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      Rendering cellulose fibers antimicrobial using cationic β-cyclodextrin-based polymers included with antibiotics

      , , , , ,
      Cellulose
      Springer Science and Business Media LLC

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          Antimicrobial-modified sulfite pulps prepared by in situ copolymerization

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            Drug carrier systems based on water-soluble cationic beta-cyclodextrin polymers.

            This study was designed to synthesize, characterize and investigate the drug inclusion property of a series of novel cationic beta-cyclodextrin polymers (CPbetaCDs). Proposed water-soluble polymers were synthesized from beta-cyclodextrin (beta-CD), epichlorohydrin (EP) and choline chloride (CC) through a one-step polymerization procedure by varying molar ratio of EP and CC to beta-CD. Physicochemical properties of the polymers were characterized with colloidal titration, nuclear magnetic resonance spectroscopy (NMR), gel permeation chromatography (GPC) and aqueous solubility determination. The formation of naproxen/CPbetaCDs inclusion complexes was confirmed by NMR and fourier transform infrared spectroscopy (FT-IR). Cationic beta-CD polymers showed better hemolytic activities than parent beta-CD and neutral beta-CD polymer in hemolysis test. The morphological study of erythrocytes revealed a cell membrane invagination induced by the cationic groups. The effects of molecular weight and charge density of the polymers on their inclusion and release performance of naproxen were also investigated through phase-solubility and dissolution studies. It was found that the cationic beta-CD polymers with high molecular weight or low charge density exhibited better drug inclusion and dissolution abilities.
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              Modified guanidine polymers: Synthesis and antimicrobial mechanism revealed by AFM

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                Author and article information

                Journal
                Cellulose
                Cellulose
                Springer Science and Business Media LLC
                0969-0239
                1572-882X
                April 2009
                December 16 2008
                April 2009
                : 16
                : 2
                : 309-317
                Article
                10.1007/s10570-008-9270-0
                ae246ef2-9593-47bd-96ee-23dfea0ec5bf
                © 2009
                History

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