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
- Keyword register: select an initial character and browse associated keywords
- 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.
Drug. Res. 35, 329-332 (1985). TLC of (14C)-ciclosidomine, (N-cyclohexane-carbonyl-3-(4-morpholine)-syduone-imine hydrochloride) and metabolites on silica with methanol - acetonitrile - acetic acid 5:4:1 (first dimension) and toluene - methanol 5:5 (second dimension). Quantification by measurement of radioactivity.
Acta Pharmaceutica Hungarica 58, 221-231 (1988). TLC on silica with chloroform - methanol 5:2, propanol - acetone - NH3 (14. 68M) - water 5:2:4:1, dichloromethane - methanol 10:2, 10:4, 12:2 and 15:2. Radioautography. After the last separation and purification step the metabolites were removed quantitatively from the TLC plate with dichloromethane - methanol 12:2 by Eluchrom. A part of the purified metabolites was silylated and/or boronated for direct MS, GC-MS and GC-IR.
(Hungarian). Acta Pharmaceutica Hungaria 59, 43-48 (1989). TLC of 1-hydroxy-1(p-chloro-phenyl)-1,2-dihydo-astriazino-(6,1a)-isoquinoline-ethane-sulfonate on silica with chloroform – methanol – acetone – water 6:1:13:1 (first dim.), butanol – acetic acid – water 4:1:1 (sec. dim.). Autoradiography.
Indian Drugs 31 (7), 333-338 (1994). Comparative evaluation of bio-assay and HPTLC fingerprints to establish shelf-life and uniformity of a herbal product. HPTLC of PHF extracts on silica, pre-washed with methanol, with benzene - butanol - methanol 95:5:2. Quantification by densitometry in fluorescence at 366/>400 nm.
Arzneim.-Forsch./Drug Res. 48, 408-414 (1998). TLC of 153Sm-Ca/Na-EDTMP (ethylenediamine tetramethylene phosphonic acid) on cellulose with NH3 25% - methanol - water 1:10:20. Detection by autoradiography.
J. Planar Chromatogr. 16, 381-385 (2003). TLC of (-)-deprenyl and metabolites (formaldehyde as dimedone adduct) on silica gel with chloroform - methanol - NH3 100:10:1 and chloroform - methanol - water 7:5:1 in the first and second dimension, respectively. Also TLC of dimedone on silica gel with 5% triethanolamine in chloroform. Visualization under UV 254 nm. Detection of radiolabeled compounds by digital autoradiography (DAR) or on X-ray film after contact autoradiography. Two-dimensional separations have improved the evaluation.
59th Indian Pharmaceutical Congress C-17, 228 (2007). HPTLC of curcumin, charantin, and swetiamarin in polyherbal formulations on silica gel with benzene - methanol 4:1 for charantin, chloroform - methanol - formic acid 74:4:1 for curcumin, and ethyl acetate - methanol - water 77:15:5 for swetiamarin. Densitometry at 536 nm for charantin, 425 nm for curcumin, and 238 nm for swetiamarin. The hRf values were 33, 89, and 54 for charantin, curcumin, and swertiamarin respectively.
60th Indian Pharmaceutical Congress PA-82, (2008). HPTLC of wedelolactone in supercritical fluid extrats of Eclipta alba Hassk. on silica gel with toluene - ethyl acetate - formic acid 50:50:1. Densitometric evaluation at 240 nm. The method is linear in the range of 100-1000 ng/spot. The method was used for estimation of wedelolactone in the raw material obtain from different regions of the country (India).