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. Chromatogr. Sci. 46 (1), 10-14 (2008). Quantitative determination of rabeprazole and mosapride in their combined pharmaceutical dosage forms by TLC on silica gel with ethyl acetate - methanol - benzene 4:1:5. Quantification by densitometry at 276 nm. Linearity was between 400 and 1200 ng/spot for rabeprazole and between 300 and 900 ng/spot for mosaprid, respectively. The limit of detection was 132 ng/spot for rabeprazole and 98 ng/spot for mosapride.
CBS 99, 14-15 (2007). HPTLC of acrylamide prechromatographically derivatized with dansulfinic acid on silica gel in a twin-trough chamber with ethyl acetate over 70 mm after focussing with methanol. Detection by dipping in a 25 % solution of propylene glycol in n-hexane. Quantitative determination by fluorescence measurement at 366/>400 nm. Precision (RSD, n=3 at 3 different concentration levels each) was 4.8 % and recovery (by standard addition) was 96 %. Linearity was between 0.1 and 0.4 µg/L. The limit of quantification was 0.08 µg/L acrylamide in drinking water. Comparison with HPLC-MS/MS showed comparable results for acrylamide in ground water.
60th Indian Pharmaceutical Congress PA-206, (2008). HPTLC of (-)hydroxy citric acid in fruits of Garcina Gummigutta on silica gel with n-propanol - water - acetic acid 50:50:1 in a twin-trough chamber saturated for 10 min. Quantitative determination by absorbance measurement at 210 nm. The method was linear in the range of 100-1000 ng/spot. Recovery was 99.8-100.9 %.
Ind. J. Pharm. Sci. 70(2), 233-236 (2008). HPTLC of duloxetine hydrochloride (in bulk drug and in tablet dosage form) on silica gel with chloroform - methanol 8:1. Quantitative determination by absorbance measurement at 235 nm. The method was linear in the range of 40-200 ng/spot. The method was suitable for routine quality control.
J. AOAC Int. 91, 1149-1153 (2008). HPTLC of berberine on silica gel prewashed with methanol using n-butanol - acetic acid - water 8:1:1 in a twin-trough chamber with chamber saturation for 5 min at 33 °C at 57 % relative humidity. Quantitative determination by absorbance measurement at 350 nm.
Indian Drugs 45(12), 948-951 (2008). HPTLC of nebivolol hydrochloride and hydrochlorothiazide on silica gel with ethyl acetate - methanol - ammonia 17:2:1. Absorbance measurement at 280 nm. The method was linear in the range of 500-1500 µg/mL and 100-500 µg/mL for nebivolol hydrochloride and hydrochlorothiazide respectively. Recovery was 99.3-101.9 % for both compounds. The method is suitable for routine quality control.
60th Indian Pharmaceutical Congress PA-194, (2008). HPTLC of bumetanide on silica gel with toluene - ethyl acetate - formic acid 14:7:1. Quantitative determination by absorbance measurement at 335 nm. In the stability test (stress conditions: acid, alkali, oxidation, dry heat, wet heat, photodegradation) the compound was well separated from degradation products. Linearity was in the range of 100 - 800 ng/spot.
J. AOAC Int. 91, 1179-1185 (2008). HPTLC of harmine, harmaline, vasicine, and vasicinone on silica gel with ethyl acetate - methanol - ammonia 70:10:3 in a twin-trough chamber at 25 °C and 40 % relative humidity. Quantitative determination by absorbance measurement at 366 nm for harmine and harmaline, at 292 nm for vasicine, and at 233 nm for vasicinone.