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.
Chinese J. Hospit. Pharm. 29 (4), 336-338 (2009). TLC of astragaloside in Tianjian capsules on silica gel with chloroform - methanol - water 13:6:2. Detection by spraying with 5 % sulfuric acid in ethanol followed by heating at 105 ºC until coloration. Quantification by densitometry at 515 nm. The linearity was between 0.98 and 4.90 µg/spot (r2 = 0.998), the %RSD was 2.4 % (n = 6) within plate and 2.3 % (n = 6) inter-plate, standard addition recovery was 99.2 % with RSD = 1.7 % (n = 6).
J. Liq. Chromatogr. Relat. Technol. 31, 2673-2685 (2008). TLC of dehydroepiandrosterone on silica gel with chloroform - acetone 17:3 with chamber saturation for 30 min. Detection by dipping into 0.05 % aqueous solutions of visualizing agents (methylene violet, gentian violet, janus blue, methylene blue, malachite green, rhodamine B) and methanolic chloramine T/methanolic sulfuric acid solution. Quantitative determination by densitometry at 200 nm (before derivatization and for methylene violet), 657 nm (gentian violet), 487 nm (janus blue), 488 nm (malachite green), 580 nm (rhodamine B), and 361 nm (chloramine T). LOD was 0.29 µg/zone (without visualizing agent, with chloramine T and with rhodamine B), 4.19 µg/ zone with methylene violet, 1.10 µg/zone with gentian violet, 2.14 µg/zone with janus blue, and 4.19 µg/zone with malachite green, all with an application volume of 5 µL.
J. Planar Chromatogr. 23, 35-39 (2010). HPTLC of ß-carotene on silica gel (prewashed with methanol) with petroleum ether - hexane - acetone 2:3:1 in a saturated twin-trough chamber. Quantitative determination by absorbance measurement at 450 nm. Linearity was between 100 and 600 ng/band. LOD and LOQ were 0.11 and 0.37 ng/band, respectively. Average intra-day precision and inter-day-precision were 0.54 % and 0.50 %, respectively.
Appl. Surf. Sci. 256, 6489-6494 (2010). TLC of naproxen released from a SBA-15 mesoporous silica drug delivery system on silica gel with benzene - tetrachloromethane - acetic acid 7:1:1. Quantitative determination by absorbance measurement at 260 nm at different time intervals. The hRf value of naproxen was 50.
Abstract No. C-97, 61st IPC (2009). Chromatographic methods are reported for identification (TLC) and quantification (HPTLC) of withaferin-A in methanolic and chloroform extract of dried fruits of Withania coagulans. Chromatographic separation on silica gel with toluene - ethyl acetate - formic acid 5:5:1. The identification of withaferin-A in both chloroform and methanolic extracts was performed by comparison of hRf values and UV absorbance maxima (209 nm). Quantification was performed by absorbance measurement at 540 nm after spraying the developed plate with Liebermann-Burchard reagent. Methanolic extracts and chloroform extracts contained 3.67 mg/g and 2.10 mg/g of withaferin-A, respectively. No withaferin-A was found in hydroalcoholic extracts.
J. Planar Chromatogr. 23, 141-147 (2010). HPTLC of p-aminobenzoic acid on silica gel (prewashed with the mobile phase) with diethyl ether - cyclohexane 5:1 in an unsaturated chamber. Quantitative determination by absorbance measurement at 270 nm. Detection by automatic spraying the following reagent solutions: 0.1 mol/L sodium nitrite solution, 0.1 mol/L hydrochloric acid, 0.03 mol/L ethanolic 8-hydroxyquinoline solution, and 10% sodium hydroxide solution. For each solution 2 spraying cycles were applied. After drying quantitative determination by densitometric scanning at 500 nm. Measured before derivatization at 270 nm calibration of p-aminobenzoic acid was perfomed between 50-1600 ng per spot. LOD was 170 ng/spot (calculated) and 50 ng/spot (estimated visually). LOQ (calculated) was 510 ng/spot. The correlation coefficient r was 0.9936 (peak area) and 0.9866 (peak height); the linear range was 200-1800 ng/spot. Measured at 500 nm after derivatization, LOD was 290 ng/spot (calculated) and 50 ng/spot (estimated visually). LOQ (calculated) was 870 ng/spot and 200 ng per spot (estimated visually). The correlation coefficient r was 0.9815 and 0.9538.
Analytical Methods 2, 521-531 (2010). An HPTLC method for determination for paliperidone in formulation as well as for in vitro release studies has been developed. HPTLC on silica gel with methanol - ethyl acetate 4:1. The hRf value was 54. Quantification was performed by densitometric evaluation at 254 nm. The method was linear in the range of 100-600 ng/band. The method was suitable for estimation of the drug in mucoadhesive microemulsion formulations, as well as for solubility and diffusion studies.
J. Planar Chromatogr. 23, 400-405 (2010). OPLC of fructose, glucose, and sucrose in 31 different types of wine (white and red; dry, semi-dry, semi-sweet, and sweet) on silica gel with acetontrile - water 13:2 (as the best of 6 mobile phases tested) under isocratic conditions in overrunning operation mode. Detection by spraying with a mixture of aniline and diphenylamine. Quantitative determination by absorbance measurement at 420 nm.