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      Drug delivery by red blood cells: vascular carriers designed by mother nature.

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      Expert opinion on drug delivery
      Informa UK Limited

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          Abstract

          Vascular delivery of several classes of therapeutic agents may benefit from carriage by red blood cells (RBC), for example, drugs that require delivery into phagocytic cells and those that must act within the vascular lumen. The fact that several protocols of infusion of RBC-encapsulated drugs are now being explored in patients illustrates a high biomedical importance for the field. AREAS COVERED BY THIS REVIEW: Two strategies for RBC drug delivery are discussed: encapsulation into isolated RBC ex vivo followed by infusion in compatible recipients and coupling therapeutics to the surface of RBC. Studies of pharmacokinetics and effects in animal models and in human studies of diverse therapeutic enzymes, antibiotics and other drugs encapsulated in RBC are described and critically analyzed. Coupling to RBC surface of compounds regulating immune response and complement, affinity ligands, polyethylene glycol alleviating immune response to donor RBC and fibrinolytic plasminogen activators are described. Also described is a new, translation-prone approach for RBC drug delivery by injection of therapeutics conjugated with fragments of antibodies providing safe anchoring of cargoes to circulating RBC, without need for ex vivo modification and infusion of RBC.

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          Author and article information

          Journal
          Expert Opin Drug Deliv
          Expert opinion on drug delivery
          Informa UK Limited
          1744-7593
          1742-5247
          Apr 2010
          : 7
          : 4
          Affiliations
          [1 ] University of Pennsylvania Medical Center, Department of Pharmacology and Program in Targeted Therapeutics of Institute of Translational Medicine and Therapeutics, IFEM, One John Morgan Building, 3620 Hamilton Walk, Philadelphia, PA 19104-6068, USA. Muzykant@mail.med.upenn.edu
          Article
          NIHMS171360
          10.1517/17425241003610633
          2844929
          20192900
          fbfd0192-f63a-49cf-935d-67118e77a150
          History

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