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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      104 156
      Simultaneous determination of tenofovir and emtricitabine in the bulk drug and tablet dosage form by HPTLC method
      M. PANDE*, Shweta GONDKAR, J. RAO, S. YADAV (*Poona College of Pharmacy, Bharati Vidyapeeth University, Pune, Maharashtra, India)

      Abstract No. F-253, 61st IPC (2009). HPTLC of tenofovir and emtricitabine on silica gel with toluene - methanol - ethyl acetate - acetic acid 40:20:50:1. Quantitative determination by absorbance measurement at 273 nm. The hRf value was 52 for tenofovir and 40 for emtricitabine. Linearity of tenofovir and emtricitabine was in the range of 120-600 ng/spot and 80-560 ng/spot, respectively. The recovery was 99.9 and 99.5 % for tenofovir and emtricitabine, respectively.

      Classification: 32a
      104 176
      (Determination of scalreol in its formulations by thin-layer chromatography) (Chinese)
      M. PENG (Peng Minjie)*, D. LI (Li Duowei), Y. WANG (Wang Yichao), SH. JIA (Jia Shaoliang) (*Inst. Life Sci., North-West University, Xi’an 710069, China)

      Chinese J. Pharm. Anal. 28 (9), 1554-1556 (2008). TLC of scalreol on silica gel with n-hexane – ethyl acetate – formic acid 32:16:1. Detection by spraying with vanillin – sulfuric acid – ethanol 1:1:18. Quantification by densitometry at 520 nm. Linearity was between 10 and 50 µg/zone with a determination coefficient of 0.9994. Recovery was 100.1 % (n = 6, %RSD = 0.9). Repeatability (%RSD, n = 6) was 2.1 % within plate and 2.3 % plate-to-plate.

      Classification: 32c
      104 196
      Quantitative analysis of losartan potassium and atenolol by high-performance thin-layer chromatography
      S. SATHE*, S. BARI (*Department of Pharmaceutical Chemistry, R. C. Patel College of Pharmacy, Karwand Naka, Shirpur Dhule, Maharashtra 425405, India, sbbari@rediffmail.com, shitalsathe@rediffmail.com)

      Indian Drugs 46(1), 78-81 (2009). HPTLC of atenolol and losartan potassium in tablets on silica gel with toluene - methanol - triethylamine 12:8:1 with chamber saturation for 45 min. Quantitative determination by absorbance measurement at 230 nm. The hRf value of atenolol was 45 and of losartan potassium 67. The method was linear in the range of 1000-4000 ng/spot for both compounds. The recovery was 98.8-98.9 %.

      Classification: 32a
      104 214
      Validated HPTLC method for the analysis of colchicine
      N. SONI*, S. MANIMARAN, N. MURUGANANTHAM, S. DHANABAL, K. ELANGO (*Dept. of Phytopharmacy & Phytomedicine, JSS College of Pharmacy, Ootacamund,The Nilgiri, Tamil Nadu, India)

      Abstract No. 9933, IHCB (2009). HPTLC of colchicines in Gloriosa superba (collected from different parts of India) on silica gel with ethyl acetate - methanol 200:27. The hRf value of colchicine was 29. Quantitative determination by absorbance measurement at 350 nm. The method was linear in the range of 50-1000 ng/spot. The sample collected from Kerala was found to contain highest level of colchicines (0.24 %).

      Classification: 32e
      104 234
      Iridoid glycoside-based quantitative chromatographic fingerprint analysis
      A. YADAV*, N. TIWARI, P. SRIVASTAVA, S. SINGH, K. SHANKER, R. VERMA, M. GUPTA (*Analytical Chemistry Div. Central Institute of Medicinal and Aromatic Plants, Lucknow 226015, India, guptammg@rediffmail.com)

      J. Pharm. Biomed. Anal. 47, 841-846 (2008). HPTLC of iridoid glycosides in the aerial part of Gambhari (Gmelina arborea) with iridoid gycoside 6-0-(2”, 3”- dibenzoyl)-o-L-rhamnopyranosylcatalpol as a chemical marker for the standardization of G. arborea plant extracts on silica gel with chloroform - methanol 4:1. Quantitative determination by absorbance measurement at 240 nm and at 430 nm after derivatization with vanillin - sulfuric acid reagent. The linear working range was between 1000-5000 ng/spot with a good correlation coefficient of 0.994.

      Classification: 32e
      105 054
      Quantitative estimation of withanolide A in marketed polyherbal spansules
      D. BAHETI*, P. SHINDE, M. AGRAWAL, R. BANGAR (*Sitabai Thite College of Pharmacy, Pune, Maharashtra, India)

      Abstract No. C-372, 61st IPC (2009). HPTLC of withanolide A in extracts and spansules dosage form on silica gel with toluene - ethyl acetate - formic acid 8:6:1. Densitometric evaluation at 254 nm. Withanolide A was well separated with an hRf value of 14. The linearity range was 40-200 ng/band.

      Classification: 32e
      105 083
      Stability-indicating validated HPTLC method for simultaneous analysis of rifabutin and isoniazid in pharmaceutical formulations
      Amelia M. AVACHAT*, S. B. BHISE (*Department of Pharmaceutics, Sinhgad College of Pharmacy, Off Sinhgad Road, Vadgaon (Bk.), Pune-411 041, India; prof_avachat@yahoo.com)

      J. Planar Chromatogr. 23, 123-128 (2010). HPTLC of rifabutin and isoniazid on silica gel with dichloromethane - acetone - methanol 20:7:2 in a twin-trough chamber previously saturated for 25 min. Quantitative determination by absorbance measurement at 504 nm for rifabutin (hRf 84) and at 262 nm for isoniazid (hRf 48). The linearity range was 10-70 and 5-35 µg/mL, the correlation coefficient was 0.9991 and 0.9989, the precision (RSD, n = 6) 0.90 % and 0.71 %, and precision on different days (RSD, n = 3) was 0.89 % and 1.01 %. LOD was 180 µg and 90 µg/zone, LOQ was 540 and 270 µg/zone, and the system suitability (RSD, n = 6) was 1.41 % and 1.86 % for rifabutin and isoniazid, respectively.

      Classification: 32a
      105 105
      Estimation of constituents from methanolic extract of Aloe vera by HPTLC technique
      Suparna ROY*, B. SINHA, MANIK (*Birla Institute of Technology, Ranchi, Jharkhand, India)

      Abstract No. C-37, 61st IPC (2009). HPTLC of methanolic leaf extracts of Aloe vera (after purification with petroleum ether (60-80 °C)) on silica gel with toluene - ethyl acetate - glacial acetic acid - methanol 4:18:1:4. Under UV 254 nm six bands with hRf values of 12, 26, 34, 44, 62, and 84 were observed. These bands correspond to well known constituents of Aloe vera: aloeresin hRf 25, barbaloin hRf 33, aloe emodin hRf 43, emodin hRf 63. The bands with hRf values of 12 and 84 could not be identified. The reported finger print profiling can serve as potential technique for authentification and batch to batch consistency of herbal drugs.

      Classification: 32e
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