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
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      109 029
      Development and validation of RP-HPLC and HPTLC method for the estimation of valsartan, hydrochlorothiazide and amlodipine besylate in combined tablet dosage form
      V. GALANDE, K. BAHETI, M. DEHGHAN* (*Dept. of Pharmaceutical Chemistry, Y. B. Chavan College of Pharmacy, Dr. Rafiq Zakaria Campus, Rauza Bagh, Aurangabad (M.S.), India, nk_baheti@yahoo.com)

      Indian Drugs 48(4), 49-55 (2011). HPTLC of hydrochlorothiazide (HCZ), amlodipine besylate (AMB) and valsartan (VAL) on silica gel with ethyl acetate - methanol - 10 % ammonia 17:4:2. The hRf value was 26 for AMB, 34 for VAL and 82 for HCZ. The linearity range was 100-700 ng/band for VAL and HCZ and 50-400 ng/band for AMB.

      Classification: 11a
      109 049
      Quantitative HPTLC analysis of palmitoyl hexapeptide
      S. SHAHI*, R. ATHAWALE (*C. U. Shah College of Pharmacy, 11/602 Mandar, Vasant Vihar Complex,Thane (W)-400 601, India; shilpa_s2000@rediffmail.com)

      J. Planar Chromatogr. 23, 365-368 (2010). HPTLC of palmitoyl hexapeptide (an antiwrinkle peptide) on silica gel with toluene - ethanol 9:1 in a twin-trough chamber with saturation for 30 min at room temperature (25 +/- 2 °C). The hRf was 33. Quantitative determination by absorbance measurement at 211 nm. Linearity was between 10 and 30 ng/band. The LOD and LOQ was 3 and 9 ng/band, respectively. The intra-day precision (%RSD, n = 6) was 0.9-1.5 % and the inter-day precision 0.9-1.4 %. The small %RSD obtained after small changes of the method conditions indicate the method is robust. The recovery of the method was in the range of 98.9-101.3 %.

      Classification: 18a
      109 076
      Quantitative analysis of oxyresveratrol on different plant parts of Morus species and related genera by HPTLC and HPLC
      S.R. AYINAMPUDI, Y.-H. WANG, B. AVULA, T.J. SMILLIE, I.A. KHAN* (*National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences and Department of Pharmacognosy, School of Pharmacy, University of Mississippi, University, MS 38677, USA; ikhan@olemiss.edu)

      J. Planar Chromatogr. 24, 125-129 (2011). HPTLC of plant extracts and oxyresveratrol on silica gel, prewashed with methanol, with hexane - ethyl acetate - chloroform - methanol 15:10:17:8 in a twin-trough chamber lined with filter paper and saturated for 20 min. Quantitative determination by densitometry at 327 nm. LOD and LOQ were 50 and 200 ng/band, respectively. The hRf value of oxyresveratrol was 31. Intra-day and inter-day variation (%RSD) were consistently below 5.0 %. Within-day precisions for the replicate analysis (n = 3) were in the range of 1.1-4.1 %. Day-to-day replicates (n = 9) were between 2.1-2.8 %.

      Classification: 32e
      109 096
      (Identification of Sanqi Jiangzhi Tongmai capsules by thin-layer chromatography) (Chinese)
      X. LAI (Lai Xinhua) *, L. TANG (Tang Lili) (*Yuebei People’s Hospital, Guangdong, Shaoguan 512026, China)

      J. Strait Pharm. 22 (12), 59-60 (2010). TLC of the extracts of the title traditional Chinese medicine 1) for red Ginseng, on silica gel with benzene - ethyl acetate - formic acid 20:16:3, detection by spraying with 3 % FeCl3 in ethanol and viewing under daylight; 2) for Chinese Taxillus twig, on silica gel with water-saturated toluene - ethyl acetate - formic acid 5:4:1, detection by spraying with 5 % AlCl3 in ethanol; 3) for Hawthorn, on silica gel with toluene - ethyl acetate - glacial acetic acid 24:8:1, detection by spraying with 3-10 % sulfuric acid in ethanol and heating at 105 °C until the zones were detected; 4) for Alisma orientale, on silica gel with toluene - ethyl acetate - formic acid 14:7:2, detection by spraying with acetic acid - concentrated sulfuric acid - ethanol 1:1:1, heating at 105 °C until the zones were detected and viewing under daylight. Identification by comparison with the standards of the individual drug.

      Classification: 32e
      109 114
      Separation and simultaneous quantification of alpha- and beta-asarone in Acorus calamus Linn from indian sub-continent on caffeine modified silica
      M. SINGH*, Y.T. KAMAL, R. PARVEEN, SAYEED AHMAD (*Bioactive Natural Product Lab., Dept. of Pharmacognosy and Phytochem. Faculty of Pharmacy, Jamia Hamdard, New Delhi, India)

      Asian Journal of Chemistry 23 (5), 2046-2048 (2011). TLC of alpha- and beta-asarone in Acorus calamus on caffeine modified silica gel (with 10 % caffeine in dichloromethane and dried at 100 °C for 10 min) with toluene - ethyl acetate 93:7. The hRf value of alpha-asarone was 67 and of beta-asarone 77. Quantitative evaluation by absorbance measurement at 313 nm. The linearity was in the range of 50-1000 ng/band for beta-asarone. The alcoholic extracts of samples from different geographical regions were found to contain 0.2-0.8 % of alpha-asarone and 8.7-11.2 % of beta-asarone.

      Classification: 32e
      110 016
      Validation of a densitometric method for the determination of theanine in tea extracts using CP atlas software
      D. CSUPOR*, K. BOROS, A. HUNYADI, K. VERES, J. HOHMANN (*University of Szeged, Faculty of Pharmacy, Department of Pharmacognosy, Eötvös u. 6, Szeged, Hungary, csupor.dezso@pharmacognosy.hu)

      J. Planar Chromatogr. 25, 571-574 (2012). HPTLC of theanine in tea extracts on silica gel with n-butanol - acetone - acetic acid - water 7:7:2:4. Detection by dipping into a ninhydrin reagent for 3 s, followed by heating at 105 °C for 5-15 min. Quantitative determination by analysis of green channels of photographs using the CP Atlas 2.0 software. The hRf of theanine was 35. Linearity was in the range of 1.4-14 ng/zone. The intermediate/inter-day/intra-day precision was below 0.7 % (n=3). Recovery (by standard addition) was between 95.7 and 102.5 %.

      Classification: 3f, 18
      110 052
      Standard addition method for the quantification of paraquat, diquat, difenzoquat, mepiquat, and chloromequat in water by thin-layer chromatography
      B. SPANGENBERG (University of Applied Sciences Offenburg, Institute of Process Engineering, Badstrasse 24, D-77652 Offenburg, Germany, spangenberg@HS-Offenburg.de)

      J. Planar Chromatogr. 25, 262-268 (2012). HPTLC of paraquat (1), diquat (2), difenzoquat (3), mepiquat (4), and chloromequat (5) in water on silica gel with 1-propanol - methanol - 2.5 N NaCl 1:1:3. Quantitative determination by absorbance measurement between 500 and 535 nm. The hRf values of compounds (1) to (5) were 21, 30 36, 52 and 56, respectively. Limits of quantification were 5 ng/zone for (1), 2 ng/zone for (2), 25 ng/zone for (3), 15 ng/zone for (4) and 9 ng/zone for (5). Recovery rates for compounds (1) to (5) were 50.7, 65.2, 59.6, 45.1 and 33.7 %, respectively.

      Classification: 29d
      110 071
      Stability-indicating HPTLC method for simultaneous estimation of amlodipine besylate, hydrochlorothiazide and olmesartan medoxomil in combined tablet dosage forms
      N. DUBEY*, A. JAIN, A. RAGHUWANSHI, D. JAIN (*College of Pharmacy, IPS Academy, Indore-452015, Madhya Pradesh, India, nitindubeympharm@yahoo.com)

      J. Planar Chromatogr. 25, 475-480 (2012). HPTLC of amlodipine besylate (1), hydrochlorothiazide (2) and olmesartan medoxomil (3) on silica gel with chloroform - ethyl acetate - toluene - methanol - glacial acetic acid 39:39:77:39:6. Quantitative determination by absorbance measurement at 230 nm. The hRf of compounds (1) to (3) were 31, 56 and 81, respectively. Linearity was in the range of 200-4800 ng/band for (1), 100-4000 ng/band for (2) and 200-5200 ng/band for (3). Limits of detection and quantification were 35 and 101 ng/band for (1), 20 and 59 ng/band for (2) and 48 and 144 ng/band for (2), respectively. Intermediate/inter-day/intra-day precision was below 1.0 % (n=6). Mean recovery was between 100.0 and 100.3 % for all active agents.

      Classification: 32a
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