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      Hydrogel nanoparticles in drug delivery.

      1 , ,
      Advanced drug delivery reviews
      Elsevier BV

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          Abstract

          Hydrogel nanoparticles have gained considerable attention in recent years as one of the most promising nanoparticulate drug delivery systems owing to their unique potentials via combining the characteristics of a hydrogel system (e.g., hydrophilicity and extremely high water content) with a nanoparticle (e.g., very small size). Several polymeric hydrogel nanoparticulate systems have been prepared and characterized in recent years, based on both natural and synthetic polymers, each with its own advantages and drawbacks. Among the natural polymers, chitosan and alginate have been studied extensively for preparation of hydrogel nanoparticles and from synthetic group, hydrogel nanoparticles based on poly (vinyl alcohol), poly (ethylene oxide), poly (ethyleneimine), poly (vinyl pyrrolidone), and poly-N-isopropylacrylamide have been reported with different characteristics and features with respect to drug delivery. Regardless of the type of polymer used, the release mechanism of the loaded agent from hydrogel nanoparticles is complex, while resulting from three main vectors, i.e., drug diffusion, hydrogel matrix swelling, and chemical reactivity of the drug/matrix. Several crosslinking methods have been used in the way to form the hydrogel matix structures, which can be classified in two major groups of chemically- and physically-induced crosslinking.

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          Author and article information

          Journal
          Adv Drug Deliv Rev
          Advanced drug delivery reviews
          Elsevier BV
          1872-8294
          0169-409X
          Dec 14 2008
          : 60
          : 15
          Affiliations
          [1 ] Faculty of Pharmacy, Shiraz University of Medical Sciences, P.O. Box 71345-1583, Shiraz, Iran. hamidim@sums.ac.ir
          Article
          S0169-409X(08)00227-5
          10.1016/j.addr.2008.08.002
          18840488
          514d7637-003e-4b35-8a29-daccfc53659d
          History

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