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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      96 079
      Study of the liquid chromatographic separation and determination of NSAID
      R. Bhushan*, S. Joshi, M. Arora, M. Gupta (*Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee-247 667, India)

      J. Planar Chromatogr. 18, 164-166 (2005). TLC of non-steroidal anti-inflammatory drugs (NSAID), i.e. mefenamic acid, naproxen, ibuprofen, flurbiprofen, ketoprofen, paracetamol, and diclofenac, on silica gel with chloroform - methanol , chloroform - ethyl acetate, acetonitrile - methanol - water, acetonitril - methanol in different proportions. Detection with iodine vapor.

      Classification: 32a
      96 109
      Identification and quantitation of polymyxin B, framycetin, and dexamethasone in an ointment by using thin-layer chromatography with densitometry
      J. KRZEK*, A. MASLANKA, P. LIPNER (*Jagiellonian University, Collegium Medicum, Department of Inorganic and Analytical Chemistry, 9 Medyczna St, 30688 Cracow, Poland)

      J. AOAC Int. 88, 1549-1554 (2005). TLC of polymyxin B, framycetin, and dexamethasone on silica gel with methanol and methanol - n-butanol - 25 % ammonia - chloroform 14:4:9:12 for framycetin and polymyxin B. Quantitative determination by densitometry at 550 nm after detection with 0.3 % ninhydrin solution. Dexamethasone was separated with cyclohexane - ethyl acetate 2:3, quantitative determination by absorbance measurement at 245 nm. Similar accuracy, relative standard deviation values from 1.49 to 2.47 % and relative error values from 0.02 to 0.81 % are comparable to those obtained with the reference methods.

      Classification: 32a
      96 135
      Quantitative analysis of ethamsylate and mefenamic acid in tablets by use of planar chromatography
      Y. S. Jaiswal, G. S. Talele*, S. J. Surana (*Department of Pharmaceutical Chemistry, R. C. Patel College of Pharmacy, Karwand Naka, Shirpur Dhule 425405, Maharashtra, India)

      J. Planar Chromatogr. 18, 460-464 (2005). HPTLC of ethamsylate and mefenamic acid on silica gel prewashed with methanol, in a pre-saturated twin-trough chamber with chloroform - methanol - acetic acid 50:40:1. After drying at 50 °C for 5 min quantitative determination by absorbance measurement at 300 nm. The validated calibration range was 500-2500 ng/spot (r = 0.998) and 500-2500 ng/spot (r = 0.997) for ethamsylate and mefenamic acid, respectively.

      Classification: 32a
      97 061
      Stability indicating HPTLC determination of curcumin in bulk drug and pharmaceutical formulations
      M.J. ANSARI*,S. AHMAD. K. KOHLI, J. ALI, R.K. KHAR (*Dept. of Pharmaceutics, Faculty of Pharmacy, Jamia Hamdard Univ., New Delhi 110062, India)

      J. Pharm. Biomed. Anal 39, 132-138 (2005). A simple, selective, precise and stability-indicating HPTLC method of analysis of curcumin both as a bulk drug and in formulations was developed and validated. HPTLC on silica gel with chloroform-methanol 37:3. This system was found to give compact spots of curcumin (Rf 0.48). Densitometric analysis of curcumin in the absorbance mode at 430 nm. The linear regression analysis data for the calibration plots showed good linear relationship with r =0.996 and 0.994 via peak height and peak area, respectively, in the concentration range of 50-300 ng per spot. The method was validated for precision, recovery, robustness. The LOD and LOQ were 8 and 25 ng per spot, respectively. Curcumin was subjected to acid and alkali hydrolysis, oxidation and photodegradation.

      Classification: 32a
      97 111
      Immunostimulant activity of Adhatoda vasica, Lawsonia inermis and Alkanna tinctoria, TLC fingerprint profile for identification
      K. JINYVARGHESE, S.T. KARPE AND S.R. KULKARNI* (*Dept. of Pharmacognosy and Phytochemistry, The Bombay College of Pharmacy, Kalina, Mumbai 400098, India)

      Indian Drugs 42 (6), 345-352 (2005). TLC fingerprint identification of methanolic extracts of Adhatoda vasica, Lawsonia inermis and Alkanna tinctoria, on silica gel. For Lawsonia inermis and Alkanna tinctoria the developing solvent toluene - acetone - acetic acid 90:10:1 was used, and for Adhatoda vasica n-hexane - acetone - diethyl ether 3:1:1 for. Detection of alkannin by spraying with 10 % methanolic KOH.

      Classification: 32a
      97 144
      HPTLC method for the estimation of fexofenadine HCl in tablet dosage form
      P. SOLAIRAJ, A. BHAT, Suvarna KINI, R. GOVINDARAJAN*, R. VENKATRAMAN (*Pharmacognosy & Ethnopharmacology Div., National Botanical Research Institute, Lucknow 226001, India)

      Indian Drugs 42 (7), 424-427 (2005) HPTLC of fexofenadine HCl from tablet dosage form on silica gel with dichloromethane - methanol 13:7. Quantitative determination by absorbance measurement at 260 nm. The linear detector response was observed between 0.2 and 1.0 µg. The method was validated to determine its accuracy and precision. The LOD was found to be 0.08 ng/µL, LOQ was 0.02 ng/µL. The recovery was carried out by standard addition method and was found to be 100.82 %.

      Classification: 32a
      98 092
      Analysis of tramadol in pharmaceutical preparations by high performance thin layer chromatography
      S. MEYYANATHAN*, P. KUMAR, B. SURESH (*J.S.S. College of Pharmacy, Ootacamund, Tamilnadu, India, meyys@rediffmail.com)

      J. Sep. Sci. 26, 1359-1362 (2003). HPTLC of tramadol and chlorzoxazone (internal standard) on silica gel with ethyl acetate - methanol 7:1 and 1 drop of ammonia. Quantitative determination by absorbance measurement at 275 nm. Linearity of determination of levofloxacin is between 1.0 and 2.5 µg and its average percentage recovery is 104.6 %.

      Classification: 32a
      99 079
      High-Performance Thin-Layer Chromatographic method for quantification of beta-Sitosterol from Cynodon Dactylon (Linn
      P. A. CHAMPANERKAR* V. V. VAIDYA, Sunita SHAILAJAN, G. R. SINGH, W. J. SHAH (*Analytical Chemistry Laboratory, S. P. Mandali’s Ramnarain Ruia College, Matunga, Mumbai 400019, vaidya_vikas@yahoo.com)

      Indian Drugs 44(1), 43-47 (2007). HPTLC of beta-sitosterol in methanolic extracts of powdered Cynodon dactylon (Linn.) Pers., on silica gel with chloroform - toulene 19:1. Detection with Libermann-Burchard reagent. Quantitative determination by densitometry at 366 nm. Beta-sitosterol response was linear over the range of 40 µg/mL to 90 µg/mL. The amount of beta-sitosterol in the whole plant powder of Canodon dactylon (Linn.) Pers was found to be 0.60 mg. The validated HPTLC method can be used for routine quality control of Cynodon dactylon (Linn.) Pers. whole plant powder and quantification of beta-sitosterol.

      Classification: 32a
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