| Literature DB >> 24486465 |
Mahasweta Das1, Chunyan Wang2, Raminder Bedi3, Shyam S Mohapatra4, Subhra Mohapatra5.
Abstract
Traumatic brain injury (TBI) causes significant mortality, long term disability and psychological symptoms. Gene therapy is a promising approach for treatment of different pathological conditions. Here we tested chitosan and polyethyleneimine (PEI)-coated magnetic micelles (CP-mag micelles or CPMMs), a potential MRI contrast agent, to deliver a reporter DNA to the brain after mild TBI (mTBI). CPMM-tomato plasmid (ptd) conjugate expressing a red-fluorescent protein (RFP) was administered intranasally immediately after mTBI or sham surgery in male SD rats. Evans blue extravasation following mTBI suggested CPMM-ptd entry into the brain via the compromised blood-brain barrier. Magnetofection increased the concentration of CPMMs in the brain. RFP expression was observed in the brain (cortex and hippocampus), lung and liver 48 h after mTBI. CPMM did not evoke any inflammatory response by themselves and were excreted from the body. These results indicate the possibility of using intranasally administered CPMM as a theranostic vehicle for mTBI. From the clinical editor: In this study, chitosan and PEI-coated magnetic micelles (CPMM) were demonstrated as potentially useful vehicles in traumatic brain injury in a rodent model. Magnetofection increased the concentration of CPMMs in the brain and, after intranasal delivery, CPMM did not evoke any inflammatory response and were excreted from the body.Entities:
Keywords: Bio-distribution; Brain; DNA delivery; LFPI; Magnetic micelle; TBI; Theranostic
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Year: 2014 PMID: 24486465 PMCID: PMC4338919 DOI: 10.1016/j.nano.2014.01.003
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307