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.
Acta Chromatographica 22 (2), 227-236 (2010), DOI:10.1556/AChrom.22.2010.2.6. TLC of piperine, the bioactive constituent of black pepper (Piper nigrum), on silica gel with dichloromethane – ethyl acetate 9:1 at 30 °C in a twin-trough chamber saturated for 30 min. Detection under UV light at 254 nm and documentation with a digital camera. Based on the image a density profile plot was established by Scion Image software, which allowed to calculate the concentration of piperine by comparison of the peak areas of samples and piperine standards. The linearity was in the range of 24-84 ng/zone (r2=0.9927). The limits of detection and quantitation were 0.35 and 1.05 ng/zone, respectively. Precision (repeatability, n=6) and intermediate precision (2 days, n=12) both are below 2.6 %RSD. Recovery is between 96.7-101.4 %.
Acta Chromatographica 22 (3), 481-489 (2010). HPTLC on silica gel with toluene – ethyl acetate – methanol – formic acid 8:10:5:2. The hRf values were 22, 19, and 81 for sennosides A and B and kaempferol, respectively. Quantification by densitometry at 270 nm. The recovery of sennosides A and B and kaempferol from Cassia fistula extract were 98.0, 98.7, and 99.1 %, respectively. The linearity was in the range of 100–400 ng/band. Instrument precision was in the range of 1.03-1.33 % and method precision in the range of 1.3-1.8 %.
Acta Chromatographica 22 (2), 259-265 (2010), DOI:10.1556/AChrom.22.2010.2.8. Description of a new, simple, precise, and accurate method for quantification of (-)-epicatechin in the leaves of Cassia fistula by HPTLC on silica gel with toluene – ethyl acetate – formic acid – methanol 205:3:1:1. Quantification by densitometry at 280 nm. The linearity was in the range of 200–800 ng/band. Method precision was 1.4 %RSD and instrumental precision 1.1 %RSD. Recovery was 98.1 % and specificity regarding matrix was given.
J. Chromatogr. A 1218 (19), 2745-2753 (2011). HPTLC of sucralose in waste water on silica gel with isopropyl acetate – methanol – water 15:3:1. The developing time was 15 min. Detection with p-aminobenzoic acid reagent. Quantification by absorbance measurement at 400 nm. The limit of quantification was 100 ng/L at a recovery rate of 80 % and the extraction of a 0.5 L water sample. An interlaboratory trial in 2008 showed good agreement of the sucralose content determined in four water samples by HPTLC and other methods (HPLC–MS/MS or HPLC–TOF-MS). The good accuracy and high sample throughput capacity proved HPTLC as a well suited method for quantification of sucralose in various aqueous matrices.
J. Planar Chromatogr. 24, 491-496 (2011). HPTLC of pentose, hexose and disaccharides in pharmaceutical formulations on silica with aqueous micellar bile salt, sodium deoxycholate in acetonitrile 1:5 with chamber saturation. This mobile phase provided the best separation of the 22 phases tested. Detection by spraying with ethanolic orcinol solution.
Asian Journal of Chemistry 23(5), 2011-2013 (2011). Methods are reported for determination of organophosphorus pesticides using TLC-cholinesterase inhibition as well as GC-FID. The powdered rice sample was initially extracted with ethyl acetate. The extract was cleaned up by GPC, eluted with cyclohexane - ethyl acetate 1:1, evaporated, and taken up in acetone. This extract was analysed by TLC on silica gel with ethyl acetate to a developing distance of 10-12 cm. After development the plate was air dried, exposed to bromine vapors, sprayed with enzyme solution and incubated at 37 °C for 30 min and sprayed with the reagent. White spots appeared against bluish-red background. The sample was also analysed by GC and the GC method was very sensitive. However, the TLC method is recommended for preliminary screening of samples.
Planta Med. 74, 1749-1750 (2008). Analytical and preparative TLC of a new monoterpene alkaloid plumerianine, (R)-4’-{(S)-1-hydroxyethyl)-5,6-dihydro-5’H-spiro[cyclopenta[c]pyridine-7,2’-furan}-5’-one, the iridoid 15-demethylplumeride, lupeol, uvaol, and ursolic acid on silica gel with toluene - ethyl acetate 8:2 or 8:3 and chloroform - methanol 9:1. Detection by spraying with vanillin-sulfuric acid reagent.
J. of Chromatogr. A 1218 (33), 5693-5704 (2011) A micro-TLC platform for the fast analysis of low-molecular mass compounds from spirulina samples was developed. The target compounds were extracted with methanol, acetone or tetrahydrofuran. HPTLC on RP-18W with acetone - n-hexane 3:7 in an unsaturated chamber using a temperature controlled micro-planar chromatographic device based on a horizontal chamber. Detection under visible light before and after exposure to iodine vapor. Pictures of the chromatograms were acquired with an office scanner and digitalized. The quantitative data was analyzed using cluster analysis and principal components analysis. With this method it was possible to distinguish genuine spirulina and non-spirulina samples as well as fresh and expired commercial products.