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      Host-guest drug delivery by β-cyclodextrin assisted polysaccharide vehicles: A review

      , ,
      International Journal of Biological Macromolecules
      Elsevier BV

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          Abstract

          <p xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="first" dir="auto" id="d2891819e77">Among different forms of cyclodextrin (CD), β-CD has been taken a special attraction in pharmaceutical science due to lowest aqueous solubility and adequate cavity size. β-CD forms inclusion complex with drugs in combination with biopolymers such as polysaccharides which plays a vital role as a vehicle for safe release of drugs. It is noticed that, β-CD assisted polysaccharide-based composite achieves better drug release rate through host-guest mechanism. Present review is a critical analysis of this host-guest mechanism for release of drugs from polysaccharide supported β-CD inclusion complex. Various important polysaccharides such as cellulose, alginate, chitosan, dextran, etc. and their association with β-CD in relevant to drug delivery are logically compared in present review. Efficacy of mechanism of drug delivery by different polysaccharides with β-CD is analytically examined in schematic form. Drug release capacity at different pH conditions, mode of drug release, along with characterization techniques adopted by individual polysaccharide-based CD complexes are comparatively established in tabular form. This review may explore better visibility for researchers those are working in the area of controlled release of drugs by carrier consist of β-CD associated polysaccharide composite through host-guest mechanism. </p>

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          Author and article information

          Journal
          International Journal of Biological Macromolecules
          International Journal of Biological Macromolecules
          Elsevier BV
          01418130
          June 2023
          June 2023
          : 240
          : 124338
          Article
          10.1016/j.ijbiomac.2023.124338
          37030461
          874dfa76-7371-4678-bc0c-08fe066eb5cb
          © 2023

          https://www.elsevier.com/tdm/userlicense/1.0/

          https://doi.org/10.15223/policy-017

          https://doi.org/10.15223/policy-037

          https://doi.org/10.15223/policy-012

          https://doi.org/10.15223/policy-029

          https://doi.org/10.15223/policy-004

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