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.
Analyst 119, (1994). TLC screening of theobromine (TB), theophylline (TP), caffeine on silica with ethyl acetate - methanol - NH3 17:2:1. Detection under UV 254 nm, and by spraying with Dragendorff- iodine reagent. Quantification by HPLC.
Asian J. Chem. 19(7), 5647-5651 (2007). HPTLC of levofloxacin hemihydrate and ornidazole on silica gel with n-butanol - water - acetic acid 3:1:1. Quantitative determination by absorbance measurement at 366 nm. The method was linear in the range of 1050-1400 µg/mL and 2600-2900 µg/mL for levofloxacin and ornidazole respectively. The recovery was between 97.3 and 98.0 % for both drugs. The method was suitable for simultaneous estimation of both drugs in combined tablet dosage form.
Determination of isoniazid in serum by thin-layer chromatography.) (Chinese). J. Pharm. Anal. (Yaowu Fenxi Zazhi) 17, 116-118 (1997). TLC on silica with chloroform - methanol 9:1. In situ spectra recording of isoniazid and its salicylaldehyde - and benzaldehyde-derivatives. Quantification by densitometry at 225 nm. Validation of the method by investigation of linearity and range, RSD, recovery and detection limits for the compounds.
Correlation of lipophilicity with affinity for alpha-adrenoceptors. J. Planar Chromatogr. 22, 141-144 (2009). Determination of the relative lipophilicity of 14 1-substituted pyrrolidin-2-one by TLC on RP-18 with mixtures of acetonitrile and pH 7.0 Tris buffer with volume fractions of acetonitrile between 20 and 80 %, with chamber saturation for 2 h. Detection under UV light. Retention data obtained by this method were exponentially dependent on acetonitrile concentration and enabled estimation of the relative lipophilicity corresponding to pH 7.0 Tris buffer as mobile phase.
Chinese J. Hosp. Pharm. (Zhongguo Yaoxue Zazhi) 18, 358-360 (1998). TLC on silica gel with 1) heptane - chloroform - ethyl acetate - ethanol 10:4:4:3. 2) chloroform - toluene - ethanol 4:6:1. Detection under UV 254 nm. Quantitation by densitometry at 263 nm or at 300 nm. Precision within plate <2.6%, plate-to-plate < 4.7% (n=5). Recovery >89.6%.
Abstract No. F-309, 61st IPC (2009). HPTLC of olopatadine HCl on silica gel with methanol - chloroform - 25 % ammonia 80:20:1. The hRf value was 46. Quantitative determination by absorbance measurement at 301 nm. The method was linear in the range of 100-900 ng/band.
Proc. Intern. Symp. on Planar Separations, Planar Chromatography 2001, pp. 395-400. OPLC of a formaldehyde-dimedone adduct (formaldemethone) on silica gel with chloroform - dichloromethane 7:13. Quantitation by densitometry at 265 nm.
60th Indian Pharmaceutical Congress PA-212 (2008). HPTLC of atomoxetine HCl on silica gel with acetone - methanol - triethylamine 30:15:2. Quantitative determination by absorbance measurement at 275 nm. The method was linear in the range of 300-2100 ng/spot and was suitable for routine quality control of pharmaceutical formulations.