert solvent which dissolves the polycarbonate film without destroying or injuring the stained cells.
  • a suitable inert solvent which dissolves the polycarbonate film without destroying or injuring the stained cells.
  • solvents will suggest themselves to those skilled in the art, and the determination of any particular solvent can be readily determined by routineexperimentation. It has been found that various halogenated hydrocarbons are particularly effective for dissolving polycarbonate films. Of those halogenated hydrocarbons that can be used, bromoform, chloroform, ethyl dichloride, methylene chloride, and l,l,2-trichloroethane are especially preferred.
  • the film is removed from the tampon as described above, and mounted on the mircoscope slide, cell side up, for permeation by the stains. After the staining is complete,
  • the slide is removed from the staining rack and the film is then inverted so that the cell side is down, viz. the cellular material faces the slide.
  • a solvent capable of dissolving the film is then droped onto the film. After the film has dissolved and all of the solvent has evaporated, the slide is then dipped into xylene and a cover slip is placed over the cellular material. The slide is then ready for examination.
  • a suitable solvent used to dissolve the polycarbonate film is not critical, and any solvent can be used that will dissolve the film and at the same time will not have a deleterious effect on the cells to be examined. Suitable solvents can be readily determined by simpile experimentation. For convenience, chloroform is the solvent of choice.
  • the presence of bacterial and fungal microorganisms can be determined by similar methods. Thus, where a bacterial determination is to be made, there is no need to place the tampon into a fixative.
  • the sample need only be air-dried and sent for cytopathological examination.
  • the dried film is removed from the supporting body as described above and Gram-stained for initial differentiation of microorganisms. The film can also be dissolved as described hereinabove. If the Gram stain reveals the presence of the pathological microorganisms the patient would then be notified with a view initiating appropriate therapy.
  • the diagnostic tampon of this invention is particularly adapted for mass screening for gonorrhea.
  • the symptoms and signs of acute infection in the adult female are frequently absent, making detection difficult.
  • the presence of N. gonorrhoeae is best determined by preparing the examining growth cultures, in which case it is necessary to keep the cellular specimen moist and relatively warm. This can be accomplished by inserting the tampon into a suitable mailer or container lined with an appropriate growth medium. At the laboratory, the tampon would be discarded, and the mailer containing the growth medium and possible gonorrhea-causing microorganisms would be placed open and flat in a Petri dish containing addi tional growth medium for continued incubation and subsequent examination.
  • the polycarbonate film is effective in adsorbing the cellular material. Nevertheless, an understanding of the mechanism is not necessary for the successful practice of the invention. It may very well be that the cellular material adheres to the surface of the film by electrostatic attraction. As mentioned hereinabove, the preferred polycarbonate film is that available under the Trademark Nucleopore. This particular material has a large number of small-sized pores. While this type of polycarbonate film is preferred, conventional polycarbonate films can be used as well.
  • porous sheet composed of the mixed esters of cellulose these latter materials cannot be as readily dissolved as can the polycarbonate film for purposes of examination, and the film therefore causes a background when the slide is viewed under the microscope.
  • the background is not, however a particularly objectionable, one, though it is not as good as that provided by a transparent film.
  • the MF-Millipore filters can be easily rendered transparent, however, by applying a few drops of immersion oil having the same index of refraction. Nevertheless, there is no real added difficulty in discerning the fine details of thestained cellular material, and in some cases the porous sheet of the mixed esters of cellulose might be preferred.
  • a tampon including a means for obtaining cell specimens for diagnosis which comprises a supporting body that is flexible, appropriately shaped and stiff enough to be inserted into a body cavity, said supporting body having a covering portion comprising an external film of polycarbonate or a porous sheet composed of biologically inert mixed esters of cellulose secured to the surface of said supporting body.
  • a vaginal tampon for obtaining cell specimens for diagnosis comprises a cylindrical shaped, supporting body having a film of polycarbonate secured to the surface thereof.
  • a method for collecting and examining cellular material from the vaginal cavity which comprises:
  • step (d) the film is dissolved with an inert solvent before examining the stained cellular material on the slide.
  • the solvent is selected from the group consisting of bromoform, chloroform, ethyl dichloride, methylene chloride, and 1,1,2- trichloroethane.

Abstract

A diagnostic tampon comprising a supporting body, the surface of which is covered with a film of polycarbonate or a porous sheet composed of pure, biologically inert mixed esters of cellulose. The tampon is particularly adapted for collecting cellular material including bacterial, fungal and parasitic elements, from body cavities, in particular the vaginal cavity, for subsequent examination.

Description

United States Patent 1191 1111 3,850,160
Denson Nov. 26, 1974 [54] DIAGNOSTIC TAMPON AND THE USE 3,521,637 7/1970 Waterbury 128/270 THEREOF FOR COLLECTING CELLULAR 3,716,430 2/ 1973 Green 128/270 MATERIAL R24,666 7 1959 Draghi 128/285 Inventor: Judy Wynne Denson, Rt. One Box 87, Tazewell, Va. 24651 Filed: Feb. 6, 1974 Appl. No.: 440,166
Related U.S. Application Data Continuation-in-part of Ser. No. 332,718, Feb. 15, 1973, abandoned.
U.S. Cl. 128/2 B, 128/270, 128/285 Int. Cl. A61f 13/20 Field of Search 128/2 B, 263, 270, 285
References Cited UNITED STATES PATENTS Richardson 128/285 Primary ExaminerAldrich F. Medbery Attorney, Agent, or FirmBacon & Thomas [5 7 ABSTRACT A diagnostic tampon comprising a supporting body, the surface of which is covered with a film of polycarbonate or a porous sheet composed of pure, biologically inert mixed esters of cellulose. The tampon is particularly adapted for collecting cellular material including bacterial, fungal and parasitic elements, from body cavities, in particular the vaginal cavity, for subsequent examination.
6 Claims, 2 Drawing Figures DIAGNOSTIC TAMPON AND THE USE THEREOF FOR COLLECTING CELLULAR MATERIAL CROSS-REFERENCE TO RELATED APPLICATIONS The present application is a continuation-in-part of application, Ser. No. 332,718, filed Feb. 15, I973 and now abandoned.
BACKGROUND OF THE INVENTION 1. Field Of The Invention The present invention relates to a diagnostic tampon for collecting cellular material, including bacterial, fungal and parasitic elements, from body cavities, in particular the vaginal cavity, wherein the tampon surface is covered with a film of polycarbonate or a porous sheet composed of pure, biologically inert mixed esters of cellulose. The tampon of the present invention is particularly adapted for the mass screening and detection of cancer of the pelvic region, in particular the female genital tract. It is of further use in detecting bacterial, fungal or parasitic elements in the female genital tract. The invention also relates to a method for collecting cellular material from the vaginal cavity.
2. Description Of The Prior Art In recent years the collection of cellular specimens from the human vaginal tract has provided an effective menans for detecting early cancer of the cervix. The cellular material thus obtained is applied, as a cervical vaginal smear, onto a microscope slide and appropriately fixed, stained, and examined. This procedure broadly describes the Papanicolaou Test, popularly known as the Pap Test. The Papanicolaou (cytological) smear is generally obtained by the physician in the office by inserting a speculum into the vagina without lubricant, thereby exposing the cervix. The surface of the external os is then scraped thoroughly and the detritus placed on a glass slide. A second specimen is obtained from the posterior fornix and placed on another glass slide. The two slides are then appropriately treated and sent to the laboratory for cytological study. Unfortunately, for reasons of modesty, many women are reluctant to present themselves periodically for gynecological examination, which usually involves an office visit which, of course, requires further effort by the patient. Many women, particularly those living in remote areas such as rural areas, also find it difficult to present themselves periodically for such examinations. Consequently, there has been a definite need for a simple means for collecting cellular material and the like from the female genital tract, which would be especially suit able for mass screening techniques. It would be desirable to be able to utilize a simple method which could be effectively employed by the patient, preferably at home, without the need for any professional assistance. Towards a means of achieving this aim, there have been proposals to use tampon-like devices adapted for cancer detection. Two of such devices are described in U.S. Pat. No. 2,905,169 and US. Pat. No. Re. 24,666.
In one of the prior art techniques, acotton fiber tampon is covered by ajacket made out of a closely woven sheercloth manufactured from a non-absorbent continuous filament yarn such as nylon. This jacket holds whatever cells are collected from the body cavity on its surface and because the cloth of the jacket is not absorbent the cells are not dehydrated. The collected cells are evenly smeared onto a microscopic slide by rotating the tampon is contact with the slide. The other prior art method involves the use of a tampon manufactured from a nylon or other synthetic sponge, which softens and swells as it adsorbs the bodily secretions.
The prior art devices suffer from various disadvantages, particularly when the collected cells are to be examined a considerable time after they are collected. There is thus a particular need for a device whereby the cellular materials can be collected unassistedly by the patient and thereafter forwarded, either directly or by mail or parcel post, .to the examining laboratory or treating physician. Such a procedure is particularly suitable for geographical areas having a shortage of physicians and cytopathological laboratories, and such a device would be extremely suitable for large scale examinations where a considerable number of such specimens could be examined at one time.
The present invention now provides a suitable diagnostic tampon which can be used directly by the patient to collect cellular material from various body cavities, in particular the vaginal cavity. The diagnostic tampon. of this invention can be given to the patient directly by the personal physician or mailed to her by a cytopathological laboratory at his request. It is also particularly adapted for dispensation by pharmacies upon a doctors prescription.
SUMMARY OF THE INVENTION The present invention provides a diagnostic tampon for obtaining cell specimens, including bacterial and fungal microorganisms and the like, for diagnosis comprising a supporting body which is flexible and stiff enough to be inserted into a body cavity wherein the surface of the supporting body is covered with either a film of polycarbonate or a porous sheet composed of pure, biologically inert mixedesters of cellulose.
The present invention also describes a vaginal diagnostic tampon for obtaining cell specimens from the vaginal cavity comprising a cylindrical shaped supporting body having a film of polycarbonate secured to the surface of the supporting body.
It is also an object of this invention to provide a method for collecting cellular material from the vaginal cavity comprising:
a.'inserting into the vaginal cavity a tampon where the tampon surface is covered with a film of polycarbonate;
b. withdrawing the tampon;
c. removing the film from the tampon and placing it on a slide;
(1. fixing and staining the cellular material on the film; and thereafter e. examining the stained cellular material.
In the preferred method of collecting and examining the cellular material, after the cellular material on the film is fixed and stained, the film is dissolved with an inert solvent, thereby leaving only the cellular material on the slide.
BRIEF DESCRIPTION OF THE DRAWING FIG. 1 is a perspective view of the herein described tampon, the surface of which is substantially completely covered with polycarbonate film.
FIG. 2 is a perspective view ofa modified form of the tampon on FIG. 1 showing only a portion of the tampon covered by the film.
DETAILED DESCRIPTION OF THE INVENTION The tampon of this invention, as shown in the accompanying figures, is of a conventional type exemplified by the catamenial'devices that are widely used. Referring to the figures, there is shown in FIG. 1 a tampon 10 which comprises a supporting body 13 similar in size and shape to the type generally used for catamenial tampons. This body is of a size and of a material sufficiently flexible and stiff enough to be inserted into a body cavity. For use in the vaginal cavity, the tamon is preferably about 2% inches long with a circumference of about 2 inches. The supporting body can be prepared from various materials, such as cotton, cellulose, nylon and the like.
Covering the supporting body 13 is a polycarbonate film or a porous sheet composed of pure, biologically inert mixed esters of cellulose 12. There is also attached at the end of the supporting body a removal string 11. Both the string and the film can be attached to the supporting body by conventional fastenings, such as stitching and the like.
FIG. 2 is a modified form of the preferred tampon shown in HO. 1, having only part of the supporting body 13 covered by the film. FlG. 2 thus shows a tampon 14 comprising a supporting body 13 partially covered by a polycarbonate or a porous sheet composed of pure, biologically inert mixed esters of cellulose 16. Attached to the end of supporting body 13 is a removal string 11. While the film is shown in the figures as having a smooth surface, the diagnostic tampon can also be manufactured so that the outer film covering has a cor- 'rugated surface, thereby presenting a larger film surface area to the body cavity.
Although either a polycarbonate or a porous sheet composed of pure, biologically inert mixed esters of cellulose can be used on the surface of the tampon, the polycarbonate film is especially preferred. As is well known. the polycarbonate used to prepare such films are the conventional. thermoplastic, linear polyesters of carbonic acid derived from the polymeric condensation of bisphenols with one or more phosgenes, such as phosgene or its derivatives. A particularly preferred polycarbonate film is that commercially available under the Trademark Nucleopore". a membrane filter available from the Nucleopore Corporation, Pleasanton, California 94566. This particular plycarbonate film contains a large number of straight-through pores, and it is understood that this film is prepared by treating conventional polycarbonate films according to the method disclosed in US. Pat. No. 3,303,085. The commercially available material is available in pore sizes of 20A to 8 microns and can contain ll pores/cm of film. A pore size of 5. 0-8. Op. (microns) is especially preferred. Nevertheless, other polycarbonate films can be used as well, even the conventional polycarbonate films that lack such pores. While the thickness of the film is not critical, a thickness of 8-13 microns is preferred, with a film thickness of 10mg. being especially preferred.
" Another preferred tampon covering is a porous sheet composed of pure, biologically inert mixed esters of cellulose. Typical mixed esters include cellulose acetate propionate and cellulose acetate butyrate. Other mixed cellulose esters can be prepared containing other combinations of lower alkanoate groups, especially low alkanoate groups containing less than 5 carbon atoms. Alternatively, the porous sheet of mixed es ters of cellulose can be derived from the mixture of the pure, simple cellulose lower alkanoate esters, such as mixtures of cellulose acetate, cellulose propionate, cellulose butyrate and the like. Cellulose nitrate can also be added to such mixtures. US. Pat. No. 2,926,104 discloses a convenient method of preparing microporous cellulose ester films.
An especially preferred series of membranes derived from the mixed esters of cellulose are the commercially available MF-Millipore filters available from the Millipore Corporation, Bedford, Massachusetts 01730. These filters come in about 12 distinct sizes containing pores ranging from 8 microns to 25 millimicrons and are microporous screens containing millions of pores/cm of surface area.
The tampon of the invention can be inserted into the desired body cavity by means of typical tampon applicators, such as for example those disclosed in U.S. Pat. No. 1,926,900 and US. Pat. No. 3,101,713.
The diagnostic tampon of this invention can be used to collect exfoliated cells originating in the epithelial, mesothelial and endothelial tissue and also foreign elements such as bacterial or fungal microorganisms and the like. Accordingly, as used herein the expression cellular material should be understood to include all of such elements.
it will therefore be seen that the tampon of this invention is particularly adapted for a wide variety of diagnostic purposes. First and foremost it is especially suitable foruse in obtaining a cervical vaginal smear for diagnosis in the Pap test. In addition, it can be used to collect pathological bacteria such as Neisseria gonorr/weae, the causative organism of gonorrhea, as well as pathogenic fungal parasites, such as Candida albicans, the causative agent of Moniliasis, which can be particularly troublesome in the vaginal tract. Other bacterial infections that can be diagnosed include Trichbmonas vagina/is and Hemoplzilus vaginalis, as well as various gonococsal, spirochetal, staphylococcal and streptococcal infections.
For vaginal use in the Pap Test, the tampon is inserted into the vagina to the point of contact with the cervix. For the Pap test, the diagnostic tampon shown in FIG. 1 is preferred since the end of the tampon is covered with the film thereby facilitating collection of cells from the external cervical os. The tampon is left in place several minutes while the patient is in an erect or semi-erect position. The tampon is then withdrawn, utilizing the attached removal string and immediately thereafter placed in a fixative. There are numerous satisfactory fixatives for use in the Pap smear which are well-known to those skilled in the art. Where it is intended that the tampon is to be sent elsewhere for examination, the tampon is inserted into an appropriate mailer which releases the fixative upon enclosing. The patients identification and history generally accompany the specimen to the laboratory.
At the laboratory, the polycarbonate film covering the tampon is removed and divided into two portions, each of which is placed on a glass slide. The film can easily be removed from the supporting body of the tampon by placing the tampon in an upright position, such as on a spindle, and then with a surgical scapel bisecting the film lengthwise, i.e. vertically, and then cutting the bottom of the film. which remains attached to the supporting body, thereby providing two film sections having rounded edges at one end. The slides are then stained with the conventional Pap smear staining reagents. The fixing and staining techniques used in preparing the cells for examination are conventional and can be found in most laboratory handbooks describing methods for carrying out the Pap test. Typical texts include Diagnostic Cytology And Its Histopathologic Basis, Leopold G. Koss, Second Ed., 1968. Since the polycarbonate film is transparent, it has the advantage of being able to be viewed directly in the microscope without causing any objectionable background. Nevertheless, if desired, the polycarbonate film can be dissolved in a suitable inert solvent which dissolves the polycarbonate film without destroying or injuring the stained cells. A wide variety of such solvents will suggest themselves to those skilled in the art, and the determination of any particular solvent can be readily determined by routineexperimentation. It has been found that various halogenated hydrocarbons are particularly effective for dissolving polycarbonate films. Of those halogenated hydrocarbons that can be used, bromoform, chloroform, ethyl dichloride, methylene chloride, and l,l,2-trichloroethane are especially preferred.
Where it is desired to dissolve the polycarbonate film, in the initial laboratory processing the film is removed from the tampon as described above, and mounted on the mircoscope slide, cell side up, for permeation by the stains. After the staining is complete,,
the slide is removed from the staining rack and the film is then inverted so that the cell side is down, viz. the cellular material faces the slide. A solvent capable of dissolving the film is then droped onto the film. After the film has dissolved and all of the solvent has evaporated, the slide is then dipped into xylene and a cover slip is placed over the cellular material. The slide is then ready for examination.
As mentioned above, the choice of a suitable solvent used to dissolve the polycarbonate film is not critical, and any solvent can be used that will dissolve the film and at the same time will not have a deleterious effect on the cells to be examined. Suitable solvents can be readily determined by simpile experimentation. For convenience, chloroform is the solvent of choice.
The presence of bacterial and fungal microorganisms can be determined by similar methods. Thus, where a bacterial determination is to be made, there is no need to place the tampon into a fixative. The sample need only be air-dried and sent for cytopathological examination. The dried film is removed from the supporting body as described above and Gram-stained for initial differentiation of microorganisms. The film can also be dissolved as described hereinabove. If the Gram stain reveals the presence of the pathological microorganisms the patient would then be notified with a view initiating appropriate therapy.
The diagnostic tampon of this invention is particularly adapted for mass screening for gonorrhea. As is well-known, the symptoms and signs of acute infection in the adult female are frequently absent, making detection difficult. The presence of N. gonorrhoeae is best determined by preparing the examining growth cultures, in which case it is necessary to keep the cellular specimen moist and relatively warm. This can be accomplished by inserting the tampon into a suitable mailer or container lined with an appropriate growth medium. At the laboratory, the tampon would be discarded, and the mailer containing the growth medium and possible gonorrhea-causing microorganisms would be placed open and flat in a Petri dish containing addi tional growth medium for continued incubation and subsequent examination.
Appropriate testing procedures for determining the presence of bacterial and fungal microorganisms and the like can be found in Diagnostic Microbiology, Robert W. Bailey and Elvyn G. Scott, 3rd. ed., l970.
The exact mechanism by which the polycarbonate film is effective in adsorbing the cellular material is not fully understood. Nevertheless, an understanding of the mechanism is not necessary for the successful practice of the invention. It may very well be that the cellular material adheres to the surface of the film by electrostatic attraction. As mentioned hereinabove, the preferred polycarbonate film is that available under the Trademark Nucleopore. This particular material has a large number of small-sized pores. While this type of polycarbonate film is preferred, conventional polycarbonate films can be used as well.
With regard to the porous sheet composed of the mixed esters of cellulose, these latter materials cannot be as readily dissolved as can the polycarbonate film for purposes of examination, and the film therefore causes a background when the slide is viewed under the microscope. The background is not, however a particularly objectionable, one, though it is not as good as that provided by a transparent film. The MF-Millipore filters can be easily rendered transparent, however, by applying a few drops of immersion oil having the same index of refraction. Nevertheless, there is no real added difficulty in discerning the fine details of thestained cellular material, and in some cases the porous sheet of the mixed esters of cellulose might be preferred.
As mentined previously, the manner in which the film is attached or secured to the tampon is not of critical importance.
While the above description has been mainly concerned with a tampon adapted for use in the vaginal cavity, it will be apparent that with slight modifications the tampon herein described can be adopted for use in other body cavities, for example, in collecting cellular material from the lower rectum, colon,and buccal cavity, and with modifications of the collection technique, cellular samples from external lesions can be obtained as well.
It will thus be apparent that equivalents or modifications of the herein described tampon may be made without departing from the scope of the invention as set forth in the following claims.
What is claimed is:
1. A tampon including a means for obtaining cell specimens for diagnosis which comprises a supporting body that is flexible, appropriately shaped and stiff enough to be inserted into a body cavity, said supporting body having a covering portion comprising an external film of polycarbonate or a porous sheet composed of biologically inert mixed esters of cellulose secured to the surface of said supporting body.
2. A vaginal tampon for obtaining cell specimens for diagnosis comprises a cylindrical shaped, supporting body having a film of polycarbonate secured to the surface thereof.
3. A method for collecting and examining cellular material from the vaginal cavity which comprises:
e. examining the stained cellular material on the slide.
4. The method of claim 3 wherein after step (d) the film is dissolved with an inert solvent before examining the stained cellular material on the slide. 7
5. The method of claim 4 wherein the solvent is selected from the group consisting of bromoform, chloroform, ethyl dichloride, methylene chloride, and 1,1,2- trichloroethane.
6. The method of claim 5 wherein the solvent is chloroform.

Claims (6)

1. A tampon including a means for obtaining cell specimens for diagnosis which comprises a supporting body that is flexible, appropriately shaped and stiff enough to be inserted into a body cavity, said supporting body having a covering portion comprising an external film of polycarbonate or a porous sheet composed of biologically inert mixed esters of cellulose secured to the surface of said supporting body.
2. A vaginal tampon for obtaining cell specimens for diagnosis which comprises a cylindrical shaped, supporting body having a film of polycarbonate secured to the surface thereof.
3. A METHOD FOR COLLECTING AND EXAMINING CELLULAR MATERIAL FROM THE VAGINAL CAVITY WHICH COMPRISES: A. INSERTING A TAMPOND, THE SURFACE OF WHICH IS COVERED WITH A FILM OF POLYCARBONATE, INTO THE VAGINAL CAVITY; B. WITHDRAWING THE TAMPOND; C. REMOVING THE FILM FROM THE TAMPOND AND PLACING IT ON A SLIDE; D. FIXING AND STAINING THE CELLULAR MATERIAL ON THE FILM; AND E. EXAMINING THE STAINED CELLULAR MATERIAL ON THE SLIDE.
4. The method of claim 3 wherein after step (d) the film is dissolved with an inert solvent before examining the stained cellular material on the slide.
5. The method of claim 4 wherein the solvent is selected from the group consisting of bromoform, chloroform, ethyl dichloride, methylene chloride, and 1,1,2-trichloroethane.
6. The method of claim 5 wherein the solvent is chloroform.
US00440166A 1973-02-15 1974-02-06 Diagnostic tampon and the use thereof for collecting cellular material Expired - Lifetime US3850160A (en)

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US3900030A (en) * 1974-06-10 1975-08-19 Dow Chemical Co Catamenial tampons
EP0018097A2 (en) * 1979-03-23 1980-10-29 The Upjohn Company Medicated device for controlled drug release
US4317454A (en) * 1977-08-04 1982-03-02 Louis Bucalo Methods and devices for obtaining specimens and for signalling when the specimen has been collected
US5231992A (en) * 1990-06-04 1993-08-03 Leon Arnaldo C Low-impact cervical cell and fluid collector
FR2724552A1 (en) * 1994-09-19 1996-03-22 Chaffringeon Bernard DEVICE FOR SINGLE USE OF COLLECTION AND, POSSIBLY, ANALYSIS OF A BODILY LIQUID
WO1996009545A1 (en) * 1994-09-22 1996-03-28 Bernard Chaffringeon Single-use device for detecting or analyzing a body fluid
FR2724837A1 (en) * 1994-09-22 1996-03-29 Chaffringeon Bernard Single-use body fluid device e.g. for detection of woman's fertile period
WO1997043955A1 (en) * 1996-05-17 1997-11-27 A.Fem Medical Corporation Method and apparatus for collecting vaginal fluid and exfoliated vaginal cells for diagnostic purposes
FR2753630A1 (en) * 1996-09-20 1998-03-27 Montmarin Jean Luc De Use of feminine sanitary protection products
US5876389A (en) * 1996-06-24 1999-03-02 Ezy-Detek (Edi) Inc. Sanitary napkins and method for collecting samples of bodily substances
US6168609B1 (en) 1997-09-12 2001-01-02 Deka Products Limited Partners Catamenial collector and methods of use
US6426227B1 (en) * 1999-08-31 2002-07-30 Common Sense Ltd. Method for analyzing secreted bodily fluids
WO2002103356A1 (en) * 2001-06-18 2002-12-27 Alexander Schoenfeld Prophylactic article useful for both protection and diagnosis and method for use and production thereof
WO2003011144A1 (en) * 2001-07-31 2003-02-13 Private Concepts, Inc. Intra-vaginal self-administered cell collecting device and method
US6583722B2 (en) 2000-12-12 2003-06-24 Kimberly-Clark Worldwide, Inc. Wetness signaling device
US6603403B2 (en) 2000-12-12 2003-08-05 Kimberly-Clark Worldwide, Inc. Remote, wetness signaling system
US6719691B2 (en) 2001-07-26 2004-04-13 Common Sense Ltd. Method, device and kit for obtaining biological samples
US20050273036A1 (en) * 2004-06-04 2005-12-08 The Procter & Gamble Company Tampon-and-applicator systems and method for in vitro testing thereof
US20070005039A1 (en) * 2004-06-30 2007-01-04 Jehann Biggs Intravaginal device with controlled expansion
WO2009129773A1 (en) * 2008-04-23 2009-10-29 Merete Medical Gmbh Test device for examining an internal body fluid and packaging thereto
US20090281514A1 (en) * 2008-05-06 2009-11-12 Playtex Products, Inc. Tampon pledget with improved by-pass leakage protection
WO2012118494A1 (en) * 2011-03-01 2012-09-07 Empire Technology Development Llc Menstrual fluid analysis
US8801628B2 (en) 2011-12-29 2014-08-12 Express Scripts, Inc. Methods and systems for medical home testing
WO2014210528A1 (en) * 2013-06-28 2014-12-31 CURRAN, Dennis, R. Endometrial sample collector
US20150065379A1 (en) * 2013-08-29 2015-03-05 Mrinal K. Sanyal Retrieval of Biological Materials from the Human Uterus, Ovary and Cervix by Suction
US20170112477A1 (en) * 2015-10-21 2017-04-27 Boston Scientific Scimed, Inc. Tissue sample device and methods
US20180064425A1 (en) * 2013-08-29 2018-03-08 Mrinal K. Sanyal Retrieval of Biological Materials from the Human Uterus, Ovary and Cervix by Suction
US10118847B2 (en) * 2017-04-11 2018-11-06 Alexander B. Howe Structures for the reduction of water impurities and methods for the deployment thereof
US20200367868A1 (en) * 2013-08-29 2020-11-26 Mrinal K. Sanyal Self-recovery of Preimplantation Stage Human Embryos and Characterization of their Morphological, Physiological and Genomic Features
WO2020260960A1 (en) * 2019-06-28 2020-12-30 Anne's Day Ltd. Vaginal detection methods and kits using a tampon

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Cited By (53)

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Publication number Priority date Publication date Assignee Title
US3900030A (en) * 1974-06-10 1975-08-19 Dow Chemical Co Catamenial tampons
US4317454A (en) * 1977-08-04 1982-03-02 Louis Bucalo Methods and devices for obtaining specimens and for signalling when the specimen has been collected
EP0018097A2 (en) * 1979-03-23 1980-10-29 The Upjohn Company Medicated device for controlled drug release
EP0018097A3 (en) * 1979-03-23 1981-09-23 The Upjohn Company Medicated device for controlled drug release
US5231992A (en) * 1990-06-04 1993-08-03 Leon Arnaldo C Low-impact cervical cell and fluid collector
US5810745A (en) * 1994-09-19 1998-09-22 Chaffringeon; Bernard Single-use body fluid analysis device
WO1996009544A1 (en) * 1994-09-19 1996-03-28 Bernard Chaffringeon Single-use body fluid analysis device
FR2724552A1 (en) * 1994-09-19 1996-03-22 Chaffringeon Bernard DEVICE FOR SINGLE USE OF COLLECTION AND, POSSIBLY, ANALYSIS OF A BODILY LIQUID
WO1996009545A1 (en) * 1994-09-22 1996-03-28 Bernard Chaffringeon Single-use device for detecting or analyzing a body fluid
FR2724837A1 (en) * 1994-09-22 1996-03-29 Chaffringeon Bernard Single-use body fluid device e.g. for detection of woman's fertile period
US5823954A (en) * 1994-09-22 1998-10-20 Chaffringeon; Bernard Single-use device for detecting or analyzing a body fluid
WO1997043955A1 (en) * 1996-05-17 1997-11-27 A.Fem Medical Corporation Method and apparatus for collecting vaginal fluid and exfoliated vaginal cells for diagnostic purposes
US5725481A (en) * 1996-05-17 1998-03-10 A. Fem Medical Corporation Method and apparatus for collecting vaginal fluid and exfoliated vaginal cells for diagnostic purposes
US6007498A (en) * 1996-05-17 1999-12-28 A.Fem Medical Corporation Method and apparatus for collecting vaginal fluid and exfoliated vaginal cells for diagnostic purposes
US6174293B1 (en) 1996-05-17 2001-01-16 A-Fem Medical Corporation Method and apparatus for collecting vaginal fluid and exfoliated vaginal cells for diagnostic purposes
GB2329843A (en) * 1996-05-17 1999-04-07 A Fem Medical Corp Method and apparatus for collecting vaginal fluid and exfoliated vaginal cells for diagnostic purposes
GB2329843B (en) * 1996-05-17 2000-10-18 A Fem Medical Corp Method and apparatus for collecting vaginal fluid and exfoliated vaginal cells for diagnostic purposes
US6689114B2 (en) 1996-06-24 2004-02-10 Ezy-Detek (Edi, Inc.) Sanitary napkin and method for collecting samples of bodily substances
US6627790B2 (en) 1996-06-24 2003-09-30 Exy-Detek (Edi) Inc. Sanitary napkin and method for collecting samples of bodily substances
US5876389A (en) * 1996-06-24 1999-03-02 Ezy-Detek (Edi) Inc. Sanitary napkins and method for collecting samples of bodily substances
WO1999047121A1 (en) * 1996-09-20 1999-09-23 Montmarin Jean Luc De Use of external or internal feminine absorbent articles as support for therapeutic or diagnostic agents
FR2753630A1 (en) * 1996-09-20 1998-03-27 Montmarin Jean Luc De Use of feminine sanitary protection products
US6168609B1 (en) 1997-09-12 2001-01-02 Deka Products Limited Partners Catamenial collector and methods of use
US6426227B1 (en) * 1999-08-31 2002-07-30 Common Sense Ltd. Method for analyzing secreted bodily fluids
US6583722B2 (en) 2000-12-12 2003-06-24 Kimberly-Clark Worldwide, Inc. Wetness signaling device
US6603403B2 (en) 2000-12-12 2003-08-05 Kimberly-Clark Worldwide, Inc. Remote, wetness signaling system
WO2002103356A1 (en) * 2001-06-18 2002-12-27 Alexander Schoenfeld Prophylactic article useful for both protection and diagnosis and method for use and production thereof
US20040231676A1 (en) * 2001-06-18 2004-11-25 Alexander Schoenfeld Prophylactic article useful for both protection and diagnosis and method for use and production thereof
US6719691B2 (en) 2001-07-26 2004-04-13 Common Sense Ltd. Method, device and kit for obtaining biological samples
WO2003011144A1 (en) * 2001-07-31 2003-02-13 Private Concepts, Inc. Intra-vaginal self-administered cell collecting device and method
US6702759B2 (en) * 2001-07-31 2004-03-09 Private Concepts, Inc. Intra-vaginal self-administered cell collecting device and method
US20040153000A1 (en) * 2001-07-31 2004-08-05 Private Concepts, Inc. Intra-vaginal self-administered cell collecting device and method
US6936013B2 (en) 2001-07-31 2005-08-30 Private Concepts, Inc. Intra-vaginal self-administered cell collecting device and method
US20050273036A1 (en) * 2004-06-04 2005-12-08 The Procter & Gamble Company Tampon-and-applicator systems and method for in vitro testing thereof
US7213466B2 (en) * 2004-06-04 2007-05-08 The Procter & Gamble Company Tampon-and-applicator systems and method for in vitro testing thereof
US20070005039A1 (en) * 2004-06-30 2007-01-04 Jehann Biggs Intravaginal device with controlled expansion
US8702670B2 (en) * 2004-06-30 2014-04-22 Mcneil-Ppc, Inc. Intravaginal device with controlled expansion
WO2009129773A1 (en) * 2008-04-23 2009-10-29 Merete Medical Gmbh Test device for examining an internal body fluid and packaging thereto
US20090281514A1 (en) * 2008-05-06 2009-11-12 Playtex Products, Inc. Tampon pledget with improved by-pass leakage protection
WO2012118494A1 (en) * 2011-03-01 2012-09-07 Empire Technology Development Llc Menstrual fluid analysis
US8911988B2 (en) 2011-03-01 2014-12-16 Empire Technology Development Llc Menstrual fluid analysis
US8801628B2 (en) 2011-12-29 2014-08-12 Express Scripts, Inc. Methods and systems for medical home testing
US9144420B2 (en) 2013-06-28 2015-09-29 Innova-Tech, Llc Endometrial sample collector
WO2014210528A1 (en) * 2013-06-28 2014-12-31 CURRAN, Dennis, R. Endometrial sample collector
US9549714B2 (en) 2013-06-28 2017-01-24 Innova-Tech, Llc Endometrial sample collector
US20150065379A1 (en) * 2013-08-29 2015-03-05 Mrinal K. Sanyal Retrieval of Biological Materials from the Human Uterus, Ovary and Cervix by Suction
US9808225B2 (en) * 2013-08-29 2017-11-07 Mrinal K. Sanyal Retrieval of biological materials from the human uterus, ovary and cervix by suction
US20180064425A1 (en) * 2013-08-29 2018-03-08 Mrinal K. Sanyal Retrieval of Biological Materials from the Human Uterus, Ovary and Cervix by Suction
US10751031B2 (en) * 2013-08-29 2020-08-25 Mrinal K. Sanyal Retrieval of biological materials from the human uterus, ovary and cervix by suction
US20200367868A1 (en) * 2013-08-29 2020-11-26 Mrinal K. Sanyal Self-recovery of Preimplantation Stage Human Embryos and Characterization of their Morphological, Physiological and Genomic Features
US20170112477A1 (en) * 2015-10-21 2017-04-27 Boston Scientific Scimed, Inc. Tissue sample device and methods
US10118847B2 (en) * 2017-04-11 2018-11-06 Alexander B. Howe Structures for the reduction of water impurities and methods for the deployment thereof
WO2020260960A1 (en) * 2019-06-28 2020-12-30 Anne's Day Ltd. Vaginal detection methods and kits using a tampon

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