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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      94 037
      TLC separation of Unicaria tomentosa alkaloids on chemically modified stationary phases
      M. GLENSK*, B. ZBIKOWSKA, W. CISOWSKI (*Department of Pharmacognosy, University of Medicine, pl. Nankiera1, 50-140 Wroclaw, Poland)

      J. Planar Chromatogr. 17, 14-17 (2004). HPTLC of oxindole alkaloids on silica gel, Diol-, CN-, NH2-, and RP-18-phases. Normal-phase TLC with 1) ethyl acetate - methanol - water 200:27:20; 2) ethyl acetate - methanol - water - acetic acid 100:2.7:5:3; 3) ethyl acetate - methanol - water - formic acid 100:2.7:5:3; 4) ethyl acetate - isopropanol - ammonia 100:2:1. RP TLC with water - methanol 7:3 containing 0.25 % ammonia; development in horizontal chamber (sandwich configuration) at room temperature. Two-dimensional TLC with mobile phase 2 in the first direction and, after drying, with mobile phase 3 in the second direction. Evaluation under UV 254 nm and after derivatization with iodine reagent or with Dragendorff reagent. TLC separations were documented by scanning. Silica and cyanopropyl layers with acidic aqueous mobile phases gave the best separation.

      Classification: 22
      94 067
      HPTLC estimation of ofloxacin & tinidazole from pharmaceutical dosage form
      K.R. GUPTA*, S.G. WADODKAR (*Department of Pharmaceutical Sciences, Nagpur University, Nagpur, India)

      Indian Drugs 41 (3), 160-164 (2004). Combinations of ofloxacin and tinidazole (1:3) are available as tablet dosage forms. Stability indicating HPTLC of ofloxacin and tinidazole on silica gel with dioxan - ethyl acetate - toluene - acetic acid - water 5.5:5:3.2:2:2 . Quantification by absorbance measurement at 307 nm. The Rf value of ofloxacin and tinidazole was found to be 0.12 and 0.85 respectively. Recovery was 99.85 % and 99.45 % for ofloxacin and tinidazole respectively. The proposed method was quantitatively evaluated in terms of calibration of concentration range, stability, and accuracy. It can be adopted for routine analysis of the formulation.

      Classification: 32a
      94 088
      Development & validation of a HPTLC method for the simultaneous estimation of cefuroxime axetil and probenecid
      K. R. SIREESHA, Deepali V. MHASKE, S. S. KADAM, S. R. DHANESHWAR (Department of Quality Assurance Techniques, Bharati Vidyapeeth Deemed University, Poona College of Pharmacy, Pune 411038, India)

      Indian J. Pharm. Sci. 66 (3), 278-282 (2004). HPTLC on silica gel with chloroform - acetonitrile - toluene - acetate buffer (pH 6.0) 50:40:10:3. Quantitative determination by absorbance measurement at 266 nm. The method was validated in terms of linearity, accuracy, precision, and specificity. The limit of detection and the limit of quantification were found to be 50 ng/spot and 100 ng/spot respectively. A simple, precise, accurate and rapid HPTLC method has been developed and validated for the simultaneous determination of cefuroxime axetil and probenecid in combined dosage form.

      Classification: 32a
      94 109
      (Study of the quality standard for sugar-free Qixuekang oral liquid
      X. ZHU (Zhu Xuan), H. TANG (Tnag Haiying), M. CHEN (Chen Man) (Jiangsu Xiansheng Pharm. Co., Ltd., Nanjing, Jiangsu 210042, China)

      Chinese J. Trad. Patent Med. (Zhongchengyao) 26 (6), 449-452 (2004). TLC of Qixuekang oral liquid extract on silica gel with 1) chloroform - ethyl acetate - methanol - water 15:40:22:10; 2) chloroform - methanol - water 28:10:1. Detection 1) by spraying with 10 % H2SO4 in ethanol and heating; 2) under UV 365 nm. Identification by fingerprint techniques. Quantification of notoginsenoside R1 by HPLC with method validation.

      Classification: 32c
      95 062
      (Study of the quality standard for Qieyou Tangjiang extract) (Chinese)
      J. GAO (Gao Jiarong)*, J. ZHANG (Zhang Junru) (*No.1 Affiliated Hosp., Anhui Coll. TCM, Anhui, Hefei 230031, China)

      Chinese J. Trad. Pat. Med. (Zhongchengyao) 27(1), 94-96 (2005). HPTLC on silica gel with 1) n-butanol - glacial acid - water 19:5:5; 2) petroleum ether (30-60 ºC) - formic acetate - formic acid 15:5:1; 3) chloroform - ethyl acetate - methanol - formic acid 200:25:50:1. Detection 1) by spraying with 0.5 % ninhydrin in ethanol; 2) under UV 365 nm; 3) by spraying with vanillin - H2SO4 solution and heating. Identification by fingerprint technique. Quantification of emodin by densitometry at 440 nm. Validation of the method by investigation of linearity (0.1 µg - 0.5 µg, r = 0.998); precision (RSD = 3.8 %, n = 15 within plate and RSD = 3.2 %, n = 5 plate to plate); reproducibility of five time assay towards the same sample (RSD = 4.4 %); standard addition recovery (99.5 %, RSD = 2.2 %, n = 5). The results for some real life samples are given.

      Classification: 32c
      95 082
      Stability indicating HPTLC determination of indapamide in tablets
      K. R. GUPTA*, A. N. MALIYE, M. R. TAJNE, S. G. WADODKAR (*Department of Pharmaceutical Sciences, Nagpur 440033, India)

      IPC 56th 2004, Abstract No. GP-11. Stability indicating HPTLC determination of indapamide in tablets on silica gel with toluene - methanol 7:3. Quantitative determination by scanning at 246 nm. Optimization of experimental parameter such as band size, chamber saturation, and slit width. The method was linear in the range of 1.4 - 3.72 g, recovery was 100.01 %. The drug was subjected to stress conditions according to ICH guidelines, degradation products were separated from the pure drug. The method was validated for accuracy, precision, linearity, and specificity.

      Classification: 32a
      95 100
      (Study of the quality standard for Funing granules) (Chinese)
      ZH. ZHAO (Zhao Zhi Qiang) (Shanghai Leiyunshang Pharm. Co., Ltd., Shanghai 201517, China)

      Chinese J. Trad. Pat. Med. (Zhongchengyao) 26 (9), App. 3-5 (2004). TLC on silica gel with 1) n-hexane - ethyl acetate 9:1; 2) chloroform - methanol 5:2; 3) n-hexane - ethyl acetate 3:1. Detection 1) under UV 365 nm; 2) by spraying with 10 % H2SO4 in ethanol and heating at 110 ºC; 3) by spraying with 5 % FeCl3 in ethanol. Identification by fingerprint technique. Quantification of icariine by HPLC.

      Classification: 32c
      96 079
      Study of the liquid chromatographic separation and determination of NSAID
      R. Bhushan*, S. Joshi, M. Arora, M. Gupta (*Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee-247 667, India)

      J. Planar Chromatogr. 18, 164-166 (2005). TLC of non-steroidal anti-inflammatory drugs (NSAID), i.e. mefenamic acid, naproxen, ibuprofen, flurbiprofen, ketoprofen, paracetamol, and diclofenac, on silica gel with chloroform - methanol , chloroform - ethyl acetate, acetonitrile - methanol - water, acetonitril - methanol in different proportions. Detection with iodine vapor.

      Classification: 32a
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