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
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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.

      94 041
      TLC and RPTLC separation of porphine, selected porphyrins, and their metalloderivatives
      M. STEFANIAK, P. KUS, J. SLIWIOK* (*Department of Chemistry, Silesian University, 9, Szkolna Street, 40-006 Katowice, Poland)

      J. Planar Chromatogr. 17, 72-74 (2004). TLC of porphine, meso-mono-tert-butylporphyrin, meso-tetra-tert-butylporphyrin and their respective Zn(II), Ni(II), and Cu(II) derivatives on silica gel with n-hexane - chloroform 7:3, and on RP-18 with methanol or methanol - water 9:1 after presaturation of the plates for 30 min. The porphyrins were detected visually.

      Classification: 23a
      56 106
      Zum nachweis der Inhaltsstoffe einer Pilzart der Gattung Panaeolus
      J. GARTZ

      (About the detection of the content of a type of mushroom of the class of panaeolus.) Pharmazie 40, 431-432 (1985). 100 samples from a panaeolus foenisecii species analyzed by TLC on silica with butanol - water - acetic acid - isopropanol 8:5:2:3; staining with Ehrlich reagent. Psilopsibine not found, but indole derivatives such as tryptamine, 5-oxy-tryptamine, 5-hydroxy-indole acetic acid.

      Classification: 23c
      107 079
      Simultaneous estimation of amlodipine besylate and telmisartan in their combined dosage form by spectophotometric and HPTLC methods
      A. BHADIVADRA*, Y. KOLADIYA, H. BHATT, P. MEHTA (*Dept. of Pharmaceutical Analysis, Institute of Pharmacy, Nirma University, Ahmedabad 382481, Gujarat, India)

      62nd Indian Pharmaceutical Congress Abstract No. F-389 (2010). TLC of amlodipine and telmisartan on silica gel with chloroform – methanol – toluene 10:7:3. The hRf values were 23 and 75 for amlodipine besylate and telmisartan respectively. Quantitative determination by absorbance measurement at 238 nm. The sample was also analysed by spectophotometry and the results by both methods were comparable.

      Classification: 23d
      106 121
      A validated high-performance thin-layer chromatographic method for simultaneous estimation of nebivolol hydrochloride and valsartan in pharmaceutical dosage form
      Shradhanjali SINGH*, Kirti TOPAGI, Mrinalini DAMLE (*Dep of Pharmaceutical Chem, AISSMS Collage of Pharmacy, Pune 411001, India, mcdamle@rediffmail.com)

      Research Journal Pharm and Tech. 2(4),746-748 (2009). A validated HPTLC method is reported for simultaneous estimation of nebivolol hydrochloride and valsartan in combined dosage form. HPTLC on silica gel with ethyl acetate - methanol - 25 % ammonia. The hRf value of valsartan was 27 and of nebivolol 75.The method was linear in the range of 800-2400 ng/band for nebivolol and 200-1000 ng/band for valsartan. Densitometric quantification at 280 nm. The method was found suitable for routine quality control of the combined dosage form.

      Classification: 23e
      107 094
      Development and validation of HPTLC method for estimation of rupatadine fumarate in formulation
      K. RAGHAVI*, M. SHAIBA, G. RAO (*KVSR Siddhartha College of Pharmaceutical Sciences, Vijayawada 520010, AP, India)

      62nd Indian Pharmaceutical Congress Abstract No. F-236 (2010). TLC of rupatadine formulation on silica gel with acetonitrile – water – formic acid 50:50:3. The hRf value was 67. Quantitative determination by absorbance measurement at 263 nm. The method was linear in the range of 1-20 µg/band.

      Classification: 23e
      113 049
      1-alkyl-3-methylimidazolium tetrafluoroborate as an alternative mobile phase additives for determination of haloperidol in pharmaceutical formulation by HPTLC UV densitometric method
      D. MIESZKOWSKI, T. SODMIAK, M. MARSZALL* (*Collegium Medicum in Bydgoszcz, Jurasza 2, 85-094 Bydgoszcz, Poland, mmars@cm.umk.pl)

      J. Liq. Chromatogr. Relat. Technol. 37, 1524-1534 (2014). HPTLC of haloperidol on RP-18 with acetonitrile - water - 1-alkyl-3-methylimidazolium tetrafluoroborate 120:80:3. Quantitative determination by absorbance measurement at 245 nm. The hRF value for haloperidol was 57. Recoveries were in the range of 99.4-106.5 %.

      Classification: 23e
      61 013
      Reversed-phase ion-pair systems to predict partition coefficients of ß-carbolines by HPLC and TLC
      M.C. PIETROGRANDE, P.A. BOREA, G. LODI, C. BIGHI, (Dep. Chem., Anal. Chem. Lab., Univ. Ferrara, Via L. Borsari 46, I-44100 Ferrara, Italy)

      Chromatographia 23, 713-716 (1987). Study of a group of 17 ß-carbolines in reversed phase ion pairing TLC system in order to predict their log p values. TLC data found comparable for log p prediction in HPLC.

      Keywords:
      Classification: 2d, 23e
      65 149
      Identification and determination of hydrochlorothiazide [Esidrex ®]
      W. BERNHARD*, A.N. JEGER, U. DE LA VIGNE, (*Wiesendamm 10a, CH-4057 Basel, Switzerland)

      J. Planar Chromatogr. 2, 77-79 (1989). HPTLC of urine extracts on silica with ethyl acetate - methanol - NH3 25% 85:10:5. Doping control by post-chromatographic derivatization. Esidrex and similar drugs as well as their metabolites are converted into azo dyes. Drug monitoring by densitometry. Determination limit of the method described is 0.2 mg/L and the sensitivity limit is 0.1 mg/L. The procedure allows the analysis of a large number of samples in a short period of time with minimal operating costs.

      Classification: 23e, 24, 32a, 32c