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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      108 110
      HPTLC densitometric evaluation of tissue culture extracts of Nothapodytes foetida compared to conventional extracts for camptothecin content and antimicrobial activity
      A.G. NAMDEO*, A. SHARMA, L. SATHIYANARAYANAN, D. FULZELE, K.R. MAHADIK (*Department of Pharmacognosy, Poona College of Pharmacy, Bharati Vidyapeeth University, Paud Road, Erandwane, 411038 Pune, Maharashtra, India; ajay_namdeo@rediffmail. com)

      Planta Med. 76, 474-480 (2010). HPTLC of camptothecin and plant material extracts (roots, stems, leaves,and fruits) on silica gel with chloroform - ethyl acetate - methanol 9:10:1 in a twin trough chamber at 25 +/- 2°C and 40 % relative humidity. Quantitative determination by densitometry at 360 nm. Linearity was between 80 and 480 ng/zone with a correlation coefficient of 0.998 +/- 0.020. Instrumental precision (%RSD) was 0.5 %. Repeatability (%RSD) of sample and standard were 1.1 and 1.0 %. The LOD and LOQ were found to be 40 and 80 ng/zone, respectively. The accuracy of the method was proven by the average percentage recovery of 99.1 %.

      Classification: 32a
      109 095
      UV densitometric HPTLC method for analysis of nitrazepam in pharmaceutical formulations
      M. KOBA*, K. KOBA, T. BACZEK (*Department of Medicinal Chemistry, Faculty of Pharmacy, Collegium Medicum of Nicolaus Copernicus University, Bydgoszcz, Poland; kobamar@wp.pl)

      J. Planar Chromatogr. 24, 44-47 (2011). HPTLC of nitrazepam on silica gel with benzene - ethanol 5:1 in a horizontal chamber with saturation for 50 min. Quantitative determination by densitometry in absorbance mode at 196 nm. The hRf of nitrazepam was 68. Linearity was in the range of 0.25-10.0 µg/zone. Mean recovery was 98.8 % and 98.8 % for tablet and pure powder, respectively. Precision and accuracy (%RSD) were 1.3 % and 1.2 %, respectively. LOD and LOQ were 0.49 and 1.52 µg/mL, respectively.

      Classification: 32a
      110 063
      A validated stability-indicating HPTLC method for the estimation of gemcitabine HCl in its dosage form
      S. BORISAGAR, H. PATEL*, C. PATEL (*Department of Quality Assurance, Shree Sarvajanik Pharmacy College, Nr. Arvind Baug, Mehsana 384001, Gujarat, India, harshaupatel@yahoo.co.in)

      J. Planar Chromatogr. 25, 77-80 (2012). HPTLC of gemcitabine on silica gel with toluene - methanol - chloroform 6:6:5. Quantitative determination by absorbance measurement at 268 nm. The hRf value of gemcitabine was 48. Linearity was in the range of 500-3000 ng/band. Intraday and interday precisions (%RSD) were 1.4-1.6 % and 1.6-1.8 %, respectively. Recovery was found to be in the range of 98.3-101.8 %.

      Classification: 32a
      110 143
      Dhule (M
      A. SHIRKHEDKAR*, D. DHUMAL, S. SURANA (*Department of Pharmaceutical Chemistry, R.C. Patel Institute of Pharmaceutical Education and Research, Shirpur, Dist

      J. Planar Chromatogr. 25, 368-373 (2012). HPTLC of rebamipide on silica gel with toluene - methanol - triethylamine 16:9:1. Quantitative determination by absorbance measurement at 230 nm. The hRf of rebamipide was 59. Linearity was in the range of 100-600 ng/band. Limits of detection and quantification were 6 and 18 ng/band, respectively. Intermediate intra-day/inter-day precision was below 1.7 % (n=3). Recovery (by standard addition) was between 100.1 and 100.9 %. The proposed HPTLC method is equivalent to a reported HPLC method.

      Classification: 32a
      111 099
      Application of an expanded model procedure for transfer of TLC screening for substandard and fake drugs designed for use in developing countries to quantitative HPTLC-densitometry methods
      K. LIANZA, J. SHERMA* (*Department of Chemistry, Lafayette College, Easton, PA, USA, shermaj@lafayette.edu)

      J. Liq. Chromatogr. Relat. Technol. 36, 2446-2462 (2013). HPTLC of amitriptyline in tablets on silica gel with acetone - ammonium hydroxide 99:1. Quantitative determination by absorbance measurement at 254 nm. The hRf value of amitriptyline was 46. Linearity was 0.70-1.30 µg/zone. The earlier model TLC to HPTLC-densitometry transfer procedure was expanded by adding sample peak identification confirmation and peak purity (specificity) tests.

      Classification: 32a
      113 084
      Use of a model procedure for transfer of Minilab qualitative screening TLC methods for lumefantrine and artemether in a combined tablet formulation to individual and simultaneous quantitative HPTLC-densitometry methods
      M. NGUYEN, J. SHERMA* (* Department of Chemistry, Lafayette College, Easton, PA 18042, USA)

      Trends in Chromatography 8, 131-135 (2013). Based on the Minilab TLC screening methods two individual and one simultaneous HPTLC methods for quantification of lumefantrine and artemether were developed. HPTLC of artemether, lumefantrine, and both substances in a combined tablet formulation on silica gel with ethyl acetate - glacial acetic acid - toluene 2:1:9 with chamber saturation. Quantitative absorbance measurement of lumefantrine at 254 nm. For artemether, detection by spraying with methanol - 96 % sulfuric acid 19:1 and heating at 100 °C for 5 minutes, evaluation in daylight and quantitative absorbance measurement at 610 nm. With the simultaneous method artemether zones were detected by heating at 160 °C for 5 min, and after cooling absorbance measurement at 254 nm was performed. This is a novel, reagent-free detection method based on thermochemical activation of fluorescence quenching. Precision (%RSD) for the artemether individual method was 0.1-0.6 % and recovery 98-103 %. Precision (%RSD) for the lumefantrine individual method was 0.9-1.8 % and recovery 100-102 %. With the simultaneous method the hRF was 34 for lumefantrine and 61 for artemether, precision (%RSD) was below 3 % and recovery was 98-100 %.

      Classification: 32a
      115 065
      Determination of moxonidine and its impurities by thin-layer chromatography
      Slavica FILIPIC, M. SHENGER, Katarina NIKOLIC, Danica AGBABA* (*Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade, Serbia, danica@pharmacy.bg.ac.rs)

      J. Liq. Chromatogr. Relat. Technol. 38, 1121-1125 (2015). HPTLC of moxonidine and impurities (1) to (4) in dosage forms on silica gel with methanol - toluene - dichloromethane - ammonia 20:30:20:1. Quantitative determination by absorbance measurement at 260 and 280 nm. Average migration distances for moxonidine and its impurities (1) to (4) were 58.5 mm, 64.4 mm, 34.5 mm, 16.1 mm and 25.6 mm, respectively. Linearity was in the range of 200-600 ng/zone for moxonidine and 20-200 ng/zone for impurities (1) to (4). LOD and LOQ for impurities (1) to (4) were 7 and 20 ng/zone. The intermediate precisions were below 4 % (n=6). Recoveries ranged between 90 and 108 %.

      Classification: 32a
      117 113
      Development and validation of a stability-indicating assay method for naftopidil
      S. EZHAVA*, S. SHAH, A. PATWARI, M. CHHABRIA (*College of Pharmacy,
      Navrangpura, Ahmedabad 380 009, India, sindhulmcp@gmail.com)

      J. Planar Chromatogr. 29, 195-202 (2016). HPTLC of naftopidil on silica gel with toluene – ethyl acetate – methanol – triethylamine 80:20:5:3. Quantitative determination by absorbance measurement at 254 nm. The hRF value was 52. Linearity was in the range of 500-2500 ng/zone. Intermediate precisions were below 1.5 %. The LOD and LOQ were 95 and 268 ng/zone. Average recovery was 100.0%.

      Classification: 32a
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