Microfluidic formulation of lipid/polymer hybrid nanoparticles for plasmid DNA (pDNA) delivery

被引:19
|
作者
Santhanes, Diviya [1 ]
Wilkins, Alex [2 ]
Zhang, Huiming [3 ]
Aitken, Robert John [2 ]
Liang, Mingtao [1 ]
机构
[1] Univ Newcastle, Sch Biomed Sci & Pharm, Callaghan, NSW 2308, Australia
[2] Univ Newcastle, Prior Res Ctr Reprod Sci, Sch Environm & Life Sci, Callaghan, NSW 2308, Australia
[3] Univ Newcastle, Res & Innovat Div, Electron Microscopy & X ray Unit, Callaghan, NSW 2308, Australia
关键词
Microfluidics; PLGA; Nanoparticles; Plasmid DNA; Gene therapy; DRUG-DELIVERY; GENE DELIVERY; LIPOSOMES; PEPTIDE; NANOPRECIPITATION; MICROSPHERES; MICELLES; DESIGN;
D O I
10.1016/j.ijpharm.2022.122223
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Lipid/polymer hybrid nanoparticles loaded with red fluorescent protein (RFP) encoded plasmid DNA (pDNA) was formulated using poly-lactic-co-glycolic acid (PLGA), cationic lipid DC-cholesterol and surfactant mPEG2000- DSPE. A lipid/ polymer ratio of 1: 10 at 1 mg/mL surfactant concentration was found to be optimal for producing nanoparticles with diameters of 100-120 nm that remained stable upon ultracentrifugation. The production of lipid/ polymer hybrid nanoparticles was investigated using microfluidics with a toroidal mixer design. Our re-sults showed that the flow parameters significantly influenced the physicochemical characteristics of nano -particles and loading of pDNA was only achieved at flow rate ratio (FRR) of 3: 1. The pDNA associated with nanoparticles was demonstrated to be structurally intact using gel electrophoresis, and the encapsulation effi-ciency (EE) was measured to be-65%. The prepared hybrid nanoparticles resulted in 20% of transfection ef-ficacy in human embryonic kidney cells (HEK293T). This study demonstrated the potential of microfluidics in the development of hybrid nanoparticles for pDNA delivery, thus facilitating the clinical translation of DNA therapeutics.
引用
收藏
页数:12
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