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.
Eur. J. Clin. Chem. Clin. Biochem. 31, 329-333 (1993). HPTLC of glaphenine, glaphenic acid, 4'-hydroxy-glaphenic acid on silica (with concentrating zone) with chloroform - isopropanol - methanol - NH3 (250g/L) 70:16:12:4.
Asian J. Chem. 19(5), 3627-3632 (2007). TLC of simvastatin and ezetimibe on silica gel with ethyl acetate - chloroform 4:1. Quantitative determination by absorbance measurement at 220 nm. The hRf value of simvastatin was 76 and of ezetimibe 89. Linearity was between 600 and 1400 µg/mL for simvastatin and ezetimibe. The recovery (by standard addition method) was in the range of 99.7 and 99.6 % for both drugs. The proposed method is precise, accurate and can be used for routine analysis of simvastatin and ezetimibe in tablets.
Biomed. Chromatogr. 10, 146-147 (1996). TLC on silica by developing twice with 1) ethyl acetate - isooctane - acetic acid 100:400:11, and 2) ethyl acetate - hexane 3:1. Detection by spraying with Triton X-100 - chloroform - petrol ether 1:9:30. Quantification by densitometry at 340 nm/> 540nm.
Indian Drugs 46(2), 150-153 (2009). HPTLC of hydrochlorthiazide (HZ) in combination with quinapril (QP) or candensartan (CD) on silica gel with toluene - ethyl acetate - glacial acetic acid 2:12:1 (for HZ and QP), or 20:50:1 (for HZ and CD), with chamber saturation for 30 min at room temperature. Quantitative determination by absorbance measurement at 273 nm. The method was linear in the range of 480-960 (HZ), 400-800 (QP) and 50-250 ng/spot (CD).
Chinese J. Pharm. (Zhongguo Yaoxue Zazhi) 33, 165-167 (1998). TLC on silica gel with heptane - chloroform - ethanol - ethyl acetate 10:4:4:3. Quantitation by densitometry. Investigation and discussion of the linear ranges, precision and recoveries of each drug. Precision < 4.89% (n=5) within plate and < 5.23% (n=5) plate-to-plate. Recovery > 91.64 ± 9.16% (n=5).
J. Planar Chromatogr. 22, 191-196 (2009). TLC of pioglitazone hydrochloride ((+/-)-5-{p-[2-(5-ethyl-2-pyridyl)ethoxy]benzyl}-2,4-thiazolidinedione hydrochloride and degradation products (after acid and alkaline hydrolysis, oxidation, photochemical and thermal treatment) on RP-18 with acetone - acetic acid - water 40:10:1 in a twin trough chamber saturated for 30 min at room temperature (25 +/- 2 °C). Quantitative determination by absorbance measurement at 225 nm. The limit of detection and quantification was 47 and 141 ng/zone, respectively.
Anal. Biochem. 271, 114-116 (1999). TLC of 10 to 20 (l of the assay mixture containing the SYBR Green II-bound reaction products AMP and ADP on silica with dioxane - NH3 - water 6:1:4. The resulting fluorescence image was directly scanned and quantitated.
J. AOAC Int. 92, 387-393 (2009). TLC of tenatoprazole - before and after acid and alkali hydrolysis, oxidation and photodegradation - on silica gel, prewashed with methanol and dried at 110 °C for 5 min, with toluene - ethyl acetate - methanol 6:4:1 in a twin trough chamber saturated with the mobile phase for 30 min at 25 °C. Quantitative determination by absorbance measurement at 306 nm. The limit of detection and limit of quantitation were 50 and 100 ng/spot, respectively.