Photolysis of thiochrome in aqueous solution: A kinetic study.

The photolysis of thiochrome (THC), an oxidation product of thiamine (vitamin B) (THE), used for its fluorimetric assay, has been studied in the pH range 7.0-12.0.

Stability-indicating spectrofluorimetric method for the assay of riboflavin and photoproducts: Kinetic applications.

A stability-indicating spectrofluorimetric method has been developed for the simultaneous assay of riboflavin (RF) and photoproducts, formylmethylflavin (FMF), lumichrome (LC) and lumiflavin (LF) in aqueous solution. The method is based on the extraction of LC formed in acid solution and LC and LF formed in alkaline solution with chloroform at pH 2.0 and their assay by fluorescence measurements at 478 and 530 nm, respectively.

Metal ion mediated photolysis reactions of riboflavin: A kinetic study.

The effect of metal ion complexation on the photolysis of riboflavin (RF) using various metal ions (Ag, Ni, Co, Fe, Ca, Cd, Cu, Mn, Pb, Mg, Zn, Fe) has been studied. Ultraviolet and visible spectral and fluorimetric evidence has been obtained to confirm the formation of metal-RF complexes. The kinetics of photolysis of RF in metal-RF complexes at pH7.

Photodegradation and stabilization of betamethasone-17 valerate in aqueous/organic solvents and topical formulations.

The effects of solvent [acetonitrile, methanol, and acetonitrile/water mixture (20:80, v/v)], buffer concentration (phosphate buffer, pH 7.5), ionic strength and commonly employed adjuvants on the photodegradation of betamethasone-17 valerate in cream and gel formulations have been studied on exposure to UV light (300-400 nm). A validated high-performance liquid chromatography method has been used to determine the parent compound and its photodegraded products.

In vitro evaluation of betamethasone esters for phototoxic potential.

The phototoxicity of Betamethasone valerate and betamethasone dipropionate has been investigated on irradiation in the wavelength range of 300-400 nm, using some basic in vitro phototoxicity tests. Both esters cause photohemolysis of mouse red blood cells and photoperoxidation of linoleic acid. The photoproducts of both esters have also been found to be phototoxic.

Photostability and interaction of ascorbic acid in cream formulations.

The kinetics of photolysis of ascorbic acid in cream formulations on UV irradiation has been studied using a specific spectrophotometric method with a reproducibility of ± 5%. The apparent first-order rate constants (k(obs)) for the photolysis of ascorbic acid in creams have been determined. The photoproducts formed in the cream formulations include dehydroascorbic acid and 2,3-diketogulonic acid.