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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      103 158
      New approach to mechanism of action of paclitaxel by means of BioArena studies
      E. TYIHÁK*, Á. MÓRICZ, P. G. OTT, M. L. HAJNOS, K. GLOWNIAK (*Plant Protection Institute, Hungarian Academy of Sciences, Herman O. u. 15, POB 102, 1525 Budapest, Hungary; etyih@nki.hu)

      J. Planar Chromatogr. 21, 331-336 (2008). TLC and OPLC of paclitaxel on silica gel with a variety of mobile phases, e. g. chloroform - methanol 9:1 with chamber saturation. After drying bioautography by immersion in the bacterial suspension of Pseudomonas savastanoi for 20 s. Visualization of the chromatograms with MTT was performed either after a short draining period or after an overnight incubation.

      Classification: 32e
      104 084
      Chromatographic analysis of an anti psoriatic herbal formulation
      Nidhi DUBEY*, N. DUBEY, R. MEHTA, A. SALUJA (*Devi Ahilya Vishwavidyalaya, School of Pharmacy, Indore, M.P., India)

      60th Indian Pharmaceutical Congress PA-226, (2008). HPTLC of Neem (active ingredient of Nimbidin capsules) on silica gel with chloroform - ethyl acetate 4:1 containing 1 % of acetic acid. Quantitative determination by absorbance measurement at 254 nm. The chromatogram showed two active constituents in Neem with hRf values of 33 and 55. Linearity was in the range of 2-20 µg. The method was suitable for estimation of different constituents of Neem in herbal formulations.

      Classification: 32e
      104 114
      High-performance thin-layer chromatography method for estimation of conessine in herbal extract and pharmaceutical dosage formulations
      A. KAUR*, V. RAVICHANDRAN, P. JAIN, R. AGRAWAL (*Pharmaceutical Chemistry Research Lab. Dept. of Pharmaceutical Sciences, Dr. Hari Singh Gour Univ. Sagar, MP 470003, India, dragrawal2001@yahoo.co.in)

      J. Pharm. Biomed. Anal. 46, 391-394 (2008). TLC of conessine on silica gel with toluene - ethyl acetate - diethyl amine 13:5:2 in a twin trough chamber saturated at 25 °C. Detection by treatment with modified Dragendorff’s reagent. Quantitative determination by absorbance measurement at 520 nm. The hRf value of conessine was 82. Linearity was in the range of 1-10 µg/zone with a correlation coefficient of 0.9998 via peak area.

      Classification: 32e
      104 152
      Densitometric HPTLC analysis of aloenin in aloe pharmaceuticals
      D.N. OLENNIKOV (Laboratory of Medical and Biological Research, Department of Biologically Active Substances, Institute of General and Experimental Biology, Siberian Division, Russian Academy of Sciences, Sakh’yanovoy St 6, 670047, Ulan-Ude, Russia; oldaniil@rambler.ru)

      J. Planar Chromatogr. 22, 359-362 (2009). HPTLC of aloenin in aloe juice, tablets, and liquid extracts on silica gel with ethyl acetate - 95 % ethanol - water 20:3:1 at room temperature in a saturated chamber. Detection by immersion for 1 s in freshly prepared 5 % sodium hydroxide solution in 95 % ethanol, followed by heating at 100 °C for 5 min. Quantitative determination by absorbance measurement at 365 nm.

      Classification: 32e
      104 207
      Qualitative and quantitative standardization of Myrica esculenta Buch
      N. SINGH, S. KHATOON*, N. SRIVASTAVA, A.K. SINGH RAWAT, S. MEHROTA (*Pharmacognosy and Ethnopharmacology Division, National Botanical Research Institute, Rana Pratp Marg, Lucknow 226001, India; neha_somvanshi@yahoo.com, sayyadak@yahoo.com)

      J. Planar Chromatogr. 22, 287-291 (2009). HPTLC of the biomarkers gallic acid, lupeol, oleanolic acid, and stigmasterol and plant extracts on silica gel with toluene - ethyl acetate - formic acid 5:5:1 for gallic acid and with toluene - ethyl acetate 4:1 for lupeol, oleanolic acid, and stigmasterol in a saturated twin trough chamber. Quantitative determination by absorbance measurement at 272 nm. Detection of oleanolic acid, lupeol, and stigmasterol by dipping in anisaldehyde reagent followed by heating at 110 °C for 5 min. Densitometric evaluation at 652 nm.

      Classification: 32e
      104 234
      Iridoid glycoside-based quantitative chromatographic fingerprint analysis
      A. YADAV*, N. TIWARI, P. SRIVASTAVA, S. SINGH, K. SHANKER, R. VERMA, M. GUPTA (*Analytical Chemistry Div. Central Institute of Medicinal and Aromatic Plants, Lucknow 226015, India, guptammg@rediffmail.com)

      J. Pharm. Biomed. Anal. 47, 841-846 (2008). HPTLC of iridoid glycosides in the aerial part of Gambhari (Gmelina arborea) with iridoid gycoside 6-0-(2”, 3”- dibenzoyl)-o-L-rhamnopyranosylcatalpol as a chemical marker for the standardization of G. arborea plant extracts on silica gel with chloroform - methanol 4:1. Quantitative determination by absorbance measurement at 240 nm and at 430 nm after derivatization with vanillin - sulfuric acid reagent. The linear working range was between 1000-5000 ng/spot with a good correlation coefficient of 0.994.

      Classification: 32e
      105 077
      Antipyretic, analgesic, anti-inflammatory and antioxidant activities of two major chromenes from Melicope lunu-ankenda
      A. JOHNSON, A. KUMAR, S. RASHEED, S. CHANDRIKA, A. CHANDRASEKHAR, S. BABY*, A. SUBRAMONIAM (*Phytochemistry and Phytopharmacology Division, Tropical Botanical Garden and Research Institute, Pacha-Palode, Kerala, India, sabulal@gmail.com)

      J. Ethnopharmacol. 130, 267-271 (2010). HPTLC of evodione and leptonol from the leaves and influorescences of Melicope lunu-ankenda on silica gel with chloroform - methanol 1:1. Detection by spraying with anisaldehyde - sulfuric acid reagent, followed by heating at 105 °C for 5 min. Quantitative determination by absorbance measurement at 580 nm.

      Classification: 32e
      105 108
      Purification of Azadirachta indica seed cake and its impact in nutritional and antinutritional factors
      M. SAXENA, K. RAVIKANTH, A. KUMAR*, A. GUPTA, B. SINGH, A. SHARMA (*Phytochemistry and Analytical Laboratory, R and D Centre, Ayurvet Limited, Baddi, H.P., India, akumar@ayurvet.in)

      J. Agric. Food Chem. 58, 4939-4944 (2010). HPTLC of azadirachtin (1) and salannin (2) in the seeds of Azadirachta indica on silica gel with hexane - ethyl acetate1:3. Quantitative determination by absorbance measurement at 220 nm. The hRf values of (1) and (2) were 18 and 30, respectively. Linearity was between 50 and 200 ppm for both (1) and (2). Recovery was 99.9 % for (1) and 99.3 % for (2). The intermediate precision was 88.5 % and 87.5 % for (1) and (2), respectively (n=3). The HPTLC and HPLC methods gave comparable results.

      Classification: 32e
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