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
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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.

      97 161
      Analysis of phthalates in plastic food-packaging bags by Thin Layer Chromatography (Chinese)
      H. CHEN (Chen Hui)*, Y. WANG (Wang Yuan), R. ZHU (Zhu Ruohua) (*Chem. Dep., Beijing Norm. Univ., Beijing 100001, China)
      Chinese J. Chromatogr. (Sepu) 24 (1), 69-72 (2006). TLC of dimethyl phthalate (DMP), diethyl phthalate (DEP), di-n-butyl phthalate (DBP) and di (2-ethylhexyl) phthalate (DEHP) in plastic food-packaging bags. Extraction with ethanol by ultrasonication, followed by filtration through a membrane of 0.45 µm. Development with ethyl acetate - anhydrous ether - isooctane 1:4:15 on silica gel. Quantitative determination by densitometry at 275 nm (reference wavelength 340 nm) by use of an external standard. Good linearities were obtained for DMP, DEP, DBP and DEHP. The detection limits were 2.1 ng for DMP, 2.4 ng for DEP, 3.4 ng for DBP and 4.0 ng for DEHP. The relative standard deviations of the four phthalates were 2.8-3.5 %. The recoveries of the four phthalate standards in real sample were 79-111 %. The method presented has the advantages of high precision, high sensitivity, small sample size, and simple pretreatment. The contents in real samples were close to the results by gas chromatography.
      Classification: 35
      106 175
      Quantitative determination of oxybutynin hydrochloride by spectrophotometry, chemometry and HPTLC in presence of its degradation product and additives in different pharmaceutical dosage forms
      N.E. WAGIEH*, Maha HEGAZY, M. ABDELKAWY, E.A. ABDELALEEM (*Analytical Chemistry Department, Faculty of Pharmacy, Beni-Suef University, Egypt)

      Talanta, 80 (5), 2007-2015 (2010). Presentation of a method for determination of oxybutynin hydrochloride (OX) in presence of its degradation product and additives in its pharmaceutical formulations. UV spectrophotometry using the first derivative of ratio spectra and measurment at 216 nm. Chemometric analysis using principal component regression and partial least-squares. HPTLC of OX and its degradation products methylparaben and propylparaben on silica gel with chloroform - methanol - ammonia - triethylamine 500:15:2.5:1. Quantitative determination by densitometry at 220 nm. Comparison of the results obtained with all three methods showed no significant differences.

      Classification: 32c
      59 141
      Metabolic fate of cinmethylin in rats
      P.W. LEE, J.M. STEARNS, W.R. POWELL, D.W. STOUTAMIRE, G.B. PAYNE, M.D. WOODWARD et al.

      J. Agric. Food Chem. 34, 162-170 (1986). TLC of cinmethylin (7-oxabicyclo (2.2.1 ) heptane, d-methyl-4-(1-methylethyl)-2- ( (2-methylphenyl) methoxy)-, exo and metabolites on silica 60 F 254 in one- and two-dimensional mode with toluene 2-propanol - acetic acid 1 50:20:1.5, hexane -2-propanol - acetic acid 20:30:1, ethyl acetate - hexane - chloroform - acetic acid 100:50:5:1.5. Detection by autoradiography; quantification by radioactivity measurement after extraction.

      Classification: 29d
      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
      98 050
      Acid hydrolysis of potato tuber sprout glykoalkaloids and kinetics of solanidine extraction in three-phase systems
      N. C. NIKOLIC*, M. Z. STANKOVIC (*Fac. of Techn., Bulevar oslobodjenja 124, 16000 Leskovac, Serbia and Montenegro)

      Ital. J. Food Sci. 18, 287-294 (2006). The ratio of alpha-solanine to alpha-chaconine of tuber sprouts was determined by TLC on silica gel with methanol – chloroform – 1 % aqueous ammonium hydroxide 2:2:1. For quantitative determination zones were isolated from the plate, extracted with 2 % aqueous acetic acid, and measured spectrophotometrically at 420 nm with methyl orange.

      Classification: 22
      106 181
      Isolation of antioxidants from Psoralea corylifolia fruits using high-speed counter-current chromatography guided by thin layer chromatography-antioxidant autographic assay
      G. XIAO, G. LI, L. CHEN, Z. ZHANG, J.J YIN, T. WU*, Z. CHENG, X. WEI, Z. WANG (*The MOE Key Laboratory for Standardization of Chinese Medicines, the SATCM Key Laboratory for New Resources and Quality Evaluation of Chinese Medicines, and the Shanghai Key Laboratory for Compound Chinese Medicines, Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Zhangjiang Hi-Tech Park, Shanghai 201210, China)

      J. Chromatogr. A 1217(34), 5470-5476 (2010). Description of a combination method using high-speed counter-current chromatography and TLC as an antioxidant assay to separate antioxidant components from the fruits of Psoralea corylifolia by dipping in a ethanolic DPPH radical solution (2.54 mM) for autography. Bands with the DPPH scavenging activity were observed as white yellow bands on a purple background. High-speed counter-current chromatography of five flavonoids and three coumarins from the fruits of P. corylifolia with n-hexane - ethyl acetate - methanol - water 10:11:13:1. Preparative TLC for clean-up improves the substance yield from the fruits.

      Classification: 35
      66 099
      Thin-layer chromatographic method for the determination of glycosyltransferase activity
      P.A. RAM, M. FUNG, C.F. MILLETTE, D.R. ARMANT, (Dep. Ant. Cell. Biol., Itarward Med. Sch., Boston, MAO2115 USA)

      Anal. Biochem. 178, 421-426 (1989). TLC of various nucleotide sugars from both high- and low-molecular-weight sugar acceptors on PEI-cellulose with 1 mM sodium phosphate buffer (pH 8.0). Determination of glycosyltransferase activity by autoradiography. Comparison of the results with those obtained by GPC and micropartitioning filtration.

      Keywords: autoradiography
      Classification: 2d, 21a
      73 071
      Quantification of type III iodothyronine, deiodinase activity using thin-layer chromatography and phosphor screen autoradiography
      J.M. KOOPDONK-KOOL*, M.C. VAN LPIK-PETERSE, G.J.M. VEENBEER, TH. J. VISSER, CH.H.H. SCHOENMAKERS, J.J.M. DE VIJLDER, (*Experim. Paediatric Endocrinol., Acad. Med. Cent., Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands)

      Anal. Biochem. 214, 329-331 (1993). TLC of title compounds on silica with 2-methylbutan-2-ol - t-butanol - 25% NH3 - acetone 1:2:2:8. Detection by exposing for 4 or 16 hrs to a storage phosphor screen. Quantification by autoradiography. Comparison of the results with those obtained by HPLC.

      Classification: 4e, 18