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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      81 120
      (The quality standard study on Xintongding Infusion
      Y. WANG (Wang Yuemin)*, S. MAO (Mao Suqing), F. WANG (Wang Fuyan), (*Liaoning Inst. Chin. Trd. Med., Shenyang 110031, P.R. China)

      J. Chinese Herb. Med. (Zhongcaoyao) 29, 93-95 (1998). TLC of tanshinone IIA on silica gel with benzene - ethyl acetate 19:1, detection under daylight; of corydalis B on silica gel with hexane - chloroform - methanol 10:6:1, detection by exposure to iodine vapor; of rutin on silica gel with ethyl acetate - formic acid - water 8:1:1, detection by spraying with AlCl3 reagent and under UV. Identification by comparison to standard. TLC of ursolic acid on silica gel with toluene - ethyl acetate - acetic acid 24:8:1. Detection by spraying with 5% sulfuric acid in ethanol and heating at 105°C for 10 min. Quantitation by densitometry at 520 nm. Precision for ursolic acid 0.9% (n=6). recovery 96.8 ± 1,2-5 (n=6),

      Classification: 32c
      93 029
      Planar chromatography for the analysis of malolactic fermentation
      D. JÄNCHEN* (Ed.) (CAMAG, Sonnenmattstr. 11, 4132 Muttenz, Switzerland, dieter.jaenchen@camag.com)

      CBS 84, 14-15 (2000). HPTLC of wine samples on silica gel with diisopropyl ether - formic acid - water 16:3:1 with chamber saturation. Detection by heating at 110 °C for 15 min, followed by cooling to room temperature and dipping in bromophenol blue reagent. Quantitative determination of malic, lactic, and succinic acid by absorbance measurement at 430 nm.

      Classification: 11a
      93 084
      Monitoring of proinsecticides (oxazolines) in biological samples
      M.BEAUFOUR*, J.-C. CHERTON, A. CARLIN-SINCLAIR (*Laboratoire Sircob, Bat. Lavoisier, 45 avenue des Etats-Unis, F-78035 Versailles Cedex, France. beaufour@chimie.uvsq.fr)

      CBS 90, 12-13 (2003). TLC of oxazoline Ia on aluminum sheets RP-18 with methanol over 10 mm, followed by water - acetonitrile 1:1 over 55 mm. Ion pair chromatography of oxazoline Ia with phosphate buffer - acetonitrile 1:1 over 60 mm after dipping in 2 mM cetyltrimethylammonium bromide. TLC of oxazoline Ib and Ic with phosphate buffer - acetonitrile - dioxane 4:3:3 over 65 mm. Determination by absorbance measurement at 200 nm (oxazoline Ia and Ib) and 262 nm (oxazoline Ic) respectively.

      Classification: 8b, 23e, 29f
      93 116
      (An improved procedure for the determination of matrine in Chinese traditional herbal drugs and preparations
      X. Li (LI XIAOYAN)*, SH. ZHAO (ZHAO SHAOHUA), X. LU (LU XIULI), ZH. LI (LI ZHENGJIE) (*Hebei Yiling Acad. Med. & Pharm., Shijiazhuang, Hebai 050035, P. R. China)

      J. Chinese Trad. Patent Med. (Zhongchengyao) 26 (2), 172-173 (2004). TLC on silica gel with 1) benzene - acetone - ethyl acetate - conc. ammonia 10:15:20:2. Detection by spraying with 5 % potassium iodobismuthate solution. Identification by comparison with the standard. Quantification by densitometry at 524 nm. The procedure is validated by investigation of its repeatability, reproducibility, and recovery. Discussion of the merits of the procedure compared to that in China Pharmacopeia (2000 ed).

      Classification: 32c
      93 145
      HPTLC - Method for quantitative determination of levamisol in tissue and organs of pigs
      M. WERTHER*, B. MUELLER, A. STREY (*Institut für Tierarzneimittel GmbH, Berliner Allee 317-321, D-13088 Berlin, Germany, margit.werther@camag-berlin.de)

      CBS 83, 12-13 (1999) HPTLC of levamisol in pig tissue on silica gel with chloroform over a developing distance of 70 mm, then with chloroform - methanol - formic acid 400:50:1 over 50 mm. Quantitative determination by absorbance measurement at 220 nm. Limits of detection are 0.6 - 1.5 µg/kg.

      Classification: 32d
      94 030
      Determination of progesterone in drug release media
      A. JAMSHIDI (Department of Novel Drug Delivery Systems, Iran Polymer and Petrochemical Institute, P.O. Box 14965/115, Tehran, Iran, a.jamshidi@ippi.ac.ir)

      CBS 93, 10-12 (2004). HPTLC of progesterone on silica gel prewashed by development in AMD2 first with chloroform - methanol 1:1 and then with the mobile phase, followed by drying at 80 °C for 15 min. Development in AMD2 with toluene - 2-propanol 10:1 without preconditioning over 60 mm. Quantitative determination by absorbance measurement at 252 nm followed by spectra recording from 200 to 360 nm. The linear working range is 25.7-154.5 ng/zone. Repeatability (standard deviation calculated from the amounts of seven simulated progesterone samples determined on the same plate at three concentration levels in the lower, middle and upper range) is 0.26-1.29 %. Recovery is 99.88-100.97 %. Reproducibility was performed with recycled HPTLC plates.

      Classification: 13a, 32a
      94 066
      Reversed-phase thin-layer chromatography of three new oral antidiabetics and densitometric determination of pioglitazone
      Anna GUMIENICZEK*, H. HOPKALA, A. BERECKA (*Department of Medicinal Chemistry, Medical University of Lublin, Chodzki 6, 20-093 Lublin, Poland)

      J. Liq. Chrom. Rel. Technol. 27, 2057-2070 (2004). HPTLC of pioglitazone hydrochloride ((±)-5-[p-[2-(ethyl-2-pridinyl)ethoxy]-benzyl]-2,4-thiazolidinedione hydrochloride), rosiglitazone maleate ((±)-5-[4-[2-[N-methyl-N-(2--pyridinyl)amino]-ethoxy]benzyl]-2,4-thiazolidinedione maleate), and repaglinide S(+)-2-ethoxy-4-[N-[1-(2-piperidinophenyl)-3-methyl-1-butyl]-aminocarbonylmethyl]benzoic acid on cyano-phase with 1,4-dioxane - buffer pH 2.8/4.4/6.4/7.9 1:4; 2:3; 1:1; 3:2; 2:1 in horizontal chambers without saturation. Quantitative determination of pioglitazone by reflectance/transmittance measurement at 266 nm.

      Classification: 32a
      94 093
      HPTLC determination of montelukast sodium in bulk drug and in pharmaceutical preparations
      R. T. SANE, A. MENEZES*, M. MOTE, A. MOGHE, G. GUNDI (*TDM laboratories, Plot no. 194, Scheme no. 6, Road no. 15, Sion (E), Koliwada, Mumbai-22, India)

      J. Planar Chromatogr. 17, 75-78 (2004). HPTLC of montelukast sodium (1-[[[(1R)-1-[3-[(1E)-2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-hydroxy-1-methylethyk)phenyl]-propyl]thio]methyl] cyclopropane acetic acid monosodium salt) and nimesulide (N-(4-nitro-2-phenoxyphenyl)methane sulfonamide or 4-nitro-2-phenoxymethanesulfonanilide) as internal standard on pre-washed silica gel with toluene - ethyl acetate - glacial acetic acid 60:34:1 in a twin-trough chamber. Quantitative determination at 344 nm.

      Classification: 32a
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