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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- 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.
CBS 114, 9-10 (2015). HPTLC of phosphodiesterase type 5 inhibitors Viagra (sildenafil), Levitra (vardenafil), Cialis (tadalafil) and their analogs (hydroxyacetildenafil, homosildenafil, thiohomosildenafil, acetildenafil, acetaminotadalafil, propoxyphenyl, hydroxyhomosildenafil, hydroxyhomosildenafil, and_x000D_
hydroxythiohomosildenafil) on silica gel with t-butyl methyl ether – methanol – 28 % ammonia 20:2:1 with chamber saturation, migration distance 70 mm. Detection under UV 254 and 366 nm. Densitometric evaluation by absorbance measurement at 232 nm. Identification of the substances based on their hRf values and distinctly different UV spectra.
J. Planar Chromatogr. 29, 184-189 (2016). HPTLC of (±)-etodolac mixed with L-Trp 1:1 as chiral inducing reagent on silica gel with acetonitrile – dichloromethane – methanol 3:1:2. Detection by using iodine vapor. The hRF values for (-)- and (+)-etodolac were 33 and 62, respectively.
J. Planar Chromatogr. 29, 341-346 (2016). HPTLC of artemisinin in the seeds of Artemisia annua on silica gel with n-hexane ‒ ethyl acetate ‒ acetic acid 20:10:1. Detection by dipping into anisaldehyde reagent (glacial acetic acid ‒ sulfuric acid ‒ anisaldehyde 50:1:0.5) followed by heating at 110 °C for 5 min. Quantitative determination by absorbance measurement at 540 nm. The hRF value for artemisinin was 43. Linearity was between 200 and 1000 ng/zone. The intermediate precision was below 0.7 % (n=3). The LOD and LOQ were 30 and 80 ng/zone, respectively. Recovery ranged from 82.9 to 87.1 %.
and chlorzoxazone toxic degradation product by different chromatographic methods
J. Planar Chromatogr. 29, 453-461 (2016). HPTLC of chlorzoxazone (1) and diclofenac potassium (2) in the presence of the nephrotoxic chlorzoxazone degradation product_x000D_
2-amino-4-chlorophenol (3) on silica gel with chloroform ‒ ethanol ‒ triethylamine 90:10:1. Quantitative determination by absorbance measurement at 230 nm. The hRF values for (1) to (3) were 63, 35 and 42, respectively. Linearities ranged between 1.5-5 μg/zone for (1), 0.5-4 μg/zone for (2) and 0.4-4 μg/zone for (3). The intermediate precisions were below 1.3 % (n=3). The LODs and LOQs were 320 and 980 ng/zone for (1), 140 and 450 ng/zone for (2) and 120 and 370 ng/zone for (3), respectively. Average recoveries were 100.2 % for (1), 99.3 % for (2) and 99.4 % for (3).
J. Planar Chromatogr. 30, 97-105 (2017). Review of current applications of room temperature ionic liquids on planar chromatography as mobile phases. Methylammonium, ethylammonium, propylammonium, isopropylammonium, butylammonium, s-butylammonium, dipropylammonium, tributylammonium were reported to be used as replacements for organic solvents in binary systems. As mobile phase additives, room temperature ionic liquids were used for the separation of peptides and basic drugs in both normal phase and reversed phase chromatography with an emphasis on their role as masking agents. The authors suggested that given the large number of possible cation and anion combinations, systematic methods that characterize solvation properties for both ionic liquids and organic solvents are required.
infected by Staphylococcus aureus – From traditional practice to scientific
approach using HPTLC-densitometry
J. Ethnopharmacol. 204, 26-35 (2017). HPTLC of quercitrin (1), isoquercitrin (2), quercitrin-3-O-β-D-xylopyranosyl-α-L-rhamnopyranoside (3) on silica gel with ethyl acetate – formic acid – acetic acid – water 100:11:11:26. Detection by spraying with NEU`s reagent (diphenylborinic acid 2-aminoethylester, natural product reagent), followed by drying at 110 °C for 2 min. Quantitative determination by absorbance measurement at 265 nm. LOD and LOQ were 31 ng/zone and 75 ng/zone for (2). Recovery was between 99.8 and 101.1 % for (2). Intermediate precision was <2 % (n=3).
Biochem. Biophys. Res. Commun. 487, 702-708 (2017). HPTLC of the reaction products of different 14C-labeled substrates of the mevalonate pathway (MVA, MVA-5-P, MVA-3-P, MVA-5-PP) and the recombinant Flavobacterium johnsoniae protein on silica gel with n-propanol – 28 % ammonia – water 6:3:1. The distribution of radioactivity on the TLC plate was detected using a suitable image analyzer.
J. Chromatogr. A 1473, 133-142 (2016). Development of a simple, accurate and precise method for the analysis of proton pump inhibitors and their co-formulated drugs, available as binary combination, by HPTLC on silica gel with toluene – iso-propranol – acetone – ammonia 50:23:25:2. Identification of 14 analytes (except for rabeprazole and lansoprazole which could not be separated) based on hRf and recorded peak spectra. Qantitative determination by densitometry at 290 nm. The linear response for the selected drugs was good with correlation coefficients ≥0.9993. The LOD and LOQ was between 7-160 ng/band and 21-478 ng/band, respectively, for all the analytes. Assessment of the method performance by analyzing different laboratory simulated mixtures and some marketed formulations of the selected drugs, and successful application of the method to investigate potential counterfeit of proton pump inhibitors through a series of simulated formulations with good accuracy and precision.