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.

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      93 016
      An LC/DAD-UV/MS method for the rapid detection of aristolochic acid in plant preparations
      J.-R. Ioset, G. E. Raoelison, K. Hostettmann* (*Institute de Pharmacognosie et Phytochimie, B. E. P., CH-1015 Lausanne, Switzerland)

      Planta med. 68, 856-858 (2002).TLC of aristolochic acid on silica gel with chloroform - methanol - acetic acid 13:4:1 before submitting to a second migration on RP-18 with methanol - water 7:13. Detection by spraying with diphenylamine reagent (0.5 % diphenylamine in 60 % sulfuric acid) followed by heating for 10 min at 100 °C. Detection limit 1 µg in visible light and 0.2 µg under UV light at 366 nm.

      Classification: 8b, 11a
      93 080
      Cleaning validation by TLC determination of norfloxacin as residue on pharmaceutical equipment surfaces
      I. VOVK*, B. SIMONOVSKA (*National Institute of Chemistry, Hajdrihova 19, SI-1000 Ljubljana, Slovenia, irena.vovk@ki.si, breda.simonovska@ki.si)

      CBS 89, 2-3 (2002). HPTLC of norfloxacin on silica gel (prewashed with methanol - chloroform 1:1) with methanol - chloroform - ammonia 51:34:15 in horizontal developing chamber with sandwich configuration. Quantitative determination by fluorescence measurement at 313/>400 nm.

      Classification: 28a, 37
      93 112
      Analysis of constituents of devil’s claw and determination of their bioactivity by HPTLC
      A. KOCH*, R. RICHTER, (*Frohme Apotheke, Frohmestrasse 14, D-22457 Hamburg, Germany, koch@frohme-apotheke.de)

      CBS 89, 4-7 (2002). HPTLC of devil’s claw extract on lichrospher silica gel with ethyl acetate - ethanol (70 %) 7:3 over 70 mm with chamber saturation. Detection by dipping in anisaldehyde - sulfuric acid reagent followed by heating at 105 °C until colors develop. Determination of bioactivity with DPPH-biotest by spraying with 0.05 % solution of (2,2-di-(4-tert-octylphenol)-1-picrylhydrazyl in methanol. Determination of antibiotic properties with Merck Chrom Biodip test by dipping in bacteria solution and incubation at 26 °C for 20 h, followed by spraying with yellow MTT tetrazolium salt.

      Classification: 32e
      93 132
      HPTLC and video-technology for stability tests of plant extracts
      A. SCHMID* (*Institute of Pharmacy, University of Basel, Switzerland)

      CBS 86, 10-12 (2001) HPTLC of valerian root extracts on silica gel (prewashed with methanol) with chloroform - ethyl acetate - propanol 15:10:1. Detection by dipping for 1 s in 15 % sulfuric acid in methanol followed by heating at 120 °C for 10 min and cooling to room temperature. Evaluation with video technology (VideoStore/VideoScan).

      Classification: 32e
      93 152
      (Study of the quality standard of Tianqi capsules
      L. XU (XU LITING), H. XIE (XIE HUA), ZH. JIA (JIA ZHENGPING), B. LIU (LIU BAIOU) (General Hosp., Lanzhou Command, PLA, Lanzhou 730050, P. R. China)

      J. Chinese Trad. Patent Med. (Zhongchengyao) 10, 807-809 (2004). TLC on silica gel plates with 1) chloroform - methanol - water 13:7:2, 2) chloroform - acetone - formic acid 25:10:4. Detection 1) by spraying with 10 % H2SO4 in ethanol and heating at 105 ºC, 2) by ammonia vapor and under UV 365 nm. Identification by fingerprint techniques. Quantitative determination of salidroside by HPLC.

      Classification: 4d, 32c
      94 043
      Purification and characterization of corrinoid compounds from a Japanese fish sauce
      F. WATANABE*, T. MICHIHATA, S. TAKENAKA, H. KITTAKA-KATSURA, T. ENOMOTO, E. MIYAMOTO, S. ADACHI (*Department of Health Science, Kochi Women’s University, Kochi 780-8515 Japan)

      J. Liq. Chrom. Rel. Technol. 27, 2113-2119 (2004). TLC of corrinoid compounds, authentic B12 and cyanocobamides (benzimidazolyl-, 5-hydroxy-benzimidazolyl- and 7-adenylcyanocobamides) on silica gel with 2-propanol - 28% ammonia - water 7:1:2 in the dark at 25 °C. Detection under daylight as pink-colored spots.

      Classification: 27
      94 072
      (Identification of Tongluo Xiaoshuan capsules by thin-layer chromatography
      F. LI (Li Fengqin) (Puyang Inst. Drug Cont., Puyang, Henan 457000, China)

      Chinese J. Trad. Patent Med. (Zhongchengyao) 26 (7), Appendix 12-14 (2004). TLC of Tongluo Xiaoshuan capsule extracts on silica gel with 1) chloroform - methanol - water 60:72:1; 2) n-hexane - ethyl acetate 3:1. Detection 1) by spraying with phosphomolybdic acid solution in ethanol and heating at 105 ºC for several min; 2) under UV 365 nm. Identification by fingerprint technique.

      Classification: 32c
      94 094
      High-performance chromatographic determination of celecoxib in its dosage form
      R. T. SANE, S. PANDIT, S. KHEDKAR* (*S. P. Mandali’s Ramnarian Ruia College, Matunga, Mumbai 400 019, India)

      J. Planar Chromatogr. 17, 61-64 (2004). HPTLC of celecoxib and loratadine (as internal standard) on silica gel after prewashing and bandwise application with n-hexane - ethyl acetate 3:2 in a twin-trough chamber and equilibration for 10 min. Quantitative determination at 262 nm. Mean recovery 100.03 %.

      Classification: 32a
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