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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      61 125
      Synthesis and some pharmacological properties of two new antagonists of oxytocin
      P. RAKOWSKI*, P. MELIN, B. LAMMEK, (*Inst. of Chemistry, Univ. of Gdansk, Sobieskiego 18, 80-952 Gdansk, Poland)

      Polish Journal of Pharmacology and Pharmacy 39, 303-307 (1987). TLC of two new 1-ß-ß-disubstituted analogues of oxytocin polypeptide hormones on silica with chloroform - methanol 7:3 or 1-butanol - acetic acid - water - pyridine 15:3:3:10 or 1-butanol - acetic acid - water 4:1:5 or ethanol - 0.1 mol/L aqueous pyridine - 0.1 mol/L aqueous acetic acid 4:1:1 or benzene - methanol - acetic acid 2:15:1 or n-hexane - ethyl ether - acetic acid 11:7:1 or benzene - methanol - acetic acid 15:2:1. Visualization with ninhydrin or iodine.

      Classification: 18b
      61 154
      Separation of amphotericin B components by combined thin-layer and high- performance liquid chromatography
      P.M. KELLY (Dep. of Science, Suny Coll. of Technology, Box 3050, Marcy Campus, Utica, N.Y. 13504, USA)

      J. Chromatogr. 437, 221-229 (1988). TLC of the major components of amphotericin B on silica with HPLC-grade methanol. The separated compounds were visualized as contrasting areas under UV 365 nm during the evaporation process. Confirmation of the results by reversed-phase HPLC.

      Classification: 28a
      61 206
      (Determination of total saponins in fiveleaf gynostemma, Gynostemma pentaphyllum
      X. HE (He Xinliang), (Shandong Provincial Inst. for Drug Control, Jinan, P.R. China)

      J. Chinese Herb Med. 18, 447-448 (1987) (Zhong Caoyao). TLC on silica with butanol - ethyl acetate - water 4:1:5. Detection by spraying with sulfuric acid - methanol 1:1, heating at 105 °C and observing under UV.

      Classification: 14, 32e
      61 228
      Instrumental TLC as routine method in pharmaceutical quality control
      B. RENGER, K. WENZ, W. ZIEGENBALG, (Mundipharma GmbH, P.O. Box 1350, D-6250 Limburg, FRG)

      H. TRAITLER, A. STUDER, R.E. KAISER (eds): Instrumental HPTLC, Institute for Chromatography, Bad Dürkheim, FRG (1987), 331-339. Introduction of the use of instrumental TLC and HPTLC as a fast, convenient analytical method for testing pharmaceutical raw materials, bulk substances and finished drugs with the results being as accurate as those obtained with many traditional methods. Instrumental TLC methods have been fully validated.

      Classification: 32a
      62 035
      Application of molecular-secondary- ion mass spectrometry for drug metabolism studies
      H. IWABUCHI, A. NAKAGAWA, KAN-ICHI NAKAMURA*, (*Anal. and Metab. Res. Lab., Sankyo Co., Ltd., Hiro-Machi 1-2-58, Shinagawaku, Tokyo 140, Japan)

      1. Direct analysis of conjugates by thin-layer chromatography-secondary-ion mass spectrometry. J. Chromatogr. 414, 139-148 (1987). Description of a method for direct molecular-secondary-ion mass spectrometry measurement of conjugates of p-nitrophenol and 4-hydroxyanti-pyrine following TLC on silica with butanol - acetic acid - ethanol - water 3:1:1:1. Discussion of the quantitative application using deuterium-labelled internal standards for p-nitrophenol conjugates.

      Classification: 4e, 32b
      62 101
      Application of various planar chromatographic techniques for the separation of iridoid glycosides from Veronica officinalis
      K. DALLENBACH-TOELKE, S. NYIREDY, O. STICHER*, (Pharm. Inst., ETH Zürich, CH-8092 Zürich, Switzerland)

      J. Chromatogr. 404, 365-371 (1987). TLC, HPTLC, OPLC and UCLC of 8 main iridoid glycosides on silica with various solvent systems. Detection by spraying with 1% vanillin in sulfuric acid and densitometry at 420 nm. Comparison of the applicability of the techniques. UCLC = Ultra-micro-chamber Centrifugal Layer Chromatography.

      Classification: 3d, 14
      62 146
      Decomposition of N-(2-chloroethyl)-N-nitroso-carbamoyl amino acid amides
      H.S. VARGA*, J. BODI, M. MESZAROS, K. MEDZIHRADSZKY, (*Research Group for Peptide Chemistry, Hungarian Academy of Sciences, H-1088 Budapest, Muzeum krt. 4/B., Hungary)

      J. of Medicinal Chemistry 31, 1492-1495 (1988). TLC on silica with butanol - acetic acid - water 4:1:1, butanol - pyridine - acetic acid - water 4:1:1:1, chloroform - methanol 9:1. Detection by spraying with ninhydrin and Cl2-tolidine.

      Classification: 18a
      62 197
      Interaction between ascorbic acid and linear and cyclized bile pigments
      M. BARBIER, (Inst. de Chimie des Substances Naturelles, CNRS, F-91190 Gif-sur-Yvette, France)

      A thin-layer chromatography study. J. Chromatogr. 440, 275-280 (1988). TLC of ascorbic adducts of bile pigments on siica with benzene - dichloromethane - methanol 5:1:1. Formation of the adducts on the plate by depositon of a sol. of ascorbic acid as a barrier on a line ca. 1.5 cm from the starting point.

      Classification: 32
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