DE138884C - - Google Patents
Info
- Publication number
- DE138884C DE138884C DENDAT138884D DE138884DA DE138884C DE 138884 C DE138884 C DE 138884C DE NDAT138884 D DENDAT138884 D DE NDAT138884D DE 138884D A DE138884D A DE 138884DA DE 138884 C DE138884 C DE 138884C
- Authority
- DE
- Germany
- Prior art keywords
- antiseptic
- mercury
- compounds
- properties
- organometallic compounds
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 230000002421 anti-septic Effects 0.000 claims description 10
- 229920000742 Cotton Polymers 0.000 claims description 5
- 150000002902 organometallic compounds Chemical class 0.000 claims description 5
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 4
- 229910052753 mercury Inorganic materials 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 2
- 238000005470 impregnation Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 231100000614 Poison Toxicity 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 200000000019 wound Diseases 0.000 description 3
- -1 B. with dermatol Chemical class 0.000 description 2
- OKJPEAGHQZHRQV-UHFFFAOYSA-N Iodoform Chemical compound IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 2
- 229960003172 iodoform Drugs 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 229960004889 salicylic acid Drugs 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N Boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- UKWHYYKOEPRTIC-UHFFFAOYSA-N Mercury(II) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 description 1
- DEJFOJWLSQJEKC-UHFFFAOYSA-N [C-]#N.[Zn+2].[Hg+].[C-]#N.[C-]#N Chemical compound [C-]#N.[Zn+2].[Hg+].[C-]#N.[C-]#N DEJFOJWLSQJEKC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000001266 bandaging Methods 0.000 description 1
- REKWPXFKNZERAA-UHFFFAOYSA-K bismuth;2-carboxyphenolate Chemical compound [Bi+3].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O REKWPXFKNZERAA-UHFFFAOYSA-K 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 231100001010 corrosive Toxicity 0.000 description 1
- 231100000078 corrosive Toxicity 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000003522 irritant Effects 0.000 description 1
- 231100000021 irritant Toxicity 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 230000000622 irritating Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910000474 mercury oxide Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000037390 scarring Effects 0.000 description 1
- 230000001954 sterilising Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- A61L15/46—Deodorants or malodour counteractants, e.g. to inhibit the formation of ammonia or bacteria
-
- 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
- A61L2300/20—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing organic materials
- A61L2300/216—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing organic materials with other specific functional groups, e.g. aldehydes, ketones, phenols, quaternary phosphonium groups
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Hematology (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Materials For Medical Uses (AREA)
Description
PATENTAMT.PATENT OFFICE.
e 138884 KLASSE 30«. e 138884 CLASS 30 «.
Bislang werden antiseptische Verbandstoffe, sei es zum Verbinden von Wunden, sei es zu chirurgischen Operationen im Allgemeinen, in der Weise dargestellt, dafs Stoffe, wie Gaze, "Watte u. s. w , mit Sublimat, Jodoform, Carbolsä'ure, Borsäure, Salicylsäure u. s. w. oder auch in neuerer Zeit mit gewissen metallorganischen Verbindungen, z. B. mit Dermatol, Quecksilberzinkcyanid, mit sulfocarbolsaurem Zink, Wismutsalicylat imprägniert werden. Diese antiseptischen Körper haben jedoch zahlreiche Nachteile:So far, antiseptic bandages are used, be it for bandaging wounds or for closing wounds surgical operations in general, presented in such a way that materials such as gauze, "Cotton wool and so on, with sublimate, iodoform, carbolic acid, boric acid, salicylic acid and so on. Or also more recently with certain organometallic compounds, e.g. B. with dermatol, mercury zinc cyanide, be impregnated with zinc sulfocarbohydrate, bismuth salicylate. These antiseptic However, bodies have numerous disadvantages:
Das Sublimat, wenn es auch einerseits aufserordentliche antiseptische Eigenschaften besitzt, ist andererseits sehr giftig, fällt Eiweifsstoffe und verzögert die Vernarbung von Wunden. Das Jodoform hat einen üblen Geruch. Die Carbolsäure und Salicylsäure haben ätzende und reizende Wirkung; die erste ist sogar giftig. Die erwähnten metallorganischen Verbindungen haben den Nachteil, dafs sie mehr oder weniger unter gewissen Einflüssen, besonders unter Einwirkung der Säuren, zersetzbar sind und das Metall leicht aus denselben ausgeschieden werden kann. Aufserdem besitzen die metallorganischen Verbindungen, ausgenommen die Verbindungen des Quecksilbers,verhältnismäfsig sehr geringe antiseptische Eigenschaften. Dagegen sind die metallorganischen Verbindungen des Quecksilbers, deren Darstellungsverfahren den Gegenstand des Patentes 132660 bildet, durch hervorragende antiseptische Eigenschaften gekennzeichnet und besitzen die vorerwähnten nachteiligen Eigenschaften nicht. Sie sind fast in demselben Grade antiseptisch wie das Sublimat, sind dabei aber nicht giftig, üben keine reizende Wirkung wie Carbolsäure aus, fällen weder Eiweifsstoffe noch organische Flüssigkeiten und haben keinen üblen Geruch. Diese vorteilhaften Eigenschaften lassen diese Verbindungen, welche durch Umsetzung zwischen Quecksilberoxyd und Phenolsulfosäuren, deren Substitutionsproducten und Homologen erhalten werden, als sehr geeignete Mittel zur Bereitung von antiseptischen Verbandstoffen erscheinen.The sublimate, even if it has exceptional antiseptic properties on the one hand, on the other hand, it is very poisonous, it drops proteins and delays the scarring of wounds. The iodoform has a foul odor. The carbolic acid and salicylic acid are corrosive and irritant effect; the first is even poisonous. The organometallic compounds mentioned have the disadvantage that they are more or less subject to certain influences, especially under the action of acids, are decomposable and the metal easily from them can be eliminated. In addition, the organometallic compounds except for the compounds of mercury, comparatively very poor antiseptic properties. They are against it organometallic compounds of mercury, the process of which is the subject matter of patent 132660, characterized by excellent antiseptic properties and do not have the aforementioned disadvantageous properties. You are almost in Antiseptic to the same degree as the sublimate, but are not poisonous, and are not irritating Effect like carbolic acid, neither proteins nor organic liquids precipitate and do not have a foul odor. These beneficial properties make these compounds, which by reaction between mercury oxide and phenol sulfonic acids, their substitution products and homologues are obtained appear to be very suitable means for preparing antiseptic dressings.
Die Bereitung der Verbandstoffe mittels dieser Verbindungen geschieht in folgender Wreise:The preparation of the dressing material by means of these compounds takes place in the following W r ation:
Nach den gewöhnlichen Methoden vorbereitete Watte wird mit einer Lösung der metallorganischen Verbindungen des Quecksilbers imprägniert. Der Ueberschufs der Lösung, deren Konzentration je nach dem Grade Antiseptizität, welche man den Verbandstoffen erteilen will, variieren kann, wird abgeprefst, die Watte im Autoclaven oder in einem Sterilisierofen getrocknet. Cotton wool prepared according to the usual methods is mixed with a solution of organometallic Impregnated compounds of mercury. The excess of the solution, whose Concentration depending on the degree of antisepticity that you want to give the bandages, can vary, is pressed, the cotton is dried in an autoclave or in a sterilization oven.
Die so bearbeitete Watte bildet einen gebrauchsfertigen antiseptischen Verbandstoff.The cotton wool processed in this way forms a ready-to-use antiseptic bandage.
Die Watte kann aber auch durch andere Körper, wie z. B. Gaze u. s. w., ersetzt werden. Man kann auch in der Lösung Fäden für chirurgische Operationen, Kanüleinlagen u. s. w., mit Vorteil präparieren und conservieren, und zwar sowohl auf kaltem Wege als auch in der Weise, dafs man den zu conservierenden Stoff in der Lösung kocht.However, the wadding can also be passed through other bodies, such as Gauze, etc., may be replaced. The solution can also contain threads for surgical operations, cannula inserts, etc., Prepare and conserve with advantage, both in the cold way and in the Make sure that the substance to be preserved is boiled in the solution.
Claims (1)
Verfahren zur Herstellung antiseptischer Verbandstoffe, gekennzeichnet durch die Imprägnierung von Watte, Gaze oder dergl. vermittelst der durch das Patent 132660 geschützten metallorganischen, mit antiseptischen Eigenschaften ausgestatteten Verbindungen des Quecksilbers. Patent claim:
Process for the production of antiseptic bandages, characterized by the impregnation of cotton wool, gauze or the like by means of the organometallic compounds of mercury protected by patent 132660 and endowed with antiseptic properties.
Publications (1)
Publication Number | Publication Date |
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DE138884C true DE138884C (en) |
Family
ID=406661
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT138884D Active DE138884C (en) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE138884C (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2423121A (en) * | 1942-05-16 | 1947-07-01 | Frank J Sowa | Reaction product of phenyl mercury salts with hydroxy alkyl amino compounds and their preparation |
DE762285C (en) * | 1938-07-15 | 1952-10-20 | Waldhof Zellstoff Fab | Process for maintaining the absorbency of pulp |
-
0
- DE DENDAT138884D patent/DE138884C/de active Active
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE762285C (en) * | 1938-07-15 | 1952-10-20 | Waldhof Zellstoff Fab | Process for maintaining the absorbency of pulp |
US2423121A (en) * | 1942-05-16 | 1947-07-01 | Frank J Sowa | Reaction product of phenyl mercury salts with hydroxy alkyl amino compounds and their preparation |
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