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.

Page
      104 140
      Quantitative HPTLC analysis of dially disulfide in garlic oil macerate
      Annie MATHEW*, R. RAVINDRA (*C. U. Shah College of Pharmacy, S.N.D.T. Women’s University, Juhu Road, Santacruz (W) Mumbai, India)

      Abstract No. 9286, IHCB (2009). HPTLC of dially disulfide in garlic oil macerate on silica gel with n-hexane - isopropyl alcohol - formic acid 196:4:3. Quantitative determination by absorbance measurement at 210 nm. The method was linear in the range of 16-48 µg/spot.

      Classification: 32e
      104 159
      Development and validation of spectrophotometric and HPTLC method for simultaneous estimation of levocetirizine dihydrochloride and montelukast sodium in their combined dosage form
      B. PATEL*, A. MODH, P. MEHTA, H. BHATT (*Institute of Pharmacy, Nirma University Science and Technology, Ahmedabad, Gujarat, India)

      Abstract No. F-311, 61st IPC (2009). HPTLC of levocetirizine dihydrochloride and montelukast sodium on silica gel with chloroform - methanol 93:7. The hRf value was 21 and 65 for levocetrizine and montelukast, respectively. Quantitative determination by absorbance measurement at 345 nm. The method was linear in the range of 100-350 ng/band for levocetrizine and 600-1100 ng/band for montelukast.

      Classification: 32a
      104 175
      A validated, stability-indicating HPTLC method for analysis of doxofylline
      N.G. PATRE, L. SATHIYANARAYANAN, M.V. MAHADIK, S.R. DHANESHWAR* (*Department of Pharmaceutical Chemistry, Bharati Vidyapeeth University, Poona College of Pharmacy, Center for Advanced Pharmaceutical Research, Erandwane, Pune 411038, Maharashtra State, India; Sunil.dhaneshwar@gmail.com)

      J. Planar Chromatogr. 22, 245-348 (2009). HPTLC of doxofylline (7-(1,3-dioxalan-2-ylmethyl)theophylline) in bulk drug and in formulations on silica gel, prewashed with methanol, with toluene - methanol 4:1 in a twin trough chamber saturated for 20 min. Quantitative determination by absorbance measurement at 275 nm.

      Classification: 32a
      104 199
      HPTLC method for the simultaneous estimation of valsartan and hydrochlorothiazide in tablet dosage form
      N. SHAH*, B. SUHAGIA, R. SHAH, N. PATEL (*Shri B. M. Shah College of Pharmaceutical Education & Research, Modasa 383315)

      Ind. J. Pharma. Sci. 71(1), 72-74 (2009). HPTLC of valsartan and hydrochlorothiazide on silica gel with chloroform - methanol - toluene - acetic acid 60:20:10:1. Quantitative determination by absorbance measurement at 260 nm. The calibration curve was linear between 300 to 800 ng/spot for valsartan and 100 to 600 ng/spot for hydrochlorothiazide. The limit of detection and the limit of quantification for valsartan were 100 and 300 ng/spot, respectively, and for hydrochlorothiazide 30 and 100 ng/spot, respectively.

      Classification: 32a
      104 219
      HPTLC method for the simultaneous estimation of itopride hydrochloride and pantoprazole in pharmaceutical dosage form
      A. SUGANTHI*, A. FATHIMUNNISA, T. RAVI (*College of Pharmacy, SRIPMS, Coimbatore, Tamil Nadu, India)

      Abstract No. F-264, 61st IPC (2009). HPTLC of pantoprazole and itopride hydrochloride on silica gel with n-butanol - chloroform - 25 % ammonia 7:2:1. The hRf value was 54 and 75 for pantoprazole and itopride hydrochloride, respectively. Quantitative determination by absorbance measurement at 291 nm. The linearity of the method was 80-240 ng/band for pantoprazole and 300-900 ng/band for itopride.

      Classification: 32a
      105 008
      Electrospun glassy carbon ultra-thin layer chromatography devices
      J.E. CLARK*, Susan OLESIK (*The Ohio State University, Department of Chemistry, 120 West 18th Ave, Columbus, OH 43210, USA)

      J. Chromatogr. A 1217 (23), 4655-4662 (2010). Development and application of electrospun glassy carbon nanofibers for ultra-thin layer chromatography (UTLC). The carbon nanofiber stationary phase was created through electrospinning and pyrolysis of SU-8 2100 photoresist, which resulted in glassy carbon nanofibers with diameters of 200-350 nm that form a mat structure with a thickness of 15 µm. The chromatographic properties of UTLC devices produced from pyrolyzed SU-8 heated to temperatures of 600, 800, and 1000 °C were investigated. By use of Raman spectroscopy and scanning electron microscopy the physical and molecular structure of the nanofibers at each temperature was determined. The carbon UTLC devices were suitable for the analysis various dye mixtures and also allowed separation of three FITC-labeled essential amino acids (lysine, threonine, phenylalanine). The electrospun glassy carbon UTLC plates showed good retention properties, plate number values above 10000, and physical and chemical robustness for a range of mobile phases.

      Classification: 3b
      105 029
      High throughput screening of mutants of oat that are defective in triterpene sythesis
      B. QIN, J. EAGLES, F. MELLON, P. MYLONA, L. PEÑA, A. OSBOURN* (*Sainsbury Laboratory, Norwich NR4 7UH, UK, anne.osbourn@bbsrc.ac.uk)

      Phytochemistry. 71, 1245-1252 (2010). TLC of squalene (1), 2,3-oxidosqualene (2) and beta-amyrin (3) in the roots of Avena strigosa on silica gel with hexane - chloroform 23:2, hexane - chloroform 1:1, and hexane - acetone 4:1 for (1), (2) and (3), respectively. Detection by exposure to iodine vapor. Quantitative determination by GC-MS.

      Classification: 15a
      105 056
      Simultaneous determination of gallic acid and piperine by high-performance thin-layer chromatography
      Bharati BARMECHA*, D. GHANAWAT, P. SHINDE, Smita SHELKE (*Sitabai Thite College of Pharmacy, Pune, Maharashtra, India)

      Abstract No. C-338, 61 IPC (2009). HPTLC of gallic acid and piperine in combined formulation on silica gel with toluene - ethyl acetate - formic acid 16:8:1. Quantitative absorbance measurement at 320 nm. The method was linear in the range of 200-800 ng/band for gallic acid and 50-350 ng/band for piperine.

      Classification: 32e
Page