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
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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.

      97 113
      Morphological, chemical, and functional analysis of Catuaba preparations
      Christa Kletter*, S. Glasl, A. Presser, J. Werner, G. Reznicek, S. Narantuya, S. Cellek, E. Haslinger, J. Jurenitsch (*Institute of Pharmacognosy, PharmaCenterVienna, University of Vienna, Althanstr. 14, 1090 Vienna, Austria; Christa.Klett@univie.ac.at)

      Planta Med. 70, 993-1000 (2004). Preparative TLC of catuabine and its hydroxymethyl derivative 7-exo-hydroxy-N-methyl-catuabine on silica gel with dichloromethane - acetone 97:3 and toluene - acetone - methanol - ammonia 45:45:7:3. Detection under UV light at 254 and 366 nm and by spraying with potassium iodoplatinate reagent (0.25 mL of 5 % hexachloroplatinic acid solution mixed with 2.25 mL of 10 % potassium iodide solution and dissolved with 5 mL water).

      Classification: 32e
      97 145
      Xanthine oxidase inhibitors from the flowers of Chrysanthemum chinense
      M. T. T. Nguyen, S. Awale, Y. Tezuka, J.-Y. Ueda, Q. L. Tran, S. Kadota* (*Institute of Natural Medicine, Toyama Medical and Pharmaceutical University, 2630 Sugitani, Toyama 930-0194, Japan. kadota@ms.toyama-mpu.ac.jp)

      Planta Med. 72, 46-51 (2006). Preparative TLC of acacetin, jaceidin, tricetin 3’,4’,5’-trimethylester, diosmetin, apigenin, eupafolin, chrysoeriol, (+-)eriodictyol, 3,4-dihydroxybenzaldehyde, p-coumaric acid, 5-O-caffeoylquinic acid methyl ester, 4,5-O-dicaffeoylquinic acid on RP18 with acetonitrile - methanol - water 1:1:3. Detection under UV at 254 nm.

      Classification: 32e
      98 067
      Quantification of eugenol, luteolin, ursolic acid, and oleanolic acid in black (Krishna Tulasi) and green (Sri Tulasi) varieties of Ocimum sanctum Linn
      S. ANANDJIWALA, J. KALOLA, M. RAJANI* (*B. V. Patel Pharmaceutical Education and Research Development Centre, Pharmacognosy and Phytochemistry Department, Thaltej, Ahmedabad-380 054, Gujarat, India; rajanivenkat@hotmail.com)

      using high-performance thin-layer chromatography. J. AOAC Int. 89, 1467-1474 (2006). HPTLC of eugenol, luteolin, ursolic acid, and oleanolic acid on silica gel in a twin trough chamber with toluene - ethyl acetate - formic acid 35:15:1 at 25 °C and 40 % relative humidity. Quantitation in absorbance mode at 280 nm for eugenol, at 350 nm for luteolin, and at 530 nm for ursolic acid and oleanolic acid after derivatization with anisaldehyde-sulfuric acid reagent and heating at 105°C. The methods were validated for precision, repeatability, and accuracy.

      Classification: 32e
      99 096
      Preparative isolation and purification of the lignan pinoresinol diglucoside and liriodendrin from the bark of Eucommia Ulmoides Oliv
      S. FENG (Feng Suomin), S. NI (Ni Shifeng), W. SUN (Sun Wenji)* (*Biomedical Key Laboratory of Northwest University , No. 229, Taibai North Road, Xi’an, Shaanxi 710069, P. R. China; fengsuomin@126.com)

      by high speed countercurrent chromatography. J. Liq. Chromatogr. & Relat. Technol. 30, 135-145 (2007). TLC of pinoresinol diglucoside and liriodendrin on silica gel (impregnated with 1 % carboxymethyl cellulose sodium) with the lower phase of chloroform - methanol - water 65:35:16. Detection by spraying with 10 % ethanolic sulfuric acid.

      Classification: 32e
      99 158
      Simple preparative isolation of salvinorin A from the hallucinogenic sage, Salvia divinorum, by centrifugal partition chromatography
      O. SHIROTA*, K. NAGAMATSU, S. SEKITA (*Laboratory of Pharmacognosy and Natural Products Chemistry, Faculty of Pharmaceutical Sciences at Kagawa Campus, Tokushima Bunri University, 1314-1 Shido, Kagawa, 769-2193, Japan; shirota@kph.bunri-u.ac.jp)

      J. Liq. Chromatogr. & Relat. Technol. 30, 1105-1114 (2007). TLC of salvinorin A, a potent naturally occuring kappa-opioid selective agonist, on silica gel and on RP-18 with n-hexane - ethyl acetate 1:1. Detection by spraying with vanillin - phosphoric acid reagent followed by heating.

      Classification: 32e
      100 096
      TLC and GC analysis of the essential oils of Stachys species
      Erzsébet HÁZNAGY-RADNAI*, S. CZIGLE, I. MÁTHÉ (*Institute of Pharmacognosy, University of Szeged, Eötvös 6, H-6720 Szeged, Hungary; haznagy.radnai@pharm.u-szeged.hu)

      J. Planar Chromatogr. 20, 189-196 (2007). TLC of sabinene, limonene, linalool, and beta-caryophyllene on silica gel with benzene - ethyl acetate 9:1. Detection by spraying with a solution of vanillin in concentrated sulfuric acid, followed by heating at 105 °C for 2 min.

      Classification: 32e
      100 157
      A Validated and Densitometric HPTLC Method for the Quantification of Withaferin-A and Withanolide-A in Different Plant Parts of Two Morphotypes of Withania somnifera
      V. SHARMA, A.P. GUPTA, Pamita BHANDARI, R.C. GUPTA, B. SINGH* (*Natural Plant Products Division, Institute of Himalayan Bioresource Technology, Palampur, 176 061, H.P, India)

      Chromatographia 66 (9-10), 801-804 (2007). HPTLC of withaferin A and withanolide A in Withania somnifera methanolic extract from different plant parts (leaf, root, stem and fruit) and of two morphotypes, on silica gel with toluene - ethyl acetate - formic acid 5:5:1. Quantification by densitometry in absorption mode at 530 nm. Linearity was between 200 and 3200 ng for both withaferin A and withanolide A. The average recovery of withaferin A and withanolide A was 96.0 and 96.7 %.

      Classification: 32e
      101 082
      Rapid TLC method for estimation of mevalonic acid in the leaves of medicinal plants
      M. RAM*, S. KHAN, P. JHA, M.A. KHAN, U. KIRAN, S. JAVED, M.Z. ABDIN (*Centre for Transgenic Plant Development, Department of Biotechnology, Jamia Hamdard, New Delhi, 110062, India)

      Chromatographi 68 (1-2), 129-133 (2008). Description of a simple, rapid, specific and sensitive method for the quantitative estimation of mevalonic acid in leaves of Artemisia annua, Psorelia corylifolia, Vinca rosea, Withania somnifera and Barleria proinites. TLC of leaf extracts on silica gel with benzene - acetone 3:2 which involved conversion of mevalonic acid to its lactone, mevalonolactone. Detection by treatment with anisaldeyde reagent. Quantitative determination of mevalonolactone by absorbance measurement at 600 nm. Linearity was between 100 and 500 ng per spot. Recovery (by standard addition) was higher than 98 % for mevalonolactone. The limit of detection was 50 ng per spot.

      Classification: 32e