Cumulative CAMAG Bibliography Service CCBS
Our CCBS database includes more than 11,000 abstracts of publications. Perform your own detailed search of TLC/HPTLC literature and find relevant information.
The Cumulative CAMAG Bibliography Service CCBS contains all abstracts of CBS issues beginning with CBS 51. The database is updated after the publication of every other CBS edition. Currently the Cumulative CAMAG Bibliography Service includes more than 11'000 abstracts of publications between 1983 and today. With the online version you can perform your own detailed TLC/HPTLC literature search:
- Full text search: Enter a keyword, e.g. an author's name, a substance, a technique, a reagent or a term and see all related publications
- Browse and search by CBS classification: Select one of the 38 CBS classification categories where you want to search by a keyword
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- Search by CBS edition: Select a CBS edition and find all related publications
Registered users can create a tailor made PDF of selected articles throughout CCBS search – simply use the cart icon on the right hand of each abstract to create your individual selection of abstracts. The saved items can be printed to PDF using the print function of your web browser.
J. Planar Chromatogr. 32, 109-114 (2019). HPTLC of fructose (1), glucose (2), maltose (3), raffinose (4) and sucrose (5) in the roots of the seven Asparagus species A. adscendens, A. racemosus, A. retrofractus, A. officinalis, A. densiflorus, A. falcatus, and A. sprengeri on silica gel with propanol - ethyl acetate - water 6:3:1. Detection by spraying with a methanolic solution of diphenylamine, aniline, and ortho-phosphoric acid, followed by heating at 140 °C for 2-3 min. Quantitative determination by absorbance measurement at 600 nm. The hRF values for (1) to (5) were 55, 50, 31, 11 and 46, respectively. Linearity was between 100 and 500 ng for (1) to (5). The intermediate precision was below 2 % (n=3). The LOD and LOQ were 22 and 66 ng for (1), 13 and 40 ng for (2), 51 and 155 ng for (3), 13 and 39 ng for (4) and 76 and 229 ng for (5), respectively. Average recovery was 97.9 % for (1), 99.9 % for (2), 99.3 % for (3), 98.3 % for (4) and 97.8 % for (5).
J. Chromatogr. A 1110 (1-2), 214-221 (2006). Presentation of a rapid, simple and inexpensive method for the analysis of fructooligosaccharides as feed additives (prebiotics) in complicated biological samples with minimal pre-treatment. TLC of fructooligosaccharides in dietetic products and in samples from intestinal tract of monogastric animals on silica gel (impregnated with sodium acetate) with butanol - ethanol - water 532 with chamber saturation. Detection by spraying with diphenylamine - aniline - phosphoric acid in acetone. Quantitative determination by absorbance measurement at 370 nm.
Acta Chimica 110, 197-202 (1982). TLC of ferric-fructose (FeCl3), ferric-fructose (FeNO3), ferric-sorbose (FeCl3 ) on silica with butanol - acetone - HCl - acetylacetone - water 604010.520. Detection with 10 % sulfuric acid and 2 % K4FeCN9.
nauk. SSSR, serija chimicheskaja 2400-2402 (1983). (Russian) (Synthesis of 3,4-di-o-benzyl-1,2,-o- (1-cyano)-ethylidcine-alpha -D-xylopyranose.) TLC of the title compound on silica with a) ether - benzene 11, 12; b) chloroform - methanol 937. Detection with 25 % sulfuric acid.
J.A.O.A.C. 72, 27,29 (1989). TLC separation of polysorbates (20, 40, 60, 65, 80) on silica with chloroform - methanol - acetic acid - water 6812123, propanol - chloroform - methanol - NH3 101052. Visualization with cobalt thiocyanate reagent.
) Koiz. Var. australis (Diels) Rehd.) (Chinese). Chinese J. Herb Med. (Zhongcaoyao) 24, 563-566(1993). Preparative TLC of saponins and monosaccharides on silica with the lower phases of a) chloroform - methanol - water 1651, and b) a solution of 9 mL of the above mixture blended with 1 mL acetic acid. Detection by spraying with 50% sulfuric acid in methanol for saponins and with naphthyl alcohol - sulfuric acid reagent for saccharides. Identification by MS and NMR.
J. Planar Chromatogr. 18, 285-289 (2005). HPTLC of glucose - after hydrolyis of starch using alpha-amylase and amyloglucosidase - on silica gel, pre-washed with methanol, treated by immersion in a 0.1 M solution of di-potassium hydrogen phosphate in methanol and activated for 30 min at 120 °C. Three-fold development was performed in a horizontal development chamber with acetonitrile - water 173. Detection by dipping in aniline-diphenylamine reagent, densitometry at 520 nm. Calibration was linear between 100 and 300 ng with a coefficient of determination r2 of 0.9959. The limits of detection and quantification for starch as glucose were 0.26 and 0.51 g/100 g, respectively.
Rapid Commun. Mass Spectrom. 25, 2201-2208 (2011). HPTLC of an equimolar mixture of malto-oligosaccharides, derivatized with p-aminobenzoic acid, on silica gel with acetonitrile – water – acetic acid 821. Quantitative determination by fluorescence measurement at 366 nm. The relative molar composition of the oligomers, determined by HPTLC, was used as a reference data for mass spectrometric analyses. For both electrospray ionization and matrix-assisted laser desorption/ionization methods, the instrumental parameters significantly influence the signal intensities and areas.