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.
Abstract No. F-277, 61st IPC (2009). HPTLC of theobromine in different extracts of tea (Camelia sinensis) on silica gel with ethyl acetate - methanol 27:3. Quantitative determination by absorbance measurement at 274 nm. The maximum content of theobromine in tea samples was 2.3 %. Linearity was in the range of 3-15 µg/zone. The limit of detection and quantification was 30 and 140 ng/spot, respectively.
Abstract No. F-259, 61st IPC (2009). HPTLC of ranolazine on silica gel with methanol - toluene 9:11 in a twin trough chamber with chamber saturation for 30 min. The hRf value was 64. Quantitative determination by absorbance measurement at 271 nm. The method was linear in the range of 2-14 µg/band. Recovery was 98.3-101.4 %.
J. Ethnopharmacol. 123, 244-249 (2009). HPTLC of kaempferol-3-O-rutinoside and astragalin in leaves of Gynura procumbens on silica gel with acetic acid – methanol – dichloromethane 1:3:7. Quantitative determination by absorbance measurement at 366 nm. The hRf values of kaempferol-3-O-rutinoside and astragalin were 43 and 72, respectively, and selectivity regarding matrix was given. Linearity was given between 16 and 1000 µg/mL and the correlation coefficients were >0.987.
pruriens. Abstract No. 9425, IHCB (2009). HPTLC of L-dopa in Mucuna pruriens seed extract and formulations on silica gel with n-butanol - acetic acid - water 4:1:1. Quantitative determination by absorbance measurement at 280 nm. The method was linear in the range of 100-1200 ng/spot with an average recovery of 100.3 %.
Abstract No. F-293, IPC (2009). HPTLC of aspirin and atorvastatin on silica gel with n-hexane - acetone - butyl acetate - formic acid 60:30:12. Quantitative determination by absorbance measurement at 242 nm. For both drugs, the method was linear in the range of 3-7 µg/band and the recovery was between 99.3 and 101.0 %.
Abstract No. F-263, 61st IPC (2009). HPTLC of repaglinide (REPA) and rosiglitazone (ROSI) on silica gel with benzene - methanol - acetone - acetic acid 80:10:9:1. Quantitative determination by absorbance measurement at 266 nm. Lienarity was in the range of 800-2800 ng/band and 400-2400 ng/band for REPA and ROSI, respectively. Recovery was 101.7 and 99.5 % for REPA and ROSI, respectively.
Abstract No. F-262, 61st IPC (2009). HPTLC of L-dopa on silica gel with n-butanol - water - actic acid 4:1:1. The hRf was 37. Detection by spraying with 0.5 % ethanolic ninhydrin solution, followed by heating at 120 °C for 2 min. Quantitative determination by absorbance measurement at 520 nm. The method was linear in the range of 600-1400 ng/band.
Abstract No. F-270, 61st IPC (2009). HPTLC of fenoverine on silica gel with methanol - butyl acetate 1:4. The hRf value of fenoverine was 67. The linearity was in the range of 50 to 500 ng/band with a correlation coefficient of 0.9976. The limit of detection and quantification was 30 ng/band and 100 ng/band, respectively. The recovery was 100.1 %.