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. Planar Chromatogr. 1, 61-64 (1988). Studies of TlC behavior of 17 diuretics on silica with neutral, basic and acidic mobile phases. Discussion of the possibility of specific identification and simultaneous quantification with a particular separation problem.
J. Planar Chromatogr. 21, 191-195 (2008). HPTLC of fluconazole and clotrimazole (as internal standard) on silica gel with toluene - chloroform - methanol 6:15:2. Quantitation by densitometry at 210 nm.
Proc. 6th Int. Symp. Instrum. Planar Chromatogr., (Interlaken 1991), Inst. Chromatogr., Bad Dürkheim, FRG, 265-271 (1991). HPTLC of xylose, 3-o-methylglucose and rhamnose in urine with arabinose as internal marker on silica with ethyl acetate - pyridine - acetic acid - water 75:15:10:10. Densitometry after three consecutive runs. Visualization by dipping into aminobenzoic acid reagent. Densitometry by absorbance at 400 nm. CV < 2.7%.
Chromatographia 69 (1-2), 157-161 (2009). TLC of amlodipine besylate (AML) and valsartan (VAL) on silica gel with toluene - methanol - acetic acid 70:30:1. Quantification by absorbance measurement at 244 nm. Linearity was between 100 - 600 ng/spot for AML and 1600 - 9600 ng/spot for VAL. For AML the RSD of intra-day precision was 1.5 - 1.8 % and of inter-day precision 1.2 - 2.0 %. For VAL the RSD of intra-day precision was 0.1 - 0.4 % and of inter-day precision 0.2 - 0.5 %. Accuracy was 98.3 % for AML and 98.7 % for VAL.
J. Chinese Herb Med. (Zhongcaoyao) 23, 633-634 (1992). TLC of cinnamyl aldehyde on silica with petrol ether - ethyl acetate 85:15. Detection under UV 254 nm and by spraying with 2,4-dinitrophenylhydrazine. Quantification by spectrophotometry at 286 nm.
J. Liq. Chromatogr. Relat. Technol. 31, 611-618 (2008). TLC of eleven new bioactive 10-substituted 2,7-diazaphenothiazines on RP-18 with acetone and aqueous TRIS (tris-(hydroxymethyl)aminomethane) buffer pH 7.4 in a saturated chamber. The concentration of acetone in the mobile phase ranged from 50-85 % in 5 % increments. Evaluation under UV 254 nm and 366 nm. The method was used for the experimental determination of lipophilicity.
J. Chromatogr. 674, 147-152 (1994). TLC of basic drugs on silica with toluene - acetone - 94% ethanol - NH3. Densitometry at 220 nm and in situ spectra recording in the range of 200 - 400 nm. Identification by correlation of corrected Rf values and spectra. (Ed.: The CAMAG Application Note A-60 is based on publications by these authors.
Ind. J. Pharm. Sci. 70(2), 251-255 (2008). HPTLC of olanzapine and fluoxetine on silica gel with methanol - toluene 2:1. Quantitative determination by absorbance measurement at 233 nm. The method was linear in the range of 100-800 ng/spot for olanzapine and 1000-1200 ng/spot for fluoxetine. Recovery was 99.4-100.4 % for both compounds. Forced degradation studies (acid, base, oxidation, photolyses and thermal) revealed that all the degradation products were well resolved from the principal compound. The method was suitable for routine quality control.