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.
J. Planar Chromatogr. 20, 275-277 (2007). HPTLC of bergenin and gallic acid on silica gel with ethyl acetate - formaldehyde - acetic acid - water 80:1:2:1 in a saturated twin-trough chamber. Quantitation was performed by scanning at 260 nm in absorption mode.
fruits. Indian Drugs 45(11), 908-910 (2008). HPTLC of embelin in ethanolic extract of dried fruits of Embelia ribes Burm. on silica gel with ethyl acetate - methanol 9:1. Quantitative determination by absorbance measurement at 365 nm. The total content in Embelia ribes fruit was 0.034 %. The proposed HPTLC method provides a good resolution of embelin from other constituents present in the ethanolic extract of dried fruits of Embelia ribes Burm.
Anal. Chim. Acta 577 (1), 46-51 (2006). HPTLC of trigonelline in herbal extracts and in pharmaceutical dosage forms on silica gel with n-propanol - methanol - water 4:1:4. Quantitative determination by absorbance measurement at 269 nm. Linearity was between 100 - 1200 ng/spot (via peak area) and the correlation coefficient was 0.9991. The trigonelline content of herbal extracts quantified and estimated from the formulation was found to be well within limits (± 5 %) of the labeled content of the formulations. The method is reproducible and selective for the estimation of trigonelline by statistical analysis of the data.
J. Planar Chromatogr. 22, 109-113 (2009). HPTLC of purpurin on silica gel with toluene - ethyl acetate - formic acid 98:2:1 in a twin trough chamber saturated for 20 min at 25 +/- 2 °C. Quantitative determination by absorbance measurement at 255 nm. The limit of detection and quantification was 50 and 100 ng/band, respectively.
Br. root powder and extract. J. Planar Chromatogr. 22, 453-456 (2009). HPTLC of 2-hydroxy-4-methoxybenzaldehyde and biological extracts on silica gel with toluene - ethyl acetate - acetic acid 7:2:1 in a twin trough chamber saturated for 20 min. Quantitative determination by absorbance measurement at 277 nm.
J. Planar Chromatogr. 22, 439-443 (2009). HPTLC of jatrorrhizine in methanolic extracts of the stem of the ’heavenly elixir’ on silica gel with ethyl acetate - isopropanol - 10 % ammonia 3:5:3 in a twin trough chamber saturated for 5 min. Detection under UV 254 nm and after derivatization with Dragendorff’s reagent. Quantitative determination by absorbance measurement at 344 nm.
Chinese J. Pharm. Anal. 28 (11), 1800-1803 (2008). TLC of adenosine and adenine in Lingzhi capsules on silica gel with chloroform – ethyl acetate – i-propanol – water 16:6:3:1. Detection under UV 254 nm. The method is simple, fast and accurate and can be used for the quality control of the medicine.
J. Planar Chromatogr. 23, 180-183 (2010). TLC of chamomile extracts on silica gel with benzene - ethyl acetate 19:1 or chloroform - methanol - water 40:10:1 in an unsaturated chamber. Detection at 254 and 366 nm. For bioautographic evaluation bioluminescent Bacillus subtilis or Pseudomonas syringae pv. maculicola were used; visualization by dye a reagent was achieved by dipping the plate in an aqueous solution of MTT. Quantitative determination by densitometric scanning at 300 nm (before biological detection) or at 590 nm (after visualization of the bioautogram with MTT).