Amani Amin, Kabiri Toraj, Shafiee Samira, Hamidi Aliasghar
Biotechnology Research Center, Department of Medicinal Chemistry, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Agronomy and Plant Breeding, Faculty of Agriculture, University of Mohaghegh Ardabili, Ardabil, Iran.
Iran J Pharm Res. 2019 Winter;18(1):125-141.
Tri-block poly (lactide) poly(ethylene glycol) poly(lactide) (PLA-PEG-PLA) copolymers are among the most attractive nano-carriers for gene delivery into mammalian cells, due to their biocompatibility and biodegradability properties. However, the low efficiency of the gene delivery by these copolymers is an obstacle to gene therapy. Here, we have investigated nanoparticles formulated using the polyethylenimine (PEI) associated with PLA-PEG-PLA copolymer for efficient DNA encapsulation and delivery. PLA-PEG-PLA/DNA and PLA-PEG-PLA/PEI/DNA nanoparticles with different concentrations of PEI were prepared by the double emulsion-solvent evaporation technique. PLA-PEG-PLA/PEI/DNA were characterized for particle size, zeta potential, morphology, biocompatibility, DNA protection, DNA release, and their ability for gene delivery into MCF-7 cells. We found that enhancing the mass ratio of PEI: (PLA-PEG-PLA) (w/w%) in the PLA-PEG-PLA/PEI/DNA nanoparticles results in an increase in particles size, zeta potential, encapsulation efficiency, and DNA release. The electrophoretic analysis confirmed that the PLA-PEG-PLA and PLA-PEG-PLA/PEI could protect DNA from ultrasound damage and nuclease degradation. MTT assay showed that the PLA-PEG-PLA/PEI/DNA had low cytotoxicity than PEI complexes. The potential of PLA-PEG-PLA/PEI/DNA nanoparticles with different concentrations of PEI as a non-viral gene delivery vector for transferring pEGFP-N1 to MCF-7 cells was examined by fluorescent microscopy and flow cytometry. The flow cytometry analysis revealed that by increasing the mass ratio of PEI: (PLA-PEG-PLA) (w/w%) in PLA-PEG-PLA/PEI/DNA nanoparticles, the efficiency of the gene delivery into MCF-7 cells was improved. The results also demonstrated that PLA-PEG-PLA/PEI/DNA nanoparticles in the serum medium improved the efficiency of gene delivery more than two-fold, compared to PEI/DNA complex.
三嵌段聚(丙交酯)-聚(乙二醇)-聚(丙交酯)(PLA-PEG-PLA)共聚物因其生物相容性和生物降解性,是用于将基因导入哺乳动物细胞的最具吸引力的纳米载体之一。然而,这些共聚物基因递送效率低是基因治疗的一个障碍。在此,我们研究了使用与PLA-PEG-PLA共聚物相关的聚乙烯亚胺(PEI)制备的纳米颗粒,用于高效DNA包封和递送。通过双乳液-溶剂蒸发技术制备了具有不同PEI浓度的PLA-PEG-PLA/DNA和PLA-PEG-PLA/PEI/DNA纳米颗粒。对PLA-PEG-PLA/PEI/DNA进行了粒径、zeta电位、形态、生物相容性、DNA保护、DNA释放以及它们将基因递送至MCF-7细胞的能力等方面的表征。我们发现,提高PLA-PEG-PLA/PEI/DNA纳米颗粒中PEI:(PLA-PEG-PLA)的质量比(w/w%)会导致粒径、zeta电位、包封效率和DNA释放增加。电泳分析证实,PLA-PEG-PLA和PLA-PEG-PLA/PEI可以保护DNA免受超声损伤和核酸酶降解。MTT分析表明,PLA-PEG-PLA/PEI/DNA的细胞毒性低于PEI复合物。通过荧光显微镜和流式细胞术检测了具有不同PEI浓度的PLA-PEG-PLA/PEI/DNA纳米颗粒作为非病毒基因递送载体将pEGFP-N1转移至MCF-7细胞的潜力。流式细胞术分析表明,通过提高PLA-PEG-PLA/PEI/DNA纳米颗粒中PEI:(PLA-PEG-PLA)的质量比(w/w%),基因递送至MCF-7细胞的效率得到提高。结果还表明,与PEI/DNA复合物相比,血清培养基中的PLA-PEG-PLA/PEI/DNA纳米颗粒将基因递送效率提高了两倍以上。