Anal. Biochem. 270, 314-422 (1999). HPTLC of the dihexadecyl phosphatidylethanolamine (DHPE) derivatives of the periodate oxidation products of disaccharides, and of oligosaccharide alditols, respectively, on silica gel with chloroform ñ methanol - water 130:50:9. Visualization after spraying with primuline reagent under long-wave UV. Quantitative estimates by fluorometric scanning densitometry. In situ analysis of the derivatives by liquid secondary ion mass spectrometry (LSIMS).

CBS 94, 14-15 (2005). HPTLC of sucralose on amino phases with acetonitrile - water 4:1 over 70 mm. Stability of sucralose in Burfi, a milk-based confection, was determined over a defined time period. The 2 products of hydrolysis have been monitored as well. Detection by heating for 20 min at 190° C. Quantitative determination by fluorescence measurement under UV 366. Limit of quantitation in the lower ng range.

The case of Bifidobacterium adolescentis MB 239. J. Planar Chromatogr. 22, 321-325 (2009). HPTLC of glucose, fructose, galactose, lactose, raffinose, 1-kestose, nystose, and fructosyl-nystose on diol phase by automated multiple development with acetonitrile - acetone - water and acetonitrile - water. Preliminary isocratic developments were performed at 22-25 °C at 65-75 % relative humidity in a twin trough chamber. Detection by vaporization with 37 % hydochloric acid vapor for 30 min followed by dipping in 4-aminobenzoic acid. Quantitative determination by fluorescence measurement at 313 nm.

J. Liq. Chromatogr. Relat. Technol. 38, 1160-1163 (2015). HPTLC of glucose and maltose in Biomphalaria glabrata after coexposure with Echinostoma caproni and Schistosoma mansoni on silica gel with 1-butanol - glacial acetic acid - diethyl ether - deionized water 27:18:5:3. Detection by spraying with 5 g 1-naphthol and 20 mL concentrated sulfuric acid in 160 mL ethanol and 13 mL deionized water, followed by heating at 110 °C for 10 min. Quantitative determination by absorbance measurement at 515 nm. The hRF values of maltose and glucose were 40 and 50, respectively.

J. Chromatogr. 328, 73-80 (1985). TLC of hyaluronate oligosaccharides on silica with isopropanol - water 66:34, containing 0.05 % NaCl. Determination of RM-values of odd- and even numbered hyaluronate-oligosaccharides. Estimation of the contribution of oligosaccharide fragments to chromatographic mobility from the difference between the RM-values of two oligomers having appropriate structures.

Planta Med. 55, 73-74 (1989). TLC of quercetin and isorhamnetin on silica with benzene - methanol - acetic acid 45:8:4. TLC of glucose and rhamnose on silica with butanol - acetic acid - water 4:1:5 and isopropanol - boric acid 85:15. Detection of flavonoids under UV 366 nm and by spraying with 1% AlCl3 in methanol followed by heating at 100°C for 5 min. Visualization of sugars with aniline hydrogenphthalate followed by heating at 110 °C for 10 min.

trivolvis (Pennsylvania and Colorado strains). J. Planar Chromatogr. 8, 184-187 (1995). HPTLC of glucose and trehalose on silica impregnated with 0.1 M sodium bisulfite and citrate buffer; development by ascending chromatography three times in the same direction with acetonitrile - water 85:15 with drying between each development. Detection with 1-naphthol-sulfuric acid reagent. Quantification by in situ reflectance scanning.

J. Liq. Chrom. & Rel. Technol. 22, 1473-1491 (1999). HPTLC of 32 variously substituted 2,5-anhydroaldohexose ethylene acetal derivatives on silica gel and RP-18 with, respectively, binary non-aqueous and aqueous mobile phases. Detection by spraying with 50% aqueous solution of sulfuric acid, followed by heating at 120°C for 10-15 min.