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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      101 090
      Validated HPTLC method of analysis for artemether and its formulations
      N.G. TAYADE*, M.S. NAGARSENKER (*Department of Pharmaceutics, Bombay College of Pharmacy, Kalina, Santacruz (E), Mumbai 400098, India)

      J. Pharm. Biomed. Anal. 43 (3), 839-844 (2007). HPTLC of artemether both as a bulk drug and in pharmaceutical formulations on silica gel aluminum plates with toluene - ethyl acetate - formic acid 80:20:3. Quantification of artemether by densitometry at 565 nm. Linearity was between 200 and 1000 ng/spot. The limit of detection and quantification was 65 and 197 ng/spot, respectively. The method was successfully applied in the analysis of lipid based parenteral formulations and marketed oral solid dosage formulation.

      Classification: 32c
      102 021
      Quantitative silver ion thin layer chromatography of triacylglycerols from sunflower oils differing in the level of linoleic acid
      Ilko MAREKOV*, R. TARANDJIISKA, S. MOMCHILOVA, B. NIKOLOVA-DAMYANOVA (*Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria)

      J. Liq. Chromatogr. Relat. Technol. 31, 1959-1968 (2008). Quantitative Ag-TLC of eight samples of sunflower oil with different linoleic acid content on silica gel (impregnated by dipping into a 0.5 % methanolic solution of silver nitrate) with petroleum ether - acetone 25:1, and petroleum ether - acetone - ethyl acetate 100:5:2, and 50:3:2. Detection by consecutive treatment with bromine and sulfurylchloride vapors (30 min each) followed by heating at 180-200 °C. Quantitative determination by absorbance measurement at 450 nm. Evaluation of authenticity and possible adulteration of edible oils.

      Classification: 11c
      102 044
      Thin layer chromatographic techniques (TLC, OPTLC) for determination of biological activated compounds from herb extracts
      Magdalena LIGOR*, B. BUSZEWSKI (*Faculty of Chemistry, Chair of Environmental Chemistry and Bioanalytics, Nicolaus Copernicus University, 7 Gagarin St., 87-100 Torun, Poland; mada@chem.uni.torun.pl)

      J. Liq. Chromatogr. Relat. Technol. 30, 2617-2628 (2007). TLC and HPTLC of monoterpenes, e. g. menthol and menthone from peppermint, on silica gel with toluene - ethyl acetate 3:7, 4:6, ... , 9:1, and 10:0 in a horizontal chamber. Detection with methanolic vanillin - sulfuric acid reagent and under UV 254 nm. Flavonoids from hawthorn, Passiflora incarnata, hop, cacao, as well as tea were also determined by TLC and OP TLC.

      Classification: 15a
      102 065
      Phosphoserine aminoacylation of tRNA bearing an unnatural base anticodon
      R. FUKUNAGA, Y. HARADA, I. HIRAO, S. YOKOYAMA* (*Department of Biophysics and Biochemistry, Graduate School of Science, The University of Tokyo, Tokyo, Japan, yokoyama@biochem.s.u-tokyo.ac.jp)

      Biochem. Biophys. Res. Commun. 372, 480-485 (2008). 2D-TLC of alpha-32P ATP or alpha-32P UTP labeled nucleotides after RNase T2 treatment of tRNA transcripts synthesized by T7 RNA polymerase, on silica gel with isobutyric acid – ammonia – water – 66:1:33 for the first dimension and isopropyl alcohol – hydrocloric acid – water 14:3:3 for the second dimension. Quantitative determination by radioactivity measurement of the labeled nucleotides.

      Classification: 21b
      102 090
      High performance thin layer chromatographic determination of the related substances in alprazolam drug
      Y. ANJANEYULU*, R. MARAYYA, D. LINGA RAO, P. KRISHNA RAO (*Natco Pharma Ltd. QC / QA Chemical Div., Road No.2, Banjara Hills, Hyderabad 500033, India, mekaguda@natcopharma.co.in)

      Asian J. Chem. 19(5), 3375-3381 (2007). The TLC method described in USP 28 does not separate all the related substances of alprazolam. An alternative HPTLC method is described for separation and estimation of starting material and synthesis related intermediates in alprazolam: 2-chloro acetamide-5-chloro benzophenone (impurity 1) i.e. starting material, nordiazepam (impurity 2), thionordiazepam (impurity 3), 2-(2-aceto hydrazinyl)-7-chloro-5-phenyl-3H-1, 4-benzodiazapine (impurity 4). The hRf values of alprazolam, impurity 4, impurity 3, impurity 2, and impurity 1 were 25, 16, 77, 45, and 83 respectively. The HPTLC method developed is capable of detecting impurities at a level of 0.05%.

      Classification: 32a
      102 108
      SIMULTANEOUS ESTIMATION OF ACECLOFENAC AND PARACETAMOL BY HPTLC IN PURE AND PHARMACEUTICAL DOSAGE FORM
      N. Harikrishnan*, V. Gunasekaran, A. Sathishbabu, G. Rao (*Dept. of Pharmaceutical Analysis, Vel’s College of Pharmacy, Old Pallavaram, Chennai 600117, India, harry74velscollege@yahoo.co.in)

      Asian J. Chem. 19(5), 3918-3922 (2007). TLC of paracetamol and aceclofenac on silica gel with toluene - isopropyl alcohol - ammonia 20:20:3. Quantitative determination by absorbance measurement at 254 nm. Linearity was between 60 and 140 µg/mL for aceclofenac and 460 and 540 µg/mL for paracetamol. Recovery (by standard addition method) of paracetamol and aceclofenac was between 98.6 and 99.3 %. The proposed method was found to be accurate, precise, simple and rapid could be used for routine analysis.

      Classification: 32a
      102 127
      Development and validation of a stability indicating HPTLC-densitometric method for satranidazole
      M.B. PATEL*, K.M. PATEL, G.S. PATEL, B.N. SUHAGIA, A.M. PRAJAPATI (*Nootan Pharmacy College , 17, Kadam Tenament, Opp. Nutan School Ghatlodia, Ahmedabad, Gujarat, India; mandev68@yahoo.com)

      J. Liq. Chromatogr. Relat. Technol. 30, 2755-2767 (2007). HPTLC of satranidazole (3-(1-methyl-5-nitroimidazol-2-yl)-1-(methylsulfonyl)imidazolidin-2-one) on silica gel (prewashed with methanol) with toluene - acetonitrile 3:2 in a twin-trough chamber saturated for 30 min at 25 °C. Quantitative determination by absorbance measurement at 314 nm. The method can effectively separate the drug from its degradation products and is therefore suitable for stability studies.

      Classification: 32a
      102 146
      Application of HPTLC in standardization of homoeopathic mother tincture Andrographis paniculata and its comparison with market products
      D. SHANBHAG, Sunita JAYARAMAN (*D. G. Ruparal College, Dept. of Chemistry, Mahim, Mumbai 400016, India, sunita_75in@yahoo.com)

      Asian J. Chem. 1, 509-513 (2008). HPTLC of andrographolide in Andrographis paniculata homoeopathic mother tincture on silica gel with chloroform - methanol 7:1. Quantitative determination by absorbance measurement at 225 nm. The standard mother tincture was found to contain 21.9 mg/100 mL andrographolide, where as 6 commercial samples contained varying amounts of andrographolide ranging from 4.89-54.62 mg/100 mL.

      Classification: 32c
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