An underestimated technique. Does pressurized and pressure-assisted capillary electrochromatography have potential in drug and pharmacological-active compounds analysis?

Pharmaceutical analysis guarantees patient safety all over the world. Thus, continuous development of existing analytical techniques is still very important. Pressurized capillary electrochromatography and pressure-assisted capillary electrochromatography are hybrid separation techniques that combine the selectivity of liquid chromatography and the high separation efficiency of capillary electrophoresis. They use a smaller amount of reagents and samples, hence, reducing the total cost of analysis. Therefore they have found application in a number of pharmaceutical and biomedical analysis. This review article focuses on the use and importance of pressurized and pressure-assisted capillary electrochromatography in pharmaceutical and biomedical analysis, taking into account types of detectors and capillaries used. Despite the fact that pressurized capillary electrochromatography and pressure assisted capillary electrochromatography offer many possibilities and have been available for over a dozen years, they are still underdevelopment and not fully explored.

Rapid Separation and Determination of Metronidazole Benzoate and Other Antiprotozoal Drugs by Pressurized Capillary Electrochromatography

A novel method for the rapid separation and determination of five polar 5-nitroimidazoles in water from different sources by pressurized capillary electrochromatography has been developed. Compared with the gradient elution mode and the packed nonpolar columns which were usually utilized for the separation of 5-nitroimidazoles, a simple isocratic elution mode and low-cost homemade polar molecularly imprinted polymer monolith were used in the experiment. Electrochromatographic conditions such as pH of buffer, organic modifier, concentration of buffer, and separation voltage were optimized. At 320 nm UV wavelengths, the five 5-nitroimidazoles could be baseline-separated rapidly in less than 11 min with the separation voltage of +20 kV in 10 mmol/L sodium dihydrogen phosphate-disodium hydrogen phosphate buffer solution (pH 4.82) containing 30% acetonitrile. Under the optimum conditions, the linear ranges of the metronidazole, secnidazole, tinidazole, ornidazole, and metronidazole benzoate were 0.50–100.00, 0.50–100.00, 0.80–500.00, 0.80–100.00, and 5.00–500.00 μg/mL, respectively, and the detection limits of these analytes were 0.11–0.73 μg/mL. Column efficiencies of 43 000, 36 000, 34 000, 14 000, and 29 000 plates/m were obtained for metronidazole, secnidazole, tinidazole, ornidazole, and metronidazole benzoate, respectively. The recoveries of different water samples were about 85.0–95.8%. Additionally, the proposed method has been successfully applied to the rapid separation of 5-nitroimidazoles in the locally available pure milk sample by simple pretreatment.