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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      104 037
      Identification of terpenes in stem of Ocimum basilicum Linn by HPTLC technique
      B. CHENGAIAH*, B. PRATAP, M. ALAGUSUNDARAM, M. RUTHU, V. SAROVAR REDDY (*Annamacharya College of Pharmacy, Rajampet, Kadapa, A.P., India)

      60th Indian Pharmaceutical Congress PA-221 (2008). HPTLC of terpenes in stem of Ocimum basilicum on silica gel with toluene - ethyl acetate 19:1. Evaluation of 5 spots under UV 254 nm and under visible light after treatment with anisaldehyde reagent followed by heating at 100 °C for 5 min: borneol (yellow, hRf 24), menthol (red, hRf 27), eugenol (blue, hRf 50), thymol (violet, hRf 57), safrole (blue, hRf 93).

      Classification: 15a
      104 064
      Development and validation of novel HPTLC method for quantitative estimation of strychnine and brucine in seeds of Strychnos Nux Vomica
      S. AHMAD*, A. KAMAL, R. PARVEEN, F. AHMAD, K. SALEEM (*JMI, Dept. of Biosciences, New Delhi, India)

      60th Indian Pharmaceutical congress PA-235 (2008). HPTLC of strychnine and brucine (in seeds of Strychnos Nux Vomica) on silica gel with chloroform - methanol - ammonia 38:2:1. Quantitative determination by absorbance measurement at 258 nm (strychnine, hRf value 29) and 271 nm (brucine, hRf value 21). The method was linear in the range of 100-1000 ng/spot (both compounds). The method was suitable for standardization of several herbal formulations containing nux vomica as an ingredient.

      Classification: 32e
      104 081
      Determination of psoralen and plumbagin from its polyherbal oil formulations by an HPTLC densitometric method
      N. DUBEY*, N. DUBEY, R. MEHTA, A. K. SALUJA (*Devi Ahilya Vishwa Vidyalaya, School of Pharmacy, Indore, India; nidhidubeympharm@yahoo.com)

      J. AOAC Int. 92, 779-784 (2009). HPTLC of psoralen and plumbagin and extracts of ayurvedic polyherbal oil formulations on silica gel at 22 °C and 55 % humidity with toluene - ethyl acetate 3:1 in a twin trough chamber with chamber saturation. UV spectra were recorded from 200 to 600 nm; densitometric measurements were performed at 302 nm (for psoralen) and 275 nm (for plumbagin).

      Classification: 32e
      104 099
      Quantitative determination of aloe-emodin in Rheum emodi using HPTLC
      P. HAMRAPURKAR*, N. LONE, K. KAMAT, T. SAMBARE (*Principal K. M. Kundnani College of Pharmacy, Mumbai, Maharashtra, India)

      60th Indian Pharmaceutical Congress PA-224 (2008). HPTLC of aloe-emodin in extract of Rheum Emodi (prepared by supercritical fluid extraction) on silica gel with toluene - acetone - formic acid 80:20:1. Quantitative determination by absorbance measurement at 254 nm. Linearity was in the range of 100-400 ng/spot. Compared with other extraction techniques supercritical fluid extraction was more effcient and less time consuming.

      Classification: 32e
      104 122
      Stability indicating HPTLC method for the determination of cinitapride hydrogen tartrate in bulk drug and pharmaceutical formulations
      M. KUMAR*, B. SRINIVASAN (*Delhi Institute of Pharmaceutical Sciences and Research (DIPASR), New Delhi, India)

      Abstract No. F-240, 61st IPC (2009). HPTLC of cinitapride hydrogen tartrate on silica gel with methanol - toluene 17:3. The hRf value was 71. Quantitative determination by absorbance measurement at 265 nm. The linearity was in the range of 90-450 ng/band. The compound was subjected to different stress conditions (acid, alkali, oxidative, photodegradation, dry and wet heat) and degradation products were well separated from the main component.

      Classification: 32a
      104 143
      Simultaneous estimation of salbutamol silphate and guaiphenesin in their combined liquid dosage form by HPTLC method
      A. MISHRA*, R. BHOMIA, S. VASANTHARAJU, A. KARTHIK, S. SAYED, K. BHAT (*L. M. College of Pharmacy, Ahmedabad, Gujarat, India)

      Abstract No. F-238, 61st IPC (2009). HPTLC of salbutamol silphate and guaiphenesin, used as pharmaceutical syrup against cough, on silica gel with ethyl acetate - methanol - 25 % ammonia 15:3:2. The hRf value was 47 and 65 for salbutamol and guaiphenesin, respectively. Quantitative determination by absorbance measurement at 280 nm. The method was linear in the range of 200-1000 ng/band for salbutamol and 10-15 µg/band for guaiphenesin.

      Classification: 32a
      104 162
      Simultaneous estimation of atorvastatin calcium, ramipril and aspirin in capsule dosage form by HPTLC
      D. PATEL*, B. SHAH, B. PATEL (*K. B. Institute of Pharmaceutical Education and Research Gandhinagar, Gujarat, India)

      Abstract No. F-245, 61st IPC (2009). HPTLC of atorvastatin (AT) calcium, ramipril (RA) and aspirin (AS) on silica gel with benzene - ethyl acetate - toluene - methanol - acetic acid 40:45:10:5:1. Quantitative determination by absorbance measurement at 220 nm. The hRf values were 45, 28 and 72 for AT, RA and AS, respectively. The linearity ranges were 0.5-2.5 µg/band (r2=0.998) for AT, 0.5-2.5 µg/band (r2=0.9978) for RA and 0.75-3.75 µg/band (r2=0.9946) for AS with mean recoveries of 100.3, 99.1 and 98.9 for AT, RA and AS, respectively.

      Classification: 32a
      104 180
      High-performance thin-layer chromatographic method for analysis of racecadotril in the bulk drug
      S.L. PRABU*, T. SINGH, C.D. KUMAR, A. JOSEPH, K.K. SRINAVASAN (*Manipal College of Pharmaceutical Sciences, Manipal 576104, India; slaxmanvel@gmail.com)

      J. Planar Chromatogr. 22, 277-281 (2009). HPTLC of racecadotril (2-{2(acetylsulfanylmethyl)-3-phenylpropanoyl}amino acetic acid benzyl ester) and its degradation products in the bulk drug and in a pharmaceutical formulation on silica gel with n-hexane - ethyl acetate 7:3 in a twin trough chamber saturated for 30 min. Quantitative determination by absorbance measurement at 230 nm. The limit of detection and quantification was 50 and 100 ng/band, respectively.

      Classification: 32a
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