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
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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. You can export your saved items to PDF by clicking the download icon.

      63 131
      (The olfactometric interaction of 1-furfurylpyrrole in sandalwood oil (East India)) (German)
      A. NIKIFOROV*, L. JIROVETZ, G. BUCHBAUER, (*Inst. für Org. Chemie der Univ. Wien, Wahringer Strasse 38, A-1090 Wien, Austria)

      Scientia Pharmaceutica 55, 101-105 (1987). TLC on silica with benzene - ethyl acetate 9:1. Detection by spraying with anisaldehyde - sulfuric acid reagent.

      Classification: 23a
      91 045
      The influence of steric effects on the TLC separation of porphyrins
      M. PODGORNA, A. SWIERK, J. SLIWIOK, (Dept. of Chem., Silesian Univ., 9 Szkolna Street, 40-006 Katowice, Poland)

      J. Planar Chromatogr. 15, 466-469 (2002). TLC of tetraphenylporphyrin derivatives belonging to two homologous series A and B on silica gel with chloroform - carbon tetrachloride and on RP-18 with methanol ñ chloroform. After drying visual detection of the spots. Optimal separations were achieved by adsorption TLC with carbon tetrachloride - chloroform 1:1 and by partition TLC on RP-18 with methanol - chloroform 2:3.

      Keywords:
      Classification: 23a
      114 049
      Thin-layer chromatography method for the detection of N,N-dimethyltryptamine in seized street samples
      B. DUFFAU*, Sonia ROJAS, S. JOFRE, M. KOGAN, I. TRIVIÑO, Paula FUENTES (*Drug Analysis Section, Institute of Public Health of Chile, Chile; and M. Kogan, Faculty of Chemical and Pharmaceutical Sciences, University of Chile, Chile, bduffau@gmail.com)

      J. Planar Chromatogr. 27, 477-479 (2014). HPTLC of N,N-dimethyltryptamine in seized street samples on silica gel with methanol – ammonia 200:3. Quantitative determination by absorbance measurement at 220 nm. The hRF value of N,N-dimethyltryptamine was 50. Linearity was in the range of 11.5-34.2 μg/zone. The intermediate precisios were below 5 % (n=3). The LOD and LOQ were 3.3 and 9.9 μg/zone, respectively. Mean recovery was 117.9 %.

      Classification: 23c
      106 117
      Thin-layer chromatography of pyridinium aldoximes using distinct techniques for development
      H. KALÁSZ*, E. MINGSOVICS, N. RAM, K. KUCA (*Department of Pharmacology and Pharmacotherapy, Faculty of Medicine, Semmelweis University, 1089 Budapest, Nagyvárad tér 4, Hungary; drkalasz@gmail.com)

      J. Liq. Chromatogr. Relat. Technol. 33, 922-935 (2010). TLC and HPTLC of 22 different pyridinium aldoximes on silica gel with water - acetonitrile - acetic acid 8:1:1, water - acetone - acetic acid 8:1:1, and acetone - 50 mM aqueous sodium acetate 1:4 using unsaturated and saturated vapor phase as well as OPLC. Detection under UV 254 nm.

      Classification: 23d
      99 057
      Quantitative determination and stress degradation studies on a biomarker trigonelline by a validated stability-indicating HPTLC method
      S. CHOPRA*, S. K. MOTWANI, Z. IQBAL, F. J. AHMAD, R. K. KHAR (*Faculty of Pharmacy, Department of Pharmaceutics, Jamia Hamdard, Hamdard Nagar, New Delhi 110 062, India; shrutichopra21@yahoo.com)

      J. Liq. Chromatogr. & Relat. Technol. 30, 557-574 (2007). TLC of trigonelline (3-carboxy-1-methylpyridinium hydrochloride) and degradation products on silica gel with n-propanol - methanol - water 4:1:4 in a twin-trough chamber. Quantitative determination by absorbance measurement at 269 nm.

      Classification: 23d
      106 116
      Development and validation for the simultaneous quantification of nebivolol hydrochloride and hydrochlorothiazide by UV spectroscopy, RP-HPLC and HPTLC in tablets
      B. DHANDAPANI*, N. THIRUMOORTHY, P. JOSH (*Dept. of Pharmaceutical Analysis, A. M. Reddy Memorial College of Pharmacy, Petlurivaripalem, Narasaraopet, Guntur 522601, A.P., India, dhandapani@gmail.com)

      E-Journal of Chemistry 7(2), 341-348 (2010). HPTLC of nebivolol hydrochloride and hydrochlorothiazide on silica gel with ethyl acetate - methanol - 25 % ammonia 17:2:1 with chamber saturation. The hRf value of hydrochlorothiazide was 21 and of nebivolol 41. Densitometric evaluation at 285 nm. The method was linear in the range of 200-1000 ng/band for nebivolol and 500-2500 ng/band for hydrochlorothiazide. The recovery was 98.9-102.4 %. Comparison of the HPTLC method with a RP-HPLC method and a UV spectroscopic method gave comparable results. The HPTLC method is suitable for routine quality control.

      Classification: 23e
      107 091
      Development and validation of HPTLC method for simultaneous estimation of gatifloxacin and ornidazole in tablets
      S. PATEL*, P. PATEL, N. PATEL, B. PATEL (*Dept. of Pharmaceutical Q. A. Shree S. K. Patel College of Pharmaceutical Education and Research, Ganapat University, Kherva, Mehsana 382711, Gujarat, India)

      62nd Indian Pharmaceutical Congress Abstract No. F-242 (2010). TLC of gatifloxacin and ornidazole on silica gel with n-butanol – ethanol – 8M ammonia 10:1:3. Quantitative determination by absorbance measurement at 299 nm. The hRf value of gatifloxacin was 27 and of ornidazole 83. The method was found to be linear between 20-100 ng/zone for gatifloxacin and 50-250 ng/zone for ornidazole (r2> 0.99). The limit of detection and quantitation were found to be 4.1 and 12.5 ng/zone, respectively for gatifloxacin and 10.3 and 31.2 ng/zone, respectively for ornidazole.

      Classification: 23e
      113 047
      Stability indicating TLC method for the determination of rosuvastatin and identification of some degradation products using electrospray ionization mass spectrometry
      F. BELAL, F. IBRAHIM, A. KHEDR, T. ELAWADY* (*Department of Pharmaceutical Chemistry, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia, tarek_elawady@yahoo.com)

      J. Liq. Chromatogr. Relat. Technol. 37, 1114-1132 (2014). HPTLC of rosuvastatin on silica gel with chloroform - n-hexane - methanol - glacial acetic acid 80:100:40:15:1. Quantitative determination by absorbance measurement at 295 nm. The hRf value for rosuvastatin was 9. Degradation products (DPs) were characterized by ESI-MS. For acidic hydrolysis, 4 major DPs with hRF values of 16, 27, 74 and 77 were obtained. For alkaline hydrolysis, one major DP of hRF 73 was detected. For thermal hydrolysis two major DPs with hRF 74 and 77 were detected. For exposure to hydrogen peroxide, 5 major DPs with hRF 15, 25, 30, 71 and 77 were obtained. For photolytic hydrolysis, 2 major DPs with hRF 70 and 78 were detected. Linearity was in the range of 500-20000 ng/zone. The intermediate/interday/intra-day precisions were below 2 % (n=3). The LOD and LOQ were 170 and 500 ng/zone. Average recovery was 99.9 %.

      Classification: 23e