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Desensitization—

Our experiments show that it is possible to obtain a general desensitisation by repeated applications to a very small surface nipple) .  [Pg.63]

What occurs on the nipples of guinea pigs (previously sensitized by the usual method) which receive multiple applications of 0.1% DNCB in acetone  [Pg.63]

To summarize, after 40 applications to one of the nipples, there is no general desensitisa-tion, but a local desensitisution on the treated nipple (N. Hunziker, 1961). It is not the acanthosis which has prevented the appearance of the lesions, since, as we have already stated (p. 19) acanthosis of the nipple due to estrogens does not prevent the appearance of spongiosis. [Pg.63]

For the present, we can say that there is a local desensitization , but we do not yet know whether or not it is specific. [Pg.63]

Fig- 34. Guinea pig sensitized to DNCB. Left nipple after 40 daily applications of 0.1% DNCB in acetone acanthosis, no spongiosis [Pg.64]


Sensitizers as well as desensitizers form a reversal oxidoreduction system with silver halides, according to both pH and pAg of the photographic emulsion. But besides the specific influence of the emulsion, the efficiency of a sensitizing dye depends on many other factors such as its adsorption, its spectral absorption, the energetic transfer yield, the dye aggregate to the silver halide, and finally on its desensitizing property in... [Pg.78]

Both RDX and HMX are substantially desensitized by mixing with TNT to form cyclotols (RDX) and octols (HMX) or by coating with waxes, synthetic polymers, and elastomeric biaders. Most of the RDX made ia the United States is converted to Composition B (60% RDX, 40% TNT, 1 part wax added). Composition A5 (RDX 98.5/stearic acid 1.5) and composition C4 (RDX91/nonexplosive plasticizer) account for the next largest uses. HMX is used as a propellant and ia maximum-performance plastic bonded explosives such as PBX 9401 and PBX N5 and the octols (147—150). [Pg.16]

The incorporation of aluminum increases the blast effect of explosives but decreases the rates of detonation, fragmentation effectiveness, and shaped charge performance. Mixes with aluminum are made by first screening finely divided aluminum, adding it to a melted RDX—TNT slurry, and stirring until the mix is uniform. A desensitizer and calcium chloride may be incorporated, and the mixture cooled to ca 85°C then poured. Typical TNT-based aluminized explosives are the tritonals (TNT + Al), ammonals (TNT, AN, Al), minols (TNT, AN, Al) torpexes and HBXs (TNT, RDX, Al) (Table 14) (223-226). [Pg.20]

C. Boyars, "Sensitivity and Desensitization of Nitroglycerin," ia Proceedings of 2nd Symposium on Chemical Problems Connected with the Stability of... [Pg.27]

Gun Propellents. Low sensitivity gun propeUants, often referred to as LOVA (low vulnerabUity ammunition), use RDX or HMX as the principal energy components, and desensitizing binders such as ceUulose acetate butyrate or thermoplastic elastomers (TPE) including poly acetal—polyurethane block copolymers, polystyrene—polyacrjiate copolymers, and glycidyl azide polymers (GAP) to provide the required mechanical... [Pg.40]

Decomposition Hazards. The main causes of unintended decompositions of organic peroxides are heat energy from heating sources and mechanical shock, eg, impact or friction. In addition, certain contaminants, ie, metal salts, amines, acids, and bases, initiate or accelerate organic peroxide decompositions at temperatures at which the peroxide is normally stable. These reactions also Hberate heat, thus further accelerating the decomposition. Commercial products often contain diluents that desensitize neat peroxides to these hazards. Commercial organic peroxide decompositions are low order deflagrations rather than detonations (279). [Pg.132]

The organic peroxides and peroxide compositions produced commercially are those that can be manufactured, shipped, stored, and used safely. Organic peroxides can be thermally and mechanically desensitized by wetting or by dilution with suitable solvents, iaert soHd fillers, or iasoluble Hquids (suspension of soHd peroxides ia Hquid plasticizers or water, and emulsions of Hquid peroxides ia water). [Pg.132]

There are probably several processes that contribute to the total desensitization process and these may be directed homologously (to own receptor) or heterologously (to other receptor). Additionally, the induences may be directed at the receptor itself and affect only that receptor, ie, specific desensitization, or may affect other receptor processes as well, ie, nonspecific desensitization. [Pg.282]

According to the electron-transfer mechanism of spectral sensitization (92,93), the transfer of an electron from the excited sensitizer molecule to the silver haHde and the injection of photoelectrons into the conduction band ate the primary processes. Thus, the lowest vacant level of the sensitizer dye is situated higher than the bottom of the conduction band. The regeneration of the sensitizer is possible by reactions of the positive hole to form radical dications (94). If the highest filled level of the dye is situated below the top of the valence band, desensitization occurs because of hole production. [Pg.496]

The opposite phenomenon, a decrease of sensitivity, is known as desensitization. The main reasons for densensitization ate the results of relative electron level positions as weU as the secondary processes of the photoelectrons, for example (97),... [Pg.496]

Aerosol adniinistration of isoproterenol produces a prompt (2—5 minutes) intense bronchodilatation of relatively short (1 h) duration. The lack of P2-selectivity leads, in many cases, to tachycardia and blood pressure elevation. Also, use of isoproterenol, like all other known P-agonists, results in a down-regulation, or desensitization, of P-adrenergic receptors. This desensitization is only partial, and after time (depending on dose, patient, and agent), a stable, less responsive state is achieved in which P-agonists remain effective. Isoproterenol has been widely used for many years. [Pg.439]

The distinctive odor of trichloroethylene may not necessarily provide adequate warning of exposure, because it quickly desensitizes olfactory responses. EataUties have occurred when unprotected workers have entered unventilated areas with high vapor concentrations of trichloroethylene or other chlorinated solvents. Eor a complete description of proper entry to vessels containing any chlorinated solvent, see ASTM D4276-84, Standard Practice for Confined Area Entry (34). [Pg.25]

Health and Safety. Cinnamyl alcohol has been evaluated by FEMA and given GRAS status (FEMA No. 2294). Two of its esters, cinnamyl cinnamate (FEMA No. 2298) and cinnamyl acetate (FEMA No. 2293), ate also used extensively in flavor and fragrance compositions. Cinnamyl alcohol has also been tested by RIFM (48) and found to be safe for use. There have been reported cases of irritation and several manufacturers market a desensitized alcohol for use in fragrance appHcations. [Pg.176]

A good sensitizing dye does not interfere with other system properties. Sensitizing dyes can sometimes influence the intrinsic response of a chemically sensitized emulsion, leading to desensitization or additional sensitization. The dye can also interfere with development rate, increase or decrease unwanted fog density, and remain as unwanted stain in the film after processing. The dye should have adequate solubihty for addition to the emulsion, but should not wander between layers in the final coating. [Pg.470]

Some alicyclic 1,2-diamine derivatives have recently been shown to have interesting CNS properties. For example, eclanamine (34) is an antidepressant with a rapid onset of action. The reasons for its potency are not as yet clear but pharmacologists note that the drug desensitizes adrenergic alpha-2 receptors and antagonizes the actions of clonidine. The synthesis of eclanamine starts with attack of cyclopentene oxide (30) by dimethylamine (to give 31). This product is converted to the mesylate by reaction with sodium hydride followed by mesyl chloride. Attack of... [Pg.5]

Phlegnia, n. phlegm, phlegmatisieren, v.t. (Expl.) desensitize, phlobaphenldsend, a. dissolving phloba-phenes. [Pg.339]


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Acetylcholine desensitization

Acetylcholine receptors desensitization

Admixtures, desensitizing

Adrenergic receptor desensitization

Agonist desensitization induced

Allergic drug reactions desensitization

Allergic reactions desensitization

Allopurinol desensitization

Antibiotics desensitization

Aspirin desensitization

Asthma desensitization

Autoreceptors desensitization

CXCR4 receptor desensitization

Cannabinoid receptor desensitization

Capsaicin desensitization

Capsaicin desensitization effects

Chemokine desensitization

Cutaneous reactions desensitization

Desensitization NSAIDs

Desensitization and Resensitization

Desensitization block

Desensitization by Preshocking

Desensitization definition

Desensitization duration

Desensitization general

Desensitization initiation

Desensitization local

Desensitization nicotinic acetylcholine receptor

Desensitization of Drug-Allergic Patients

Desensitization of receptors

Desensitization phenomenon

Desensitization vancomycin

Desensitization variability

Desensitized

Desensitized Composition

Desensitizers

Desensitizers

Desensitizing

Desensitizing

Desensitizing agents

Desensitizing gums

Drug-allergic patients desensitization

Exposure Intervention and Systematic Desensitization

Eye movement desensitization and reprocessing

Eye-movement desensitization reprocessing

Heterologous desensitization

Homologous desensitization

Insulin Desensitization

Metabotropic glutamate receptors desensitization

Model based on desensitization of the cAMP receptor

Neuronal nicotinic acetylcholine receptors desensitization

Nitroglycerin mixture, desensitized, solid

Opioid receptor desensitization

Opioid-chemokine receptor interaction desensitization

Opioids desensitization

Penicillin desensitization

Penicillins allergy desensitization

Pentaerythritol tetranitrate desensitized PETN

Pharmacodynamics receptor desensitization

Prostacyclin desensitization

Receptor Desensitization and Down-Regulation

Receptor Desensitization, Internalization, and Recycling

Receptor-class desensitization

Receptors desensitization

Reversal of desensitization

Sensitivity desensitize

Sensitization desensitization

Sensitizing dyes desensitization

Signal transduction desensitization

Solid desensitized explosives

Switching Off and Desensitization of 7-Helix Transmembrane Receptors

Systematic desensitization

Tolerance and Desensitization

Trafficking desensitization, internalization

Trimethoprim-sulfamethoxazole desensitization

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