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.

      77 084
      Determination of allantoin in biological, cosmetic, and pharmaceutical samples
      X.B. CHEN, W. MATUSZEWSKI, J. KOWALZYK, (Rowett Research Inst., Bucksburn, Aberdeen AB2 9SB, UK)

      J. AOAC Int. 79, 628-635 (1996). TLC of allantoin in pharmaceuticals on silica with e.g. methanol - acetone - formic acid - water 40:2:1:6 and in urine on cellulose with butanol - acetic acid - water 2:1:1. Detection with pDMAB (Ehrlich's reagent). Quantification by densitometry at 445 nm. TLC as fast and inexpensive semiquantitative method for estimation of allantoin in natural samples.

      Classification: 23e
      99 059
      Automatic selection of mobile phases - VI) Thin-Layer Chromatography on silica of libraries of piperidinones
      N. T. BURDZHIEV, C. E. PALAMAREV, M. D. PALAMAREVA* (*Department of Chemistry, University of Sofia, 1, James Bouchier Avenue, Sofia 1164, Bulgaria; mpalamareva@chem.uni-sofia.bg)

      J. Liq. Chromatogr. Relat. Technol. 29, 2045-2057 (2006). TLC of substituted trans-piperidinones comprising 15 amidolactames and 7 aminolactames on silica gel with 13 mobile phase systems with LSChrom software. The procedure takes into account the adsorption properties of the mobile phase (parameter epsilon), stationary phase, and sample structure expressed by the relevant group.

      Classification: 3d, 23e
      106 114
      HPLC, TLC, and first-derivative spectrophotometry stability-indicating methods for the determination of tropisetron in the presence of its acid degradates
      L.S. ABDEL-FATTAH, Z. EL-SHERIF, K.M. KILANI, Dalia A. EL-HADDAD* (*National Organization for Drug Control & Research, 6&7 AboHazem St, Pyramids, P. O. Box 29, Giza, Egypt; daliaelhaddad@hotmail.com)

      J. AOAC Int. 93, 1180-1191 (2010). TLC of tropisetron and its acid-induced degradation products on silica gel with methanol - glacial acetic acid 22:3 with chamber saturation for 45 min. Detection under UV light at 254 nm. Quantitative determination by scanning at 285 nm. The hRf values were 44, 84, and 92 for tropisetron and degradates I and II, respectively. Linearity was between 1 and 10 µg/zone. Mean accuracy was 100.2 %. The precision was 0.64 %.The limit of detection and quantification for tropisetron was 0.26 and 0.80 µg/zone, respectively. The intraday and interday precisions were evaluated by assaying freshly prepared samples of tropisetron in triplicate concentrations, i. e. 3, 5, and and 9 µg/zone, resulting in 99.8 %, 100.3 %, and 100.4 %, respectively, for interday precision and 99.7 %, 100.2 %, and 99.7 %, respectively, for intraday precision (with a precision of 0.9 %, 0.6 %, 0.8 % and 0.6 %, 0.4 %, 0.6 %, respectively).

      Classification: 23
      54 089
      Magyar Kemini Folyoirat 90, 124-129 (1984)
      G. KORANYI, E. SZEBENYI-GYOERI, A. VELIN-PRIKIDANOVICS, J. BERLIK

      (Hungarian). (Electrochemical studies on benzimidazole derivatives. I. Anodic oxidation of 2-amino-benzimidazole.) TLC of 2-amino-benzimidazole on silica with chloroform - CCl4 - methanol 8:5:1.

      Keywords:
      Classification: 23
      73 015
      Reversed phase liquid chromatography of some benzimidazole derivatives
      S.M. PETROVIC*, M. ACANSKI, N.U. PERISIC-JANJIC, D.J. VLAOVIC, (*Dept. Anal. Chem., Fac Technol., Univ. Novi Sad, Cara Lazaral, P. O. Box 340, 21000 Novi Sad, Yugoslavia)

      Chromatographia 37, 98-104 (1993). RP TLC of title compounds on RP-18 silica with aqueous NH3 (pH 11.19-11.69) - methanol 25:75. Determination of Rf values and calculation of k values. Study of the retention behavior of the compounds as a function of the pH values. Investigation of the effect of composition of the aqueous phase, the molecular structure of the aqueous phase, and the type of organic modifier on the relationship between the retention constant (log k) and the pH of the aqueous phase.

      Keywords:
      Classification: 2c, 23
      63 129
      Review - High-performance liquid chromatography of porphyrins
      C.K. LIM*, F. LI, T.J. PETERS, (*Div. Clin. Cell Biol., MRC Clin. Res. Cent., Watford Road, Harrow, Middlesex HAI 3UJ, UK)

      J. Chromatogr. 429, 123-153 (1988). A section of the review on TLC of porphyrins with 9 references emphasizing its advantages.

      Keywords:
      Classification: 23a
      91 043
      Thin-layer chromatographic mobility of some tetraphenylporphyrin derivatives
      P. KUS, (Dept. of Chem., Silesian Univ., 9, Szkolna Street, 40-006 Katowice, Poland)

      J. Planar Chromatogr. 15, 383-386 (2002). TLC of 7 meso-tetraphenylporphyrin derivatives on silica gel, alumina, cellulose, polyamide and silica gel with Cu and chiral reagent with several single- or two-component mobile phases. Detection of spots visually.

      Keywords:
      Classification: 23a
      96 058
      Use of selected structural descriptors for evaluation of the lipophilicity of bile acids investigated by RP HPTLC
      Alina PYKA*, M. DOLOWY, D. GURAK (*Department of Analytical Chemistry, Faculty of Pharmacy, Silesian Academy of Medicine, Jagiellonska 4, 41-200 Sosnowiec, Poland)

      J. Planar Chromatogr. 18, 465-470 (2005). HPTLC of cholic, glycocholic, glycodeoxycholic, chenodeoxycholic, deoxycholic, lithocholic, and glycolithocholic acid on RP-18 W, RP-2, and cyano phases in a presaturated chamber with mixtures of an organic modifier (methanol, dioxane, acetonitrile, acetone) and water in different volume proportions which were varied in steps of 5 % from 35 to 80 %. Detection by spraying with a 10 % aqueous solution of sulfuric acid or by dipping in a 10 % solution of phosphomolybdic acid in ethanol and heating at 120 °C for 20 min. Investigation of relationships between lipophilicity obtained by use of RP-HPTLC, experimental and theoretical partition coefficients, and selected structural descriptors.

      Classification: 2d, 23b