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. You can export your saved items to PDF by clicking the download icon.
J. Planar Chromatogr. 24, 232-235 (2011). HPTLC of darunavir ethanolate in tablets on silica gel, prewashed with methanol, with toluene - ethyl acetate - methanol 7:2:1 in a twin-trough chamber lined with filter paper and saturated with mobile phase for 30 min at room temperature (25 +/- 2 °C). Quantitative determination by densitometry in absorbance mode at 267 nm. The hRf of darunavir ethanolate was 47. Linearity was between 250 and 1750 ng/band with r = 0.9994. The limits of detection and quantification were 15 and 46 ng/band, respectively. The intra-day and inter-day precision was (%RSD, n = 6) between 0.5-0.9 % and 1.1-1.3 %. Recovery (n = 6) was 99.3-101.2 %.
J. Planar Chromatogr. 24, 264-267 (2011). TLC of crebanine on silica gel with toluene - ethyl acetate - methanol 14:3:3 in a twin-trough chamber saturated for 1 h at 25 +/- 2 °C. Detection under UV light at 254 nm. Quantitative determination by densitometry in absorbance mode at 286 nm. The method precision (%RSD, n = 3) and the instrument precision (%RSD, n = 6) were 0.9 and 0.5 %, respectively. The repeatability (%RSD, n = 5) was 0.8; the accuracy as average recovery was 100.1 %. The limit of detection and quantification was 10 and 15 ng/zone, respectively. Linearity was between 100-500 ng/zone. The hRf value was 54.
J. Planar Chromatogr. 23, 315-319 (2010). HPTLC of polyphenols (extracted from Quercus robur) and quercetin, chlorogenic acid, gallic acid, and rutin as standards on silica gel with ethyl acetate - water - formic acid 87:3:10 in an unsaturated twin-trough chamber. Detection by spraying with 1 % 2-aminoethyl diphenylborinate (natural products reagent) followed by 2 % polyethylene glycol 4000 solution as well as by spraying with 2 % phosphomolybdic acid reagent followed by heating at 120 °C for 5 min. Evaluation by densitometry in absorption mode at 700 nm.
Der Pharmacia Letter 2(4), 440-446 (2010). TLC of glibenclamide on silica gel with toluene - ethyl acetate - methanol 16:1:2. The hRf value was 45. Quantitative determination by densitometry in absorbance mode at 229 nm. The method was linear in the range of 40-200 ng/band. The recovery was 99.8 %.
J. Planar Chromatogr. 24, 534-538 (2011). HPTLC of clarithromycin in plasma on silica gel (prewashed with methanol) with ethyl acetate - methanol - 15 % ammonium acetate (pH 10.6) 7:2:1 in a twin-trough chamber with saturation for 15 min. Detection by dipping into xanthydrol solution (10 % in methanol). Quantitative determination by densitometry in absorbance mode at 506 nm. The hRf was 62. The method was linear over the range of 0.1-3.0 µg/mL (r2 = 0.9974). The recovery (by standard addition) was over 85 %. The intra-day and inter-day precision (%RSD) of the assay was in the range of 0.8-4.6 %. The recovery was above 95 %.
J. Planar Chromatogr. 24, 130-135 (2011). TLC of Juniperus essential oils (containing terpenoids, monoterpenes, sesquiterpenes and alcohols) with guaiazulene and cineole as standards on silica gel with ethyl acetate - toluene 1:19. Detection by spraying with anisaldehyde reagent followed by heating for 5 min at 100 °C and examination under daylight. The hRf values were 42 and 89 for cineole and guaiazulene, respectively.
J. Liq. Chromatogr. Relat. Technol. 34, 1783-1799 (2011). HPTLC of isotretinoin in topical formulations on silica gel with toluene - methanol 9:1. Quantitative determination by absorbance measurement at 340 nm. The hRf of glycyrrhizin was 43. Linearity was 100-500 ng/zone. LOD and LOQ were found to be 13 and 42 ng/zone. The intra-day and inter-day precision precisions (n = 5) were 1.8 % and 1.6 %, respectively. Recovery (by standard addition) ranged from 99.1-100.6 %.
J. Liq. Chromatogr. Relat. Technol. 32, 2437-2450 (2009). HPTLC calliterpenone (1) and calliterpenone monoacetate (2) in the leaves of Callicarpa macrophylla on silica gel with methanol - water 9:11. Quantitative determination by absorbance measurement at 210 nm. The hRf values of (1) and (2) were 43 and 73, respectively. Linearity was between 1-5 µg/zone for (1) and (2). LOD and LOQ were 230 and 780 ng/zone for (1) and 220 and 730 ng/zone for (2). Intra-day and inter-day precisions ranged between 1.3-1.7 % for (1) and 1.1-1.7 % for (2). Recoveries (by standard addition) were between 97.5-100.8 % for both.