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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      94 060
      Spectrophotometric, spectrofluorimetric, and densitometric methods for the determination of indapamide
      NADIA F. YOUSSEF (National Organization for Drug Control and Research, 6 Abo Hazem St. Pyramids Ave, PO Box 29, Cairo, Egypt)

      J. AOAC Int. 86, 935-940 (2003). TLC of indapamide (4-chloro-N-(2-methylindolin-1-yl)-3-sulfamoylbenzamide), its degradation product, and related substance 2-methylnitrosoindoline on silica gel using toluene - ethyl acetate - glacial acetic acid 69:30:1 after pre-saturation for 1 h. Detection under UV light at 254 nm. Quantitative determination at 424 nm. Limit of detection 0.11 µg/spot. The method was validated according to the guidelines of the USP.

      Classification: 32a
      94 091
      TLC densitometric determination of bromhexine hydrochloride in pharmaceuticals, and its validation
      E. SUMARLIK, G. INDRAYANTO* (*Assessment Service Unit, Faculty of Pharmacy, Airlangga University, Surabaya, Indonesia)

      J. Liq. Chrom. Rel. Technol. 27, 2047-2056 (2004). TLC of bromhexin on silica gel with n-butanol - glacial acetic acid - water 260:77:75 in a twin-trough chamber after at least 3 h of saturation. Quantitative determination at 325 nm by absorbance measurement. The method is selective, precise, and accurate and can be used for routine analysis of pharmaceutical preparations in pharmaceutical industry quality control laboratories.

      Classification: 32a
      95 021
      Analysis of glycosides and aglycones of flavonoid compounds by double-development thin-layer chromatography
      E. SOCZEWINSKI*, M. WOJCIAK-KOSIOR, G. MATYSIK (*Department of Chemistry, Medical University, Staszica 6, 20-081 Lublin, Poland)

      J. Planar Chromatogr. 17, 261-263 (2004). HPTLC of aglycones and glycosides (flavone, hesperetin, naringenin, apigenin, kaempferol, quercetin, myricetin, tiliroside, apigenin 7-glucoside, myricitrin, kaempferol 3,7-dirhamnoside, hyperoside, hesperidin, rhoifolin, rutin, naringin) on silica gel by using mixtures of dichloromethane and ethyl acetate for aglycones and mixtures of ethyl acetate and formic acid for glycosides. The plates were conditioned for 15 min and developed face down in a horizontal chamber. To separate mixtures of flavonoids two-step gradient devlopment was used. In the first step (for gycosides) the plates were developed to a distance of 65 mm with ethyl acetate - formic acid - water 170:30:1. In the second step (for aglycones ) the plates were developed to a distance of 95 mm with dichloromethane - ethyl acetate - formic acid 170:30:1. Quantitation by densitometry at 254 nm.

      Classification: 8a
      95 052
      Test of the stability of olibanum resins and extracts
      S. BASAR, Angelika KOCH* (*Frohme-Apotheke, Frohmestrasse 14, 22457 Hamburg, Germany)

      J. Planar Chromatogr. 17, 479-482 (2004) HPTLC of beta-boswellic acid (BA), acetyl-beta-BA, keto-BA, and acetyl-keto-BA and ethanolic extracts of olibanum resin on silica gel with toluene - ethyl acetate - formic acid - heptane 80:20:3:10 in a twin trough chamber without chamber saturation. Quantitative determination by reflectance measurement at 245 and 285 nm. Also two dimensional development with the same mobile phase in the second direction.

      Classification: 32e
      95 078
      Normal-phase TLC separation of some antiarrhythmics
      R. PIETRAS*, H. HOPKALA, D. KOWALCZUK, A. MALYSZA (*Department of Medicinal Chemistry, Medical University, Chodzki 6, 20-093 Lublin, Poland)

      Densitometric determination of mexiletine hydrochloride in capsules. J. Planar Chromatogr. 17, 213-217 (2004). TLC of disopyramide, flecainide, mexiletine, tocainide, and verapamil on aluminium oxide and silica gel in horizontal chambers. The best mobile phase for separation on the alumina plates was tetrahydrofuran - hexane - 25 % ammonia 25:24:1 and on silica chloroform - tetrahydrofuran - ethanol - 25 % ammonia 81:19:20:1. Detection under UV light at 210 nm and by use of different reagents. Quantification of mexiletine hydrochloride in capsules was performed densitometrically at 254 nm.Correlation coefficient in the concentration range 20 - 45 µg per band was 0.9974, with RSD of 5.23 %.

      Classification: 32a
      95 097
      (Study of the quality standard for Buxie Danggui extract) (Chinese)
      M. XIN (Xin Meiyu) (Guangdong Wannianqing Pharm. Co., Ltd., Shantou, Guangdong 515031, China)

      Chinese J. Trad. Pat. Med. (Zhongchengyao) 27 (2), 225-227 (2004). TLC on silica gel with 1) petroleum ether (30 - 60 ºC) - ethyl acetate 9:1; 2) benzene - glacial acetic acid 4:1. Detection 1) by spraying with 1 % vanillin solution and heating at 105 ºC for 10 min; 2) under UV 365 nm. Identification by fingerprint technique. Quantification of ferulic acid by densitometry at 325 nm. Validation of the method by investigation of linearity (0.16 µg - 1.6 µg, r = 0.9992); precision (RSD = 1.8 %, n= 5 within plate and RSD = 2.3 % plate to plate); reproducibility of five time assay towards the same sample (RSD = 0.5 %); and standard addition recovery (97.17 %, RSD = 0.9 %, n = 5). The results for three real life samples are given.

      Classification: 32c
      96 038
      Separation of complex fructo-oligosaccharides (FOS) and inulin mixtures by HPTLC-AMD
      T. BERNARDI, Elena TAMBURINI*, G. VACCARI (*Chemistry Department, University of Ferrara, Via L. Borsari 46, 44100 Ferrara, Italy)

      J. Planar Chromatogr. 18, 23-27 (2005). HPTLC-AMD of fructo-oligosaccharides and inulin mixtures (sucrose, 1-kestose, nystose, and fructosylnystose) on diol phases at 55-65 % relative humidity in a twin-trough chamber with an acetonitrile - acetone - water polarity gradient. Detection by derivatization with 4-aminobenzoic acid reagent and quantitation by scanning at 366 nm.

      Classification: 10a
      96 069
      High-performance thin-layer chromatographic determination of carbamate residues in vegetables
      F. TANG, S. GE, Y. YUE*, Rimao Hua, Rong Zhang (*International Centre for Bamboo and Rattan, 100102 Beijing, China)

      J. Planar Chromatogr. 18, 28-33 (2005). HPTLC and TLC of four carbamate residues (pirimicarb, methomyl, carbofuran, carbaryl) in vegetables on silica gel (prewashed with chloroform - methanol 1:1 followed by drying at 110 °C for 30 min) with system I (two fold development with first toluene - acetone 4:1, and second dichloromethane - acetone 4:1), and system II (two fold development with first ethyl acetate - petroleum ether 3:2, and second chloroform - petroleum ether 9:1). Quantitative determination by densitometric scanning at 254 and 366 nm.

      Classification: 29c
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