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Critical Reviews™ in Therapeutic Drug Carrier Systems

 

ISSN for PRINT: 0743-4863

Institutional price:

$1014.00

Issues per year:

6

For Online Access

Best Paper Award Selection - Editorial Board Site

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2005, Volume22

Issue 5

  82 pages  

   

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Issue price - $161.00  

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  • Polymeric Nanoparticles for Oral Delivery of Drugs and Vaccines: A Critical Evaluation of In Vivo Studies
  • Sergio A. Galindo-Rodriguez
    Pharmapeptides,Geneva-Lyon Interuniversity Center, Archamps; UMR-CNRS 5007,Faculty of Pharmacy,Claude Bernard University Lyon I,Lyon, France; and School of Pharmaceutical Sciences,Ecole de Pharmacie Geneve-Lausanne,University of Geneva,Geneva, Switzerland

    Eric Allemann
    School of Pharmaceutical Sciences, Ecole de Pharmacie Geneve-Lausanne, University of Geneva; and Bracco Research SA, Plan-les-Ouates, Geneva, Switzerland

    Hatem Fessi
    UMR-CNRS 5007, Faculty of Pharmacy, Claude Bernard University Lyon I, Lyon, France

    Eric Doelker
    School of Pharmaceutical Sciences, Ecole de Pharmacie Geneve-Lausanne, University of Geneva, Geneva, Switzerland


    ABSTRACT

    Oral drug delivery is the preferred route of administration of drugs. Because of their versatility, nanoparticles often have been investigated for the delivery of a wide number of drugs by this route. This article first examines the physicochemical, pharmaceutical and technological aspects that make nanoparticles a potential oral delivery system for drugs and active biomolecules. Next, upon consideration of in vivo studies, the pharmacokinetic, pharmacological and therapeutic aspects of orally administered nanoparticles are described. Special emphasis is placed on improvement of oral bioavailability of drugs incorporated into nanoparticles. Two main mechanisms involved in enhancing drug absorption are discussed: the protection of drug by nanoparticles against harsh conditions in the gut and the prolongation of gastrointestinal transit of nanoparticles by using bioadhesive polymers. Furthermore, nanoparticle uptake by intestinal cells and oral vaccination by these colloidal carriers are also covered. In this context, the immune responses elicited as well as the protection against pathogens induced by antigen-loaded nanoparticles administered by the oral route are presented. Finally, the main limitations and perspectives of these colloidal carriers as oral drug delivery systems are discussed.

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