Class dissolution

Medicine Highest oral strength according to WHO Essential Medicines List" Solubility Permeability BCS class Dissolution test (for biowaiver)" Potential risks Indication(s) according to WHO Essential Medicines List" Comments and special dosage form indications"... 

Broadly speaking, melt extrusion is used to produce pharmaceutical products that can be broken down into four application classes dissolution-enhanced prodncts, controlled released prodncts, foamed products, and shaped delivery systems. The subsequent sections describe the design of drug products to achieve the desired controlled release characteristics. 

Compounds which dissolve in concentrated sulphuric acid may be further subdivided into those which are soluble in syrupy phosphoric acid (A) and those which are insoluble in this solvent (B) in general, dissolution takes place without the production of appreciable heat or colour. Those in class A include alcohols, esters, aldehydes, methyl ketones and cyclic ketones provided that they contain less than nine carbon atoms. The solubility limit is somewhat lower than this for ethers thus re-propyl ether dissolves in 85 per cent, phosphoric acid but re-butyl ether and anisole do not. Ethyl benzoate and ethyl malonate are insoluble. 

Suitable inlets commonly used for liquids or solutions can be separated into three major classes, two of which are discussed in Parts A and C (Chapters 15 and 17). The most common method of introducing the solutions uses the nebulizer/desolvation inlet discussed here. For greater detail on types and operation of nebulizers, refer to Chapter 19. Note that, for all samples that have been previously dissolved in a liquid (dissolution of sample in acid, alkali, or solvent), it is important that high-purity liquids be used if cross-contamination of sample is to be avoided. Once the liquid has been vaporized prior to introduction of residual sample into the plasma flame, any nonvolatile impurities in the liquid will have been mixed with the sample itself, and these impurities will appear in the results of analysis. The problem can be partially circumvented by use of blanks, viz., the separate examination of levels of residues left by solvents in the absence of any sample. 

Positive-Tone Photoresists based on Dissolution Inhibition by Diazonaphthoquinones. The intrinsic limitations of bis-azide—cycHzed mbber resist systems led the semiconductor industry to shift to a class of imaging materials based on diazonaphthoquinone (DNQ) photosensitizers. Both the chemistry and the imaging mechanism of these resists (Fig. 10) differ in fundamental ways from those described thus far (23). The DNQ acts as a dissolution inhibitor for the matrix resin, a low molecular weight condensation product of formaldehyde and cresol isomers known as novolac (24). The phenoHc stmcture renders the novolac polymer weakly acidic, and readily soluble in aqueous alkaline solutions. In admixture with an appropriate DNQ the polymer s dissolution rate is sharply decreased. Photolysis causes the DNQ to undergo a multistep reaction sequence, ultimately forming a base-soluble carboxyHc acid which does not inhibit film dissolution. Immersion of a pattemwise-exposed film of the resist in an aqueous solution of hydroxide ion leads to rapid dissolution of the exposed areas and only very slow dissolution of unexposed regions. In contrast with crosslinking resists, the film solubiHty is controUed by chemical and polarity differences rather than molecular size. 

On dissolution in water, peroxohydrates Hberate hydrogen peroxide into solution. Some peroxo salts also Hberate hydrogen peroxide when dissolved in water, and before the introduction of x-ray crystallography, compounds within these classes were often confused with each other. 

The first three classes are called available chlorine compounds and are related to chlorine by the equilibria in equations 1—4. These equilibria are rapidly established in aqueous solution (6), but the dissolution of some hypochlorite salts and A/-chloro compounds can be quite slow. 

In addition to simple dissolution, ionic dissociation and solvolysis, two further classes of reaction are of pre-eminent importance in aqueous solution chemistry, namely acid-base reactions (p. 48) and oxidation-reduction reactions. In water, the oxygen atom is in its lowest oxidation state (—2). Standard reduction potentials (p. 435) of oxygen in acid and alkaline solution are listed in Table 14.10- and shown diagramatically in the scheme opposite. It is important to remember that if or OH appear in the electrode half-reaction, then the electrode potential will change markedly with the pH. Thus for the first reaction in Table 14.10 O2 -I-4H+ -I- 4e 2H2O, although E° = 1.229 V,... 

This PUCI3 also acts as a salt-phase buffer to prevent dissolution of trace impurities in the metal feed by forcing the anode equilibrium to favor production (retention) of trace impurities as metals, instead of permitting oxidation of the impurities to ions. Metallic impurities in the feed fall into two classes, those more electropositive and those less electropositive than plutonium. Since the cell is operated at temperatures above the melting point of all the feed components, and both the liquid anode and salt are well mixed by a mechanical stirrer, chemical equlibrium is established between all impurities and the plutonium in the salt even before current is applied to the cell. Thus, impurities more electropositive than the liquid plutonium anode will be oxidized by Pu+3 and be taken up by the salt phase, while impurities in the electrolyte salt less electropositive than plutonium will be reduced by plutonium metal and be collected in the anode. 

Scientists initially approached structure-function relationships in proteins by separating them into classes based upon properties such as solubility, shape, or the presence of nonprotein groups. For example, the proteins that can be extracted from cells using solutions at physiologic pH and ionic strength are classified as soluble. Extraction of integral membrane proteins requires dissolution of the membrane with detergents. 

The principal member of the first class is tributyl phosphate (TBP). It is convenient to use this organic reagent in the refining of yellow cake consequent to nitric acid dissolution. After dilution, the solution is subjected to filtration through vacuum filters prior to intro-... 

While most polymer/additive analysis procedures are based on solvent or heat extraction, dissolution/precipita-tion, digestions or nondestructive techniques generally suitable for various additive classes and polymer matrices, a few class-selective procedures have been described which are based on specific chemical reactions. These wet chemical techniques are to be considered as isolated cases with great specificity. 

From the characteristics of the methods, it would appear that FD-MS can profitably be applied to poly-mer/additive dissolutions (without precipitation of the polymer or separation of the additive components). The FD approach was considered to be too difficult and fraught with inherent complications to be of routine use in the characterisation of anionic surfactants. The technique does, however, have a niche application in the area of nonpolar compound classes such as hydrocarbons and lubricants, compounds which are difficult to study using other mass-spectrometry ionisation techniques. 

Drugs in Class II have low aqueous solubility (but high membrane permeability), and any factor affecting dissolution rate would be expected to have an impact on the absorption of such compounds. Factors that are noted in Fig. 11, such as fluid pH, volume and viscosity, and bile secretion (especially in response to fatty foods), might be expected to play a role in dissolution rate and thereby affect absorption. Compounds that fall into this class include carbamazepine, cyclosporin, digoxin, griseofulvin, and spironolactone. Food would be expected to exert a potentially significant affect on... 

These mixing motions will tend to improve drug absorption for two reasons. Any factor that increases rate of dissolution will increase the rate (and possibly the extent) of absorption, especially for poorly water-soluble drugs (BCS Classes II and IV). Since rate of dissolution depends on agitation intensity, mixing movements will tend to increase dissolution rate and thereby influence absorption. As rate of absorption depends directly on membrane surface area, and since mixing increases the contact area between drug and... 

Class III recalls are those that involve violations of the law, but for which a health hazard is remote. Examples in this case include insect parts or droppings in flour, the marketing of a product without an approved NDA, unacceptable disintegration or dissolution of tablets, or swollen cans of certain food products [23],... 

The rapid dissolution class boundary is defined in terms of the in vitro dissolution being greater than 85% in 30 min in 900 mL aqueous media at pH 1, 4.5, and 6.8, using USP Apparatus I (100 rpm) or Apparatus II [50 rpm (revolutions/min)] [104]. A similar guideline has been introduced in the European Union [105]. Examples of molecules from the various four classes are presented in Fig. 2.9 [102,104]. 

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