| Literature DB >> 28300659 |
Ashish K Agrawal1, Farrukh Aqil2, Jeyaprakash Jeyabalan3, Wendy A Spencer4, Joshua Beck4, Beth W Gachuki5, Sara S Alhakeem5, Karine Oben5, Radha Munagala2, Subbarao Bondada5, Ramesh C Gupta6.
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. Published by Elsevier Inc.Entities:
Keywords: Antitumor efficacy; Exosomes; Immunological responses; Lung cancer; Systemic toxicity; Taxol
Mesh:
Substances:
Year: 2017 PMID: 28300659 DOI: 10.1016/j.nano.2017.03.001
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307