US2408818A - Medicated surgical dressings - Google Patents
Medicated surgical dressings Download PDFInfo
- Publication number
- US2408818A US2408818A US423475A US42347541A US2408818A US 2408818 A US2408818 A US 2408818A US 423475 A US423475 A US 423475A US 42347541 A US42347541 A US 42347541A US 2408818 A US2408818 A US 2408818A
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- Prior art keywords
- sulfa
- compound
- surgical
- gauze
- dressing
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- Expired - Lifetime
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- 150000001875 compounds Chemical class 0.000 description 66
- 239000000463 material Substances 0.000 description 38
- 239000004753 textile Substances 0.000 description 18
- 206010052428 Wound Diseases 0.000 description 16
- 208000027418 Wounds and injury Diseases 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- 238000010410 dusting Methods 0.000 description 11
- 230000001954 sterilising effect Effects 0.000 description 10
- 238000010521 absorption reaction Methods 0.000 description 9
- 238000005470 impregnation Methods 0.000 description 8
- 238000004659 sterilization and disinfection Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 229920000609 methyl cellulose Polymers 0.000 description 7
- 239000001923 methylcellulose Substances 0.000 description 7
- 235000010981 methylcellulose Nutrition 0.000 description 7
- SKIVFJLNDNKQPD-UHFFFAOYSA-N sulfacetamide Chemical compound CC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 SKIVFJLNDNKQPD-UHFFFAOYSA-N 0.000 description 7
- 229960002673 sulfacetamide Drugs 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- 238000011065 in-situ storage Methods 0.000 description 6
- 238000002386 leaching Methods 0.000 description 6
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 6
- 229940124530 sulfonamide Drugs 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- 229920003086 cellulose ether Polymers 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Natural products CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000001856 Ethyl cellulose Substances 0.000 description 3
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 3
- 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 3
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 3
- 229920001249 ethyl cellulose Polymers 0.000 description 3
- 235000019325 ethyl cellulose Nutrition 0.000 description 3
- 230000002070 germicidal effect Effects 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000002421 anti-septic effect Effects 0.000 description 2
- 230000003385 bacteriostatic effect Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 150000007529 inorganic bases Chemical class 0.000 description 2
- OKJPEAGHQZHRQV-UHFFFAOYSA-N iodoform Chemical compound IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000007530 organic bases Chemical class 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 1
- 206010021143 Hypoxia Diseases 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 229920006063 Lamide® Polymers 0.000 description 1
- 229920003091 Methocel™ Polymers 0.000 description 1
- 208000002565 Open Fractures Diseases 0.000 description 1
- -1 Prontosil Red Chemical class 0.000 description 1
- 206010053615 Thermal burn Diseases 0.000 description 1
- 230000003187 abdominal effect Effects 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- JAONZGLTYYUPCT-UHFFFAOYSA-K bismuth subgallate Chemical compound OC(=O)C1=CC(O)=C2O[Bi](O)OC2=C1 JAONZGLTYYUPCT-UHFFFAOYSA-K 0.000 description 1
- 229960000199 bismuth subgallate Drugs 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 208000031513 cyst Diseases 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 230000002439 hemostatic effect Effects 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 206010034674 peritonitis Diseases 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- ABBQGOCHXSPKHJ-WUKNDPDISA-N prontosil Chemical compound NC1=CC(N)=CC=C1\N=N\C1=CC=C(S(N)(=O)=O)C=C1 ABBQGOCHXSPKHJ-WUKNDPDISA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229950008188 sulfamidochrysoidine Drugs 0.000 description 1
- 229960002211 sulfapyridine Drugs 0.000 description 1
- GECHUMIMRBOMGK-UHFFFAOYSA-N sulfapyridine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=CC=CC=N1 GECHUMIMRBOMGK-UHFFFAOYSA-N 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/44—Medicaments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
- A61L2300/404—Biocides, antimicrobial agents, antiseptic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
- A61L2300/432—Inhibitors, antagonists
- A61L2300/434—Inhibitors, antagonists of enzymes
Definitions
- the present invention relates to the manufacture of an improved surgical dressing, and more particularly to a non-dusting medicated sur ical dressing that is especially adapted to supply co trolled and safe amounts of one of the sulfa compounds directly to a wound where it can be effective in creating or maintaining an antiseptic condition and at the same time can be absorbed into the circulation without producing undesired after effects.
- Sulfanilamide and its numerous derivatives and related compounds of high germicidal activity have come to be used to some extent by local application in powdered form in wounds and in the surgical operating field.
- sulfa compounds in powder form in abdominal operations, wher the danger of infectious peritonitis has been greatly reduced by the introduction of, say, 5 grams of a sulfa compound at operation.
- sulfa compounds The local application of sulfa compounds is accompanied by absorption of the compound, which produces as a side effect the distribution of the drug through the circulation. While this effect is by no means undesirable, the sudden absorption of large quantities introduced in solid form often causes the appearance of the sulfa compound in the blood stream in higher quantities than those considered safe. Anoxemia, liver and kidney damage may result.
- the sulfa compound When the sulfa compound is applied in solid form to certain types of Wounds, for instance in pyelonidal cysts, the compound will tend to dissolve rapidly and drain down or away from the wound.
- the present procedure of dusting the powdered sulfa compound into the Wound or field of operation has the further disadvantage that the distribution is not uniform or sufficiently controlled in amount.
- sulfanilamide itself has a relatively low water solubility, only about 0.7% dissolving at room temperature, the amount of the compound that can be introduced into a surgical gauze by means of an aqueous solution is necessarily very limited. If a non-aqueous liquid such as ethyl or methyl alcohol is used, then there is a tendency for the sulfa compound to crystallize out on the fibers of the gauze or other textile material with resultant dusting.
- My invention has for a further object a method of impregnating surgical gauze and similar materials with a sulfa compound and the fixing of the compound in the fibers of th textile material so that it will be released in controlled and regulated amounts when the dressing made therefrom is applied to a wound. At the same time the sulfa compound is prevented from being dissolved away by the moisture present in the conventional sterilizing autoclaving treatment.
- My invention in certain of its broader aspects is based upon my discovery that the relatively water soluble sulfa compounds, such for example as various salts formed by reaction of the sulfa compounds with inorganic or organic bases, for example, sodium hydroxide or diethanolamine, when used in a solution of 2 or higher to impregnate surgical gauze, will be retained within and on the surfaces of the fibers of the textile material to such an extent as to insure a highly satisfactory result when th gauze is used as a surgical dressing.
- the sulfa compounds retained in the gauze show no tendency to dusting on drying and are not washed out or drained away during the autoclaving treatment.
- the amount of sulfa compound that may be retained in the gauze may be markedly increased by adding a small amount of a compound having the effect of increasing the viscosity of the solution.
- This compound should also be selected from those that are inert in respect to the sulfa compound as well as bland in their effect on body tissues or wounds with which they may come in contact on application ofthe surgical auze.
- methyl cellulose serves very well for this purpose, particularly when the sulfa compound is introduced into the gauze in the form of an aqueous solution. When an alcohol solution is used, ethyl cellulose may be added to bring about the desired viscosity and thereby promote retention of the sulfa compound on the fibers of the gauze or dressing material.
- the impregnated gauze may now be strilized like ordinary surgical gauze which is usually autoclaved for 20 minutes with steam at 20 lbs. per square inch. As is customary with the autoclaving of ordinary gauze, here too additional moisture is removed by evacuating the autoclave during the cooling period.
- Various grades of methyl cellulose may be used. The particular methyl cellulose used in my work is a product of the Dow Chemical Commm; of Midland, Michigan, known as Methocel XX High. Methyl cellulose of various other viscosity types may be used with appropriate adjustment of the proportion added so as to insure the desired viscosity in the impregnating solution.
- ethyl cellulose when used in an alcohol solution or other suitable solvent, the ethyl cellulose will be selected from the various viscosity types available and proportioned in the amount added to the solution to insure the desired ultimate viscosity in the impregnating bath.
- a solution may be obtained, for example, by using sodium sulfacet (N -acetyl sulfanilamide) as the sulfa derivative.
- the pH of the impregnating solution may be reduced, preferably to between 7 and 8, by adding thereto a suitable proportion of th corresponding free acidic sulfa compound.
- a course grade surgical gauge was impregnated with sodium sulfacet in a 10% solution containing 0.1% of Methoce] XX High. After impregnating and drying, the dressing had, gained 19% in Weight. Sections of the padsso prepared were set aside before and after autoclaving and extracted with water. They contained 10% of sulfacet by chemical analysis before autoclaving and 12.0% after autoclaving. Using the same impregnating solution on finer surgical gauze material, there was an increase in weight, of about 15% after impregnating and drying, and th impregnated gauze contained 10.8%. and. 13.1% of sulfacet before and after autoclaving, respectively. It will be understoodv that the apparent increase during autoclaving is. due to the more thorough drying resulting from the auto-. claving treatment. It will be understood that the impregnation process may be carried on either as a, continuous or batch process.
- sulfa drugs have a tendency to turn yellow, especially when exposed. to light and air. This may be counteracted by wrapping the impregnated surgical dressing in a light-proof cover, such as colored Cellophane, that will keep out the actinic rays, and. by placing the material in evacuated containers. that the addition of small amounts, e. g., at least about one part to onethou'sand. parts of the sulfa compound, of. sodium sulfite to the impregnating bath serves to prevent discoloration.
- aqueous solutions of the relatively soluble types. of, sulfa compounds as, for example, the sodium and diethanolamine salts of N -acetyl sulfanilamide the sulfa compound stays on the fibers of. the dressing material and shows no tendency to. crystallize and falloff as dust even whenv stored over considerable. periods.
- the relatively'water soluble sulfa compounds While I prefer to. use the relatively'water soluble sulfa compounds, it will be understood that the sulfav compounds. that are less soluble in water, and more particularly the free acid sulfa compounds, may be.used invariousnon-aqueous solutions, especially in ethyl or methyl alcohol solutions of suitabl concentration. When used in such a non-aqueous; medium, a binding or controlling agent suchas methyl cellulose should be added since otherwise there will be a rather marked tendency'for the sulfadrug to crystallize out on the textile material.
- sulfanilamide and its numerous derivatives having germicidal or bacteriostatic properties and produced by substitutions effected either in the ring or in the functional groups, particularly the amide nitrogen, usually referred to as N also germicidally active or bacteriostatic derivatives of these compounds, such as Prontosil Red, where the amino group N is replaced for instance by an azo group which is reconverted in the body to NH2.
- N germicidally active or bacteriostatic derivatives of these compounds, such as Prontosil Red
- sulfa compound as used herein those germicidally active or bateriostatic salts which are formed from the sulfa compounds by reaction with inorganic as well as organic bases, for example, sodium hydroxide or diethanolamine.
- a surgical dressing material comprising a dry textile material havin a feel and flexibility similar to that of untreated surgical gauze and carrying on the fibres thereof an impregnation of a sulfa compound in a proportion at least equalling 5% of the weight of said textile material and a binding agent consisting essentially of a cellulose ether present in an amount sufficient to hold said sulfa compound in situ in said material without leaching during steam sterilization and substantially Without dusting during handling while at the same time permitting gradual absorption of said sulfa compound from the dressing When applied to a wound.
- a surgical dressing material comprising a dry textile material having a feel and flexibility similar to that of untreated surgical gauze and carrying on the fibres thereof an impregnation of a sulfa compound in a proportion between and 20% of the Weight of said textile material and a binding agent consisting essentially of a cellulose ether present in an amount sufficient to hold said sulfa compound in situ in said material without leaching during steam sterilization and substantially without dusting during handling while at the same time permitting gradual absorption of said sulfa compound from the dressing when applied to a wound.
- a surgical dressing material comprising a dry textile material having a feel and flexibility similar to that of untreated surgical gauze and carrying on the fibres thereof an impregnation of a sulfa compound in a proportion at least equalling 5% of the weight of said textile material and a binding agent consisting essentially of methyl cellulose in an amount sufficient to hold said sulfa compound in situ in said material without leaching during steam sterilization and substantially without dusting during handling while at the same time permitting gradual absorption of said sulfa compound from the dressing when applied to a wound.
- a surgical dressing material comprising a dry textile material having a feel and flexibility similar to that of untreated surgical gauze and carrying on the fibres thereof an impregnation of a mixture of an alkaline salt of a sulfa compound and an acid sulfa compound having a pH value of less than 9 when brought into solution in water and said sulfa compound being further associated with a binding agent consisting essentially of a cellulose ether present in an amount suflicient to hold said sulfa compound in situ in said material without leaching during steam sterilization and substantially Without dusting during handling while at the same time permitting gradual absorption of said sulfa compound from the dressin when applied to a wound.
- a surgical dressing material comprising a dry textile material having a feel and flexibility similar to that of untreated surgical gauze and carrying on the fibres thereof an impregnation of sulfanilamide in a proportion at least equalling 5% of the weight of said textile material and a binding agent consisting essentially of a cellulose ether present in an amount suflicient to hold said sulfanilamide in situ in said material without leaching during steam sterilization and substantially without dusting during handling while at the same time permitting gradual absorption of said sulfam'lamide from the dressing when app-lied to a wound.
- a surgical dressing material comprising a dry textile material having a feel and flexibility similar to that of untreated surgical gauze and carrying on th fibres thereof an impregnation of a Water-soluble salt of N -acetyl sulfanilamide in a proportion at least equalling 5% of the weight of said textile material and a binding agent consist-ing essentially of a cellulose ether present in an amount sufficient to hold said salt in situ in said material without leaching during steam sterilization and substantially without dusting during handling while at the same time permitting gradual absorption of said salt from the dressing when applied to a wound.
Description
Patented Oct. 8, 1946' UNITED STATES PATENT OFFICE MEDICATED SURGICAL DRESSINGS No Drawing. Application December 18, 1941, Serial No. 423,475
6 Claims.
The present invention relates to the manufacture of an improved surgical dressing, and more particularly to a non-dusting medicated sur ical dressing that is especially adapted to supply co trolled and safe amounts of one of the sulfa compounds directly to a wound where it can be effective in creating or maintaining an antiseptic condition and at the same time can be absorbed into the circulation without producing undesired after effects.
Sulfanilamide and its numerous derivatives and related compounds of high germicidal activity, hereinafter more particularly defined and usually referred to as sulfa compounds, in addition to their systemic use by peroral and parenteral administration, have come to be used to some extent by local application in powdered form in wounds and in the surgical operating field. Among uch applications, one may especially mention the use of sulfa compounds in powder form in abdominal operations, wher the danger of infectious peritonitis has been greatly reduced by the introduction of, say, 5 grams of a sulfa compound at operation. These compounds have likewise been used locally in the treatment of extensive burns and in compound fractures.
The local application of sulfa compounds is accompanied by absorption of the compound, which produces as a side effect the distribution of the drug through the circulation. While this effect is by no means undesirable, the sudden absorption of large quantities introduced in solid form often causes the appearance of the sulfa compound in the blood stream in higher quantities than those considered safe. Anoxemia, liver and kidney damage may result. When the sulfa compound is applied in solid form to certain types of Wounds, for instance in pyelonidal cysts, the compound will tend to dissolve rapidly and drain down or away from the wound. The present procedure of dusting the powdered sulfa compound into the Wound or field of operation has the further disadvantage that the distribution is not uniform or sufficiently controlled in amount.
I am aware of the earlier use of surgical gauze drenched with ferric chloride for hemostatic purposes or impregnated with iodoform or bismuth subgallate for minor wounds and dressings, but so far as I know no one has previously produced a surgical gauze impregnated with a sulfa compound for use as a medicated surgical dressing. There are several factors that would tend to dis courage the use of a sulfa compound in surgical dressings, among which may be mentioned the fact that in order to introduce an effective amount of the sulfa compound into the dressing the impregnating solution in which the gauze is immersed must carry a high concentration of the sulfa compound. Since sulfanilamide itself has a relatively low water solubility, only about 0.7% dissolving at room temperature, the amount of the compound that can be introduced into a surgical gauze by means of an aqueous solution is necessarily very limited. If a non-aqueous liquid such as ethyl or methyl alcohol is used, then there is a tendency for the sulfa compound to crystallize out on the fibers of the gauze or other textile material with resultant dusting. Judging by the behavior of various of the Water soluble germicides and bacteriostats of the prior art, it was to have been expected that if a relatively water soluble sulfa compound were used instead of the relatively insoluble sulfanilamide, such compound would tend to be dissolved out in sterilizing and after application to various types of draining wounds. A still further deterrent to the use of the sulfa derivatives generally is the tendency of many of them to discolor a textile material when the impregnated textile material is exposed to light and air.
I have found that these apparent obstacles to the use of sulfa compounds in surgical dressings may be overcome in several ways which I will describe below, and it is therefore a principal object of my invention to produce a surgical dressing impregnated with a sulfa compound in an effective amount for direct application to wounds and in other situations where it is desired to effect or maintain antiseptic conditions or to effect direct absorption of th compound into the circulation.
It is a further object to provide a sulfa compound-impregnated surgical dressing which is dry and substantially non-dusting and at the same time retains essentially the feel and flexibility of untreated surgical gauze.
My invention has for a further object a method of impregnating surgical gauze and similar materials with a sulfa compound and the fixing of the compound in the fibers of th textile material so that it will be released in controlled and regulated amounts when the dressing made therefrom is applied to a wound. At the same time the sulfa compound is prevented from being dissolved away by the moisture present in the conventional sterilizing autoclaving treatment.
My invention in certain of its broader aspects is based upon my discovery that the relatively water soluble sulfa compounds, such for example as various salts formed by reaction of the sulfa compounds with inorganic or organic bases, for example, sodium hydroxide or diethanolamine, when used in a solution of 2 or higher to impregnate surgical gauze, will be retained within and on the surfaces of the fibers of the textile material to such an extent as to insure a highly satisfactory result when th gauze is used as a surgical dressing. The sulfa compounds retained in the gauze show no tendency to dusting on drying and are not washed out or drained away during the autoclaving treatment.
I have further found that the amount of sulfa compound that may be retained in the gauze may be markedly increased by adding a small amount of a compound having the effect of increasing the viscosity of the solution. This compound should also be selected from those that are inert in respect to the sulfa compound as well as bland in their effect on body tissues or wounds with which they may come in contact on application ofthe surgical auze. I have found that methyl cellulose serves very well for this purpose, particularly when the sulfa compound is introduced into the gauze in the form of an aqueous solution. When an alcohol solution is used, ethyl cellulose may be added to bring about the desired viscosity and thereby promote retention of the sulfa compound on the fibers of the gauze or dressing material.
By way of example, I have found that a marked improvement in the ability of surgical gauze to retain sulfa compounds is brought about by adding as little as one part per thousand of methyl cellulose to a relatively concentrated aqueous solution of a sulfa compound. Due to the increased viscosity of the solution, it is pos-, sible, by merel soaking the gauze and then subjecting it to gentle wringing comparable to that obtained by wringing the gauze in the hands, to obtain an average increase in the weight of the gauze, of 209%. Hence if a solution carrying two and; one-half parts by Weight of the sulfa compound is used to impregnate the gauze, it, is possible to insure a minimum saturation of around 5% of the sulfa compound. After the soaking and gentle wringing the moisture or other solvent is removed from the padding by evaporation, as for instance by a current of warm air or the use of a warm light such as an infrared lamp, care being taken, however, not to apply sufficient centrifugal or similar mechanical force to remove the solute as well as the solvent. Slight stiffness at this stage may be eliminated by rubbing and working the gauze. The impregnated gauze may now be strilized like ordinary surgical gauze which is usually autoclaved for 20 minutes with steam at 20 lbs. per square inch. As is customary with the autoclaving of ordinary gauze, here too additional moisture is removed by evacuating the autoclave during the cooling period. Various grades of methyl cellulose may be used. The particular methyl cellulose used in my work is a product of the Dow Chemical Commm; of Midland, Michigan, known as Methocel XX High. Methyl cellulose of various other viscosity types may be used with appropriate adjustment of the proportion added so as to insure the desired viscosity in the impregnating solution. Likewise, when ethyl cellulose is used in an alcohol solution or other suitable solvent, the ethyl cellulose will be selected from the various viscosity types available and proportioned in the amount added to the solution to insure the desired ultimate viscosity in the impregnating bath.
Lil
I have further found that the tendency of the treated gauze to become discolored during autoclaving can be overcome by using an impregnating solution having a pH value below 9. Such a solution may be obtained, for example, by using sodium sulfacet (N -acetyl sulfanilamide) as the sulfa derivative. In case th sulfa derivative employed has a higher alkalinity as, for example, one of the more alkaline sodium salts, e. g., the sodium salt of sulfapyridine, the pH of the impregnating solution may be reduced, preferably to between 7 and 8, by adding thereto a suitable proportion of th corresponding free acidic sulfa compound.
Byv following this procedure I have prepared surgical dressings containing as much as 20% by weight of a sulfa compound without altering the appearance and the mechanical properties of the surgical dressing material before and after sterilization. The followin demonstrates that the sulfa compound is not altered by th process, especially by the sterilization;
A course grade surgical gauge was impregnated with sodium sulfacet in a 10% solution containing 0.1% of Methoce] XX High. After impregnating and drying, the dressing had, gained 19% in Weight. Sections of the padsso prepared were set aside before and after autoclaving and extracted with water. They contained 10% of sulfacet by chemical analysis before autoclaving and 12.0% after autoclaving. Using the same impregnating solution on finer surgical gauze material, there was an increase in weight, of about 15% after impregnating and drying, and th impregnated gauze contained 10.8%. and. 13.1% of sulfacet before and after autoclaving, respectively. It will be understoodv that the apparent increase during autoclaving is. due to the more thorough drying resulting from the auto-. claving treatment. It will be understood that the impregnation process may be carried on either as a, continuous or batch process.
Some of the sulfa drugs have a tendency to turn yellow, especially when exposed. to light and air. This may be counteracted by wrapping the impregnated surgical dressing in a light-proof cover, such as colored Cellophane, that will keep out the actinic rays, and. by placing the material in evacuated containers. that the addition of small amounts, e. g., at least about one part to onethou'sand. parts of the sulfa compound, of. sodium sulfite to the impregnating bath serves to prevent discoloration.
Contrary to what might have been expected, I have found that when I have used more or less concentrated. aqueous solutions of the relatively soluble types. of, sulfa compounds as, for example, the sodium and diethanolamine salts of N -acetyl sulfanilamide, the sulfa compound stays on the fibers of. the dressing material and shows no tendency to. crystallize and falloff as dust even whenv stored over considerable. periods.
While I prefer to. use the relatively'water soluble sulfa compounds, it will be understood that the sulfav compounds. that are less soluble in water, and more particularly the free acid sulfa compounds, may be.used invariousnon-aqueous solutions, especially in ethyl or methyl alcohol solutions of suitabl concentration. When used in such a non-aqueous; medium, a binding or controlling agent suchas methyl cellulose should be added since otherwise there will be a rather marked tendency'for the sulfadrug to crystallize out on the textile material.
Where herein the term sulfa compound is I have also found.
used in the specification and claims, it is to be understood as including sulfanilamide and its numerous derivatives having germicidal or bacteriostatic properties and produced by substitutions effected either in the ring or in the functional groups, particularly the amide nitrogen, usually referred to as N also germicidally active or bacteriostatic derivatives of these compounds, such as Prontosil Red, where the amino group N is replaced for instance by an azo group which is reconverted in the body to NH2. I also intend to include within the term sulfa compound as used herein those germicidally active or bateriostatic salts which are formed from the sulfa compounds by reaction with inorganic as well as organic bases, for example, sodium hydroxide or diethanolamine.
It will be understood that where herein I have referred to surgical gauze and surgical dressing material, I mean to include any and all of the textile materials heretofore used for such purposes, such as cotton, wool and the various synthetic fibers. Th impregnation treatment may, of course, be applied to the material at any stage in its manufacture or even after it has been completely converted into one of the conventional forms for use as surgical dressings such as gauze, bandages, packing, absorbent cotton and related products.
I claim:
1. A surgical dressing material comprising a dry textile material havin a feel and flexibility similar to that of untreated surgical gauze and carrying on the fibres thereof an impregnation of a sulfa compound in a proportion at least equalling 5% of the weight of said textile material and a binding agent consisting essentially of a cellulose ether present in an amount sufficient to hold said sulfa compound in situ in said material without leaching during steam sterilization and substantially Without dusting during handling while at the same time permitting gradual absorption of said sulfa compound from the dressing When applied to a wound.
2. A surgical dressing material comprising a dry textile material having a feel and flexibility similar to that of untreated surgical gauze and carrying on the fibres thereof an impregnation of a sulfa compound in a proportion between and 20% of the Weight of said textile material and a binding agent consisting essentially of a cellulose ether present in an amount sufficient to hold said sulfa compound in situ in said material without leaching during steam sterilization and substantially without dusting during handling while at the same time permitting gradual absorption of said sulfa compound from the dressing when applied to a wound.
3. A surgical dressing material comprising a dry textile material having a feel and flexibility similar to that of untreated surgical gauze and carrying on the fibres thereof an impregnation of a sulfa compound in a proportion at least equalling 5% of the weight of said textile material and a binding agent consisting essentially of methyl cellulose in an amount sufficient to hold said sulfa compound in situ in said material without leaching during steam sterilization and substantially without dusting during handling while at the same time permitting gradual absorption of said sulfa compound from the dressing when applied to a wound.
4. A surgical dressing material comprising a dry textile material having a feel and flexibility similar to that of untreated surgical gauze and carrying on the fibres thereof an impregnation of a mixture of an alkaline salt of a sulfa compound and an acid sulfa compound having a pH value of less than 9 when brought into solution in water and said sulfa compound being further associated with a binding agent consisting essentially of a cellulose ether present in an amount suflicient to hold said sulfa compound in situ in said material without leaching during steam sterilization and substantially Without dusting during handling while at the same time permitting gradual absorption of said sulfa compound from the dressin when applied to a wound.
5. A surgical dressing material comprising a dry textile material having a feel and flexibility similar to that of untreated surgical gauze and carrying on the fibres thereof an impregnation of sulfanilamide in a proportion at least equalling 5% of the weight of said textile material and a binding agent consisting essentially of a cellulose ether present in an amount suflicient to hold said sulfanilamide in situ in said material without leaching during steam sterilization and substantially without dusting during handling while at the same time permitting gradual absorption of said sulfam'lamide from the dressing when app-lied to a wound.
6. A surgical dressing material comprising a dry textile material having a feel and flexibility similar to that of untreated surgical gauze and carrying on th fibres thereof an impregnation of a Water-soluble salt of N -acetyl sulfanilamide in a proportion at least equalling 5% of the weight of said textile material and a binding agent consist-ing essentially of a cellulose ether present in an amount sufficient to hold said salt in situ in said material without leaching during steam sterilization and substantially without dusting during handling while at the same time permitting gradual absorption of said salt from the dressing when applied to a wound.
HARRY SOBOTKA.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US423475A US2408818A (en) | 1941-12-18 | 1941-12-18 | Medicated surgical dressings |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US423475A US2408818A (en) | 1941-12-18 | 1941-12-18 | Medicated surgical dressings |
Publications (1)
Publication Number | Publication Date |
---|---|
US2408818A true US2408818A (en) | 1946-10-08 |
Family
ID=23679033
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US423475A Expired - Lifetime US2408818A (en) | 1941-12-18 | 1941-12-18 | Medicated surgical dressings |
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Country | Link |
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US (1) | US2408818A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2464755A (en) * | 1946-07-09 | 1949-03-15 | Vodol Company | Coated gauze |
US2480532A (en) * | 1945-09-05 | 1949-08-30 | Allied Lab Inc | Stabilized 2-sulfanilamido-5-carboxythiazole |
US2804424A (en) * | 1951-04-24 | 1957-08-27 | American Cyanamid Co | Method of preparing a tetracycline type antibiotic-containing wound dressing |
-
1941
- 1941-12-18 US US423475A patent/US2408818A/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2480532A (en) * | 1945-09-05 | 1949-08-30 | Allied Lab Inc | Stabilized 2-sulfanilamido-5-carboxythiazole |
US2464755A (en) * | 1946-07-09 | 1949-03-15 | Vodol Company | Coated gauze |
US2804424A (en) * | 1951-04-24 | 1957-08-27 | American Cyanamid Co | Method of preparing a tetracycline type antibiotic-containing wound dressing |
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