Capillary electrophoresis methods for impurity profiling of drugs:A review of the past decade / 药物分析学报

Capillary electrophoresis(CE)is widely used for the impurity profiling of drugs that contain stereo-chemical centers in their structures,analysis of biomolecules,and characterization of bio-pharmaceuticals.Currently,CE is the method of choice for the analysis of foodstuffs and the determination of adulterants.This article discusses the general theory and instrumentation of CE as well as the classification of various CE techniques.It also presents an overview of research on the applications of different CE techniques in the impurity profiling of drugs in the past decade.The review briefly presents a comparison between CE and liquid chromatography methods and highlights the strengths of CE using drug compounds as examples.This review will help scientists,fellow researchers,and students to understand the applications of CE techniques in the impurity profiling of drugs.

Optimization of microwave-assisted extraction technique for isolation of betulinic acid from Dillenia indica Linn. and its quantification using developed HPTLC method

Modern extraction technique was investigated for the separation of betulinic acid from the bark of Dillenia indicaLinn. Betulinic acid, a pentacyclic triterpenoid, is a potent anticancer compound and possesses other pharmacologicalactions. The objective of the present study was to investigate the optimum extraction conditions for betulinic acidusing microwave-assisted extraction by applying response surface methodology based on three factors three levelsBox–Behnken experimental design. The extraction was performed by considering three different independent variables:extraction temperature (70°C–90°C), microwave power (100 W), and extraction time (10–20 minutes) and quantifiedusing developed High-performance thin layer chromatography method. The maximum yield of betulinic acid at optimizedexperimental conditions, i.e., 90°C, 200 W, 15 minutes was found to be 0.91%w/w. Analysis of variance showed that the“p-value” was 0.0004 which indicate that the models were statistically significant (p ˂ 0.05). The value of the “coefficientof determination” (R2) for microwave-assisted extraction was 0.94 which indicate that the model shows the goodness offit. To conclude, Microwave Extraction technique along with response surface design proved to be efficient compared toconventional methods which could be applied to isolate active constituents from plant sources.