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.
J. Chinese Trad. Patent Med. (Zhongchengyao) 22 (9), 618-621 (2000). TLC on silica gel with 1) cyclohexane - chloroform - ethyl acetate - acetic acid 40:10:16:1, 2) hexane - ethyl acetate 17:3, 3) petroleum ether (30-60°C) - ethyl formate - formic acid 15:5:1. Detection 1) by spraying with 10% sulfuric acid in ethanol and heating at 100°C for 5 min, 2) by spraying with 5% vanillin in sulfuric acid, 3) under UV 254 nm. Identification by finger print. Quantitation of paeoniflorin by HPLC.
JAOAC Int. 84, 1219-1231 (2001). Compilation of the role of planar chromatography (PC) in medicinal and aromatic plant (MAP) research and development, and demonstration of the importance of the technique, after extraction, in the analysis of MAP (identification and quantitative determination of the separated compound/s), in the purification and isolation process, and in different types of screening procedure. Special attention is paid to analytical, micropreparative and preparative forced-flow techniques, for example OPLC and rotation planar chromatography (RPC). Purification and isolation procedures are shown in flowcharts. Some applications, relating to different classes of substance, are presented to demonstrate the versatility of various planar chromatographic techniques.
J. Liq. Chrom. Rel. Tech. 38, 271-282 (2015). HPTLC of (1) terazosin, (2) doxazosin, (3) prazosin, and (4) alfuzosin in plasma on silica gel with acetonitrile - phosphate buffer 3:7 at pH 3. Quantitative determination by absorbance measurement at 332 nm. The hRF values of (1) to (4) were 52, 47, 53 and 41, respectively. Linearities were between 10 and 100 ng/zone for (1) and (2), between 15 and 75 ng/zone for (3) and between 5 and 100 ng/zone for (4). The LOD and LOQ were 4 and 9 ng/zone for (1), 5 and 10 ng/zone for (2), 7 and 14 ng/zone for (3) and 4 and 5 ng/zone for (4), respectively. The intermediate intra-day and inter-day precisions were below 2.6 % (n=6). Mean recoveries were found in the range of 94.2-99.9 %.
J. Planar Chromatogr. 20, 335-339 (2007). TLC of etoricoxib (rofecoxib as internal standard) on silica gel in a filter-paper-lined twin-trough chamber previously saturated with mobile phase vapor for 30 min with toluene - 1,4-dioxane - methanol 17:2:1. Densitometric analysis of etoricoxib was performed in absorbance mode at 235 nm. The limits of detection and quantitation were 30 and 100 ng/zone, respectively.
Determination by using autoradio - layer chromatographic recorder.
J. Planar Chromatogr. 20, 149-152 (2007). HPTLC of nebivolol hydrochloride on silica gel prewashed with methanol with toluene - ethyl acetate - methanol - formic acid 8:6:4:1 in a saturated twin-trough chamber. Densitometric quantification at 285 and 298 nm.
J. Chromatogr. 445, 385-392 (1988). TLC on silica with hexane - ethyl acetate - acetone 5:4:1. Immersion for 10-20 s in a fluorogenic reagent containing 100 mL ethanol, 100 mL ether and 4 mL concentrated sulfuric acid. Development in the 2nd direction with hexane - ethyl acetate - dichloromethane 1:2:2. Detection under UV 366 nm. Detection limit, 0.5 µg for both.
J. Planar Chromatogr. 21, 107-112 (2008). Optimization and comparison of the acidic visualization methods most often used for steroids. OPLC of ethinyl estradiol, ’dienolether’ (3-methoxyestra-2,5(10)-dien-17b-ol), norethisterone, norethisterone acetate, norethisterone enanthate, nandrolone, and nandrolone decanoate on HPTLC silica gel with cyclohexanone - ethyl acetate - chloroform 1:1:1. Detection with sulfuric acid at three different concentrations, phosphomolybdic acid, and phosphoric acid with different heating temperatures for different times. Evaluation under UV 366 nm (sulfuric acid, phosphoric acid) and in white light (phosphomolybdic acid). It was found that derivatization at higher temperatures for shorter periods usually results in greater sensitivity, although heating for longer periods at lower temperatures leads to a more stable and robust result. Evaluation by videodensitometry.