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. Chinese Herb Med. (Zhongcaoyao) 20, 303-305 (1989). TLC of phospholipids on silica with chloroform - methanol - acetic acid - water 50:25:10:2. Detection by spraying with Vaskovsky’s reagent and Dragendorff’s reagent. Identification by comparison of the Rf values with those of standards.
Acta Alimentaria 19, 237-2609 (1990). TLC of non polar lipids on silica with ether – toluene – ethanol – acetic acid 40:50:2:0.2 or ether – hexane 6:94, TLC of glycolipids on silica with chloroform – acetone – acetic acid – water 10:90:2:3 or ether – acetic acid 99:1, TLC of phospholipids on silica with chloroform – methanol – NH3 (33%) – water 65:35:5:2.5.
J. Liquid Chromatogr. 13, 2771-2781 (1990). HPTLC of mixtures on glycosphingolipid acceptors on silica with chloroform - methanol - 0.2% CaCl2· 2 H2O 55:45:10. Incubation with enzyme solution and a radio active sugar nucleotide donor. Determination of the radioacivities by using a liquid scintillation counter after elution or by autoradiography.
Acta Alimentaria, 21, 11-21 (1992). TLC of nonpolar lipids, glycolipids and phospholipids on polyamide. Detection by exposure to iodine vapor. Quantitative determination by spraying with 45 % sulfuric acid and heating at 120 °C
Jap. Oil Chem. (Yukagaku) 41, 1049-1054 (1992). Description of a new method for the determination of lysophosphatidyl choline and phosphatidyl choline, consisting of preparative TLC and enzymatic detection by choline oxidase - phenol. Comparison with the conventional 2D-TLC method.
J. Chromatogr. B, 664, 311-316 (1995). An optimized gradient enabling the separation of all stratum corneum lipids by automated multiple development on HPTLC plates is presented. An initial isocratic step with toluene separates sebum lipids. This is followed by a 25-step development using a gradient with a polarity range of methanol - water to hexane. Post-chromatographic derivatization by spraying with 10% cupric sulfate pentahydrate in 8% o-phosphoric acid solution and heating for 10 min at 110 °C. Densitometric scanning by absorbance at 450 nm.
Chinese J. Chromatogr. (Sepu) 14, 249-252 (1996). Two-dimensional TLC of lipids in erythrocyte membranes on silica with chloroform - methanol - NH3 - water 80:26:15:3 for the 1st direction, and chloroform - methanol - acetone - acetic acid - water 78:20:4:3:0.4 for the 2nd. Detection by exposure to iodine vapor. Quantification by GC after elution with chloroform - methanol 1:1.
J. Planar Chromatogr. 11, 214-221 (1998). Optimization of a stable solvent mixture for monitoring oils from plant sources, including blended oils used in frying. HPTLC of mono-, di-, and triacylglycerides on RP-18 with dichloromethane - ethyl acetate - methanol - acetic acid 27:22:38:13. A wide range of detection reagents was assessed for applicability to the detection of neutral lipids on the reversed phase. Phosphomolybdic acid gave the most stable results and the sensitivity was comparable with that of the other reagents. The detection limit for individual components was 0.4 µg.