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

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      117 114
      (Study of the method for the quality control of Shengxinfa Jiaonang capsules) (Chinese)
      W. FAN (Fan Weifeng), SH. WANG (Wang Shiyong)*, D. HE (He Danxuan), ZH. YE (Ye Zhiwen), Q. LI (Li Qin) (*Yulin Pharm. Group Co. Ltd., Guangxi, Yulin 537001, China)

      Chinese J. of Inform. on TCM 20 (7), 59-61 (2013). Shengxinfa Jiaonang capsule is a herbal TCM preparation for treatment of hair loss caused by blood deficiency and kidney essence deficiency, scalp pruritus, alopecia areata, and postpartum alopecia. For quality control, TLC on silica gel (1) for Fallopia multiflora (Thunb.) Harald, with toluene – ethyl acetate – formic acid 15:2:1, detection in daylight; (2) for Psoralea corylifolia Linn., with n-hexane – ethyl acetate 4:1, detection by spraying with 10 KOH in methanol and viewing under UV 366 nm; (3) for Gastrodia elata Bl., with chloroform – ethyl acetate 1:1, detection by spraying with 10 % sulfuric acid in ethanol and heating at 105 °C until the zones are visible. Quantification of 2,3,5,4'-tetrahydroxy stilbene-2-Ο-β-D-glucoside by HPLC.

      Classification: 32e
      118 019
      Trilinear analysis of thin-layer chromatography retention of 35 model compounds chromatographed on nine adsorbents with 20 pure solvents
      L. KOMSTA*, R. SKIBINSKI, N. BEZPALKO, A. MIELNICZEK, B. STEPKOWSKA (*Department of Medicinal Chemistry, Medical University of Lublin, Jaczewskiego 4, 20–090 Lublin, Poland, lukasz.komsta@umlub.pl)

      J. Sep. Sci. 39, 4258-4262 (2016). TLC of 35 model compounds on RP-2, RP-8, RP-18, alumina, cellulose, cyano, diol, amino phase, and silica gel with 20 pure solvents (acetone, acetonitrile, 1-butanol, 1-chlorobutane, chloroform, cyclohexane, 1,2-dichloroethane, dichloromethane, dioxane, ethanol, ethyl acetate, heptane, hexane, methanol, isooctane, 1-propanol, 2-propanol, t-butyl methyl ketone, tetrahydrofuran, and toluene). Parallel factor analysis was used to study the retention phenomena in quantitative manner.

      Classification: 2c
      118 048
      The effect of mutation in the clpX gene on the synthesis of N-acyl-homoserine lactones and other properties of Burkholderia cenocepacia 370
      M. VESELOVA, Y. ROMANIVA, V. LIPASOVA, O. KOKSHAROVA, Y. ZAITSEVA, M. CHERNUKHA, A. GINTSBURG, I. KHMEL* (*Institute of Molecular Genetics, Russian Academy of Sciences, Kurchatov Square 2, Moscow 123182, Russia, khmel@img.ras.ru)

      Microbiol. Res. 186-187, 90-98 (2016). TLC of N-acyl-homoserine lactones from Burkholderia cenocepacia strains on RP-18 with methanol - water 3:2. TLC plates were then overlaid with the biosensor strain A. tumefaciens NTL4/pZLR4 in soft agar (0.6 % M9 medium supplemented with glucose 0.2 % and X-gal 40 µg/mL), followed by incubation overnight at 30 °C. N-acyl-homoserine lactones were visually identified as blue zones.

      Classification: 8b
      118 085
      Comparison of analytical methods in chemometric fingerprinting of metallicolous
      and non-metallicolous populations of Echium vulgare L
      S. DRESLER*, T. KUBRAK, E. RUTKOWSKA, M. GAGOS, A. BOGUCKA, R. SWIEBODA, M. WOJCIK (*Department of Plant Physiology, Maria Curie-Sk?odowska University,
      Akademicka 19, 20-033 Lublin, Poland, slawomir.dresler@poczta.umcs.lublin.pl)

      Phytochem. Anal. 27, 239-248 (2016). HPTLC of Echium vulgare from different sites (characterized by varied heavy metal contamination in the substrates) on silica gel with ethyl acetate – 98-100 % formic acid – glacial acetic acid – water 100:11:11:26. Qualitative identification under UV light at 366 nm. Pre-processing of TLC plate images was performed using open architecture software.

      Classification: 32e
      119 024
      Laser desorption-ion mobility spectrometry as a useful tool for imaging of thin-layer chromatography surface
      V. ILBEIGI, M. SABO, Y. VALADBEIGI, S. MATEJCIK*, M. TABRIZCHI**, (*Comenius Univ. in Bratislava, Fac. of Math., Phys. & Inform., Dep. of Exp. Phys., Mlynska dolina, F2 842 48, Slovakia; **Dep. of Chem., Isfahan Univ. of Technology, Isfahan, 84156-83111, Iran)

      J. Chromatogr. A 1459, 145-151 (2016). Presentation of a novel method for coupling TLC with ion mobility spectrometry (IMS) using laser desorption technique (LD). Sampling of the compounds (explosives like trinitrotoluene, 1,3,5-trinitro-1,3,5-triazacyclohexane, pentaerythritol tetranitrate, 2,4-dinitrotoluene and 3,4-dinitrotoluene; amino acids like alanine, proline and isoleucine, nicotine and diphenylamine mixtures) on the layer surface within less than 80 s after TLC separation by using the LD-IMS technique without the need of any further manipulation or preparation. The TLC plate was moved in desired directions by the motorized micro-positioning stage towards the right position of the fixed laser. TLC-LD-IMS offers an additional separation dimension, allowing separation of overlapping TLC analytes, and reveals possibility for fast and effective analysis of the mixtures due to the scan rate for LD being adjustable.

      Classification: 4e, 15
      119 081
      Fengycin produced by Bacillus subtilis 9407 plays a major role in the biocontrol of apple ring rot disease
      H. FAN (Fan Haiyan), J. RU (Ru Jinjiang), Y. ZHANG (Zhang Yuanyuan), Q. LI (Qi Wang), Y. LI (Li Yan)* (*Department of Plant Pathology, College of Plant Protection, China Agricultural University, No. 2 Yuanmingyuan West Road, Haidian District, Beijing,100193, China, fanhaiyan6860@163.com)

      Microbiol. Res. 199, 89-97 (2017). HPTLC bioautography of lipopeptide crude extracts from wild-type strain Bacillus subtilis 9407 on silica gel with chloroform – methanol – water 65:25:4. The plates were laid on the surface of a potato dextrose agar containing fungal spores at room temperature for 2 h and then removed. Incubation at 28 °C for 5 days. The hRF value for fengycin was 15.

      Classification: 28a
      120 005
      Quantification techniques for important environmental contaminants in milk and dairy products
      N. RAZA, K. KIM* (*Department of Civil & Environmental Engineering, Hanyang University, 222 Wangsimni Ro, Seoul 04763, South Korea, kkim61@hanyang.ac.kr)

      Trends. Anal. Chem. 98, 79-94 (2018). Review of essential protocols for the quantification of dairy-related contaminants, including the application of HPTLC for the determination of residual pesticides such as chlorpyrifos, bifenthrin, deltamethrin, cyhalothrin and imidacloprid and antibiotics such as cephalosporin.

      Classification: 1
      120 026
      Effect-directed analysis of Pimpinella saxifraga L
      Gertrud MORLOCK*, T. LAPIN (*Justus Liebig University Giessen, Chair of Food
      Science, Institute of Nutritional Science, Interdisciplinary Research Center
      (IFZ), Heinrich-Buff-Ring 26–32, 35392 Giessen, Germany, Gertrud.Morlock@uni-giessen.de)

      root extract via HPTLC–UV/Vis/FLD–EDA–MS. J. Planar Chromatogr. 31, 79-86 (2018). HPTLC with effect-directed analysis (EDA) for (bio)profiling of Pimpinella saxifraga root. HPTLC on silica gel with 1) ethyl acetate – methanol – acetic acid 8:3:1 for polar separation, and 2) toluene – ethyl acetate – acetic acid 20:5:1 for apolar separation. Ten different detections were shown on one HPTLC plate cut into sections. Detection of absorbing compounds under A) white light and B) UV 254 nm and C) fluorescent ones under UV 366 nm. Three plate sections were used for microchemical derivatizations for D) detection of flavonoids after derivatization with diphenylborinic acid 2-aminoethylester reagent, followed by dipping into a polyethylene glycol 400 solution, E) universal detection with anisaldehyde sulfuric acid reagent, and F) detection of glycosides with diphenylamine aniline reagent. Effect-directed detection of G) DPPH scavenging compounds, antimicrobials via H) A. fischeri and I) B. subtilis bioassays, and J) AChE inhibitory compounds was also performed. Multi-detection showed multi-potent zones with hRF values of 19, 24, 49 and 78, which were exemplarily further characterized by HPTLC–ESI–MS in both ionization modes. A weak estrogen-effective zone was also observed via HPTLC–planar yeast estrogen screen (pYES) bioassay on RP-18 with n-hexane – toluene – ethyl acetate 6:3:4 or, after optimization, toluene – ethyl acetate 1:1.

      Classification: 4e, 7, 28a
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