J. Agric. Food Chem. 48, 1000-1008 (2000). Analytical TLC of the triflate derivative of di-o-isopropylidene-2,3:4,5-b-D-fructopyranose on silica gel with chloroform - methanol - water 95:35:2; TLC of phospholipids on silica gel with chloroform - methanol - water 65:25:4. Detection by spraying with 5% phosphomolybdic acid in ethanol and heating for 5 min at 60°C. Also TLC separation and detection of phosphatidylethanolamine-linked glucosylamines; Amadori products and similar compounds. Preparative TLC on silica gel with chloroform - methanol - NH3 (25%) 75:25:1. Detection (on the plate margins) by spraying with 2,7-dichlorofluorescein solution (0.1% in methanol).

J. Agric. Food Chem. 49, 5852-5856 (2001). Preparative TLC of triglycerides (1,3-dilinoleoyl-2-olein, 1,3-dioleoyl-2-linolein, 1,2,3-trilinolein) and linoleic acid, oleic acid, and their esters on silica gel with hexane - ether 6:1.

J. Planar Chromatogr. 19, 167-170 (2006). HPTLC of standards (cholesterol, oleic acid, triolein, methyl oleate, and cholesteryl oleate as marker compounds for free sterols, free fatty acids, triacylglycerols, methyl esters, and steryl esters, respectively, as well as cholesterol, phosphatidylethanolamine, phosphatidylcholine, and lysophosphatidylcholine for the analysis of polar lipids) and prepared samples of leeches on silica gel (with preadsorbent zone and prescored lanes) in a pre-saturated twin-trough chamber with petroleum ether - diethyl ether - glacial acetic acid 80:20:1 (for neutral lipids) and hexane - petroleum ether - diethyl ether - glacial acetic acid 50:25:5:1 (for steryl esters). Visualization by spraying with 5 % ethanolic phosphomolybdic acid solution and heating for 10 min at 110 °C. HPTLC of polar lipids on equal layer with chloroform - methanol - water 65:25:4. Visualization by spraying with 5% aqueous cupric sulfate solution and heating for 10 min at 140 °C. Quantification of neutral lipids at 610 nm and of polar lipids at 370 nm.

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.

Chromatogr. 686, 155-157 (1994). Description of a TLC developing tank designed to give optimal saturation conditions, with the title compounds as example, resulting in highly reproducible chromatograms, on silica with chloroform - methanol - 0.2% aqueous CaCl2 60:37:8. Visualization by orcinol reagent.

J. Liq. Chrom. & Rel. Technol. 20, 1149-1157 (1997). Preparative TLC of gangliosides (for the removal of the non-polar lipids) on silica gel with chloroform - methanol - 0.3% calcium chloride solution. After elution HPTLC on silica gel with chloroform - methanol - 0.1 M sodium lactate 11:8:2. Visualization by spraying with orcinol reagent (0.5% solution in 20% sulfuric acid).

J. Chromatogr. A 1218 (19), 2754-2774 (2011). HPTLC for lipid analysis is particularly useful for smaller, apolar compounds and offers some advantages over HPLC. Description of stationary phases, solvent systems and detection methods for the individual lipid classes (cholesterol and its derivates, glycerides, sphingo- and glycolipids, phospholipids). In comparison with common staining methods the combination of HPTLC and mass spectrometric detection methods is a very powerful method to investigate the identities of the HPTLC zones in detail.

J. High Resol. Chromatogr. 5, 635-636 (1982). HPTLC of lipids (pg, pm, pc, dgdg, sqdg, mgdg, pe, ps, pi, n-ape, pa, dpg) on silica-CaSO4 or magnesium silicate with 1) chloroform - acetone - methanol - formic acid -water 100:40:20:20:8, 2)acetone - benzene - formic acid-water 200:30:3:10. Detection with molybdate or malachite green reagent.