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.

Page
      97 126
      Stability indicating HPTLC determination of etoricoxib in formulations
      G. MAHESHWARI, G. SUBRAMANIAN, A. RANJITH KUMAR, Tara CHAND TAK* (*Dept. of Pharmacy, Manipal College of Pharm. Sci., Manipal, India)

      Abstract GP-74 IPC (2005). HPTLC of etoricoxib in tablets on silica gel with toluene - 1,4 dioxane - methanol 17:2:1. Quantitative determination by absorbance measurement at 235 nm. Linearity range was 500-1500 ng/spot. For stability studies the sample was subjected to acid and alkali hydrolysis, thermal, oxidaline and photo degradation. The peaks of all the degraded products were well resolved with significant different Rf values. The method was validated for different parameters and found suitable for routine quality control.

      Classification: 32a
      97 154
      A simple and sensitive HPTLC method for the determination of content uniformity of atorvastatin calcium tablets
      Savita YADAV, Deepali MHASKE, A. KAKAD, B. PATIL, S. KADAM, S. DHANESHWAR* (*Dept. of Quality Assurance Techniques, Bharati Vidyapeeth Deemed University, Poona College of Pharmacy, Erandwane, Pune 411038, India)

      Indian J. Pharm. Sci. 67 (2), 182-186 (2005). HPTLC of atorvastatin calcium in its commercial single component tablet formulations (10 mg/tablet), on silica gel with benzene-methanol 7:3. The Rf value was 0.46. Quantitative determination by absorbance measurement at 281 nm. The method was validated in terms of linearity (200-600 ng/spot), precision (intraday variation: 0.25 - 1.01 %, interday variation: 0.21 - 0.88 %), accuracy and specificity. The LOD for atorvastatin calcium was 40 ng/spot, the LOQ was 200 ng/spot. The proposed method was successfully applied to determine atorvastatin calcium content of 10 individual tablet units of two market formulations after extracting atorvastatin calcium with methanol. All formulations were compliant with USP specifications (RSD less than or equal to 6 %) of the content uniformity test. The proposed HPTLC method can analyse ten or more formulation units simultaneously on a single plate and provides a faster and cost effective quality control tool for routine analysis of atorvastatin calcium formulation.

      Classification: 32a
      98 068
      Estimation of trans-resveratrol in herbal extracts and dosage forms by high-performance thin-layer chromatography
      S. BABU, K. KUMAR, G. SUBBARAJU* (*Laila Impex Research Center, Vijayawada, India, subbarajugottumukkala@hotmail.com)

      Chem. Pharm. Bull. 53, 691-693 (2005). HPTLC of trans-resveratrol in the roots of Polygonum cuspidatum and in dosage forms on silica gel with chloroform – ethyl acetate – formic acid 25:10:1. Quantitative determination by absorbance measurement at 313 nm. Linearity of determination of trans-resveratrol is between 0.5 and 3.0 µg with a correlation coefficient of 0.9989. LOD is 9 ng, and LOQ is 27 ng. The average percentage recovery is 99.9 - 100.7 %.

      Classification: 32a
      98 108
      Determination of gatifloxacin and ornidazole in tablet dosage forms by high-performance thin-layer chromatography
      B. SUHAGIA, S. SHAH, I. RATHOD, H. PATEL*, D. SHAH, B. MAROLIA (*Department of Quality Assurance, L.M. College of Pharmacy, Gujarat, India, patelhary2001@yahoo.com)

      Anal. Sci. 22, 743-745 (2006). HPTLC of gatifloxacin and ornidazole on silica gel with n-butanol – methanol 8:1 and 1 drop ammonia with chamber saturation for 45 min. Quantitative determination by absorbance measurement at 302 nm. Linearity of determination of gatifloxacin is 100 – 500 ng and of ornidazole 250 – 1250 ng, with a correlation coefficient of more than 0.9850. The intra-day and inter-day coefficients of variation are found to be in the range of 0.68 - 2.58 % and 0.37 - 3.62%, respectively.

      Classification: 32a
      99 091
      Two new benzofurans and other constituents from Ligularia przewalskii
      W. D. XIE (Xie Wei-Dong), X. GAO (Gao Xue), T. SHEN (Shen Tong), Z. J. JIA (Jia Zhong-Jian)* (*Department of Chemistry, Lanzhou University, Lanzhou, 730000, P. R. China; jiazj@lzu.edu.cn)

      Pharmazie 61, 556-558 (2006). Preparative TLC of two benzofurans euparin, friedelin, and beta-sitosterol on silica gel with petroleum ether - ethyl acetate 20:1. Detection under UV light.

      Classification: 32e
      99 132
      Simultaneous HPTLC determination of Frusemide and Spironolactone from pharmaceutical formulation
      M. M. BAING*, V. V. VAIDYA, P. A. CHAMPANERKAR, W. SHAH (*Dept. of Chemistry, S.P. Mandali’s Ramnarain Ruia College, Matunga, mumbai 400019, vaidya_vikas@yahoo.com)

      Indian Drugs 44 (3), 205-208 (2007). HPTLC of frusemide (= furosemide) and spironolactone on silica gel with toluene - acetonitrile - glacial acetic acid 70:30:2, with chamber saturation for 15 min at room temperature. Development over 8 cm, followed by air drying. Quantitative determination by densitometry at 254 nm. Linearity was between 8 - 32 ng/µL and 20 - 80 ng/µL for frusemide and spironolactone respectively. The method was validated for accuracy and precision. The limit of detection and quantification for frusemide was 3 ng/µL and 8 ng/µL respectively, and for spironolactone 2 ng/µL and 6 ng/µL, respectively. Recovery by standard addition was 99.4-101% for both compounds.

      Classification: 32a
      99 170
      Quality control of Shajun Zhiyang lotion (Chinese)
      J. YU* (Yu Jiaqi), Z. YANG (Yang Zhonglan), H. JIAN (Jian Hongjun), Y. ZHANG (Zhang Yongping), L WEI (Wei Ling) (*Guizhou Zunyi Hosp., Zhunyi, Guizhou 563000, China)
      J. Chinese Trad. Patent Med. (Zhongchengyao), 27 (8), 900 - 903 (2005). TLC of Shajun Zhiyang lotion on silica gel with 1) benzene - ethyl acetate - isopropanol - methanol - ammonia 12:6:3:3:1; 2) benzene - ethyl acetate 30:1; 3) ethyl acetate. Detection 1) under UV 365 nm; 2) by spraying with 5% vanillin in H2SO4 solution and heating at 105 °C. Identification by fingerprint techniques. Quantification of matrine by HPLC.
      Classification: 32c
      100 072
      Determination of valdecoxib from its bulk drug and pharmaceutical preparations by HPTLC
      D.T. BAVISKAR*, S.C. JAGDALE, N.O. GIRASE, A.Y. DESHPANDE, D.K. JAIN (*M. A. H. College of Pharmacy, Dhule, India)

      Indian Drugs 44(10), 734 (2007). HPTLC of valdecoxib on silica gel with toluene - ethyl acetate 1:1. Quantitative evaluation by densitometry at 262 nm. Valdecoxib was well separated from rofecoxib. Linearity was between 800 and 1000 ng/zone. Recovery was 98.9 %.

      Classification: 32a
Page