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.

      72 114
      Micropreparative chromatography of some quaternary alkaloids from the roots of Chelidonium majus L
      W. GOLKIEWICZ, M. GADZIKOWSKA, J. KUCZYNSKI, L. JUSIAK,, (Dep. of Inorg. and Analytical Chemistry, Medical Academy, Staszica 5, 200081 Lublin, Poland)

      J. Planar Chromatogr. 6, 382-385 (1993). Investigation of the system silica gel and aqueous buffer - methanol eluent for the chromatography of alkaloids. TLC of quaternary alkaloids on silica buffered at different pH and eluted with mobile phases of pH similar to that of the silica. Detection under UV at 366 nm of with Dragendorff's reagent. Quantification by scanning in absorbance at 280 nm. Quaternary alkaloids: sanguinarine, chelerithrine, chelilutine, chelirubine, dihydrosanguinarine, dihydrochelerithrine, berberine.

      Classification: 22
      73 086
      Alkaloids of Stemona japonica
      Y. YE, G.-W. QIN, R.S. XU*, (*Shanghai Institute of Materia Medica, Academia Sinica, Shanghai 200031, P.R. China)

      J. of Natural Products 57, 665-669 (1994). TLC of alkaloids in crude plant extracts on silica with petrol ether - acetone 2:1, dichloromethane - methanol 95:5 and hexane - acetone 1:1. Detection by spraying with Dragendorff's reagent. Excellent separation of closely related alkaloids.

      Classification: 22
      76 107
      (Comparative study of the extraction process for the preparation of Maxingshigan pills by thin-layer chromatography
      Q. HE (He Qun)*, J. LUO (Luo Jieying), Q. DENG (Deng Qingping), (*Hunan Coll. Trad. Chin. Med., Chagsha 410007, P.R. China)

      J. Chinese Herb. Med. 26, 463-464 (1995). TLC on silica with chloroform - methanol - NH3 100:8:1. Detection by spraying with 0.5% ninhydrin in ethanol. Quantification of ephedrine by densitometry at 510 nm.

      Classification: 22
      78 083
      Pyrrolizidine alkaloids of Cynoglossum officinale and Cynoglossum amabile (Family Baraginaceae)
      A. El-SHAZKY*, T. SARG, A.A.TEYA, E. ABDEL AZIZ, L. WITTE, M. WINK, (*Dept. of Pharmacogn., Fac. of Pharm., Zagazig Univ., Zagazig, Egypt)

      Biochemical Systematics and Ecology 24, 415-421 (1996). TLC of 3'-acetylheliosupine, heliosupine, viritiflorine, heliosupine N-oxide on silica with dichloromethane - methanol - NH3 85:15:2 or 75:23:2.

      Classification: 22
      80 063
      Transfer of alkaloids from Delphinium to Castilleya via Root Parasitism
      M.D. MARKO*, F.R. STERMITZ, (*Dept. of Biol., Colorado State Univ., Fort Collins CO 80523, USA)

      Norditerpenoid alkaloid analysis by electrospray mass spectrometry. Biochemical Systematics and Ecology 25, 279-285 (1997). TLC of alkaloids on silica with chloroform - methanol 9:1. Detection by spraying with Dragendorff's or iodoplatinate reagent.

      Keywords:
      Classification: 22
      83 075
      Preparation and characterization of acid hydrolysis products of the tomato glycoalkaloid
      M. FRIEDMAN*, N. KOZUKE, L.A. HARDEN, (Western Reg. Res. Center, Agric. Res. Service, U.S. Dept. of Agric., 800 Buchanan Str., Albany, California, 94710 USA)

      J. Agric. Food Chem. 46, 2096-2101 (1998). TLC of a-tomatine and hydrolysis products (i.a. tomatidine) on silica gel with chloroform - methanol - 1% NH3 2:2:1, bottom layer, chloroform - methanol - 2% NH3 14:6:1, and chloroform - methanol - 1% NH3 13:7:1; 5:5:1. Visualization by spraying with anisaldehyde solution followed by heating at 120°C for 5 min.

      Keywords:
      Classification: 22
      87 059
      TLC and HPTLC assay of quinoline and quinuclidine alkaloids in Cinchonae Cortex and pharmaceutical preparations
      T. MROCZEK, K. GLOWNIAK*, (*Dept. of Pharmacogn., Med. Univ., 12 Peowiaków St, 20.007 Lublin, Poland)

      J. Planar Chromatogr. 13, 457-462 (2000). TLC and HPTLC of extracts and standards (quinine, quinidine, cinchonine, cinchonidine) on silica gel with 7 different mobile phases. The quaternary mobile phase toluene - chloroform - diethyl ether - diethylamine 8:3:7:2 enabled the determination of alkaloids in a variety of preparations and extracts. Two different modes of densitometric evaluation (absorbance and fluorescence) were used. Results from quantitative analysis were statistically assessed by use of a calibration procedure, a calibration equation, the correlation coefficient, and the relative standard deviation.

      Keywords:
      Classification: 22, 32e
      88 088
      Retention behavior of some alkaloids in thin layer chromatography with bonded stationary phases and binary model phases
      M. WAKSMUNDZKA-HAJNOS*, A. PETRUCZNIK, (*Dept. of Inorg. and Anal. Chem., Med. Univ., Staszica 6, 20-081 Lublin, Poland)

      J. Planar Chromatogr. 14, 364-370 (2001). TLC of 24 alkaloids (aconitine - yohimbine) on silica gel and aminopropyl-modified silica gel plates as well as on cyanopropyl-, diol- and RP 18-modified silica gel plates using a variety of binary mobile phases prepared from n-hexane and polar modifiers - 2-propanol, ethyl acetate, methyl ethyl ketone, tetrahydrofuran, dioxane - in different concentrations for NP chromatography and reversed-phase systems with buffered aqueous -acetonitrile mobile phases (pH 9.15). Visualization at 254 nm.

      Keywords:
      Classification: 22