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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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.
CBS 97, 6-7 (2006). HPTLC of absinthe (a beverage of the wormwood plant, Artemisia absinthium) on silica gel with acetone - acetic acid (98 %) - toluene - dichloromethane 1:1:3:5 over 70 mm. Detection by dipping in a solution of acetic anhydride - sulphuric acid - ethanol 1:1:10 followed by heating at 104 °C for 5 min. Quantitative determination by absorbance measurement at 554 nm. The hRf value of absinthin was 64 and selectivity regarding matrix was given. Linearity was between 0.1 and 10 g/L. The limit of detection and quantification for absinthin was 0.05 and 0.11 g/L, respectively. The precisions were better than 13.5 % (intraday) and 15.8 % (interday).
59th Indian Pharmaceutical congress F-146, 424, (2007). HPTLC of paracetamol, acetofenac and chlorzoxazone on silica gel with toluene - chloroform - methanol - ethyl acetate 6:2:2:1. Densitometric quantification at 225 nm. The hRf values of aceclofenac, paracetamoland chorzoxazole was 22, 42, and 73, respectively. Linearity was between 700-2400, 1000-3200, and 300-1000 ng/zone for aceclofenac, paracetamol and chorzoxazole, respectively. Recovery was between 100.5 and 101.5 % for all compounds.
J. Planar Chromatogr. 20, 179-182 (2007). HPTLC of apigenin on silica gel with chloroform - acetone - formic acid 76:16:8 in a twin-trough chamber saturated for 30 min. Quantification by densitometric scanning at 340 nm.
59th Indian Pharmaceutical congress C- 260, 287, (2007). HPTLC of artemisinin, quercitin and rutin from Artemisia dracunculus (Asteraceae) on silica gel with ethyl acetate - dichloromethane - formic acid - glacial acetic acid - water 100:25:10:10:1 for artemisinin, and n-hexane - acetone - ethyl acetate 16:1:1 for quercitin and rutin. Evaluation under UV 254 nm. The hRf values were 15, 26 and 91 for quercitin, artemisinin, and rutin, respectively. The alcoholic extract (dried) of the plant was found to contain 0.84 % artemisinin, 0.14 % quercitin, and 0.019 % rutin.
59th Indian Pharmaceutical congress F-23, 395, (2007). HPTLC of aspirin and cilostazol in synthetic mixture on silica gel with methanol - ethyl acetate - toluene - ether 2:4:4:1. Linearity was between 75 and 600 ng/mL for aspirin and 100 and 800 ng/mL for cilostazol. Recovery was between 98 and 101 %.
J. Planar Chromatogr. 20, 149-152 (2007). HPTLC of nebivolol hydrochloride on silica gel prewashed with methanol with toluene - ethyl acetate - methanol - formic acid 8:6:4:1 in a saturated twin-trough chamber. Densitometric quantification at 285 and 298 nm.
J. Planar Chromatogr. 20, 437-441 (2007). HPTLC of the 4 biomarkers bergapten, psoralen, rutin, and chlorogenic acid, on silica gel with ethyl acetate - formic acid - acetic acid - water 20:2:2:5 for chlorogenic acid and rutin and with petroleum ether - diethyl ether - acetic acid 5:5:1 for bergapten and psoralen in a saturated twin-trough chamber. Quantitative determination at 317 nm.
Phytochem. Anal. 19, 2-16 (2008). Recent developments in the phytochemical analysis of Panax ginseng are described, including different approaches such as the determination of the total saponin content and target compound and group-specific analysis using HPTLC-MS. In metabolite profiling, the paper describes the use of nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry.