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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Planta Med. 75, 12-17 (2009). HPTLC of swertiamarin and the ethyl acetate extract of Enicostemma axillare on silica gel with ethyl acetate - butanol 1:1 in a twin trough chamber. Quantitative determination by densitometric absorbance measurement at 254 nm.
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.
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, 503-506 (2011). HPTLC of oleanolic acid in extracts of dried roots on silica gel with toluene - ethyl acetate - glacial acetic acid 70:30:1 in a saturated twin-trough chamber. Detection by spraying with anisaldehyde-sulfuric acid reagent and heating in an oven at 110 °C for 5 min. Quantification was performed by immediate densitometric absorbance measurement at 529 nm. The average recovery was 98.9 %. LOD and LOQ were 10 and 30 ng/zone, respectively. The hRf value was 58. Linearity was between 100 and 1000 ng/zone. Precision (%RSD) was 1.4 %.
J. Liq. Chromatogr. Relat. Technol. 34, 1664-1675 (2011). HPTLC of pramipexole in pharmaceutical formulations on silica gel with ethyl acetate - toluene - methanol 16:3:1 + 1 drop ammonia. Quantitative determination by absorbance measurement at 263 nm. The hRf value of pramipexole was 32. Precision was below 2 %. Linearity was 200-2000 ng/zone. LOD and LOQ were found to be 30 and 200 ng/zone. The intermediate/inter-day/intra-day precision (n = 6) was 0.4 %. Recovery (by standard addition) was in the range of 98.5-99.1 %.
J. Planar Chromatogr. 25, 509-515 (2012). HPTLC of textile dyes Lanasyn Blue F-L 150 (1), Lanasyn Dark Brown M-GLN (2), Lanasyn Red M-GA (3), Nylosan Dark Brown S-MBL (4), and Nylosan Red N-2RBL (5) on RP-18 with n-butanol - ethyl acetate - 5 % ammonium hydroxide 4:4:1. Quantitative determination by absorbance measurement at 550 nm. Linearity was in the range of 20-60 ng/band. Limits of detection for (1) to (5) were 7, 6, 3, 5 and 1 ng/band, respectively.
J. Planar Chromatogr. 25, 394-402 (2012). 2D-HPTLC of kaempferol, quercetin, rutin, hyperoside, ferulic acid, gallic acid, caffeic acid, chlorogenic acid, chinic acid, p-coumaric acid, catechin, epicatechin, and resveratrol in the flowers of Eupatorium cannabinum on cyano phase with propan-2-ol mixed with n-heptane, and ethyl acetate mixed with n-heptane as non-aqueous mobile phases in the first direction and after turning the plate 90 ° with methanol mixed with water in the second direction of development. Detection by spraying with diphenylborinic acid 2-aminoethylester and PEG 4000 or DPPH radical reagent. Evaluation under UV 254 nm and 366 nm. The 2D-HPTLC system allowed the separation of the phenolic fractions.
J. Planar Chromatogr. 25, 388-393 (2012). HPTLC of alternariol (1), alternariol monomethyl ether (2), altenuene (3), L-tenuazonic acid (4) in Alternaria alternata strains isolated from foodstuffs on silica gel pre-coated with oxalic acid in methanol with toluene - ethyl acetate - formic acid 6:3:1. Quantitative determination by absorbance measurement at 254 nm. The hRf values of compounds (1) to (4) were 25, 36, 49 and 30, respectively. The %RSD of repeatability were 7–19. Limit of detection for compounds (1) to (3) was 0.3 mg/kg and limit of quantification for (1) to (4) was 5.0 mg/kg in rice cultures with Alternaria alternata mycelium.