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.
Chinese Anal. Chem. (Fenxi Huaxue) 26, 81-84 (1998). TLC on silica, development twice with 1) chloroform - methanol - acetic acid - acetone - water 35:25:4:14:2, 2) hexane - ether 4:1. Detection by spraying with 10% phosphomolybdic acid in ethanol and heating at 120°C for 10 min, and with Dittmer reagent. Quantitation of phosphatidylcholine (pc), cholesterol (ch), and glycerolipid (gly) by densitometry at 650 nm. Detection limit <0.2 mg/spot. Recovery 104% (n=5) for pc.
Chinese J. Modern Appl. Pharm. (Zhongguo Xiandai Yingyong Yaoxue) 15, 51-52 (1998). TLC on silica gel with benzene - ethyl acetate 9:1. Detection under UV. Quantitation by densitometry at 322 nm. Precision = 1.17% (n=6). Recovery 98.0 ± 0.68% (n=4).
J. Chinese Herb. Med. (Zhongcaoyao) 28, 723-725 (1997). TLC on silica gel by double development with hexane - ethyl acetate - ether - formic acid 100:80:20:1. Detection under UV 254 nm. Precision within plate 1.92% (n=5), plate-to-plate 2.64% (n=5). Recovery 98.10 ± 2.25% (n=5).
CBS 90, 2-4 (2003). HPTLC-AMD on silica gel with a 11-step gradient with chloroform - ethanol - acetone followed by 3 isocratic steps with chloroform for separation of cholesterol, cholesterol sulfate and various ceramide classes. For separation of cholesterol, fatty acids, triacylglycerol, cholesteryl esters, and squalene a 2-step gradient with n-hexane - ethyl acetate followed by an isocratic step with n-hexane. Conditioning between single runs with 4 M acetic acid. Detection by dipping in copper sulfate reagent followed by heating at 150 °C for 20 min. Quantitative determination by absorbance measurement at 546 nm.
CBS 89, 10-11 (2002). HPTLC on silica gel with 1) ethyl acetate - chloroform 1:1 over 30 mm followed by drying at room temperature for 15 min and 2) ethyl acetate - chloroform 9:1 over 50 mm in horizontal development chamber. Detection by dipping in anisaldehyde - sulfuric acid reagent followed by heating at 60 °C for 5 min. Quantitative determination by absorbance measurement at 440 nm. Precision (n=6 at 100 mg/kg feed) is found to be 2.7 %.
CBS 81, 14-15 (1998). HPTLC-AMD of extracts on silica gel with 16-step gradient based on methanol containing 0.1 % acetic acid via dichloromethane to n-hexane. Quantification by absorbance measurement at 255, 260, 290 and 310 nm (multi wavelength scan). Precision is determined to be 3%.
CBS 83, 14-15 (1999) HPTLC of a mixture of the reaction product and its educts on cyano phase with cyclohexane - ethyl acetate - acetic acid 400:100:1 over 40 mm. Quantitative determination by absorbance measurement at 233 nm.
J. Liq. Chrom. Rel. Technol. 27, 2039-2045 (2004). HPTLC of cholesteryl oleate, methyl oleate, triolein, oleic acid, and cholesterol on pre-washed silica gel with petroleum ether - diethyl ether - glacial acetic acid 80:20:1 in a twin-trough chamber with saturation. Detection with phosphomolybdic acid reagent. Quantitative determination at 610 nm.