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
  • A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
  • A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
  • A61L2/18—Liquid substances or solutions comprising solids or dissolved gases
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
  • A01N35/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aliphatically bound aldehyde or keto groups, or thio analogues thereof; Derivatives thereof, e.g. acetals
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
  • A61C9/00—Impression cups, i.e. impression trays; Impression methods

Definitions

• rigid impression materials In dentistry, a distinction is made between rigid and elastic impression materials. While rigid impression materials such as plaster, zinc oxide eugenol pastes, waxes and gutta-percha are mainly used to determine the position of the teeth with respect to one another, i.e. to carry out the bite registration, elastic impression materials based on synthetic or natural ones are mainly used for the production of dental models Polymers used in which the solidification is brought about by physical or chemical crosslinking reactions.
• silicones are silicones, polyethers and polysulfides, all of which are cross-linked chemically.
• silicone materials a distinction is made in principle between the condensation-crosslinking silicone compositions (the hardening here is carried out using organic tin or titanium compounds as catalysts which bring about the crosslinking of the starting polysiloxanes after cleavage of end groups); secondly, so-called addition-crosslinking silicone impression compositions are used, in which the curing takes place by reaction of a polysiloxane with vinyl end groups with a polysiloxane with SiH groups using certain platinum catalysts.
• the polyether materials In addition to the polysulfides, the polyether materials also play an important role due to their hydrophilic material properties, since the good wetting possible here means that the dental situation in the mouth can also be reproduced particularly well in an aqueous environment.
• the crosslinking reaction here is based on the polymerization of epimine-terminated polyether prepolymers, which is initiated by sulfonium salt catalysts.
• the most important natural polymers are polymeric carbohydrates, of which the alginates are of the greatest importance. With these materials, water-containing elastic gels are formed in the solidification reaction, and their durability is less than that of the synthetic materials.
• Alginate impression materials are known to provide jaw impressions with sufficient accuracy and are widely used due to their cheap manufacture.
• This impression material is supplied to the user in the form of an alginate-containing powder, which he mixes with a defined amount of water before use.
• the reactants then leave Alginic acid salt and calcium salt in solution, react with each other and form an insoluble, elastic hydrogel.
• a soluble alginic acid salt such as potassium or sodium alginate and a moderately soluble calcium salt such as calcium sulfate
• retarders such as sodium phosphate or sodium pyrophosphate
• fillers such as diatomaceous earth and complex transition metal fluorides such as potassium hexafluorotitanate are generally used.
• compositions of the alginate impression materials can vary in relatively wide ranges. So 10-30% by weight of sodium or potassium alginate, 10-30% by weight of calcium sulfate, 0.5-5% by weight of sodium phosphate and / or sodium pyrophosphate, as well as the rest of the usual fillers, flavorings and thixotropy aids be included. Particularly suitable fillers are diatomaceous earth, sodium or potassium hexafluorotitanate, and zinc oxides.
• impression compounds based on agar-agar are reversible materials (so-called hydrocolloids), which in principle can be used again and again.
• hydrocolloids reversible materials
• the strongly water-containing agar-agar gel is brought into the sol state in a water bath, the impression material is brought into a mouth in a spoon and, by supplying cold water through the spoon, converted back into a solid, elastic state.
• the negative form and the actual model are generally not made by the same person. Rather, after the original has been accepted, the negative form is passed on to a model workshop via more or less long transport routes, where the model is then produced by specially trained personnel becomes. Due to the manufacturing process, the negative form can be contaminated with germs, whereby pathogenic germs cannot be excluded. Contamination with hepatitis viruses represents a particular danger in dentistry. It was therefore proposed very early on to disinfect the negative form before passing it on, in order to rule out any danger to persons who would come into contact with it later.
• the invention therefore relates to a method for disinfecting medical impression materials, in which the impression materials are brought into contact with the aqueous solution of a disinfectant after solidification and removal of the original, characterized in that this solution contains 0.1 to 15 percent by weight of a contains soluble alcohol.
• the new method not only quickly and thoroughly kills all relevant germs and viruses, but also reduces the negative effects on the dimensional accuracy, surface quality and pourability of the negative to such an extent that they no longer interfere in practice. This also applies to polyethers and hydrophilized silicones and even to the extremely sensitive polymeric carbohydrates, especially the alginates, which have found widespread use in dentistry as impression materials.
• the method is usually carried out in such a way that the negative form is immersed in a prepared solution of the disinfectant immediately after removal from the organ to be imaged or, preferably, after a brief rinse with water, so that all possibly contaminated surfaces are wetted by the solution .
• the solution is generally at room temperature, but if the impression material allows it, it can also be disinfected at elevated temperatures.
• the contact times depend on the desired degree of disinfection and are usually at room temperature in the range between 1 and 20 minutes, preferably between 1 and 10 minutes and in particular between 1 and 5 minutes.
• the mold is then removed, usually rinsed again with water and stored in a suitable manner until further use.
• the disinfection does not necessarily have to be carried out after the production of the negative form, but can also be carried out at a later time, if necessary in addition to a disinfection cycle immediately after production.
• the mold can also be sprayed with the active ingredient solution for disinfection.
• the alcohols to be used according to the invention should be water-soluble in the respective use concentration.
• butanediol, butanol, triethylene glycol, polyethylene glycols and mixed polyethylene polypropylene glycols are suitable.
• the alcohols are preferably infinitely miscible with water.
• Alcohols with 1 to 3 C atoms and ether alcohols with 3 to 6 C atoms are therefore preferably used.
• Examples of alcohols with 1 to 3 carbon atoms are ethanol, isopropanol, n-propanol, 1,2-propylene glycol and glycerin.
• Examples of ether alcohols with 3 to 6 carbon atoms are diethylene glycol, triethylene glycol and butyl glycol.
• the addition of the alcohols to the aqueous disinfectant solutions surprisingly results in a far lower impairment of the dimensional accuracy and the surface quality when disinfecting the negative form than can be achieved with purely aqueous solutions or predominantly alcoholic solutions of the disinfectants.
• the concentration of alcohol is generally between about 0.1 and 15 percent by weight, based on the weight of the finished disinfectant solution, preferably between 1 and 10% by weight. The most suitable concentration depends on the type of alcohol and is, for example, about 1% by weight for isopropanol, about 2 to 5% by weight for n-propanol and glycerol, and about 1.2 for propylene glycol 1 to 3% by weight and in the case of ethanol approximately 2 to 6% by weight.
• the disinfectant solutions additionally contain customary disinfectant agents.
• the selection of the active substances and the choice of the concentration is primarily determined by the spectrum of germs to be combated but also by the intended disinfection time.
• suitable broadly active disinfectants are, for example, aldehydes, phenols, quaternary ammonium compounds, biguanides, active hologue compounds and peroxidic compounds, alone or in a suitable combination.
• suitable active substances from these classes are glutaraldehyde, o-phenylphenol, p-chloro-m-cresol, didecyldimethylammonium chloride, benzyldimethylalkylammonium chloride, oligohexamethylene biguanide hydrochloride, hydrogen peroxide and peracetic acid.
• active ingredients with a narrow spectrum of germs, for example fungicides, such as undecylenic acid derivatives.
• Particularly preferred active ingredients for the process according to the invention are aldehydes, in particular succinedialdehyde and glutardialdehyde, and peroxidic compounds.
• concentrations of 0.1 to 10% by weight, preferably 0.5 to 7% by weight, of disinfectant substance are sufficient, but in special cases it is also possible to work outside these limits. If the disinfection readings contain both glutardialdehyde and glyoxal - a preferred embodiment of the invention - these aldehydes are preferred. • - 8 -
• the disinfectant solution preferably contains the two aldehydes in an amount of 0.5 to 7% by weight, in particular 1 to 5% by weight, calculated as the sum of the two aldehydes.
• up to 3% by weight, preferably 0.01 to 2% by weight, of other disinfectant active ingredients can be present, but in many cases the addition of further disinfectant active ingredients can also be dispensed with.
• the disinfectant solutions can contain other customary auxiliary substances.
• surfactants are to be mentioned here, which should facilitate the wetting of the negative form.
• Nonionic and, preferably, anionic surfactants are primarily used, but other types of surfactants can also be used if they are sufficiently compatible with the materials to be disinfected.
• Nonionic surfactants ie in general addition compounds composed of ethylene oxide and long-chain alcohols or phenols, are not alcohols in the context of this invention.
• pH-regulating substances and buffer substances can be present in order to determine the preferred pH of the solution of 2 to 11, especially 3 to 9, safe to set.
• auxiliaries include substances having a sequestering effect, fragrances, dyes, foam inhibitors and hydrotropes, and agents which facilitate the moldability of the negative with gypsum, such as inorganic fluorides, for example a2TiFs.
• the amount of auxiliary substances in the disinfection solution is preferably between 0.01 and 10% by weight and, in particular, between 0.1 and 5% by weight.
• the amount of surfactants preferably makes up 0 to about 1% by weight, in particular 0 to 0.5
• the disinfectant solutions can be prepared from the individual components immediately before application of the method, however
• a disinfectant solution which is particularly suitable for the method according to the invention has the following composition:
• alcohol from the group consisting of ethanol, n-propanol and mixtures thereof,
• aldehyde from the group succinic dialdehyde, glutaraldehyde and mixtures thereof,
• the preferred area of application of the method according to the invention is the disinfection of impression materials in the field of dental and jaw medicine.
• the method is by no means limited to this area, but is also very widely applicable, not least because of the exceptional material compatibility. In no case was it observed that the addition of the alcohols would have restricted the usefulness of the agents also for other disinfection measures.
• aqueous solutions used for the following tests had the following composition (in percent by weight, remainder water):
• the impression was rinsed under a weak stream of tap water for 10 seconds.
• the impression was then poured out with plaster (Moldano, Bayer, Leverkusen, DE).
• plaster Mioldano, Bayer, Leverkusen, DE
• To completely harden the plaster model the model and negative mold were kept in a hygrophor (23 ° +/- 1 ° C, 100% relative atmospheric humidity) for 30 minutes.
• the alginate form was then carefully separated from the gypsum and the gypsum model was measured under the microscope for dimensional changes and examined for surface properties.
• alginate impression material made from water and the product Palgat (from Espe, Seefeld, DE) was mixed in a rubber cup according to the manufacturer's instructions and processed into lenticular test specimens of approximately 22 mm in diameter and 5 mm in thickness by spreading on a spot made of Prozellan ⁇ tet (hardening time 5 minutes). The contamination then took place by placing these bodies in a germ suspension which contained more than 10 nucleating units of Staphylococcus aureus per milliliter.
• the germ carriers were stored in open petri dishes in a desiccator over water for 30 minutes, then placed in the disinfection solution for a certain time (5 or 10 minutes), taking care to ensure complete wetting. To count the still viable germs, the germ carriers were then individually shaken together with 10 g of glass beads for 2 minutes in 20 ml of an inactivation solution and the germ count was then determined from this solution in the usual way by inoculation on agar and broods.

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• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Dentistry (AREA)
• Veterinary Medicine (AREA)
• Epidemiology (AREA)
• Animal Behavior & Ethology (AREA)
• Oral & Maxillofacial Surgery (AREA)
• Wood Science & Technology (AREA)
• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Agronomy & Crop Science (AREA)
• Plant Pathology (AREA)
• Engineering & Computer Science (AREA)
• General Chemical & Material Sciences (AREA)
• Zoology (AREA)
• Environmental Sciences (AREA)
• Dental Preparations (AREA)
• Apparatus For Disinfection Or Sterilisation (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Percussion Or Vibration Massage (AREA)

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• 1989
  • 1989-09-11 DE DE8989116773T patent/DE58904328D1/de not_active Expired - Lifetime
  • 1989-09-11 ES ES89116773T patent/ES2054963T3/es not_active Expired - Lifetime
  • 1989-09-11 WO PCT/EP1989/001052 patent/WO1990003191A1/de active IP Right Grant
  • 1989-09-11 AU AU42187/89A patent/AU628391B2/en not_active Ceased
  • 1989-09-11 BR BR898907663A patent/BR8907663A/pt not_active Application Discontinuation
  • 1989-09-11 US US07/663,818 patent/US5190724A/en not_active Expired - Fee Related
  • 1989-09-11 JP JP1509610A patent/JPH04500617A/ja active Pending
  • 1989-09-11 EP EP89910090A patent/EP0434717A1/de active Pending
  • 1989-09-11 EP EP89116773A patent/EP0360118B1/de not_active Expired - Lifetime
  • 1989-09-15 PT PT91732A patent/PT91732B/pt not_active IP Right Cessation
  • 1989-09-18 MX MX017578A patent/MX172107B/es unknown
  • 1989-09-18 CA CA000611811A patent/CA1322155C/en not_active Expired - Fee Related
• 1991
  • 1991-03-05 NO NO910869A patent/NO178287C/no unknown
  • 1991-03-15 FI FI911296A patent/FI97023C/fi not_active IP Right Cessation
  • 1991-03-18 DK DK199100480A patent/DK173960B1/da not_active IP Right Cessation

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