Biochem. Biophys. Res. Commun. 525, 61-66 (2020). HPTLC of complete precursors of glycosylphosphatidylinositol (GPI) in Gpi8 deficient strains of Candida albicans on silica gel with chloroform - methanol - water 4:4:1. Metabolic labeling was performed using [2-3H]-myo-inositol. Detection of radiolabeled glycolipid intermediates by scanning for 5 min.

J. Sep. Sci. 44, 387-402 (2021). Review of current methods for the analysis of disperse, acid, basic and reactive dyes from 2009 to present, including the identification and characterization of synthetic dyes by employing chromatographic methods.

J. Sep. Sci. 43, 3885-3901 (2020). HPTLC of erianin and gigantol in the stems of Dendrobium hercoglossum on polyamide film with methyl benzene - ethyl formate - formic acid 6:3:1. Detection by spraying with 10 % ethanol solution of sulfuric acid, followed by heating at 105 ºC.

J. Sep. Sci. 43, 2981-2988 (2020). HPTLC of citicoline (1) and piracetam (2) in presence of their degradation products on silica gel with methanol - chloroform - ammonium chloride buffer 9:1:2. Quantitative determination by absorbance measurement at 230 nm. The hRF values for (1) and (2) were 15 and 85, respectively. Linearity was between 0.2 and 4 µg/zone for both (1) and (2). Intermediate precision was below 2 % (n=3). The LOD and LOQ were 56 and 180 ng/zone for (1) and 53 and 170 ng/zone for (2), respectively. Average recovery was 100.9 % for (1) and 99.8 % for (2).

J. of Chromatogr. Sci. 58 (5), 418 - 426 (2020). Development of a method for the quantitation of glibenclamide (GLIBEN), rosiglitazone maleate (ROSI) and metformin hydrochloride (MET) from a combined dosage form by HPTLC on RP-18 F254s aluminum layer with methanol - tetrahydrofuran - water - glacial acetic acid 40:9:10:1. Detection under UV light. The hRf for GLIBEN, ROSI and MET was 54, 62 and 80, respectively. Quantification and photodocumentation by densitometry. For GLIBEN and  ROSI the LOD and LOQ was 80 and 200 ng/zone, for MET the LOD and LOQ was 48 and 120 ng/zone, respectively. The linearity for GLIBEN and ROSI was 200 - 1000 ng/zone (r = 0.9991 for GLIBEN and r = 0.9993 for ROSI) and for MET 120 - 600 ng/zone (r = 0.9988). The method was precise and accurate for all three drugs, and well suitable for the analysis of triglucored tablets, and reliable quality control for GLIBEN, ROSI and MET in a combined dosage form.

J. Chinese Trad. Patent Med. 41 (3), 516-521 (2019). Yiqi Tongmai Capsule is a herbal TCM for activating blood circulation and regulating veins, as to relieve dizziness, chest tightness, chest pain caused by blood stasis. HPTLC for quality control on silica gel (1) for Ligusticum chuanxiong hort, with n-hexane - ethyl acetate 3:1 after presaturation of plates for 20 min, detection under UV 366 nm; (2) for Radix paeoniae rubra, with chloroform - ethyl acetate - methanol - formic acid 80:10:40:1 after presaturation of plates for 20 min, detection by spraying with 5 % vanilline in sulfuric acid - ethanol 1:4 and heating at 105 ˚C until the zones are detected in daylight, comparison with the standard  paeoniflorin; (3) for Panacis Quinquefolii Radix and Panaxnotoginseng (Burk.) F.H.Chen with trichloroform - anhydrous ethanol - water 10:10:1 after presaturation of plates for 15 min, detection by spraying with 10 % solution of sulfuric acid - ethanol 1:4 and heating at 105 ˚C until the zones are detected in daylight and under UV 366 nm, identification by comparison with the standards notoginsenoside R1, ginsenoside Rg1, Re, Rb1 and pseudoginsenoside F11.

J. of Chromatogr. Sci. 58 (5), 411 - 417 (2020). Analysis of a binary mixture of silymarin (SR) and vitamin E (VE) acetate in their pure forms, pharmaceutical formulation and spiked human plasma, by HPTLC on silica gel with hexane - acetone - formic acid 140:60:3, detection at UV 215 nm, and quantification by densitometry. The linearity was 0.2 - 2.5 and 0.2 - 4.5 μg/band for SR and VE, respectively. Accuracy was 99.9 ± 1.2 % and 100.2 ± 1.6 % for SR and VE, respectively. The method was successfullly used for the determination of the studied drugs in their pharmaceutical formulation without any interference from excipients, and in spiked plasma samples. Statistical comparison of the results obtained by this HPTLC method showed no significant difference to the results obtained by the reported HPLC method.

J. of Chromatogr. Sci. 58 (4), 303 - 308 (2020). Determination of dapoxetine hydrochloride (DAP) and tadalafil (TAD) in their binary mixtures either as raw materials or in pharmaceutical formulations, by HPTLC on silica gel with ethanol - ethyl acetate 1:9. Quantitative determination by densitometry at 222 nm. The linear range was 0.1 - 1.6 and 0.2 - 2.5 μg/band for dapoxetine and tadalafil, respectively, with accuracies of 98.9 % ± 0.6 and 99.3 6% ± 1.4, respectively.