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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      102 088
      Evaluation of the water and organic liquids extraction efficiency of Spirulina maxima dyes using thermostated micro thin-layer chromatography
      P.K. ZARZYCKI*, M.B. ZARZYCKA (*Koszalin University of Technology, Section of Toxicology and Bioanalytics, Department of Environmental Biology, Koszalin Sniadeckich 2, 75-453 Koszalin, Poland; pkzarz@wp.pl or pawel_k_z@hotmail.com)

      J. AOAC Int. 91, 1196-1202 (2008). Thermostated micro HPTLC of Spirulina maxima dyes on RP18 with acetone - n-hexane 3:7 in a homemade temperature-controlled removable horizontal micro TLC chamber at 40 °C with chamber saturation. Detection by direct digital scan under visible light conditions. Experimental data indicated that under such conditions, with an office scanner used for chromatogram digitalization, spot quantification could be accurately performed within the analyte mass range of two orders of magnitide.

      Classification: 3d, 30b
      102 111
      Effect of hydrolysis on the yield of hederagenin and high-performance thin-layer chromatography densitometric quantification of hederagenin in fruit pericarp of Sapindus spp
      J. KALOLA, S. ANANDJIWALA, H. SRINAVASA, M. RAJANI* (*B. V. Patel Pharmaceutical Education and Research Development Center, Pharmacognosy and Phytochemistry Department, Thaltej, Ahemdabad 380 054, Gujarat, India; rajanivenkat@hotmail.com)

      J. AOAC Int. 91, 1174-1178 (2008). HPTLC of hederagenin on silica gel with toluene - ethyl acetate - formic acid 7:3:5 in a twin-trough chamber. Detection with anisaldehyde - sulfuric acid reagent by dipping for 1 s and heating for 7 min at 100 °C. Quantitative determination by absorbance measurement at 595 nm.

      Classification: 32e
      102 131
      Thin-layer chromatography-densitometric analysis of alpha-mangostin content in Garcina mangostana fruit rind extracts
      W. POTHITIRAT, W. GRITSANAPAN* (*Mahidol University, Department of Pharmacognosy, Faculty of Pharmacy, 447 Sri-Ayudhaya Rd, Ratchatewi, Bangkok 10400, Thailand; pywgs@mahidol.ac.th)

      J. AOAC Int. 91, 1145-1148 (2008). TLC of alpha-mangostin on silica gel with dichloromethane - methanol 24:1 in a saturated twin-trough chamber. Quantitative determination by absorbance measurement at 320 nm.

      Classification: 32e
      102 149
      Development and validation of a HPTLC method for the estimation of trandolapril in tablet dosage form
      A. SINGH*, P. OM, R. SINGH, G. SINGH, B. GANESH (*Central Indian Pharmacopoeia Laboratory, Research & Development Div., Indian Pharmacopoeia Commission, Govt. of India, Ministry of Health & Family Welfare, Sector-23, Rajnagar, Ghaziabad, India)

      60th Indian Phamaceutical Congress PA-196, (2008). HPTLC of trandolapril on silica gel with chloroform - methanol - acetic acid 16:3:1 in a saturated chamber. Quantitative determination by absorbance measurement at 210 nm. Linearity was in the range of 200-1000 ng/spot. The method was suitable for routine quality control of drug in tablet dosage form.

      Classification: 32a
      103 055
      Easy ambient sonic-spray ionization mass spectrometry combined with thin-layer chromatography
      R. HADDAD, H.M.S. MILAGRE, R.R. CATHARINO, M.N. EBERLIN* (*Thomson Mass Spectrometry Laboratory, Institute of Chemistry, State University of Campinas, 13084-971, Campinas SP, Brazil; eberlin@iqm.unicamp.br)

      Anal. Chem. 80, 2744-2750 (2008). TLC of mixtures of semipolar nitrogenated compounds as well as pharmaceutical drugs (allyl phenylamine, phenylamine, ethylpyridine, propanolol hydrochloride, and amlodipine besylate) on silica gel with ethyl acetate - hexane 1:4; detection under UV 254 nm. On-spot detection and analyte characterization via easy ambient desorption and sonic-spray ionization (EASI) and (tandem) mass spectrometry detection.

      Classification: 4e, 17
      103 112
      Estimation of apigenin, an anxiolytic constituent, in Turnera aphrodisiaca
      S. KUMAR*, R. MADAAN, A. SHARMA (*S. D. College of Pharmacy, Barnala 148101, India)

      Ind. J. of Pharma Sci. 70(6), 847-851 (2008). HPTLC of apigenin in segregated parts (leaves, stems, flowers and fruits) of Turnera aphrodisiaca on silica gel with toluene - ethyl acetate 1:4. Quantitative determination by absorbance measurement at 336 nm. Flowers were found to contain maximum amount of apigenin whereas leaves contained the least. Apigenin contents in methanolic extracts of aerial plant parts were fourteen times lower than in acid hydrolyzed methanolic extracts, indicating the presence of most of apigenin in glycosidic form. The plant material collected in September showed maximum contents of apigenin.

      Classification: 32e
      103 138
      Efficient and sensitive method for quantitative analysis of 6-gingerol in marketed Ayurvedic formulation
      K.K. ROUT*, S.K. MISHRA (*Pharmacognosy and Phytochemistry Division, University Department of Pharmaceutical Sciences, Utkal University, Vani Vihar, Bhubaneswar 751004, Orissa, India; kd_rout@yahoo.co.in)

      J. Planar Chromatogr. 22, 127-131 (2009). HPTLC of 6-gingerol, extracts of Suprabha and market samples of ginger on silica gel (prewashed with methanol) with n-hexane - acetone 18:7 in a twin trough chamber saturated for 4 min at 20 +/- 4 °C and 36 +/- 3 % relative humidity. Quantitative determination by absorbance measurement at 286 nm. The limit of detection and quantification was 40 and 150 ng/band, respectively.

      Classification: 32e
      103 165
      (Study of the quality standard for Fangji Guanjie pills) (Chinese)
      S. ZHANG (Zhang Songan)*, Y. CAI (Cai Yaling), J. YUAN (Yuan Jinlan), X. WU (Wu Xiaohui), CH. FENG (Feng Chao), L. ZHOU (Zhou Lumin), Y. YAO (Yao Youqi), D. ZHOU (Zhou Daonian) (*Pharm. Coll., Tongji Med. Inst., MidChina Univ. Technol., Wuhan, Hubei 430030, China)

      J. Chinese Trad. Patent Med. 30 (10), 1478-1482 (2008). TLC of Fangji Guanjie pill extracts on silica gel with 1) petroleum ether (60-90 ºC) - ethyl acetate 10:1; 2) ethyl acetate - formic acid - glacial acetic acid - water 15:1:1:2; 3) petroleum ether (60-90 ºC) - ethyl acetate 17:3; 4) chloroform - methanol - water 40:10:1; 5) diethyl ether - chloroform - methanol 4:2:1. Detection 1) under UV 254 nm; 2) by spraying with 10 % sulfuric acid in ethanol; 3) by spraying with dinitrophenylhydrazine in ethanol and heating at 105 ºC; 4) by spraying with 5 % potassium iodobismuthate solution. Identification by comparison with the standards fangchinoline and tetrandrine.

      Classification: 32e
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