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.A.O.A.C. 69, 699-703 (1986). TLC of deoxynivalenol, fusarenon X, nivalenol, T-2 toxin, HT-2 toxin, neosolaniol, diacetoxyscirpenol on silica with ethyl acetate - methanol 20:1. Detection after drying by spraying with 20 % methanolic AlCl3-solution and heating 10 min at 130 °C. Examination under UV. Detection limits 300 ng - 800 ng.
Elelmezési Ipar 41, 324-326 (1987). OPLC of zearalenons on silica with chloroform - acetone 9:1 or with toluene - ethyl acetate - formic acid 30:14:2. Detection by UV 254 nm. Sensitivity 40-60 ng/spot. Spraying with Sarudi reagent (1% 4- methoxy-benzene-diazonium-fluoroborate). Sensitivity 20 ng/spot. Recovery:62.5-84.6%.
J. Chromatogr. 432, 407-411 (1988). TLC on silica with ethyl acetate - acetone - water - acetic acid 50:25:15:10. Detection by fluorimetry after reacting the spots with fluorescamine. Detection limit, 8 ng for both.
J. AOAC Int. 73, 584-589 (1990). TLC of aflatoxin B1 and B2 according to CB-TLC method of AOAC (26.050). Good agreement of TLC method: high level of variability in TLC values in any individual test, however, average TLC results are highly correlated with the actual aflatoxin content present in the sample.
J. AOAC Int. 75, 474-480 (1992). TLC of wortmannin on silica 60 with chloroform - methanol 97:3. Detection by spraying with 20 % aqueous sulfuric acid or freshly prepared acidic p-anisaldehyde solution and heating at 60-70 °C. Bioassay after cutting the TLC plate.
J. AOAC Int. 77, 1179-1183 (1994). TLC of fusarochromanone on silica with chloroform - methanol - NH3 45:5:1 or 40:10:1. Detection under UV 254 (limit 5 ng) of UV 366 nm (Detection limit 3 ng). Fusarochromanone gives a positive (turns pink) ninhydrin reaction; it turns yellow-green when sprayed with either 20% sulfuric acid in methanol or p-anisaldehyde solution. Detection limit of these 3 colorimetric reagents is 250 ng. Fusarochromanone is relatively unstable when exposed to fluorescent light; standards should be stored in the dark in the freezer.
J. Chromatogr. A 815, 75-92 (1998). A review with 135 references on TLC, HPLC and other methods for monitoring studies of ochratoxin A in food chain and for studies dealing with the OA carryover, including sampling, sample storage, extraction, spiking procedures, clean-up, detection, determination and confirmation.
J. Planar Chromatogr. 13, 328-332 (2000). OPLC of aflatoxin B1, B2, G1 and G2 on silica gel (TLC and HPTLC plates) with chloroform - toluene - tetrahydrofuran 15:15:1. Quantitation of aflatoxins by densitometry at 365/>436 nm. The validation procedure includes tests on specificity and determination of the retention factor, resolution, asymmetry, linearity, accuracy, precision, detection limit, and quantitation limit of the method according to ICH III/5626/94. The robustness of the procedure was also determined and found to be critically dependent on the type of plate used (TLC or HPTLC).