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 J. Hosp. Pharm. (Zhongguo Yiyuan Yaoxue Zazhi) 23 (1), 31-32 (2003). TLC on silica gel with petroleum ether (60-90°C) - ethyl acetate 19:1. Detection under UV 365 nm. Quantitation by densitometry at 290 nm and with the standard addition calibration method.
J. Planar Chromatogr. 16, 396-401 (2003). HPTLC of gallic acid and tannin on cellulose with iso-butanol - acetic acid - water 14:1:3.5 and on silica gel with chloroform - ethanol - formic acid 5:4:1 in a saturated chamber. After drying visualization under UV light at 254 nm. Quantitation by densitometry at 280 nm in absorbance mode. The validated method was found to be simple, reliable, and convenient for routine analysis. Establishment of a validated procedure.
CBS 89, 4-7 (2002). HPTLC of devil’s claw extract on lichrospher silica gel with ethyl acetate - ethanol (70 %) 7:3 over 70 mm with chamber saturation. Detection by dipping in anisaldehyde - sulfuric acid reagent followed by heating at 105 °C until colors develop. Determination of bioactivity with DPPH-biotest by spraying with 0.05 % solution of (2,2-di-(4-tert-octylphenol)-1-picrylhydrazyl in methanol. Determination of antibiotic properties with Merck Chrom Biodip test by dipping in bacteria solution and incubation at 26 °C for 20 h, followed by spraying with yellow MTT tetrazolium salt.
J. AOAC Int. 86, 909-915 (2003). In quality control and stability testing of herbal medicinal products, fingerprint chomatograms are used as powerful tools to evaluate and compare the composition of compounds in such products. To fulfill the ICH- and GMP-based regulatory requirements in pharmaceutical QC, chromatographic fingerprint analysis needs to be validated. By considering the stationary phase, sample application, developing solvents, chromatogram development, plate labeling, derivatization, documentation, and chromatographic equipment the paper provides a comprehensive concept for evaluating validation parameters for planar chromatographic fingerprinting based on a standardized methodology. Validation parameters addressed include stability of the analyte, selectivity, robustness testing, and method reproducibility.
(Malvaceae). J. Planar Chromatogr. 18, 264-268 (2005). TLC in horizontal chambers of phenolic acids (caffeic, p-coumaric, ferulic, protocatechuic, gentisic, chlorogenic, isovanillic, gallic, syringic, vanillic and p-hydroxybenzoic acid) from Lavatera trimestris flowers on cellulose with water - acetic acid 3:17, toluene - ethyl formate - formic acid 5:4:1, chloroforrm - acetic acid - water 4:1:1 and of flavonoids (rutoside, kaempferol 3-rhamnoglucoside, hyperoside, isoquercetin, luteolin 7-glucoside, quercitrin, isorhamnetin 3-glucoside, luteolin, apigenin, quercetin, kaempferol) on silica gel with n-propanol - ethyl acetate - water 7:2:1, ethanol - 25 % ammonia - water 20:1:4, ethyl acetate - formic acid - water 10:2:3, ethyl acetate - formic acid - glacial acetic acid - water 100:11:11:27 and 50:5:5:9. Also two-dimensional TLC of phenolic acids on cellulose (after conditioning in the chamber for 5 min with benzene - methanol - acetic acid 94:1:5) with benzene - methanol - acetic acid - acetonitrile 16:2:1:1 in the first direction and with sodium formate - formic acid - water 1:0.1:20 in the second direction. Detection under UV light at 254 and 366 nm before and after treatment with ammonia vapor. Also derivatization by spraying with a 2 % aqueous solution of iron(III) chloride, diazotized sulfanilic acid in 20 % sodium carbonate solution, and diazotized p-nitroaniline for phenolics and with a 1 % methanolic solution of natural products reagent A for flavonoids.
Planta Med. 71, 1036-1039 (2005). Preparative TLC of ent-18-hydroxytrachyloban-3beta-ol on silica gel with toluene - ethyl acetate - acetonitrile 5:2:3 and 40:9:1. Visualization by spraying with anisaldehyde - sulfuric acid reagent followed by heating at 105 °C for 5 min.
J. pharmac. Sci. 70, 415-418 (1981). TLC of dexamethasone, betamethasone and impurities on silica with chloroform - acetone 9:1. Detection by UV 254. Densitometry.
Planta Med. 70, 509-514 (2004). Analytical and preparative TLC of a new iridolactone (4R,5R,7S,8S,9S)-7-hydroxy-8-hxdroxymethyl-4-methyl perhydrocyclopenta[c]pyran-1-one) on silica gel and RP18 with acetonitrile - water 1:1. Detection by dipping in phosphomolybdic acid or vanillin - sulfuric acid reagent followed by heating at 110 °C for 5 min.