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      Milk-derived exosomes for oral delivery of paclitaxel.

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          Abstract

          In this report milk-derived exosomes have been investigated for oral delivery of the chemotherapeutic drug paclitaxel (PAC) as an alternative to conventional i.v. therapy for improved efficacy and reduced toxicity. PAC-loaded exosomes (ExoPAC) were found to have a particle size of ~108 nm, a narrow particle size distribution (PDI ~0.190), zeta potential (~ -7 mV) and a practical loading efficiency of ~8%. Exosomes and ExoPAC exhibited excellent stability in the presence of simulated-gastrointestinal fluids, and during the storage at -80 °C. A sustained release of PAC was also observed up to 48 h in vitro using PBS (pH 6.8). Importantly, ExoPAC delivered orally showed significant tumor growth inhibition (60%; P<0.001) against human lung tumor xenografts in nude mice. Treatment with i.p. PAC at the same dose as ExoPAC, however, showed modest but statistically insignificant inhibition (31%). Moreover, ExoPAC demonstrated remarkably lower systemic and immunologic toxicities as compared to i.v. PAC.

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          Author and article information

          Journal
          Nanomedicine
          Nanomedicine : nanotechnology, biology, and medicine
          Elsevier BV
          1549-9642
          1549-9634
          Jul 2017
          : 13
          : 5
          Affiliations
          [1 ] James Graham Brown Cancer Center, University of Louisville, Louisville, KY.
          [2 ] James Graham Brown Cancer Center, University of Louisville, Louisville, KY; Department of Medicine, University of Louisville, Louisville, KY.
          [3 ] Department of Medicine, University of Louisville, Louisville, KY.
          [4 ] 3P Biotechnologies, Inc., Louisville, KY.
          [5 ] Department of Microbiology, Immunology & Molecular Genetics, and Markey Cancer Center, University of Kentucky, Lexington, KY.
          [6 ] James Graham Brown Cancer Center, University of Louisville, Louisville, KY; 3P Biotechnologies, Inc., Louisville, KY; Department of Pharmacology and Toxicology, University of Louisville, Louisville, KY. Electronic address: rcgupta@louisville.edu.
          Article
          S1549-9634(17)30043-6
          10.1016/j.nano.2017.03.001
          28300659
          6ffb9b03-e761-4da9-a505-3b69089c8b19
          History

          Antitumor efficacy,Taxol,Systemic toxicity,Lung cancer,Immunological responses,Exosomes

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