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.

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      52 137
      Thin-layer chromatographic identification of phenothiazine derivative drugs
      K. STEINBRECHER

      J. Chromatogr. 260, 463-470 (1983). TLC of twenty different phenothiazine bases on silica with a) ether - ethyl acetate - NH3 (1:1 saturated), b) methanol - butanol 6:4, c) dichloromethane - methanol 5:1 and d) chloroform - isopropanol - NH3 70:30:1. Detection with 10 % H2SO4 in ethanol. The system permits to distinguish all phenothiazines from each other.

      Keywords:
      Classification: 32
      97 121
      Eremophilane sesquiterpenes from Ligularia myriocephala
      J. LIN (Jun-Xi Lin), X. WEI (Xiao-Ning Wei), Y. SHI* (Yan-Ping Shi) (*Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730 000, China. shiyp@lzb.ac.cn)

      Planta Med. 72, 175-179 (2006). Preparative TLC of 1beta,6beta-diangeloyloxy-8beta,10beta-dihydroxyeremophil-(11)-en-8alpha,12-olide, 1beta,6betadiangeloyloxy-8alpha,10alpha-dihydoxyeremophil-7(11)-en-8beta,12olide, 1beta-angeloyloxy-8-oxoeremophil-6,9-diene-12-oic acid methylester on silica gel with petroleum ether (60-90°) - acetone 3:1. Detection under UV light at 254 nm or by spraying with 98 % sulfuric acid - ethanol 1:19 followed by heating.

      Classification: 32e
      53 166
      Zur Stabilität von Oxyethyltheophyllin-Injektionslösungen
      R. POHLOUDEK-FABINI, G. DOEGE, D. KOTTKE

      (About the stability of oxyethyltheophylline-injections.) Pharmazie 39, 24-26 (1984). TLC of theophylline and ethophylline on silica with ethyl acetate - methanol -25 % NH3 8:2:1. Detection with diazo-reagent.

      Keywords:
      Classification: 32
      97 158
      Determination of resveratrol in Polygonum cuspidatum Siebet Zucc by thin-layer chromatography (Chinese)
      R. ZHAO (Zhao Ruizhi), (TCM Lab., No.2 Clinical Hosp., Guangzhou Univ. Trad. Chinese Med. & Pharm., Guangzhou 510120, China)
      et Zucc by thin-layer chromatography) (Chinese). J. Chinese Trad. Patent Med. (Zhongchengyao) 27 (5), 605-607 (2005). TLC of resveratrol on silica gel with petroleum ether (30 ºC-90 ºC) - ethyl acetate - methanol - glacial acetic acid 200:50:35:1. Detection under UV light. Identification by comparison with the standard. Quantification by densitometry at 293 nm. Validation of the method by investigation of its linearity range (0.5 µg - 5.0 µg, r = 0.999); precision (RSD = 0.98 %, n = 5); its reproducibility of five time assay towards the same sample (RSD = 2.52 %); standard addition recovery (101.6 %, RSD = 0.26 %, n = 5). The results for three real life samples are given. Discussion of the application of the procedures for the quality control of the medicine.
      Classification: 32e
      53 184
      Is urine a suitable material for the preliminary screening of drugs in autopsy cases? Forensic Science Int
      G. THELANDER, J. JONSSON, J. SCHUBERTH

      22, 189-194 (1983). TLC of urine samples on silica, two plates differently chromatographed with, plate A) ethyl acetate - methanol - NH3 85:10:5 after exposure to NH3, plate B) methanol - NH3 100:1. 5. Detection by spraying with different reagents.

      Keywords:
      Classification: 32
      99 082
      New compounds from Commiphora myrrha (Nees) Engl
      F. AHMED, M. ALI*, O. SINGH (*Phytochemistry Research Laboratory, Faculty of Pharmacy, Jamia Hamdard (Hamdard University), New Delhi-62, India; mali_chem@yahoo.co.in)

      Pharmazie 61,728-731 (2006). TLC of myrracadinol A, myrracalamene A, myrracalamene B, myrracadinol B. triacont-1-ene, myrracalamene C, and myrracadinol C on silica gel with petroleum ether, toluene, petroleum ether - chloroform 4:1, toluene - chloroform 4:1, benzene, benzene - ethyl acetate - diethyl amine 6:3:1, or chloroform- methanol 17:3. Detection under UV light, by exposure to iodine vapors and by spraying with ceric ammonium sulfate.

      Classification: 32e
      54 156
      Eine wirtschatliche HPTLC Methode zur simultanen Bestimmung von Antiepileptica in kleinen Serien
      T. MUELLER, I. STEINBACH, S. KAPP

      (An economical HPTLC method for simultaneous determination of antiepileptica in small series.) Fresenius Z. Anal. Chem. 218, 261-263 (1984). HPTLC of antiepileptics on silica with chloroform -2-propanol - NH3 80:20:1. Densitometry at 210 nm.

      Keywords:
      Classification: 32
      99 122
      TLC-Densitometric analysis of artemisinin for the rapid screening of high-producing plantlets of Artemisia annua L
      T. KOOBKOKKRUAD, A. CHOCHAI, C. KERDMANEE, W. DE-EKNAMKUL* (*Department of Pharmacognosy, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Thailand, dwanchai@chula.ac.th)

      Phytochem Anal. 18, 229-234 (2007). HPTLC of Artemisia annua leaves on silica gel with hexane – ethyl acetate – acetone 16:1:1. Detection by exposing to ammonia vapor at 100ºC for 2 hours. Quantitative determination by absorbance measurement at 320 nm. Linearity is between 0.5 and 12 µg/mL and the limit of detection is 0.5 µg/mL. The method is as sensitive and accurate as the HPLC-UV method involving a pre-column reaction.

      Classification: 32e
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