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.
62nd Indian Pharmaceutical Congress Abstract No. F-335 (2010). TLC of ampicillin and dicloxacillin on silica gel with n-butanol – water – formic acid 63:6:4. Quantitative determination by absorbance measurement at 220 nm. The hRf values of ampicillin and dicloxacillin were 85 and 69 respectively. The linearity was in the range of 1-6 µg/zone for both ampicillin and dicloxacillin. The recovery for ampicillin was 98.5-101.9 % and that for dicloxacillin was 98.3-101.3 %.
62nd Indian Pharmaceutical Congress Abstract No. F-290 (2010). TLC of ranolazine on silica gel with methanol – 10 mM ammonium acetate 3:2. The hRf value was 54. Quantitative determination by absorbance measurement at 271 nm. The recovery was 99.9 %.
62nd Indian Pharmaceutical Congress Abstract No. F-262 (2010). TLC of carbamazepine on silica gel with ethyl acetate – toluene – methanol 5:4:1. Quantitative determination by absorbance measurement at 285 nm. The hRf value was 47. The linearity was in the range of 100-600 ng/zone with r2 = 0.9995. The limit of detection was found to be 17 ng/zone, whereas the limit of quantitation was found to be 50 ng/zone.
Chinese J. Food R & D, Test & Anal. 31 (10), 134-138 (2010). TLC of chlorogenic acid on silica gel with ethyl acetate – water – formic acid 17:2:2. Detection by spraying with 2 % FeCl – 1 % KFe(CN) 4:1.
J. Trad. Chinese Veterinary Med. (5), 53-55 (2010). TLC on silica gel with acetone – ethanol – hydrochloric acid 10:6:1. Detection by spraying with bismuth potassium iodide – 1 % FeCl3 in ethanol 5:1 and heating at 100 ºC. Quantitative determination of stachydrine by absorbance measurement at 510 nm. The precision was 3.7 %RSD within plate (n=8), and the stability of the measurement within 120 minutes was 4.5 %RSD (n=5). The linearity range was 3.2-38.3 µg/zone (r=0.997, n=6) and standard addition recovery was 96.6 % (RSD=2.0 %, n=6).
Analytical Chemistry, An Indian Journal 9(3) (2010). HPTLC of a racemic mixture of oxybutynin chloride on chiral phase with toluene – acetone – methanol 8:1:1. Both enantiomers were well separated with hRf values of 47 and 63. The identity of the isomers was established by on-line UV, NMR and MS data. The method was validated using NP-TLC and the same mobile phase. The method was linear in the range of 50-350 µg/band with a recovery of 98.2-101.7 %.
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.
J. Planar Chromatogr. 24, 487-490 (2011). HPTLC of vitamin D3 in fish oil after saponification and purification on silica gel with chloroform - diethyl ether 9:1 with chamber saturation for 20 min. Quantitative determination at 280 nm. Linearity was between 200 and 1000 ng/band. The LOD and LOQ were 29 and 232 ng/band, respectively. The repeatability (RSD) was 4.6 %; the %RSD for intermediate precision was 0.9; the %RSD for intra-day precision (n = 6) was between 2.9-5.9 % and the %RSD for inter-day precision (n = 6) was between 3.2-6.4 %. Recovery was 97.6 - 104.2 % with a %RSD of 3.9 - 4.8 %.