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. 13, 187-190 (2000). RPTLC of eleven derivatives of 1-[2-hydroxy or 1-[2-acetoxy-3-(4-aryl-1-piperazinyl)propyl]pyrrolidin-2-one on RP 18 with mixtures of acetone - methanol - water, with acetone content between 21.4 and 78.5 %, in 7.1 % increments, and methanol content 14.3 %. Detection under UV.
J. Planar Chromatogr. 14, 188-190 (2001). TLC of finasteride and loratadine on silica gel plates (prewashed with methanol) with chloroform - ethyl acetate 3:2. Evaluation by densitometry at 228 nm. The linear range of the analysis was 0.2 - 2.0 µg, recovery 101.28%. New simple, precise, rapid, selective TLC method.
J. Liqu. Chromatogr. 24, 321-328 (2002). HPTLC of acetaminophen, caffeine, salicylamide and potassium salicylate on HPTLC silica gel containing a preadsorbent zone after pre-washing with dichloromethane -methanol 1:1 with a double-development for a distance of 6 cm with ethyl acetate - methanol - NH3 16:3:1. Quantitation of potassium salicylate by densitometry at 302 nm. Precision was 1.11% and relative standard deviation 1.45% for samples analyzed with six replicates; the limit of detection was 1.50 µg of potassium salicylate.
J. Planar Chromatogr. 15, 274-279 (2002). TLC of 6 p-substituted propanoic acid amides on silica gel with chloroform - ethyl acetate 1:24 and chloroform - acetone and on paraffin oil impregnated silica gel with methanol - water and acetone - water in different ratios. Detection under UV 254 nm.
J. Planar Chromatogr. 15, 380-383 (2002). HPTLC of 24 2-(2,4-dihydroxyphenyl)benzothiazols on RP-8 and RP-18 modified silica gel in a horizontal sandwich chamber. The mobile phases used were water - methanol mixtures with amounts of methanol in the range 0.50-1.0 v/v at intervals of 0.05. Detection at 325 nm.
J. Liq. Chrom. & Rel. Technol. 26, 2673-2685 (2003). TLC of 6 veterinary fluoroquinolones (difloxacin, ciprofloxacin, norfloxacin, sarafloxacin, enrofloxacin, and flumequine) by 1- and 2-dimensional development on silica gel and on diol-, amino-, and cyanopropyl-modified silica gel with six different mobile phases like e.g. dichloromethane - methanol - 2-propanol - 25% NH3 3:3:5:2 and 4:4:5:2. Detection under UV 254 or 366 nm. Optimization procedure.
J. Planar Chromatogr. 16, 438-441 (2003). TLC on silica gel with ethanol (96%) - toluene - chloroform - acetic acid 12:40:28:1 after saturation for at least 2 h at ambient temperature (25°C). Densitometry in absorbance mode between 200 and 400 nm. Quantification at 250 nm for betamethasone dipropionate and at 310 nm for salicylic acid. The method was validated for linearity, homogeneity, detection limit, accuracy, and working range. A cheap, rapid, and simple validated TLC method.
J. Pharm. Biomed. Anal. 34, 525-530 (2004). HPTLC of busulfan, an alkylating agent in pharmaceutical preparations, on Lichrospher silica gel with ethyl acetate - chloroform - methanol 13:4:3 in horizontal sandwich chamber. After development the plate was soaked in 2 % ethanolic solution of 4-nitro benzyl pyridine, followed by heating at 193 °C for 10 min. Quantitative determination by absorbance measurement at 600 nm. The method was validated for accuracy, precision, linearity (100-500 µg/mL), and specificity. The method was suitable for stability studies of busalfan in pharmaceutical preparations.