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.
Food Addit Contam Part A. 38, 1778-1787 (2021). HPTLC of deoxynivalenol (1), 3-acetyldeoxynivalenol (2), 15-acetyldeoxynivalenol (3), zearalenone (4) and nivalenol (5) in Chilean cereals on silica gel with toluene - ethyl acetate - formic acid 1:8:1. Detection by dipping into a solution of 10 % aluminium trichloride in 50% methanol, followed by heating at 120 °C for 15 min. Quantitative determination by absorbance measurement at 366 nm. The hRF values for (1) to (6) were 39, 50, 45, 60 and 20, respectively. Linearity was between 20 and 160 ng/zone for (1) to (5). The LOD and LOQ were 120 and 160 µg/Kg for (1), 120 and 200 µg/kg for (2) and (3), 80 and 120 µg/kg for (4) and 120 and 160 µg/kg for (5), respectively. Recovery was between 88.6 and 111.5 % for (1), 93.6 and 108.3 % for (2), 91.0 and 111.0 % for (3), 84.3 and 114.2 % for (4) and 86.0 and 112.5 % for (5).
J. Liq. Chromatogr. Relat. Technol. https://doi.org/10.1080/10826076.2021.1930556 (2021). HPTLC of patulin in apple juice on silica gel with methyl tert-butylether - n-pentane 9:5. Detection by spraying with 0.25 % methyl-benzothiazolinone hydrazone hydrochloride monohydrate in methanol, followed by heating at 105 °C. Quantification was performed using a 48-bit flatbed scanner for color measurements (in red, green, and blue). Quantification in fluorescence mode by use of a 16-bit CCD-camera and UV-366 nm illumination as well as a HPTLC DAD-scanner. The hRF value for patulin was 58. Linearity was between 5 and 800 ng/zone. The LOD and LOQ were 33 and 67 ng/zone, respectively.
Anal. Bioanal. Chem. 411, 6655-6665 (2019). HPTLC of lovastatin present in lactone (1) and hydroxy acid forms (2) and mycotoxin citrinin (3) in red yeast rice on silica gel with n-hexane - acetone - 10 % acetic acid 60:40:1. Quantitative determination by absorbance measurement at 238 nm for (1) and (2) and fluorescence measurement at 313/> 400 nm for (3). The hRF values for (1) to (3) were 35, 23 and 7, respectively. Linearity was between 50 and 500 ng/zone for (1) and (2) and 5 and 50 ng/zone for (3). Intermediate precision was below 2 % (n=5). The LOD and LOQ were 10 and 50 ng/zone for (1) and (2) and 1 and 4 ng/zone for (3). Average recovery was 109.9 % for (1) to (3).
J. Planar Chromatogr. 33, 617-630 (2020). HPTLC of aflatoxin B1 in marketed samples of corn, groundnut, rice, wheat and dried chillies on silica gel with chloroform - acetone 9:1. Quantitative determination by absorbance measurement at 366 nm. The hRF value for aflatoxin B1 was 36. Linearity was between 10 and 120 ng/zone. Intermediate precision was below 2 % (n=3). The LOD and LOQ were 1 and 3 ng/zone. Average recovery was 85.2 %.
J. Planar Chromatogr. 33, 209-217 (2020). HPTLC of patulin in fruit-based food on silica gel with toluene - ethyl acetate - formic acid 5:4:1. Quantitative determination by absorbance measurement at 254 nm. The hRF value for patulin was 53. Intermediate precision was below 4 % (n=5). The LOD and LOQ were 0.66 and 1.99 ng/zone, respectively. Recovery was between 106.0 and 108.6 %.
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.