| Literature DB >> 27530524 |
Luís F Neves1, Jinghua Duan2,3, Adrienne Voelker1, Anil Khanal4, Lacey McNally4, Jill Steinbach-Rankins1,2,3, Brian P Ceresa1,4.
Abstract
Drug delivery to corneal epithelial cells is challenging due to the intrinsic mechanisms that protect the eye. Here, we report a novel liposomal formulation to encapsulate and deliver a short sequence peptide into human corneal epithelial cells (hTCEpi). Using a mixture of Phosphatidylcholine/Caproylamine/Dioleoylphosphatidylethanolamine (PC/CAP/DOPE), we encapsulated a fluorescent peptide, resulting in anionic liposomes with an average size of 138.8 ± 34 nm and a charge of -18.2 ± 1.3 mV. After 2 h incubation with the peptide-encapsulated liposomes, 66% of corneal epithelial (hTCEpi) cells internalised the FITC-labelled peptide, demonstrating the ability of this formulation to effectively deliver peptide to hTCEpi cells. Additionally, lipoplexes (liposomes complexed with plasmid DNA) were also able to transfect hTCEpi cells, albeit at a modest level (8% of the cells). Here, we describe this novel anionic liposomal formulation intended to enhance the delivery of small cargo molecules in situ.Entities:
Keywords: Peptide; liposomes; ophthalmic delivery; plasmid DNA
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Year: 2016 PMID: 27530524 PMCID: PMC5033054 DOI: 10.1080/02652048.2016.1202343
Source DB: PubMed Journal: J Microencapsul ISSN: 0265-2048 Impact factor: 3.142