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Milk-derived exosomes for oral delivery of paclitaxel.
Agrawal, Ashish K; Aqil, Farrukh; Jeyabalan, Jeyaprakash; Spencer, Wendy A; Beck, Joshua; Gachuki, Beth W; Alhakeem, Sara S; Oben, Karine; Munagala, Radha; Bondada, Subbarao; Gupta, Ramesh C.
Afiliación
  • Agrawal AK; James Graham Brown Cancer Center, University of Louisville, Louisville, KY.
  • Aqil F; James Graham Brown Cancer Center, University of Louisville, Louisville, KY; Department of Medicine, University of Louisville, Louisville, KY.
  • Jeyabalan J; Department of Medicine, University of Louisville, Louisville, KY.
  • Spencer WA; 3P Biotechnologies, Inc., Louisville, KY.
  • Beck J; 3P Biotechnologies, Inc., Louisville, KY.
  • Gachuki BW; Department of Microbiology, Immunology & Molecular Genetics, and Markey Cancer Center, University of Kentucky, Lexington, KY.
  • Alhakeem SS; Department of Microbiology, Immunology & Molecular Genetics, and Markey Cancer Center, University of Kentucky, Lexington, KY.
  • Oben K; Department of Microbiology, Immunology & Molecular Genetics, and Markey Cancer Center, University of Kentucky, Lexington, KY.
  • Munagala R; James Graham Brown Cancer Center, University of Louisville, Louisville, KY; Department of Medicine, University of Louisville, Louisville, KY.
  • Bondada S; Department of Microbiology, Immunology & Molecular Genetics, and Markey Cancer Center, University of Kentucky, Lexington, KY.
  • Gupta RC; 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.
Nanomedicine ; 13(5): 1627-1636, 2017 07.
Article en En | MEDLINE | ID: mdl-28300659
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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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Paclitaxel / Exosomas / Antineoplásicos Fitogénicos Límite: Animals / Humans Idioma: En Revista: Nanomedicine Asunto de la revista: BIOTECNOLOGIA Año: 2017 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Paclitaxel / Exosomas / Antineoplásicos Fitogénicos Límite: Animals / Humans Idioma: En Revista: Nanomedicine Asunto de la revista: BIOTECNOLOGIA Año: 2017 Tipo del documento: Article