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
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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.

      109 061
      A simple, rapid, and sensitive HPTLC method for the estimation of clarithromycin
      P. LOYA, P. D. HAMRAPURKAR* (*Principal K. M. Kundnani College of Pharmacy, Plot no. 23, Joy Building, Rambhau, Salgaonkar Marg, Cuffe parade, Colaba, Mumbai - 400 005, India; phamrapurkar@gmail.com)

      J. Planar Chromatogr. 24, 534-538 (2011). HPTLC of clarithromycin in plasma on silica gel (prewashed with methanol) with ethyl acetate - methanol - 15 % ammonium acetate (pH 10.6) 7:2:1 in a twin-trough chamber with saturation for 15 min. Detection by dipping into xanthydrol solution (10 % in methanol). Quantitative determination by densitometry in absorbance mode at 506 nm. The hRf was 62. The method was linear over the range of 0.1-3.0 µg/mL (r2 = 0.9974). The recovery (by standard addition) was over 85 %. The intra-day and inter-day precision (%RSD) of the assay was in the range of 0.8-4.6 %. The recovery was above 95 %.

      Classification: 28a
      113 057
      Development and validation of a thin-layer chromatographic–densitometric method for the analysis of clotrimazole vaginal tablets
      B. NYAMWERU, J. SEMPOMBE, E. KAALE*, T. LAYLOFF (*Medicinal Chemistry School of
      Pharmacy, Muhimbili University of Health and Allied Sciences, PO Box 65013,
      Dar es Salaam, Tanzania, elia.kaale@lycos.com)

      J. Planar Chromatogr. 27, 47-51 (2014). HPTLC of clotrimazole in vaginal tablets on silica gel with toluene - acetone 3:2. Quantitative determination by absorbance measurement at 215 nm. The hRF value for clotrimazole was 27. Linearity was in the range of 1000-2400 ng/zone. The intermediate/interday/intra-day precisions were below 1.3 % (n=6). Recovery was between 99.1 and 100.1 %.

      Classification: 28a
      117 100
      Use of thin-layer chromatography to detect counterfeit sulfadoxine/pyrimethamine tablets with the wrong active ingredient in Malawi
      F. KHULUZA, S. KIGERA, R.W.O. JAEHNKE, L. HEIDE* (*Pharmaceutical Institute, Eberhard-Karls-University Tuebingen, Auf der Morgenstelle 8, 72076 Tuebingen, Germany, heide@uni?tuebingen.de)

      Malaria J. 15, 215 (2016). TLC of methanol extracted tablets and the standards sulfadoxine and pyrimethamine with the GPHF Minilab (procedure for sulfadoxine) on silica gel with ethyl acetate – methanol 3:1 for approximately 15 min. Detection under UV 254 nm, and by exposure to iodine vapor. Documentation with a commercial digital camera. For comparison to authentic paracetamol and co-trimoxazole samples, the GPHF Minilab solvent systems for paracetamol (acetone – toluene – acetic acid 20:20:1), pyrimethamine (ethyl acetate – methanol – acetone – conc. aqueous ammonia 24:12:4:1) and co-trimoxazole (ethyl acetate – methanol 3:1) were used. 28 market samples were collected and analyzed, 10 samples were further analyzed by HPLC according to the USP. One sample was falsified, the box contained a mixture of paracetamol tablets and co-trimoxazole tablets and none of the tablets contained any anti-malarial drugs.

      Classification: 28a
      120 075
      Bioassay-guided detection and identification of an antibacterial compound from greater burdock
      Agnes MORICZ*, D. KRUZSELYI, P. OTT (*Plant Protection Institute, Centre for
      Agricultural Research, Hungarian Academy of Sciences, Herman O. Street 15,
      1022 Budapest, Hungary, moricz.agnes@agrar.mta.hu)

      J. Planar Chromatogr. 31, 87-91 (2018). HPTLC-direct bioautography of the ethanolic leaf extract of greater burdock (Arctium lappa L.) on silica gel with chloroform – methanol – water 36:4:1. Direct bioautography by dipping into a bacterial suspension of Bacillus subtilis F1276 and Pseudomonas maculicola, followed by incubation for 2 h and dipping into an aqueous solution of 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) vital dye. The main antibacterial compound was analyzed by HPLC-MS.

      Classification: 28a
      56 119
      Thin-layer chromatographic analysis of adriamycinone in fermentation broths
      K. DORNBERGER, C. STENGEL, N. MIOSGA

      J. Chromatogr. 328, 432-435 (1985). TLC of anthracyclinones obtained from hydralized fermentation broths on silica impregnated with a 0.5 N oxalic acid solution with chloroform - acetone 7:3. Fluorimetric determination at 589/483 nm after scraping of the spots from the plate.

      Classification: 28a
      59 116
      Isolation and liquid chromatographic determination of the cyclic peptide mycotoxin cyclosporin A from rice
      J.V. EDWARDS, E.B. LILLEHOJ

      J.A.O.A.C. 70, 126-129 (1987). TLC of cyclosporin A on silica with 3 solvent systems: butanol - acetic acid - water 4:1:1, chloroform - acetic acid - methanol 85:10:5, ethyl acetate - hexane - acetone 2:1:1. Detection with iodine, spraying with 6N HCl, oven-drying at 110 °C for 30 min and spraying with 0.1 % ninhydrin in butanol.

      Keywords: food analysis
      Classification: 28a
      61 159
      (Determination of biozamycin in chicken eggs and meat by fluorescence densitometry and high performance thin-layer chromatography
      K. SAITO, M. HORIE, Y. HOSHINO, N. NOSE, H. NAKAZAWA, (Saitama Profct. Inst. Public Health, Urawa, Japan 338)

      Jap. Hygienic Chem. 32, 442-446 (1986) (Eisei Kagaku). TLC on silica with acetonitrile - water 7:1. Determination by fluorescence densitometry at 365 nm. Detection limit 0.2 µg/g.

      Classification: 28a
      64 230
      TLC-UV spectrometric determination of the capreomycon sulfate component
      G. WANG (Wang Guiyin), (Hennan Inst. Drug Cent., Zhengzhou, P.R. China)

      Chinese J. Antibiotics 13, 376-377 (1988). TLC on silica with 10% ammonium acetate - 10% NH3 - acetone 9:1:10. Detection under UV 254 nm. Quantification by spectrometry at 269 nm after removal from plate and elution with citric buffer.

      Classification: 28a