Pharmaceuticals water-solubility

Pharmaceutical Water-soluble coating for tablets Suspending agent to inhibit settling of ceramic lotion... 

Considerable interest has been shown ia poly(ethylene oxide) for diverse appHcations ia food, drug, and cosmetic products. Such uses fall within the scope of the Federal Food, Dmg, and Cosmetic Act. The U.S. FDA has recognized and approved the use of poly(ethylene oxide) for specific food and food packaging uses. USP/NF-grades of Polyox water-soluble resins (Union Carbide Corp.) are available for pharmaceutical appHcations. 

Cross-linked versions of water-soluble polymers swollen in aqueous media are broadly referred to as hydrogels (52) and have a growing commercial utility in such apphcations as oxygen-permeable soft contact lenses (qv) (53) (Table 4) and controUed-release pharmaceutical dmg deflvery devices (54). Cross-linked PVP and selected copolymers fit this definition and are of interest because of the following stmcture/performance characteristics ... 

Other apphcations for VP/VA copolymers are uses as water-soluble or remoistenable hot melt adhesives (140), pharmaceutical tablet coatings, binders, and controUed-release substrates. 

Carmine [1390-65-4] is the trade name for the aluminum lake of the red anthraquinone dye carminic acid obtained from the cochineal bug. The dye is obtained from the powdery form of cochineal by extraction with hot water, the extracts treated with aluminum salts, and the dye precipitated from the solution by the addition of ethanol. This water-soluble bright red dye is used for coloring shrimp, pork sausages, pharmaceuticals, and cosmetics. It is the only animal-derived dye approved as a colorant for foods and other products. 

Ascorbic acid commonly known as vitamin C, is one of the most important water soluble vitamins. Ascorbic acid is involved in many biological processes and it is an essential compound in the human diet [1]. The determination of ascorbic acid has gained increase significance in pharmaceutic, clinical, and food applications. So far, different methods have been developed for determination of ascorbic acid [2, 3]. 

A number of water-soluble cellulose ethers are marketed." Methyl cellulose is prepared by a method similar to that used for ethyl cellulose. A degree of substitution of 1.6-1.8 is usual since the resultant ether is soluble in cold water but not in hot. It is used as a thickening agent and emulsifier in cosmetics, as a paper size, in pharmaceuticals, in ceramics and in leather tanning operations. 

The first clinical trials were performed in the 1970 s using a sodium salt derivative with an open E-ting (Fig. 1). However, the clinical efficacy was limited and severe bladder toxicity led to the termination of the clinical trials. The poor efficacy of the camptothecin sodium salt in those clinical trials was probably due to the fact that the open E-ring form of camptothecin (carboxylate derivative) is inactive as a Topi inhibitor. Following the identification of Topi as a target of camptothecin, water-soluble derivatives were produced by the pharmaceutical industry. Two of these water-soluble derivatives have been approved by the FDA for cancer treatment in the early 2000s topotecan and irinotecan. 

Cellulose is also commercially modified by acetylation to produce a material suitable for X-ray and cine film. Commercially cellulose ethers are also prepared, such as methylcellulose. This material is water-soluble and gives a highly viscous solution at very low concentrations. Hence it is widely used as a thickener in latex paints and adhesives, in cosmetics and for coating pharmaceutical tablets. 

Indeed, these reactions proceed at 25 °C in ethanol-aqueous media in the absence of transition metal catalysts. The ease with which P-H bonds in primary phosphines can be converted to P-C bonds, as shown in Schemes 9 and 10, demonstrates the importance of primary phosphines in the design and development of novel organophosphorus compounds. In particular, functionalized hydroxymethyl phosphines have become ubiquitous in the development of water-soluble transition metal/organometallic compounds for potential applications in biphasic aqueous-organic catalysis and also in transition metal based pharmaceutical development [53-62]. Extensive investigations on the coordination chemistry of hydroxymethyl phosphines have demonstrated unique stereospe-cific and kinetic propensity of this class of water-soluble phosphines [53-62]. Representative examples outlined in Fig. 4, depict bidentate and multidentate coordination modes and the unique kinetic propensity to stabilize various oxidation states of metal centers, such as Re( V), Rh(III), Pt(II) and Au(I), in aqueous media [53 - 62]. Therefore, the importance of functionalized primary phosphines in the development of multidentate water-soluble phosphines cannot be overemphasized. 

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