Chromatographia 40, 96-98 (1995). Study of the behavior and separation ability of cellulose, starch and aminoplast thin-layers with aqueous and non-aqueous mobile phases by measuring the retention of a homologous series of benzamides. Discussion of the retention behavior and separation ability in terms of the nature of the solute, support and eluent.

J. Planar Chromatogr. 10, 18-25 (1997). Study of the distribution of different ion-pairing reagents, e.g. tetramethylammonium (TMA), tetrabutylammonium (TBA), cetyltrimethylammonium (CTMA), and trioctylmethylammonium (TOMA) by measurement of the absolute concentrations of the compounds in the stationary phase after chromatography (OPLC) on silica impregnated by immersion into a methanolic solution (0.05 M) of the reagents with methanol - water mixtures in different ratios. The behavior of acidic, neutral, and basic compounds were studied simultaneously. The chromatographic results showed good correlation with the concentration of the reagents measured on the layer.

J. Planar Chromatogr. 13, 37-41 (2000). TLC of phenol derivatives (2-amino-, 3-amino-, 4-amino-, o-, m-, p-nitrophenol, o-, m-, p-cresol, 2,3-, 2,4-, 2,5-, 2,6-, 3,4-, 3,5-dichlorophenol) on chitin with water - aliphatic alcohol, water - carboxylic acid, water - mineral acid, water - inorganic base and water - mineral salt mixtures.

J. Planar Chromatogr. 15, 324-331 (2002). Further investigation of the possibility that aliphatic ligands on chemically bonded TLC phases are partially aromatized at considerably elevated temperatures (considerably higher than 100°C). After heating in closed systems and extraction analysis was performed by HPLC-DAD.

J. Chromatogr. A 1170 (1-2), 91-100 (2007). Use of three modes of sample application on the chromatographic plate at present investigations of pressurized planar electrochromatography (PPEC) systems taking into special attention their influence on performance of the separating system: 1) application directly with microsyringe, 2) deposition of sample solution on scrap of adsorbent layer followed by location of this scrap on the chromatographic plate, 3) application with a commercially available aerosol applicator. All three modes were combined with prewetting of the chromatographic plates in order to accomplish equilibration of the stationary phase - mobile phase system. Best results were obtained when the plate was prewetted and when application was performed with commercially available aerosol applicator.

J. Planar Chromatogr. 12, 373-377 (1999). Development and evaluation of a new TLC manual multi-applicator for simultaneous deposition of up to 15 samples, successively on several plates of different sizes. Acepromethazine was used as test analyte, and plates were scanned at 375 nm. The multi-applicator furnished good inter-capillary reproducibility (relative standard deviation smaller or equal 4 %) and quantitatively satisfactory linearity (r = 0.996) and reproducibility (RSD = 4 %). HPTLC of acepromethazine maleate on silica gel with methanol. Quantitation by densitometry at 375 nm in absorbance mode.

J. AOAC Int. 91, 1196-1202 (2008). Thermostated micro HPTLC of Spirulina maxima dyes on RP18 with acetone - n-hexane 3:7 in a homemade temperature-controlled removable horizontal micro TLC chamber at 40 °C with chamber saturation. Detection by direct digital scan under visible light conditions. Experimental data indicated that under such conditions, with an office scanner used for chromatogram digitalization, spot quantification could be accurately performed within the analyte mass range of two orders of magnitide.

J. Liq. Chromatogr. Relat. Technol. 35, 294-307 (2012). A new chamber configuration, in which the feeding of the mobile phase to the TLC plate is carried out directly over the sorption layer of the plate, was proposed. The chamber is suitable for linear and circular TLC in ascending, horizontal, and descending modes of development.