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.

      73 152
      (Determination of dolantin in plasma by thin-layer chromatography
      Y. WANG (Wang Yujin), CH ZHOU (Zhou Changying), (Dept. Forensic Med., Shanxi Coll. Med., Taiyuan 030001, P.R. China)

      Chinese J. Pharm. Anal. (Yaowu Fenxi Zazhi) 14, 40-42 (1994). TLC on silica with chloroform - methanol 9:1. Detection by spraying with potassium iodobismuthate reagent. Quantification by densitometry at 500 nm. Comparison of the results with those from fluorometry.

      Classification: 32f
      78 082
      Pyrrolizidine alkaloids from Senecio jacalensis and Senecio callosus
      A.M. DE VIVAR*, A.L. PEREZ, P. VIDALES, D.A. NIETO, L. VILLASENOR, (*Inst. de Quimica, Univ. Nat. Autonome de Mexico, Cindad Univ., Coyocan, 045510 Mexico D.F.)

      Biochemical Systematics and Ecology 24, 175-176 (1996). TLC of alkaloids on silica with chloroform - methanol 4:1.

      Classification: 22
      94 050
      A simple and sensitive HPTLC method for estimation of gatifloxacin in tablet dosage forms
      S. A. SHAH, I. S. RATHOD, B. N. SUHAGIA, Meeta BALDANIYA (Department of Quality Assurance, L. M. College of Pharmacy, Navarangpura, Ahmedabad 380009, India)

      Indian J. Pharm. Sci. 66 (3), 306-308 (2004). HPTLC on silica gel with n-butanol - methanol - 6 M ammonia 5:1:2. Gatifloxacin showed Rf values of 0.47 ± 0.03. Quantitative determination by absorbance measurement at 292 nm. The method was validated in terms of linearity (400-1200 ng/spot), precision (intra-day variation 1.3 to 3.2 %, inter-day variation 3.9 to 5.0 %), accuracy (93.3 to 99.4 %), and specificity. The limit of detection and limit of quantification for gatifloxacin were found to be 10 ng/spot and 50 ng/spot respectively. The method is simple, sensitive, precise, and can be used for the routine quality control testing of marketed tablet formulations (400 mg).

      Classification: 32a
      95 060
      Development and validation of a new sensitive method for the simultaneous estimation of amlodipine - atenolol in tablets by HPTLC
      M. G. PAI*, Dattesh VEREKAR, K. VENKATESHWAR RAO (*Goa College of Pharmacy, Panaji, Goa, India)

      IPC 56th 2004, Abstract No. GP-5. Simultaneous HPTLC determination of amlodipine and atenolol on silica gel with ethyl acetate - methanol - ammonia 60:40:3. Quantitative determination by scanning at 254 nm. The method was found linear in the range of 0.5 – 5.0 mg/mL amlodipine and 5.0 mg – 50 mg/mL atenolol. Recovery was 98.11 – 101.5 % for both of the compounds. The method was validated for accuracy, precision, linearity, specificity, LOD, and LOQ.

      Classification: 32a
      96 088
      Fluorescence detection combined with either HPLC or HPTLC for pharmaceutical quality control in a hospital chemotherapy production unit
      G. EDMOND, B. PHILIPPE, M. LIONEL, P. ANGELO* (*Dept. of Clinical Pharmacy, Institut Gustave Roussy, 39, rue Camille Desmoulins, 94800 Villejuif, France)

      J. Pharm. Biomed. Anal. 39, 581-586 (2005). For post-production quality control of camptothecin derivatives irinotecan (CPT 11) and topotecan (TPT), HPLC and HPTLC methods have been developed which were suitable for identification, determination of purity and quantification. HPTLC on silica gel with methylene chloride - methanol - formic acid - water 82:24:2:1. After development, the plate was soaked in 15 % paraffin in n-heptane. Quantitative determination by fluorescence measurement at 366/>400 nm. The method was linear within the range of 100-1000 ng/mL for both CPT-11 and TPT. The method was validated for accuracy, precision, LOD, and LOQ.

      Classification: 32a
      97 096
      Development of stabililty indicating HPTLC method for determination of satranidazole in bulk, its formulations and to study degradation kinetics
      B. H. PATEL*, K.M. PATEL, A.M. PRAJAPATI, M. PATEL, D.S. SANKHIA (*Dept. of Pharm. Chem, S. K. Patel College of Pharm. Edu. Research, Vidyanagar, Kherva, Gujarat, India)

      Abstract GP-75, IPC (2005). HPTLC of satranidazole and its degradation products on silica gel with toluene - acetonitrile 3:2. For stability studies, the sample was treated with NaOH, HCl, H2O2 and photolysis. Degradation products were well resolved with significant different Rf values. The method had a linearity range of 100-500 ng. The proposed method suitable to investigate the kinetics of hydrolysis and photodegradation processes with first order in NaOH, and zero order for photolysis.

      Classification: 32a
      98 043
      Separation methods for phytoecdysteroids
      M. BATHORI*, H. KALASZ (*Dept. of Pharmacognosy, Fac. of Pharm., Univ. of Szeged, Hungary)

      LC-GC Europe 14, Issue 10, 626-631 (2001). TLC of 20-hydroxyecdysone on silica gel, pre-washed with methanol. Different mobile phases are investigated, the mixture of chloroform — methanol — benzene 25:5:3 was used for quantification. Densitometry at 254 nm. TLC of ecdysteroids under the same conditions, detection at 254 nm, in white light and at 366/>400 nm (fluorescence) after spraying with a vanillin-sulphuric acid reagent. Identification was facilitated with two-dimensional TLC, displacement TLC (D-TLC) and forced flow TLC (FF-TLC). Comparison with HPLC.

      Classification: 13
      99 135
      Quantitative determination of haloperidol in tablets by high performance thin-layer chromatography
      S. MENNICKENT*, L. PINO, M. VEGA, C. GODOY, M. DIEGO (*Department of Pharmacy, Faculty of Pharmacy, University of Concepción, Concepción, Chile, smennick@udec.cl)

      J. Sep. Sci. 30, 772-777 (2007). HPTLC of haloperidol in tablets on silica gel with acetone – chloroform – n-butanol – acetic acid – water 2:4:4:1:1. Quantitative determination by absorbance measurement at 254 nm. Linearity was between 10 and 100 ng/µL, detection limit was 0.89 ng/µL, and the quantification limit was 2.71 ng/µL. Coefficient of variation is 2.35% and 4.50% for precision and accuracy, respectively. Successful comparison with HPLC measurements.

      Classification: 32a