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.
60th Indian Pharmaceutical Congress PA-220 (2008). HPTLC of domperidone and esomeprazole on silica gel with chloroform - methanol 9:1 with chamber saturation for 30 min. The hRf value was 25 for domperidone and 46 for esomeprazole. Quantitative determination by absorbance measurement at 295 nm. The method was linear in the range of 60-300 ng/spot for domperidone and 80-400 ng/spot for esomeprazole.
J. Pharm. Biomed. Anal. 46, 391-394 (2008). TLC of conessine on silica gel with toluene - ethyl acetate - diethyl amine 13:5:2 in a twin trough chamber saturated at 25 °C. Detection by treatment with modified Dragendorff’s reagent. Quantitative determination by absorbance measurement at 520 nm. The hRf value of conessine was 82. Linearity was in the range of 1-10 µg/zone with a correlation coefficient of 0.9998 via peak area.
Abstract No. 9966, IHCB (2009). HPTLC of root tuber extracts of Asparagus gonoclados Baker on silica gel with ethyl acetate - methanol - water 15:3:2. Detection by spraying with anisaldehyde reagent. Quantitative determination by absorbance measurement at 425 nm. Shatavarin IV was used as marker.
J. Planar Chromatogr. 22, 265-271 (2009). HPTLC of atorvastatin calcium, ramipril, and aspirin and extracts of pharmaceutical formulations on silica gel, prewashed with methanol, with methanol - benzene - ethyl acetate - glacial acetic acid 9:140:100:1 in a twin trough chamber, saturated with mobile phase for 30 min at room temperature. Quantitative determination by absorbance measurement at 210 nm. The limit of detection was 5 ng/zone for atorvastatin calcium, 3 ng/zone for ramipril, and 19 ng/zone for aspirin.
Chinese J. Hosp. Pharm. 29 (4), 1246-1247 (2009). TLC of TCM drug extracts on silica gel with 1) chloroform - methanol - acetone 10:1:1; 2) toluene - chloroform - acetone - methanol - formic acid 4:6:8:1:4; 3) chloroform - methanol 4:1. Detection 1) after exposure to ammonia vapor under UV 254 nm; 2) under UV 254 nm; 3) by spraying with 10 % sulfuric acid in ethanol followed by heating at 105 °C until coloration.
60th Indian Pharmaceutical Congress PA-231 (2008). HPTLC of voriconazole on silica gel with toluene - ethyl acetate 1:3. Quantitative determination by absorbance measurement at 255 nm. The linearity range was 10-1200 ng/spot, recovery was 99.5 %. The method was suitable for routine quality control of formulations.
Abstract No. F-365, 61st IPC (2009). HPTLC of rivastigmine hydrogen tartrate on silica gel with methanol - 25 % ammonia - acetic acid 200:7:2. The hRf value was 54. Quantitative determination by absorbance measurement at 215 nm. The method was linear in the range of 1-10 µg/band.
Rapid Commun. Mass Spectrom. 24, 2295-2304 (2010). HPTLC of glycosphingolipids (GSLs) on silica gel with chloroform - methanol - water 120:70:17. The plate was overlaid with Shiga toxin (Stx), and the microbes were detected with primary anti-Stx and appropriate alkaline phosphatase labeled secondary antibodies. Bound antibodies were visualized by color development using 0.05 % 5-bromo-4-chloro-3-indolyl phosphate p-toluidine salt in glycine buffer. The GSLs were extracted from the plate and analyzed by electrospray ionization mass spectrometry (ESI-MS). Using the combination of a TLC overlay assay and nanoESI-QTOF-MS, the structural characterization of the functional Stx1 receptors of Raji and THP-1 cells is reported.