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. Chromatogr. A 815, 3-20 (1998). A review with 136 references on the status of TLC of mycotoxins in various sample matrices, stressing on the merits of TLC in qualitative and quantitative determination of the toxins. General comparison between different TLC methods, TLC with HPLC, ELISA and GC, etc.
J. Planar Chromatogr. 14, 53-56 (2001). RP-OPLC of fumonisin B1, B2, B3, and B4 on RP-18 using a two-step development. The first step with acetonitrile - 1% KCl 1:9 served for sample clean-up, the second with acetonitrile - 4% KCl 5:2 for separation. Visualization by use of fluorescamine as derivatization agent. Densitometry in fluorescence mode at 365 nm. Quick and efficient procedure.
Quim. Nova 33, 43-47 (2010). HPTLC of aflatoxin B1 in peanuts on silica gel with chloroform - acetone 99:1. Quantitative determination by absorbance measurement at 366 nm, using a CCD camera followed by image processing using the software ImageJ. Linearity was between 0.8 and 4.8 ng/zone. The intra-day and inter-day precisions had a RSD lower than 5.2 %. LOD was 0.4 ng/zone while LOQ was 1.2 µg/kg. The average recovery was 94.9 %. The proposed method is a simple, efficient and low cost tool for quantitative analysis of aflatoxin B1 in peanut samples.
Food Control. 72, 110-122 (2017). Review of the methodologies reported on mycotoxin analysis in Sub-Saharan Africa. The review highlights the analytical methods reported for monitoring of toxic contaminants in food and feedstuffs, including references on the application of TLC and quantitative densitometry. _x000D_
J.A.O.A.C. 67, 580-582 (1984). HPTLC of zearalenone and zearalenol on silica with a) chloroform - ethanol 95:5 and b) benzene - acetone 9:1. Detection by spraying with 0.7 % Fast Violet B solution, followed by borate buffer solution. Sensitivity > 80 ng/g for zearalenone and > 200 ng for zearalenol.
J.A.O.A.C. 68, 136-137 (1985). TLC of aflatoxins on silica with chloroform - acetone 9:1in the first dimension and ether - methanol - water 96:3:1 in the second. Assay by viewing under 360 nm UV light and comparing with standards at 1 to 2 ng per spot.
J.A.O.A.C. 69, 690-696 (1986). TLC of aflatoxins B1, B2, G1, G2 on silica with a) water - saturated chloroform - acetone 88:12, b) toluene - ethyl acetate - formic acid 48:40:12. Quantification by fluorescence densitometry. Detection limit 1 ppb.
J.A.O.A.C. 70, 654-657 (1987). TLC of T-2 mycotoxin, HT-2, T-2 triol and T-2 tetraol on silica with 2 sequential solvent systems: 1. chloroform - ethyl acetate - ethanol 50:25:25 and 2. chloroform - ethyl acetate - ethanol 80:10:10. Detection of unlabelled mycotoxin standards by reacting with 4-(p-nitrobenzyl)pyridine; radiolabelled standards by autoradiography.