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, 435-438 (2001). TLC of streptomycin, kanamycin, gentamycin, and tobramycin on silica gel and RP-18 with acetone - 2% sodium acetate - acetic acid - butanone 7:6:4:1 for normal-phase TLC, and acetonitrile - 5mM sodium acetate buffer (pH 4.6) 2:9 for reversed-phase TLC. Visualization by iodine vapor. The minimum detection limits were in the range of 0.4 - 0.6 µg.
J. Planar Chromatogr. 18, 203-206 (2005). TLC of primycin (a mixture of related compounds), streptomycin, dihydrostreptomycin on silica gel with A) n-butanol - water - methanol - acetic acid 4:2:1:1; and B) chloroform - methanol - water - 35% formic acid - n-butanol - formaldehyde 160:53:9:6:3:3. When using phase B repeated development improved the resolution. After development the plates were dried in a vacuum chamber at 100 °C. An efficient prewashing technique (with methanol - 35 % formic acid 1:1 followed by drying with hot air) made the TLC plates suitable for densitometric measurements at short wavelengths. Quantitative determination by absorbance measurement at 200 nm.
J. Planar Chromatogr. 20, 69-71 (2007). TLC of mycotoxins (aflatoxin B1, B2, G1, ochratoxin A, sterigmatocystin, chaetomins, roquefortine C, penicillic acid, trichothecenes) on silica gel, prewashed with methanol, with chloroform - xylene - acetone 6:3:1. Detection under UV and by spraying with 0.5 % anisaldehyde in sulfuric acid followed by heating at 110 °C for 10 min.
Food Control. 59, 700-707 (2016). HPTLC of aflatoxin B1 conjugated with carboxymethoxylamine hemihydrochloride (aflatoxin B1-CMO) on silica gel with chloroform - methanol 9:1 and 15 % acetic acid. Identification under UV light at 366 nm. The method was applied for conjugation with bovine serum albumin.
J.A.O.A.C. 67, 1108-1110 (1984). TLC of mycotoxins after extraction and preliminary clean up chromatography on silica with toluene - ethyl acetate - 90 % formic acid 6.3:1. In-situ conversion of ochratoxin A, citrinin, penicillic acid and zearalenone to new fluorescent compounds. Sterigmatocystin separated on silica impregnated with 0.6 N sulfuric acid or 10 % oxalic acid, developed with methanol. Detection by UV, short-wave and long-wave.
J.A.O.A.C. 68, 458-458 (1985). TLC of aflatoxins on silica with toluene - ethyl acetate - 90 % formic acid 6:3:1. Measurement of radioactivity by liquid scintillation counting.
J.A.O.A.C. 68, 1128-1130 (1985). TLC of ochratoxin A on silica with toluene - ethyl acetate - formic acid 5:4:1 and visualization under longwave UV. Semiquantitative estimation against standards.
J. Agric. Food Chem. 35, 445-448 (1987). TLC of deoxynivalenol, fusarenon-x, and nivalenol after extraction, purification, filtration. Chromatography on aluminium chloride impregnated silica with chloroform - acetone - 2-propanol 1.8:1:1, 2.7:1.5:1.5 and fluorodensitometric quantification after heating to 120 °C for 8 min. Determination limit: 50 ng/g; average recovery 83 %.