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.
Anal. Letters 31, 475-489 (1998). HPTLC of plant tissues, dansylated in a microwave oven, on silica with chloroform - triethylamine 2:1. Quantitation by in situ densitometry at 338/>502 nm. Detection limit 1.8 - 3.0 ng. Precision 0.75-1.39%.
J. Planar Chromatogr. 13, 257-260 (2000). Description of the combined use of overpressured layer chromatography with digital autoradiography for qualitative and quantitative determination of metabolites depending on the complexity and radioactivity content of the matrix investigated. OPLC of extracts of metabolite solutions on HPTLC silica gel layers. Detection by autoradiography.
Proc. Intern. Symp. on Planar Separations Plan. Chrom. 149-152 (2003). Description of an on-line system which provides computer controlled elution of spots from the TLC plate and injection of the eluted substances into MS. All flexibility of TLC is retained, small fraction of MS working time is needed, and any spot on an unlimited number of plates can be selected.
LC-GC Europe 16, Issue 4, 225-229 (2003). A technique for the direct determination of substances from TLC plates by MALDI-MS is discussed. Methods for the generation of quantitative data by adding an internal standard to the development solvent are described and the use of post-source decay-MALDI experiments in conjunction with TLC-MALDI-MS for compound identification is reported.
Proceedings of Sino/West German Symposium on chromatography, Science Press, Beijing, China148-167 (1983). With the availability of cheap and powerful "personal computers" in the laboratory, chromatographic signal and data treatment undergoes a most remarkable change due to its perfection in mathematics, graphics display, dialog possibilities, memory capabilities and chromatographic signal and data treatment.
J. Chromatogr. Sci., 30, 192-196 (1992). The method is demonstrated with seven naphthalene compounds, four PAH’s and some other thermally stable substances.
J. Planar Chromatogr. 2, 53-61 (1989). Construction of the new instrument with the principle of five rotation planar chromatographic methods. The efficiency of the RPC methods demonstrated with the separation of saponin glycosides from Panax ginseng and some furocoumarin isomers from Pastinaca sativa. For preparative separation, an extract from Peucedanum palustre was chosen.
J. Planar Chromatogr. 28, 126-132 (2015). TLC of 17 morphine derivatives on RP phase with 3 different mobile phases, (1) methanol - 0.02 M ammonium hydroxide, (2) methanol - 0.7 M ammonium hydroxide, and (3) methanol - 0.02 M acetic acid. In each case, the individual mobile phases contained 30-90 % (v/v; in 10 % increments) of methanol as an organic modifier. Detection by absorbance measurement at 254 nm. RP-TLC can be used for the characterization of the lipophilicity of semisynthetic derivatives of morphine.