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
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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.
by direct fluorimetry on thin-layer plates. J. Chromatogr. 462, 442-447 (1989). TLC of phallotoxins on silica with chloroform - methanol - 28% NH3 64:40:10. Detection by spraying with 2.5% 4-dimethyl-aminobenzaldehyde in methanol, then with a solution of 2 mL sulfuric acid in 10 mL of methanol - glycerol 6:4, and heating at 110°C for 10 min. Quantification by fluorimetry.
J. AOAC Int. 73, 581-584 (1990). TLC of aflatoxin B1 on silica with ether – methanol – water 96:3:1. Detection and quantification by fluorescence. Quantitative TLC results in good agreement with LC.
J. AOAC Int. 75, 307-312 (1992). The American Oil Chemists Society method (AOCS Official Method Ah 1-72) was used for TLC analysis of aflatoxin B1; quantification by densitometry. Good correlations for results obtained by using ELISA with TLC, and TLC with LC. Comparison of advantages and disadvantages of ELISA, TLC and LC.
Appl. Environm. Microbiol. 59, 2864-2867 (1993). TLC of fumonisin B1 on silica 60 with a) 1-butanol - acetic acid - water 2:1:10 and b) chloroform - methanol - water - acetic acid 55:36:8:1. Densitometry after derivatization with p-anisaldehyde at 600 nm.
China. J. AOAC Int. 82, 657-662 (1999). TLC of aflatoxins on silica gel with toluene - acetone 1: 1; visualization under UV 365 nm. The limit of detection was 20 ng/g.
Proc. Intern. Symp. on Planar Separations, Planar Chromatography 2001, pp. 343-349. HPTLC of aflatoxins (B1, B2, G1, G2, M1), ochratoxin A, patulin, deoxynivalenol, fumonisins, sterigmatocystin, cyclopiazonic acid and altenuene on silica gel with chloroform - acetone 22:3, benzene - methanol - acetic acid 18:1:1, toluene - ethyl acetate - formic acid 5:4:1, chloroform - acetone - 2-propanol 8:1:1, chloroform - methanol - water - acetic acid 55:36:8:1, acetonitrile - 2-propanol - 0.25 M phosphoric acid 4:5:10, ethyl acetate - 2-propanol - NH3 6:3:2 and toluene - ethyl acetate - formic acid 6:3:1, respectively. Detection under UV or by spraying with aluminium chloride, 4-methoxybenzaldehyde, trifluoroacetic acid - aluminium chloride, and 4-dimethylaminobenzaldehyde. Quantitation by densitometry at different wavelengths in absorbance or fluorescence mode.
Brazilian Journal of Microbiology 42, 172-180 (2011). TLC of patulin on silica gel with toluene – ethyl acetate – formic acid 5:4:1. Detection by spraying with 0.5 % aqueous methyl-benzothiazolinone hydrazone hydrochloride monohydrate, followed by heating at 130 °C for 15 min. Quantitative determination by absorbance measurement at 366 nm. Linearity was between 45 and 2100 µg/kg. The limits of detection and quantification were 0.005 µg/kg and 14 µg/kg. The relative standard deviation for repatibility was 6.2 %. Recovery (by standard addition) was 88 % for patulin.
Food Chem. 233, 290-301 (2017). Review of analytical methods for the effective control of patulin contamination, including TLC validated methodologies. The paper included a reference of standard methods, including the official AOAC method where detection is achieved by spraying with 3-methyl-2-benzothiazolinone hydrazone with a limit of detection of approximately 20 mg/L.