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.
Abstract No. F-234 61st IPC (2009). A stability-indicating HPTLC method is reported for estimation of diacerein in the presence of its degradation products. HPTLC on silica gel with toluene - ethyl acetate - formic acid 50:30:1. The hRf value of diacerein was 39. Densitometric analysis at 254 nm. The method was found to be linear in the range of 100-600 ng/band. The method was validated regarding stability. The sample was subjected to different stress conditions (acid/base hydrolysis, oxidation, photolysis, thermal) and showed extensive degradation in alkaline medium and mild degradation under acidic and oxidative conditions. The method allowed separation of diacerein from different degradation products.
J. Liq. Chromatogr. Relat. Technol. 33, 748-760 (2010). HPTLC of mercury(II), copper(II), nickel(II), cadmium(II), mercury(II), lead(II), cobalt(II), manganese(II), palladium(II), platinum(II), and zinc(II) as porphyrin complexes using newly synthesized tetra-(bromo-4-hydroxyphenyl) porphyrin (TBHPP), tetra-(4-phenoxyphenyl) porphyrin (TPPP) and tetra-p-chloromethylphenyl porphyrin (CMPP) on silica gel with acetone - chloroform 1:4 for TBHPP and TPPP and dichloromethane - chloroform - hexane 1:1:3 for CMPP. The hRF values were determined for the metal-TBHPP, -TPPP, and -CMPP chelates. Detection was performed by absorbance measurement at 420 nm. The linear range was 3.6-60, 3.6-30, 1.2-30, 0.6-30, 0.6-30, 2.4-60 ng/µL, LOD was 0.90, 0.92, 0.36, 0.19, 0.16, and 0.41 ng/µL, and LOQ was 3.01, 3.06, 1.11, 0.54, 0.54, 0.54, and 1.36 ng/µL. Intermediate precision (RSD%, n = 5) (6 ng/µL) was 3.55, 4.25, 3.20, 3.85, 2.25, 0.45 % and the regression coefficient was 0.9908, 0.9904, 0.9944, 0.9961, 0.9972, and 0.9942. The hRf values were 68, 16, 83, 42, 67, and 76 for Hg-TBHPP, Zn-TBHPP, Cu-TBHPP, Co-TBHPP, Hg-TBHPP, and Cu-CMPP, respectively.
Analytical Chemistry - An Indian Journal 8(1), 29-33 (2009). A sensitive and accurate HPTLC method has been developed for the determination of eugenol from the leaf and berry powder of Pimenta dioica (L) Merr. The leaf and berry powders were extracted with methanol. HPTLC on silica gel with ethyl acetate - methanol - water 6:2:1. Detection and quantification by densitometry at 280 nm. Linear response to eugenol was found to be in the concentration range of 200-600 ng/band. The developed method can be used for routine quantitative monitoring of eugenol from the dried leaf and berry powder of Pimenta dioica (L) Merr.
Rasayan J. Chem. 2(3), 720-723 (2009). HPTLC of cefetamet on silica gel with toluene - chloroform - methanol 3:6:1. The hRf value of cefetamet was 35. Densitometric evaluation at 236 nm. The method was linear in the range of 1-5 µg/band. The recovery was 99.3-101.5 %. The method was found suitable for routine quality control.
Asian Journal of Plant Sciences 9(1), 44-50 (2010). Beta-sitosterol is one of the major phytoconstituents in cornsilk (style and stigma of Zea mays Linn.). An HPTLC method for the standardization of cornsilk as a bioavailable source of beta-sitosterol is reported. HPTLC of methanolic extracts of dried cornsilk and plasma of rabbits (1 h after injection of plant slurry) on silica gel with toluene - ethyl acetate - methanol - glacial acetic acid 80:10:5:3 with chamber saturation for 30 min. Detection by treatment with Liebermann-Burchard reagent. Beta-sitosterol was well resolved with an hRf value of 48. Quantitative determination by fluorescence measurement at 366 nm. The method was suitable for the pharmacokinetic study (absorption - elimination). The study confirmed the bioavailability of beta-sitosterol from cornsilk, which is therefore a potential natural source of beta-sitosterol.
Eurasian J. Anal.Chem. 5(1), 21-24 (2010). A stability-indicating HPTLC method has been developed for simultaneous estimation of amlodipine besylate and nebivolol hydrochloride. HPTLC on silica gel with ethyl acetate - methanol - 25% ammonia 17:2:2. The hRf value of amlodipine besylate was 40 and of nebivolol hydrochloride 60. Densitometric quantification at 240 nm for amlodipine and 260 nm for nebivolol. The method was linear in the range of 500-2000 ng/band for both compounds. Degradation products formed under stress conditions (acid, alkali, oxidative, dry heat, photo degradation) were well separated from the main compound. The method was suitable for quality control and stability studies.
International Journal of ChemTech Research 2(2), 1042-1046 (2010) HPTLC on silica gel with dichloromethane - methanol 9:1 in a twin-trough chamber saturated for 30 min. The hRf value was 70. Densitometric evaluation in absorbance mode at 254 nm. The method was linear in the range of 400-2000 ng/band. The average recovery was 101.2 %.
J. Planar Chromatogr. 23, 304-308 (2010). Chromatographic investigation of ranitidin and degradation products by TLC on silica gel, RP-18, alumina, cellulose, and amino phase and by HPTLC on silica gel and amino phase. HPTLC of ranitidin and degradation products in pharmaceutical preparations on silica gel with pure solvents (methanol, ethyl acetate, acetonitrile, and DMSO) and binary mixtures (acetonitrile - DMSO, acetonitrile - methanol, and ethyl acetate - methanol) with chamber saturation. The best separation of ranitidine and its photolytic degradation products was obtained on RP-18 W with methanol - water mixtures in a wide range of concentrations as mobile phase. Detection by spraying with sulfuric acid - methanol 1:4 and heating for 10 min at 120 °C.