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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      104 117
      A vlidated stability indicating HPTLC method for simultaneous estimation of irbesartan and hydrochlorothiazide
      A. KHODKE*, M. DAMLE, K. BOTHARA (*AISSMS College of Pharmacy, Pune, Maharashtra, India)

      Abstract No. F-269, 61st IPC (2009). HPTLC of hydrochlorothiazide and irbesartan on silica gel with acetonitrile - chloroform 5:6. The hRf value was 27 and 45 for irbesartan and hydrochlorothiazide, respectively. Quantitative determination by absorbance measurement at 270 nm. The sample was exposed to different stress conditions (acid, alkali, oxidative, photodegradation, thermal). Neither of the compounds showed degradation under thermal and photodegradation conditions, but both compounds showed significant degradation under acid, alkali and hydrolytic conditions. Degraded products were well resolved from the parent compounds.

      Classification: 32a
      104 136
      Determination of harmalin in Passiflora edulis leaves by HPTLC
      T. MANI*, S. BADAMI, N. MAHADEVAN, S. MANIMARAN, B. SURESH (*Bharathi College of Pharmacy, Bharathi Nagara, Karnataka, India)

      Abstract No. 9274, IHCB (2009). HPTLC of harmalin from ethanolic leaf extracts of Passiflora edulis on silica gel with ethyl acetate - acetic acid - formic acid - water 100:11:11:27. The hRf value of harmalin was 39. The method was linear in the range of 200-1600 ng/spot, recovery was 98.4-99.2 %.

      Classification: 32e
      104 153
      Specrofluorometry, thin-layer chromatography, and column high-performance liquid chromatography determination of rabeprazole sodium in the presence of its acidic and oxidized degradation products
      A. OSMAN*, M. OSMAN (*National Organization for Drug Control and Research, 6 Abu Hazem St Pyramids, PO Box 29, Cairo, Egypt; afaf_osmanelteti@yahoo.com)

      J. AOAC Int. 92, 1373-1381 (2009). TLC of rabeprazole sodium and its degradation products on silica gel with isopropanol - 30 % ammonia 40:1 with chamber saturation. Quantitative determination by absorbance measurement at 284 nm.

      Classification: 32a
      104 169
      Quality control of polyherbal formulations used in diabetes mellitus
      P. PATEL*, N. PATEL, R. GOYAL (*Shri B. M. Shah College of Pharmaceutical Education & Research, Modasa, Gujarat, India)

      60th Indian Pharmaceutical Congress PG-246 (2008). HPTLC of biomarkers such as curcumin, charantin, and swertiamarin in some polyherbal formulations on silica gel with benzene - methanol 4:1 (for charantin), chloroform - methanol - formic acid 74:4:1 (for curcumin), and ethyl acetate - methanol - water 77:15:5 (for swertiamarin). Quantitative determination by absorbance measurement at 536 for charantin (hRf value 33), 425 nm for curcumin (hRf value 89), and 238 nm for swertiamarin (hRf value 54).

      Classification: 32e
      104 192
      Standardization of Ayurvedic formulations containing Aloe vera by quantification of a marker compound
      K.K. ROUT*, O.P. ROUT, S.K. MISHRA (*Pharmacognosy and Phytochemistry Division, University Department of Pharmaceutical Sciences, Utkal University, Vani Vihar, Bhubaneswar 751004, Orissa, India; kd_rout@yahoo.co.in)

      J. Planar Chromatogr. 22, 381-384 (2009). TLC of aloin in commercial Ayurvedic preparations on silica gel (prewashed with methanol) with ethyl acetate - methanol - water 50:7:2 in a twin trough chamber with chamber saturation for 5-7 min at 30 +/- 4 °C and a relative humidity of 57 +/- 3 %. Quantitative determination by absorbance measurement at 360 nm. The limit of detection and quantification was 10 and 20 ng/band, respectively.

      Classification: 32e
      104 210
      A validated stability indicating method for determination of aspirin and clopidogrel bisulphate
      P. SINHA*, M. DAMLE, K. BOTHARA (*AISSMS College of Pharmacy, Pune, Maharashtra, India)

      60th Indian Pharmaceutical Congress PA-208 (2008). TLC of aspirin and clopidogrel bisulphate on silica gel with carbon tetrachloride - acetone 5:2. The hRf value of aspirin was 15 and of clopidogrel bisulphate 80. Quantitative determination by absorbance measurement at 220 nm. The method was linear in the range of 2-6 µg/spot for aspirin and 3-6 µg/spot for clopidogrel.

      Classification: 32a
      104 226
      HPTLC method development for estimation of rivastigmine hydrogen tartrate in pharmaceutical dosage form
      D. VASA*, N. VASA, P. GIDE, V. VAGHELA (*A. R. College of Pharmacy & G. H. Patel Institute of Pharmacy, Anand, Gujarat, India)

      Abstract No. F-365, 61st IPC (2009). HPTLC of rivastigmine hydrogen tartrate on silica gel with methanol - 25 % ammonia - acetic acid 200:7:2. The hRf value was 54. Quantitative determination by absorbance measurement at 215 nm. The method was linear in the range of 1-10 µg/band.

      Classification: 32a
      105 030
      Micro scale procedure for analysis of andrographolide in Andrographis paniculata leaves
      A. VARMA, Neeta SHRIVASTAVA* (*B. V. Patel Pharmaceutical Education and Research Development (PERD) Centre, Sarkhej-Gandhinagar Highway, Thaltej, Ahmedabad-380054, Gujarat, India; neetashrivastava_perd@yahoo.co.in)

      J. Planar Chromatogr. 23, 50-55 (2010). HPTLC of andrographolide on silica gel with chloroform - methanol - ethyl acetate 12:3:2 in a twin-trough chamber previously saturated for 15 min. Quantitative determination by absorbance measurement at 223 nm. The relative standard deviation of intra-day and inter-day analysis was in the range of 0.56-1.33 %. Lineartiy was given between 200-700 ng/band; the correlation coefficient was 0.9998 and the RSD 0.97 %. The limits of detection and quantification were 60 and 150 ng/band. Average recovery was 98.8 +- 0.41 %.

      Classification: 15a
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