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:

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      112 108
      Validated specific densitometric method for simultaneous estimation of telmisartan and atorvastatin in presence of degradation products formed under ICH-recommended stress conditions
      R. THANGAVELU*, S. MAKAPOTHULA, N. GOWDA (*Analytical Research Laboratory, Department of Pharmaceutical Analysis, PES College of Pharmacy, Hanumanthanagar, Rajiv Gandhi University of Health Sciences, Bengaluru-560050, Karnataka, India, nraj_msubaroda@yahoo.co.in)

      J. Planar Chromatogr. 26, 445-451 (2013). HPTLC of telmisartan (1) and atorvastatin (2) on silica gel with methanol - chloroform 1:7. Quantitative determination by absorbance measurement at 280 nm. The hRf values for (1) and (2) were 64 and 27, respectively. Linearity was between 1.2-7.2 µg/zone for (1) and 0.4-2.4 µg/zone for (2). LOD and LOQ were 3 and 8 ng/zone. Recoveries (by standard addition) were 98-101 % for (1) and 99-101 % for (2). Intermediate intra- and inter-day precision was below 2 %. Comparable results were obtained with HPLC and UV methods.

      Classification: 32a
      114 047
      Effect of multiple development techniques on the chromatographic parameters and separation selectivity of some alkaloids on C18 and CN-silica layers
      Anna PETRUCZYNIK*, Adriana KARCZMARZ, Monika WAKSMUNDZKA-HAJNOS (*Department of Inorganic Chemistry, Medical University of Lublin, Chod?ki 4A, 20-093 Lublin, Poland, anna.petruczynik@poczta.onet.pl)

      J. Planar Chromatogr. 27, 333-339 (2014). TLC of alkaloids such as (1) papverine, (2) quinine, (3) berberine, (4) brucine, (5) emetine, (6) chelidonine, (7) boldine, (8) protopine and (9) allocryptopine on CN or RP18W phase with mixture of acetonitrile and water containing: acetic buffer at pH 3.6, 1 % acetic acid, 1 % ammonia, 0.01 M octane sulfonic acid sodium salt or methanol, and water containing 0.01 M diethylamine. On C18 plates, the best conditions for the separation of alkaloids were obtained with the mobile phase containing addition of octane sulfonic acid sodium salt, diethylamine, or aqueous ammonia; as for the CN plates, with aqueous eluents containing diethylamine or ammonia and nonaqueous eluent containing mixture of methanol, diidopropyl ether, and 2% ammonia. The efficiency of the system was increased by using a combination of two-dimensional thin-layer chromatography with multiple development chromatogram methods.

      Classification: 22
      119 052
      Determination of fatty acids and lipid classes in salmon oil by near infrared spectroscopy
      M. CASCANT, C. BREIL, A. FABIANO, F. CHEMAT, S. GARRIGUES*, M. DE LA GUARDIA (*Department of Analytical Chemistry, University of Valencia, 50 Dr. Moliner Street, Research Building, 46100 Burjassot, Valencia, Spain, salvador.garrigues@uv.es)

      Food Chem. 239, 865-871 (2018). NIR spectroscopy for the analysis of oleic, palmitic, linoleic, linolenic, omega-3 and omega-6 acids, unsaturated and saturated fatty acids, and triacylglycerides was compared with HPTLC and GC methods. HPTLC of polar (1) and neutral (2) lipids in salmon oil on silica gel with methyl acetate – isopropanol – chloroform – methanol – potassium chloride (0.25 % solution) 25:25:25:10:9 for (1) and with n-hexane – diethyl ether – glacial acetic acid 35:15:1. Detection by dipping into primulin reagent (10 mg primuline, 40 mL water, 160 mL acetone) for 2 s. The NIR method permits the simultaneous quantification of several fatty acids, but the accuracy and robustness of the method remain at the screening level for palmitic and linolenic acids and monounsaterated fatty acids. The method is not sensitive enough to detect low concentrations of fatty acids, therefore direct measurements on salmon tissue samples were not considered. The NIR method requires a previous extraction of the lipids, similar to the chromatographic techniques. Still the NIR method is a fast, direct and not destructive technique for salmon oil sample screening purposes.

      Classification: 11c
      122 075
      Reversed-phase high-performance liquid chromatography and high-performance thin-layer liquid chromatography methods for simultaneous determination of theophylline, guaifenesin and guaifenesin impurity (guaiacol) in their bulk powders and in dosage form
      E.A. ABDELALEEM, I.A. NAGUIB, S.A. FARAG*, H.E. ZAAZAA (*Anal. Chem. Dep., Faculty of Pharm., Nahda Univ., Beni-Suef, Egypt, shosho_5005eg@yahoo.com)

      J. Chromatogr. Sci., 56 (9), 846–852 (2018). Simultaneous determination of theophylline (THP), guaifenesin (GUI) and guaiacol (GUA, a guaifenesin impurity) by HPTLC on silica gel with ethyl acetate – hexane – methanol - ammonia 65:35:10:2. Detection and quantification by densitometry at 275 nm. The hRf values were 13, 35 and 80 for THP, GUI and GUA, respectively. The linearity range was 0.4–2 μg/band for both THP and GUI, and 0.4–1.2 μg/band for GUA. Validation of the proposed method according to ICH guidelines. Statistical comparison of the results with RP-HPLC showed no difference regarding accuracy and precision.

      Classification: 32c
      56 103
      Magyar Kemiai Folyoirat 91, 126-130 (1985)
      S. HOSZTAFI, S. MAKLEIT, T. TIMAR

      (Hungarian). (N-demethylation of morphine alkaloids III. Some new reactions of the N-demethyl derivatives.). TLC on silica with benzene - methanol 8:2, chloroform - methanol 9:1 and chloroform - acetone - diethylamine 5:4:1. Visualization by UV or by Dragendorff reagent. Identified substances: N-demethylneopine, N-demethylneomorphine.

      Classification: 22
      58 022
      Thin-layer chromatographic separation of optical, geometrical and structural isomers
      A. ALAK, D.W. ARMSTRONG

      Anal. Chem. 58, 582-584 (1986). TLC of 9 racemic mixtures, 3 diasteomeric mixtures and 6 structural isomers on-cyclodextrin-bonded silica with methanol -1 % aqueous triethylammonium acetate (pH 4.1) 5:5. Detection under UV at 254 nm. Evaluation of different silica preparations.

      Classification: 3d
      60 088
      Erarbeitung eines dünnschichtchromatographischen Analysenverfahrens zu quantitativen Erfassung der fäkalen Gallensäurezusammensetzung
      G. FRIEMANN. Dissertation Univ. Goettingen (1984)

      (TLC chromatographic analysis for the quantitative estimation of the fecal bile acid composition). TLC of cholic acid, chenodesoxy cholic acid, desoxy cholic acid, lithocholic acid and ursodesoxy cholic acid on silica with isooctane - isopropanol - acetic acid 30:10:1 and/or isooctane - ethyl acetate - acetic acid 10:10:2. Derivatization with 2 % ethanolic solution of 2,7-dichlorofluoresceine. Densitometric quantification by fluorescence. Fiber rich polysaccharides (dietary fibers) elevate fecal bile acids and their metabolites. The possible role of this diet in relation to fecal bile acid concentration and large bowel cancer is discussed.

      Classification: 13d, 13c
      63 136
      Liquid column chromatography using thin-layer chromatographic silica gel
      D.J. BEVERIDGE, D.M. HARRISON, R.M. MC GRATH*, (*Dep. Biochem., Univ. Witwatersrand, P.O. WITS 2050, Johannesburg, South Africa)

      J. Chromatogr. 450, 443-447 (1988). TLC of cyclopiazonic acids on silica with ethyl acetate - methanol - conc. NH3 60:35:5. Detection under UV 254 nm. Comparison of the results with those obtained by CC on the same TLC silica. Also TLC of nutmeg oil on silica with petrol ether (80-100°C) - ether 8:2. Detection under UV or by exposure to iodine vapor.

      Classification: 28b