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
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      104 124
      HPTLC estimation of cefixime and cloxacillin in tablet dosage form
      N. LADKAT*, M. ANRUTKAR, J. JAGADE, A. KALE, S. PAWAR, A. BHOSALE (*Poona Dist. Education Asso. Seth Govind Raghunath Sable College of Pharmacy, Pune, Maharashtra, India)

      Abstract No. F-260, 61st IPC (2009). HPTLC of cefixime and cloxacillin on silica gel, prewashed with methanol, with n-butanol - methanol - water - formic acid 80:60:40:3. The hRf values were 28 and 45 for cefixime and cloxacillin, respectively. Quantitative determination by absorbance measurement at 293 nm for cefixime and 343 nm for cloxacillin. The linearity range was 150-600 ng/band for both compounds.

      Classification: 32a
      104 145
      Estimation of glycyrrhizic acid and withanolide A in polyherbal formulation by HPTLC
      S. MISHRA*, Sunita CHAUDHARY, K. GADHVI (*Saraswati Institute of Pharmaceutical Sciences, Ahmedabad, Gujarat, India)

      60th Indian Pharmaceutical Congress PA-233 (2008). HPTLC of glycyrrhizic acid on silica gel with toluene - ethyl acetate - glacial acetic acid 25:15:1. The hRf value of glycyrrhizic acid was 52, linearity was between 500-1000 ng/mL and recovery was 99.2 %. Withanolide A was separated with toluene - ethyl acetate - glacial acetic acid 20:20.1. The hRf value of withanolide A was 44, linearity was in the range of 400-1000 ng/mL and recovery was 99.4 %.

      Classification: 32e
      104 164
      Determination of camylofin dihydrochloride in bulk and tablet by liquid chromatography and HPTLC
      F. PATEL*, J. DONGA, N. PATEL, V. GANDHI (*Dharmaj Degree Pharmacy College, Dharmaj, Gujarat, India)

      Abstract No. F-267, 61st IPC (2009). HPTLC of camylofin dihydrochloride on silica gel with chloroform - ethyl acetate - methanol - 25 % ammonia 50:30:20:1. Quantitative determination by absorbance measurement at 215 nm. Linearity was in the range of 1.5-7.5 µg/band. The proposed method is suitable for routine quality control of bulk drug and tablets.

      Classification: 32a
      104 185
      Development and validation of HPTLC method for simultaneous estimation of olmesartan medoxomil and hydrochlorothiazide in their combined tablet dosage form
      P. RAJA* , K. BHATT, V. JOSHI, K. AMIN (*A. R. College of Pharmacy and G. H. Patel Institute of Pharmacy, Anand, Gujarat, India)

      60th Indian Pharmaceutical Congress PA-232 (2008). HPTLC of olmesartan medoxomil and hydrochlorothiazide on silica gel with methanol - toluene - ethyl acetate 5:11:4 with chamber saturation for 30 min. The hRf value of olmesartan medoxomil was 27 and of hydrochlorothiazide 44. The method was linear in the range of 300-1800 ng/spot for both drugs.

      Classification: 32a
      104 204
      Stability-indicating TLC-densitometric determination of nebivolol hydrochloride in bulk and pharmaceutical dosage form
      A.A. SHIRKHEDKAR*, P.M. BUGDANE, S. SURANA (*R.C. Patel College of Pharmacy, Shirpur Dist. Dhule, (M.S.) 425 405 India)

      J. Chromatogr. Sci. 48 (2), 109-113 (2010). HPTLC of nebivolol hydrochloride on silica gel with toluene – methanol - triethylamine 19:6:1. The hRf value of nebivolol hydrochloride was 33. Quantification by densitometry in the absorbance mode at 281 nm. Linearity was between 500 and 3000 ng/spot with r2= 0.9994. The limit of detection and quantification was 63 and 191 ng/spot, respectively. Nebivolol hydrochloride was subjected to acid and alkali hydrolysis, oxidation, thermal degradation, and photodegradation. The degradation products were well-resolved from the main component.

      Classification: 32c
      104 225
      Simultaneous estimation of nebivolol hydrochloride and S-amlodipine besylate by high-performance thin-layer chromatography
      J. VADHAVANA*, B. PATEL, R. PATEL (*K. B. Institute of Pharmaceutical Education and Research, Gandhinagar, Gujarat, India)

      Abstract No. F-247, 62st IPC (2009). HPTLC of nebivolol HCl and S-amlodipine besylate on silica gel (prewashed with methanol) with chloroform - toluene - methanol - acetic acid 50:20:1. The hRf value was 33 and 48 for S-amlodipine and nebivolol, respectively. Quantitative determination by absorbance measurement at 271 nm. The method was linear in the range of 500-2500 ng/band for nebivolol and 250-1280 ng/band for S-amlodipine, respectively.

      Classification: 32a
      105 013
      Differently complex oligosaccharides can be easily identified by matrix-assisted laser desorption and ionization time-of-flight mass spectrometry directly from a standard thin-layer chromatography plate
      K. NIMPTSCH, R. SUESS, T. RIEMERA, A. NIMPTSCH, M. SCHNABELRAUCH, J. SCHILLER (* University of Leipzig, Medical Faculty, Institute of Medical Physics and Biophysics, Härtelstr. 16-18, 04107 Leipzig, Germany)

      J. Chromatogr. A 1217 (23), 3711-3715 (2010). Oligosaccharides (derived from dextran, alginate, hyaluronan and chondroitin sulfate) were characterized by matrix-assisted laser desorption and ionization time-of-flight (MALDI-TOF) mass spectrometry (MS) directly on a normal phase TLC plate. The applied oligosaccharides were either commercially available or obtained from the polysaccharides by HCl-induced hydrolysis. TLC was followed by MALDI-TOF MS subsequent to matrix deposition. The high quality mass spectra obtained allow for unequivocal assignments. The high content of formic acid in the solvent does not cause major problems but is responsible for the partial formylation of the analyte and a minor N-acetyl loss from hyaluronan and chondroitin sulfate.

      Classification: 4e
      105 037
      Effect of chromatographic conditions on separation and system efficiency in HPTLC of selected quinoline standards on cyanopropyl stationary pases
      Anna PETRUCZYNIK (Department of Inorganic Chemistry, Medical University of Lublin, Staszica 6, 20-081 Lublin, Poland; annapetruczynik@poczta.onet.pl)

      J. Planar Chromatogr. 23, 56-64 (2010). HPTLC of thirteen quinolines (quinoline, isoquinoline, 2,4-dihydroxyquinoline, 8-hydroxyquinoline, 5,6-benzoquinoline, 2,2’-diquinoline, 8-methylquinoline, 5-aminoquinoline, 1-ethylquinoline, 2-chlorquinoline, 6-nitroquinoline, 2,6-dimethylquinoline, 5-hydroxyquinoline) on cyano phase with different mobile phases prepared from mixtures of methanol, acetonitrile, 2-propanol, tetrahydrofuran, and dioxane with addition of buffer at different pH, ion-pairing reagents, or silanol blockers. Detection under UV light at 254 nm and by densitometric absorbance measurement at 254 nm. Improved peak symmetry was observed for mobile phases containing ion-pairing reagent. The most symmetrical peaks were obtained by use of mobile phase containing diethylamine as silanol blocker.

      Classification: 23e
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