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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J. Liqud Chromatogr. 7, 1321-1340 (1984). TLC of 30 organic acids on calcium sulfate, calcium sulfate + charcoal, + p-dimethylaminobenzaldehyde, + fly ash, + silica, etc. Detection with 1 % ninhydrin, 1 % ethanolic alkaline bromophenol blue solution.
J. Liquid Chromatogr. 6, 179-192 (1983). TLC of phospholipids (lysolecithin, sphingomyelin, dipalmitoyl lecithin, phosphatidylserine, phosphatidylinositol, phosphatidyl ethanolamine, phosphatidylglycerol). Two times predeveloped with chloroform - methanol 1:1. Development with chloroform - ethanol - triethylamine - water 80:30:34:8. Detection with 10 % copper(II)sulfate in 8 % H3PO4 or 3 % copper(II)acetate in 8 % H3PO4. Densitometry.
J. Planar Chromatogr. 5, 45-49 (1992). HPTLC of phospholipids (distearoylphospatidylglycerol, -lecithin, -ethanolamine, -ethanolmaleimidocaproate, cholesterol) on silica with chloroform – methanol 12:4. Detection with cupric sulfate – phosphoric acid reagent (20 g cupric sulfate pentahydrate in phosphoric acid (8%, 200 mL). Quantification by densitometry (absorbance at 290 nm).
Hanzaigaku Zasshi (Acta Criminol. Med. Legalls Jap.) 60, 149-154 (1994). Simultaneous TLC detection of spermine and choline from human semen, and semen of some other animals, and of a number of fruit and vegetable juices. Discussion of the distinction between the chromatograms for human semen and those for other samples.
Anal. Biochem. 257, 67-70 (1998). HPTLC of cardiolipin, phosphatidic acid, phosphatidylcholine, phosphatidylethanolamine, phosphatidylglycerol, phosphatidylinositol, phosphatidylserine, and sphingomyelin on silica gel by fourfold automated multiple development with chloroform - methanol - 2-propanol - triethylamine - 0.25% aqueous KCl 60:18:50:36:9, chamber precondition with 0.1 N NH4OH. Visualization by spraying with 1) 1,6-diphenyl-1,3,5-hexatriene, and after intermediate drying with 2) molybdenum blue reagent according to Dittmer and Lester. Quantification by densitometry at 370/>460 nm. Visual detection limits of down to 10 ng.
Food Chem. 110, 538-546 (2008). TLC of wax esters of oilfish (Ruvettus pretiosus) and escolar (Lepidocybium flavobrunneum) on silica gel with xylene. Detection by spraying with 40 % sulfuric acid in ethanol - anisaldehyde 9:1, followed by heating at 100 °C for 2 min or until color is observed. The hRf value of wax esters was 60. The method was compared with DNA sequencing and GC-MS. The TLC method is inexpensive, provides a reliable result within 30 min, and is suitable for screening of numerous samples.
by HPTLC. Abstract No. 9191, IHCB (2009). HPTLC of (-)hydroxy citric acid (the main constituent of Garcinia gummigutta fruits) on silica gel with n-propanol - water - glacial acetic acid 50:50:1. Quantitative determination by absorbance measurement at 210 nm. The hRf value was 46. The method was linear in the range of 100-1000 ng/spot, recovery was 99.8-100.9 %.
Research J. Pharm. and Tech. 3(3), 825-827 (2010). TLC on silica gel (plates pre-washed with methanol) with chloroform - methanol 4:1. The hRf value of aceclofenac was 38 and of diacerein 66. Densitometric evaluation at 256 nm. The linearity range was 10-50 µg/band for aceclofenac and 5-25 µg/band for diacerein. The recovery was in the range of 99.3-101.8 % for both compounds. The method was suitable for routine quality control of combined dosage forms without any interference from the excipients.