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
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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. The saved items can be printed to PDF using the print function of your web browser.

      124 047
      Lipophilicity estimation of anti-proliferative and anti-inflammatory 6-substituted 9-fluoroquino[3,2-b]benzo[1,4]thiazines
      Malgorzata JELEN, K. PLUTA, B. MORAK-MLODAWSKA* (Department of Organic Chemistry, School of Pharmacy with the Division of Laboratory Medicine, The Medical University of Silesia, Sosnowiec, Poland,

      J. Liq. Chromatogr. Relat. Technol. 42, 563-569 (2019). TLC of 17 new anti-proliferative and antiinflammatory tetracyclic 6-substituted 9-fluoroquinobenzothiazines on RP-18 with acetone - aqueous TRIS (tris(hydroxymethyl)-aminomethane) buffer pH 7.4 (ionic strength 0.2 M), where the concentration of acetone was from 50 to 85 % in 5 % increments. Lipophilicity parameters were determined (RM0 and logPTLC) and compared with computationally calculated lipophilic parameters. Relation of lipophilicity with predicted and experimental biological activities was discussed.

      Classification: 2c
      124 023
      Differences in the efficiency of separation of analgesic drugs by high-performance thin-layer chromatography with similar octadecyl silica-based adsorbents
      M. TRZEBIATOWSKI*, R. GWARDA, T. DZIDO (*Department of Physical Chemistry, Medical University of Lublin, Chodźki Str. 4A, 20-093 Lublin, Poland,

      J. Planar Chromatogr. 32, 517-520 (2019). HPTLC of tramadol (1), caffeine (2), paracetamol (3), ibuprofen (4), naproxen (5), and diclofenac (6) on RP-18 WF, LiChrospher RP-18 WF, and RP-18 WF with concentration zone, developed with various ratios of methanol in water with 0.1 M potassium chloride. Qualitative identification under UV light at 254 nm. Potassium chloride may be used to suppress ion–ion interactions between the solutes and the silica gel surface.  HPTLC RP-18WF plates with concentration zone and developed with methanol - water 13:7 with addition of 0.15 mol/L KCl were suitable for the qualitative and quantitative analyses of tramadol, paracetamol, caffeine, naproxen, and ibuprofen or diclofenac. The method allowed to study subtle differences in the efficiency of the separation of analgesic drugs by HPTLC with similar octadecyl silica-based adsorbents.  

      Classification: 2c, 32a
      123 022
      Reversed-phase Thin-Layer Chromatography of inorganic anions on tri-n-butyl amine impregnated silica gel-G layers: separation of coexisting I–, IO3– and IO4–, Fe(CN)64– and Fe(CN)43-
      S. SHARMA*, C. SHARMA (*Department of Chemistry, School of Sciences, IFTM University, Delhi Road, Moradabad 244102, India,

      J. Planar Chromatogr. 32, 265-271 (2019). HPTLC of 24 anions on tri-n-butyl amine (TBA) impregnated silica gel with 13 mobile phases (methanol, dimethylformamide, diisopropyl ether, tetrahydrofuran, 2-propanol, dimethylformamide - methanol 1:1, dimethylformamide - diisopropyl ether 1:1, dimethylformamide - tetrahydrofuran, 1:1, dimethylformamide - 2-propanol 1:1, 0.1 M oxalic acid, 0.1 M tartaric acid, 0.1 M citric acid and 0.1 M succinic acid). The retention behavior was analyzed in aqueous and non-aqueous mobile phases. The hRF values were also correlated with their lyotropic numbers. 20 % TBA-impregnated silica gel was found very effective for binary and ternary separations of anions.

      Classification: 2c, 33b
      100 004
      Partial least-squares study of the effects of organic modifier and physicochemical properties on the retention of some thiazoles
      Tatjana DJAKOVIC-SEKULIC*, N. PERISIC-JANJIC, C. SARBU, Z. LOZANOV-CRVENKOVIC (*Department of Chemistry, Faculty of Sciences, University of Novi Sad, Trg D. Obradovica 3, 21000 Novi Sad, Serbia;

      J. Planar Chromatogr. 20, 251-257 (2007). TLC with aqueous ammonia-organic modifier (acetonitrile, dioxane, acetone) mobile phases has been used to study the effect on retention of the chromatographic system and the physicochemical properties of twelve 2,4-dioxotetrahydro-1,3-thiazoles. Principal-component analysis and partial least-squares regression were used to determine the molecular properties with the greatest effect on retention for each modifier. Good correlation was obtained between experimental and calculated retention data. HPTLC on RP-18 without chamber saturation. Detection under UV 254 nm.

      Classification: 2c
      111 002
      A comparative study of the lipophilicity of 1,2,4-triazoles by reversed-phase and micellar TLC and OPLC
      M. JANICKA*, K. STEPNIK, A. PACHUTA (*Maria Curie-Skodowska University, Department of Physical Chemistry, Faculty of Chemistry, Maria Curie-Skodowska Sq. 3, 20-031 Lublin, Poland,

      J. Planar Chromatogr. 26, 153-159 (2013). TLC lipophilicities of 21 newly synthesized 1,2,4-triazoles on RP-8 and RP-18 with buffered solutions of acetone, 1,4-dioxane, tetrahydrofuran and acetonitrile as well as on cyano phase with solutions of 0.03, 0.04, 0.06, 0.08 and 0.1 M sodium dodecyl sulfate modified with the constant (20 %) addition of organic modifier (acetone, 1,4-dioxane, tetrahydrofuran and acetonitrile). Partitioning lipophilicity indices showed mobile phase composed of sodium dodecyl sulfate and tetrahydrofuran as the system providing the best linear correlations between chromatographic and partitioning lipophilicities of tested 1,2,4-triazoles.

      Classification: 2c
      115 002
      A comparative quantitative structure-retention relationships study for lipophilicity determination of compounds with a phenanthrene skeleton on cyano-, reversed phase-, and
      normal phase-thin layer chromatography stationary phases
      K. CIURA*, J. NOWAKOWSKA, P. PIKUL, W. STRUCK, M. MARKUSZEWSKI (*Medical University of Gda?sk, Faculty of Pharmacy, Department of Physical Chemistry, Al. Gen. J. Hallera 107, 80-416, Gda?sk, Poland,

      J. AOAC Int. 98, 345-353 (2015). HPTLC of 14 derivatives containing the phenanthrene skeleton on RP, CN and NP phases. Quantitative structure-retention relationship analysis determined that the best conditions to predict log P was RP with acetone–water ranging from 30 to 80 % in 10 % increments of the organic modifier.

      Classification: 2c
      119 012
      Quantitative structure–retention relationship modeling of the retention behavior of selected antipsychotic drugs in normal-phase thin-layer chromatography
      K. CIURA*, A. RUTECKA, P. KAWCZAK, J. NOWAKOWSKA (*Medical University of Gda?sk, Faculty of Pharmacy, Department of Physical Chemistry, Al. Gen. J. Hallera
      107, 80-416, Gda?sk, Poland,

      J. Planar Chromatogr. 30, 225-230 (2017). HPTLC of chlorpromazine, chlorprothixene, clozapine, quetiapine, perazine, perphenazine, prochlorperazine, promazine and trifluoperazine on silica gel (1) and amino phase (2) with tetrahydrofuran – petroleum ether ranging from 40 % to 100 % and methanol – petroleum ether ranging from 10 % to 50 % for (1) and a mixture of tetrahydrofuran – water ranging from 50 % to 100 % for (2). Detection by spraying with a mixture of concentrated sulfuric acid – methanol 1:4, followed by heating_x000D_
      at 120 °C for 10 min. A statistical analysis was used for the development of the quantitative structure‒retention relationship (QSRR) model._x000D_

      Classification: 2c
      122 016
      Applying multivariate methods in the estimation of bioactivity properties of acetamide derivatives
      G. VASTAG*, Suzana APOSTOLOV, B. KAURINOVIC, L. GRBOVIC (*University of Novi Sad, Faculty of Sciences, Department of Chemistry, Biochemistry and Environmental Protection, Trg D. Obradovi?a 3, 21000 Novi Sad, Serbia,

      J. Planar Chromatogr. 31, 497-504 (2018). HPTLC of chloroacetamide derivatives on RP-18 with ethanol and tetrahydrofuran as organic modifiers with water. Lipophilicity was examined by cluster analysis and principal component analysis. The obtained chromatographic parameters of the examined acetamides were correlated with the standard measure of lipophilicity, log P.

      Classification: 2c