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.
Acta Alimentaria 17, 309-317 (1988). TLC method for the determination of zearalenone in ground paprika. Two-dimensional TLC on silica with petrol ether - ether 1:1 and chloroform - ethanol 95:5. Detection under UV 254 nm and 366 nm, spraying with 2% 4-methoxybenzene-diazonium fluoroborate solution. Detection limit, 20 ng per spot.
J. AOAC Int. 73, 579-581 (1990). TLC of aflatoxin B1, B2 according to AOAC CB method 968.22. Quantification by densitometry. Good correlation between LC and TLC for aflatoxin B1.
Prehrambeno-tehnoloska i biotehnoloska revija 27 (4), 209-212 (1989). TLC of zearaleone on silica with toluene - ethyl acetate - water 6:3:1. Quantification by densitometry in fluorescence at 365 nm and in absorbance for fluorescence quenching at 254 nm. Comparison of both methods. The advantage of fluorescence quenching is its sensitivity, in particular at low toxin concentrations. The method also provides detection without previous spraying with a reagent. Spots are very stable for several days.
J. Agric. Food. Chem. 42, 195-199 (1994). HPTLC of visaltricin (3-(1-methyl-4-(3-methyl-2-butenyl)imidazol-5-yl)-2-propenoic acid) with benzene - acetone 12:7; chloroform - methanol 9:1; chloroform - methanol 90:10:1. Detection by spraying with p-anisaldehyde solution and heating at 110 °C for 5 min.
J. AOAC Int. 80, 1215-1219 (1997). TLC of aflatoxins B1, B2, G1, and G2 on silica with chloroform - acetone 9:1. Visualization under UV 366 nm; quantification by densitometry.
J. Liq. Chromatogr. 23, 2727-2738 (2000). HPTLC on silica gel with chloroform - ethanol 7:1. Quantitation by fluorodensitometry by 318/>400 nm after drying 10 min at room temperature. The method is linear from 3 to 12 µg/g and the limit of determination is 3.0 µg/g.
J. Planar Chromatogr. 17, 372-374 (2004). TLC of aflatoxins B1, B2, G1, and G2 on silica gel with chloroform - acetone 23:2 in unsaturated chambers. Detection under UV light at 366 nm. Selection of the optimum mobile phase composition by software programs.
Anal. Chem. 81, 3858-3866 (2009). HPTLC of microcystin LR and nodularin on silica gel with 1-propanol - ethyl acetate - water 3:5:2 with 5 % acetic acid. Detection and quantification by UV spectroscopy at 232 nm and direct identification of separated analytes on the HPTLC plate by IR-MALDI-o-TOF MS. The detection limit was 3-5 ng/zone. For detection of peptides, plates were cut and sprayed with a solution of p-anisaldehyde, followed by heating at 105 °C until purple-blue peptide spots appeared.