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. 14, 350-354 (2001). TLC of troleandomycin, tylosin, rifamycin B, vancomycin, erythromycin, and rifampicin on polyamide 11 plates with five binary solvent mixtures methanol - water, ethanol - water, propanol - water, acetonitrile - water, and tetrahydrofuran - water. Detection by spraying with anisaldehyde - methanol - acetic acid - orthophosphoric acid - sulfuric acid 1:100:10:10:5 and heating at 110°C for 10 min.
J. Planar Chromatogr. 18, 423-426 (2005). HPTLC of antibiotics (sulfadimidine, sulfadiazine, sulfaguanidine, trimethoprim) on silica gel without chamber saturation in a twin-trough chamber with chloroform - methanol 89:11. Quantification by videodensitometry at 254 nm. Limit of detection was 0.05 µg per spot for sulfadimidine, sulfadiazine, and sulfaguanidine, and 0.1 µg per spot for trimethoprim.
typical fruit of Cerrado in Minas Gerais State, Brazil
Acta Scientiarum 37, 367-374 (2015). HPTLC of ochratoxin A from Aspergillus carbonarius on silica gel with ethyl acetate - toluene - 90 % formic acid 5:4:1. Qualitative determination under UV light at 366 nm.
Method for the analysis of aflatoxins, ochratoxin A, zearalenone, vomitoxin and secalonic acid D. J.A.O.A.C. 67, 963-967 (1984). TLC of aflatoxins on silica with ether - methanol - water 96:3:1 and of ochratoxin with toluene - acetic acid 95:5. Quantification by fluorescence measurement. Minimum detectable amount for aflatoxins: less than 0.5 ng/g; ochratoxin: l0 ng/g.
J.A.O.A.C. 68, 839- 842 (1985). Rapid TLC procedure for mycotoxin determination on silica with various solvent combinations (two-dimensional). Detection by viewing under longwave UV light and spraying with various spray reagents. Assay by visual comparison with standards.
J.A.O.A.C. 69, 35-36 (1986). TLC of deoxynivalenol (DON, 3,7,15-trihydroxy-12, 13-epoxytrichothec -9- en-8 -one) on silica, impregnated with15 % AlCl3 -solution with chloroform - acetone - isopropanol 8:1:1. Quantification by fluorodensitometry after heating of the TLC plate at 120 °C for 7 min. Limit of detection: abt. 50 ng/g. Modification of a TLC method published by Trucksess at al., J.A.O.A.C. 67, 40-43 (1984).
J.A.O.A.C. 70, 123-126 (1987). TLC of cyclopiazonic acid on silica with benzene -methanol - acetic acid 90:7:5. Detection by spraying with 1 % p-dimethylaminobenzaldehyde in ethanol - HCl 3:1. TLC of aflatoxin on silica with ethyl ether - methanol - water 96:3:1. And TLC of patulin and griseofiulvin on silica with toluene - ethyl acetate - 90 % formic acid 5:4:1. Detection under DV and then spraying with 0.5 % 3-methyl-2-benzothiazolinone hydrazone and heating at 130 dwgr. C.
Chromatographia 25, 875-880 (1988). HPTLC on silica with chloroform - xylene - acetone 6:3:1 (two runs). Quantification by fluorodensitometry at 366/>400 nm and evaluation via peak height. Optimum sensitivity, accuracy and precision resulted when a combination of a fully automated TLC sampler, an unsaturated glass developing chamber and a monochromatic densitometer were employed. Benzene - acetonitrile 98:2 was found to be the most suitable sample application solvent. Influence of instrumental and operating parameters monitored and documented CV and CI.