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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      104 128
      (Identification of leaf of Vitex negundo L
      H. LU (Lu Hui)*, H. XIE (Xie Hongping), SH. YANG (Yang Shilin), B. GU (Gu Bing) (*Pharm. Coll., Suzhou Univ., Suzhou, Jiangsu 215123, China)

      var. cannabifolia (Sieb. et Zucc.) Hand. -Mazz. and Oleum Viticis Negundo by thin-layer chromatography) (Chinese). J. Chinese Trad. Med. & Pharm. (Shizhen Guoyi Guoyao) 20 (11), 2799-2800 (2009). TLC of TCM drug extracts on silica gel with petroleum ether (60-90 ºC) – ethyl acetate 100:3. Detection by spraying with a solution of 5 % vanillin – 10 % sulfuric acid in ethanol 1:10 followed by heating at 105 °C until coloration, evaluation in visible and UV light.

      Classification: 32e
      104 144
      Stability-indicating HPTLC method for the estimation of tolterodine in bulk drug
      A. MISHRA*, R. BHOMIA, S. VASANTHARAJU, A. KARTHIK, S. SYED, K. BHAT (*Manipal College of Pharmaceutical Sciences, Manipal Univeristy, Manipal, Karnataka, India)

      Abstract No. F-237, 61st IPC (2009). HPTLC of tolterodine on silica gel with toluene - methanol - 25 % ammonia 250:250:1. The hRf value was 40. Quantitative determination by absorbance measurement at 284 nm. The method was linear in the range of 200-1000 ng/band. The compound was subjected to different stress conditions (acid, alkali, oxidation, thermal) and degradation under alkaline conditions was observed. The degradation products were well separated from the main component.

      Classification: 32a
      104 161
      Development and validation of a simultaneous HPTLC method for the estimation of atorvastatin calcium and amlodipine besilate in tablet dosage form
      C. PATEL*, B. PATEL, P. PATEL, C. PATEL (*Shri Sarvajanik Pharmacy College, Hemchandracharya North Gujarat University, Mehsana, Gujarat, India)

      60th Indian Pharmaceutical Congress PA-213 (2008). HPTLC of atorvastatin calcium and amlodipine besilate on silica gel with chloroform - toluene - methanol - water 55:10:20:2. Quantitative determination by absorbance measurement at 242 nm. The calibration curve was found to be linear between 400 and 1200 ng/spot for both atorvastatin calcium and amlodipine besilate. The limit of detection and the limit of quantification for atorvastatin calcium were 100 and 400 ng/spot, and for amlodipine besilate 200 and 400 ng/spot, respectively.

      Classification: 32a
      104 179
      Application of a stability-indicating HPTLC method for the quantitative determination of hesperidin in pharmaceutical dosage form
      Kirti PRABHU*, R. LOBO, Richa AGRAWAL, A. SHIRWAIKAR, A. SHIRWAIKAR, Mamatha BALLAL (*Dept. of Pharmacognosy, Manipal College of Pharmaceutical Science, Manipal University, Manipal, India)

      Abstract No. 9324, IHCB (2009). HPTLC of hesperidin in orange peel extract and formulation on silica gel with ethyl acetate - methanol - water 100:17:13. Quantitative determination by absorbance measurement at 287 nm. The method was linear in the range of 10-1000 ng/spot. Hesperidin was subjected to degradation studies (acid, alkali, hydrolysis, oxidation, and thermal stress) and was found susceptible to different stress condition. The method was suitable for determination of hesperidin and its degradation products in bulk drug as well as formulations.

      Classification: 32e
      104 200
      Simultaneous estimation of mosapride citrate and pantoprazole in solid dosage form by HPTLC method
      R. SHAH*, H. BHATT, G. PATEL, C. SHARASTRY (*Shree Dhanvantary Pharmacy College, Surat, Maharashtra, India)

      Abstract No. F-236, 61st IPC (2009). HPTLC of pantoprazole and mosapride citrate on silica gel (pre-washed with methanol) with ethyl acetate - benzene - methanol - 25 % ammonia 48:35:15:2 at room temperature. Quantitative determination by absorbance measurement at 250 nm or 276 nm. The method was linear in the range of 3-7 µg/band for both drugs. Recovery was between 99.0 and 103.5 %.

      Classification: 32a
      104 217
      High-performance thin-layer chromatographic analysis of bicalutamide in bulk drug and liposomes
      G.S. SUBRAMANIAN*, A. KARTHIK, A. BALIGA, P. MUSMADE, S. KINI (*Department of Pharmaceutical Quality Assurance, Manipal College of Pharmaceutical Sciences, Manipal University, Manipal, Karnataka, India 576104; ganrajesh@gmail.com)

      J. Planar Chromatogr. 22, 273-276 (2009). HPTLC of bicalutamide and leflunomide (as internal standard) on silica gel with toluene - ethyl acetate 4:5 in a twin trough chamber saturated for 30 min at room temperature. Quantitative determination by absorbance measurement at 273 nm. The limit of detection and quantification was 50 and 200 ng/band, respectively.

      Classification: 32a
      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
      105 031
      Arginase activity in mitochondria – an interfering factor in nitric oxide synthase activity assays
      P. VENKATAKRISHNAN, E. NAKAYASU, I. ALMEIDA, R. MILLER* (*Department of Biological Sciences, University of Texas at El Paso, El Paso, Texas, The United States of America, tmiller2@utep.edu)

      Biochem. Biophys. Res. Commun. 394, 448-452 (2010). HPTLC of [14C]-L-arginine and [14C]-L-citrulline of a nitric oxide synthase conversion assay in mitochondria rat liver, on silica gel with butanol - acetic acid - water 3:1:1. Detection by dipping in a solution of 2 % ninhydrin in acetone, followed by heating on a plate heater for 1 min. After visualization, the plates were exposed to X-ray film for 4.5 days.

      Classification: 18a
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