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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J. Planar Chromatogr. 20, 447-450 (2007). HPTLC of piperine on silica gel, prewashed with methanol, with hexane - acetone 13:7 in a twin-trough chamber with chamber saturation for 5 min. Quantification by densitometry at 340 nm in absorbance mode.
59th Indian Pharmaceutical Congress C-42, 234, (2007). HPTLC of E-guggulsterone (a steroidal ketone present in oily resin of Commiphora mukul) and five marketed ayurvedic tablet formulations, on silica gel with toluene - propane-1-ol - glacial acetic acid 8:1:1. Densitometry at 254 nm. The hRf of E-guggulsterone was 61. Several marketed formulations were evaluated for E-guggulsterone, the UV spectra of the standard and that of the formulations were comparable in respect of E-guggulsterone. The TLC pattern showed several other zones corresponding to unknown phytochemicals. The method was suitable for quantitative evaluation of formulation in respect of E-guggulsterone in presence of other phyto chemicals.
J. Chromatogr. A 1187 (1-2), 250-259 (2008). Description of a simple, fast and robust temperature-controlled system for non-forced-flow micro-planar chromatography. Micro-TLC plates can be developed in horizontal position under controlled temperature and with temperature gradients between - 20 and 80 ºC. Saturated or unsaturated chamber conditions are possible and only small amounts of mobile phase are required (0.3 to 1 mL). Plate temperature equilibration is obtained within 5 to 12 min and a typical non-forced flow run can be finished within only 5 to 20 min. On the micro-plate more than 10 spots can be separated in one direction or up to 180 spots per plate for two-dimensional and multi-development runs. Demonstration of fast and efficient separation of a number of analytes including fullerenes, cyclodextrins and steroids as well as complex samples obtained from natural products and pharmaceutical formulations. Thermostated micro-planar chromatography can be applied in retention and quantification studies.
J. Chromatogr. A 1188 (2), 295-300 (2008). Determination of food dyes (tartrazine, azorubine and sunset yellow) in different products by HPTLC combined with image processing of scanned chromatograms, on 3-aminopropyl modified silica gel with isopropanol - diethyl ether - ammonia 2:2:1. Quantification by using digital processing of images with special-purpose software. The limit of detection was between 5 and 9 ng/spot and the limit of quantification was between 10 and 18 ng/spot. Recovery was between 96.4 and 102.7 %.
J. Planar Chromatogr. 21, 191-195 (2008). HPTLC of fluconazole and clotrimazole (as internal standard) on silica gel with toluene - chloroform - methanol 6:15:2. Quantitation by densitometry at 210 nm.
J. Sep. Sci. 31, 237-241 (2008). HPTLC of chlorogenic acid in green coffee beans on silica gel with ethyl acetate - dichloromethane - formic acid - acetic acid - water 100:25:10:10:11. Quantitative determination by absorbance measurement at 330 nm. The hRf value was 27 and selectivity regarding matrix was given. Linearity was between 550 and 1750 ng/spot. The limits of detection and quantification were 80 and 250 ng, respectively. Recovery was 97.1 %. The intermediate/interday/intra-day precision was between 1.06 % and 1.35 % (n=6). The data showed no statistically significant differences for HPTLC and HPLC methods.
J. Liq. Chromatogr. Relat. Technol. 31, 1959-1968 (2008). Quantitative Ag-TLC of eight samples of sunflower oil with different linoleic acid content on silica gel (impregnated by dipping into a 0.5 % methanolic solution of silver nitrate) with petroleum ether - acetone 25:1, and petroleum ether - acetone - ethyl acetate 100:5:2, and 50:3:2. Detection by consecutive treatment with bromine and sulfurylchloride vapors (30 min each) followed by heating at 180-200 °C. Quantitative determination by absorbance measurement at 450 nm. Evaluation of authenticity and possible adulteration of edible oils.
J. Liq. Chromatogr. Relat. Technol. 30, 2617-2628 (2007). TLC and HPTLC of monoterpenes, e. g. menthol and menthone from peppermint, on silica gel with toluene - ethyl acetate 3:7, 4:6, ... , 9:1, and 10:0 in a horizontal chamber. Detection with methanolic vanillin - sulfuric acid reagent and under UV 254 nm. Flavonoids from hawthorn, Passiflora incarnata, hop, cacao, as well as tea were also determined by TLC and OP TLC.