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.

      127 036
      Influence of cation transporters (OCTs and MATEs) on the renal and hepatobiliary disposition of [11C]metoclopramide in mice
      I. HERNANDEZ, S. MAIRINGER, M. SAUBERER, J. STANEK, T. FILIP, T, WANEK, G. CIARIMBOLI, N. TOURNIER, O. LANGER* (*Department of Clinical Pharmacology, Medical University of Vienna, 1090 Vienna, Austria,

      Pharm. Res. 38, 127-140 (2021). HPTLC of [11C]metoclopramide in plasma, kidney, urine and liver extracts on silica gel with ethyl acetate - ethanol - 25 % ammonium hydroxide 16:4:1. Detection using a multisensitive phosphor screen. The hRF value for [11C]metoclopramide was 60. The method allowed kinetic analysis in different organs after radiotracer injection in mice.


      Classification: 32c, 34
      102 161
      Knockdown of JNK rescues 3T3-L1 adipocytes from insulin resistance induced by mitochondrial dysfunction
      T. KIM, W. LEITNER, R. ADOCHIO, B. DRAZNIN* (*Department of Medicine, University of Colorado Denver School of Medicine, Mail Stop 8106, Colorado, USA,

      Biochem. Biophys. Res. Commun. 378, 772-776 (2009). TLC of lipids from adipocytes on silica gel pre-treated with a solution containing methanol – water – potassium oxide – EDTA 60:40:1%:1mM and activated at 100 °C for 1 hour. The plate was developed with n-propanol – water – glacial acetic acid 65:34:1. Detection and quantitative determination by autoradiography using storage phosphor technology.

      Classification: 34
      72 174
      The advantages of a new bio-imaging analyzer for investigation of the metabolism of 14C-radiolabeled pesticides
      O. KLEIN, T. CLARK, (Bayer AG, Crop Protection Center, Monheim Institute for Metabolism Research, D-51368 Leverkusen-Bayerwerk, Germany)

      J. Planar Chromatogr. 6, 368-371 (1993). Investigation of the linearity, sensitivity, and resolution of a new bio-imaging analyzer TLC plate scanner and comparison of the results with those obtained using a linear analyzer or conventional X-ray autoradiography. The instrument has a wide linear dynamic range: from 10 to 11'000 dpm for an individual component; the sensitivity was significantly, i.e. 50 to 100 times, higher; the resolution was far better than that of the linear analyzer and comparable with that of autoradiography.

      Classification: 3f, 34
      114 102
      Review of advances in planar radiochromatography
      J. SHERMA*, Dolcie DEGRANDCHAMP (*Department of Chemistry, Lafayette College, Easton, PA 18042, USA,

      J. Liq. Chromatogr. Relat. Tech. 38, 381-389 (2015). Review of the materials, techniques and instruments for the detection and quantification of radiolabeled compounds by planar radiochromatography. Special reference is made to sample preparation, stationary phases (including instant TLCD sheets), initial zone application, mobile phases, stationary phase development, and zone detection and quantification.

      Classification: 1, 34
      76 061
      Vernolic and cyclopropenoic fatty acids in Piper nigrum seed oil
      C.D. DAULATABAD*, G.M. MULLA, A.M. MIRAJKAR, (*Dept. of Chem., Karnatak University, Dharwad-580 003, Karnataka , India)

      Fat Sci. Technol. 97, 453-454 (1995). Analytical TLC of fatty acids (i. a. cyclopropenoic acid, vernolic acid) on silica with ether - hexane 2:8; 3:7. In addition preparative TLC of mixed fatty acids for separation into oxygenated and nonoxygenated fractions. Detection by spraying with dichlorofluorescein and visualization under UV.

      Classification: 11a, 11e, 34
      116 037
      Lipid exchange between Borrelia burgdorferi and host cells
      J.T. CROWLEY, A.M. TOLEDO, T.J. LA ROCCA, J.L. COLEMAN, E. LONDON, J.L. BENACH* (*Center for Infectious Diseases, Stony Brook University, Stony Brook, New York, USA;

      PLoS ONE 9(1), e1003109 (2013). In order to understand how Borrelia burgdorferi acquires cholesterol from its host, five experiments were performed. HPTLC on silica gel with chloroform – methanol 17:3, the lipids were extracted through the Bligh and Dyer method: (1) from the spirochete incubated 4 h in a medium containing 4 mg/L BODIPY-cholesterol (fluorescing only in hydrophobic environment), (2) from the spirochete incubated 2 h in a medium containing 10 µCi/L tritiated cholesterol, (3) from HeLa cells incubated with the spirochete itself charged with tritiated cholesterol (after removal of all spirochetes). The same analysis was applied (4) to the purified outer membrane vesicles of the spirochete previously charged with BODIPY-cholesterol. In cases (1) and (4), UV detection showed that the BODIPY-cholesterol is incorporated into the cholesterol glycolipids of B. burgdorferi, whereas without incubation it has the same hRf as cholesterol. In cases (1), (2) and (4), iodine staining made free cholesterol and cholesterol-glycolipids (galactopyranosides) visible, but no other (cholesterol-free) lipids. In case (2), the chromatogram was sprayed with EN3HANCE Spray (DuPont), exposed using BioMax MR Film (Kodak) for 4 and 14 days at −80 °C and developed using a Medical Film Processor Model SRX-101A (Konica); the radiolabelled cholesterol was shown incorporated into the cholesterol-glycolipids. In cases (2) and (3), the radiolabelled zones on the layer were scraped off and analyzed by liquid scintillation counting; cholesterol-glycolipids were found (more than free cholesterol) transferred from the spirochete to the HeLa plasmalemma.

      Classification: 11c, 13c, 34
      76 103
      Comparison of TLC- and HPLC- 32P-postlabelling assay for cisplatin-DNA adducts
      A. FOERSTI, J. STAFFAS, K. HEMMINKI, (Cent. Nutrition Toxicol., Karolinski Inst., S-14157 Huddinge, Sweden)

      Carcinogenesis 15, 2829-2834 (1994). Separation of the title compounds, postlabelled with [g-32P] ATP, by TLC and HPLC with on-line detection of 32P.

      Classification: 21b, 34
      116 056
      Pharmacokinetic properties of a novel D-peptide developed to be therapeutically active against toxic ?-amyloid oligomers
      L. LEITHOLD, N. JIANG, J. POST, T. ZIEHM, E. SCHARTMANN, J. KUTZSCHE, J. SHAH, J. BREITKREUTZ, K. LANGEN, A. WILLUWEIT, D. WILLBOLD* (*Institute of Complex Systems, Structural Biochemistry, Jülich, Germany,

      Pharm. Res. 33, 328-336 (2016). HPTLC of a derivative of a novel D-peptide with improved binding to Aβ oligomers (3H-radioactively labelled RD2) on silica gel with 2-butanol - pyridine - ammonia (28 %) - water 39:34:10:26. 3H detection by placing the plates on phosphor imaging plates for autoradiography. The method was useful to determine the stability of 3H-labelled RD2 in mouse plasma.

      Classification: 18b, 34