Anal. Biochem. 242, 152-155 (1996). HPTLC of phosphatidylinositol 3,4,5-trisphosphospate, phosphatidylinositol 3,4-bisphosphosphate and phosphatidylinositol 4,5-bisphosphosphate on silica gel impregnated with 5% boric acid solution in methanol, and of phospatidylinositol 4-phosphate and phosphatidylinositol 3-phosphate on NH2 impregnated with 5% boric acid solution in methanol. Development with 1-propyl acetate - 2-propanol - ethanol - 6% NH3 1:3:1:3. Visualization by immersion in 5% CuSO4 solution in 8% aqueous H3PO4 and heating at 180°C for 15 min. Quantitative determination by autoradiography and by densitometry at 366nm.

J. Chinese Trad. Patent Med. (Zhongchengyao) 20 (1), 22-32 (2000). A review with 65 references involving testing methods, TLC as well as GC and HPLC. Stressing on the advantages, such as suitability for complex medicine, simpleness of sample preparation, flexibility in detection, etc.

Chinese Anal. Chem. (Fenxi Huaxue) 30 (1), 38-41 (2002). TLC on polyamide with cyclodextrins (0-8 x 10-3 mol/L) as mobile phase and NH3(H2O-NH4Cl, pH 9.7 as buffer. Detection under UV. Investigation of the interaction between emodin, aloe-emodin and six cyclodextrins. Comparison of the inclusion capacity of different cyclodextrins. Calculation of the thermodynamic parameters of the interaction. Discussion of use of this interaction to modify the biological properties of emodin and aloe-emodin.

J. Proteome Res. 14, 567-577 (2015). HPTLC of (1) lipids and (2) cholesterol from urinary exosomes on silica gel predeveloped in chloroform - methanol 1:1. (1) was developed with with two mobile phases: chlorofom - ethanol - triethylamine - water 30:35:35:8, and hexane - ether 200:9; (2) with chloroform - acetone 19:1. Detection by dipping in 10 % copper sulfate followed by heating at 185 °C for 5 min.

59th Indian Pharmaceutical congress F-152, 426, (2007). HPTLC of rosiglitazone on silica gel aluminum layer with chloroform - ethyl acetate - ammonia 70:30:1. The hRf value of rosiglitazone was 40. Densitometric analysis in absorbance mode at 230 nm. Linearity was between 100 and 1000 ng/zone. Recovery (by standard addition method) was 99.6 %. Limit of detection and quantification was 10 ng and 50 ng/zone, respectively.

(A method for quantitative determination of retinol in blood serum by HPTLC.) Mikrochimica Acta (Wien) I, 235-238 (1984). HPTLC separation of retinol in blood serum of animals on silica with petrol ether - ether 1:1. Quantitative determination by absorbance at 330 nm.

J. Planar Chromatogr. 20, 373-380(2007). Investigation of the chromatographic behavior of the phenolic drugs niclosamide, hexachlorophene, ibuprofen, pentazocine, ethamivan, bithionol, salicylanilide, caffeic acid, p-coumaric acid, 4-aminosalicylic acid, ferrulic acid, and methyldopa on RP-8 and RP-18 phase prewashed with methanol, with methanol - water mixtures in different volume proportions, with chamber saturation for 20 min.The results calculated using seven different software products indicate, that chromatographic lipophilicity can be used as a measure of the lipophilicity of the compounds investigated. Spectra were acquired with the densitometer in absorbance mode. Densitometric scanning was performed at the respective absorption maxima.

(Japanese). Shimadzu Review 44, 243-246 (1987) (Shimazu Hyoron). TLC after esterification with G-anthryldiazomethane on silica with benzene - acetone system and on chemically bonded silica with methanol. Quantification by fluorodensitometry.