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Preparation and optimisation of anionic liposomes for delivery of small peptides and cDNA to human corneal epithelial cells

机译:阴离子脂质体的制备和优化,用于向人角膜上皮细胞传递小肽和cDNA

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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 +/- 34nm and a charge of -18.2 +/- 1.3mV. After 2h 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.
机译:由于保护眼睛的内在机制,将药物递送至角膜上皮细胞具有挑战性。在这里,我们报道了一种新颖的脂质体制剂,可以将短序列肽封装并传递到人角膜上皮细胞(hTCEpi)中。使用磷脂酰胆碱/己酰胺/二油酰磷脂酰乙醇胺(PC / CAP / DOPE)的混合物,我们封装了荧光肽,得到的阴离子脂质体的平均大小为138.8 +/- 34nm,电荷为-18.2 +/- 1.3mV。与肽包封的脂质体温育2小时后,66%的角膜上皮(hTCEpi)细胞将FITC标记的肽内在化,证明了该制剂有效地将肽传递至hTCEpi细胞的能力。另外,脂质复合物(与质粒DNA复合的脂质体)也能够转染hTCEpi细胞,尽管水平适中(占细胞的8%)。在这里,我们描述了这种新颖的阴离子脂质体制剂,旨在增强小货物分子的就地递送。

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