Preparation and Characterization of PLA-PEG-PLA/PEI/DNA Nanoparticles for Improvement of Transfection Efficiency and Controlled Release of DNA in Gene Delivery Systems.

基因传递 生物相容性 PEG比率 Zeta电位 聚乙烯亚胺 化学 转染 乙二醇 纳米颗粒 材料科学 纳米技术 生物化学 有机化学 基因 财务 经济
作者
Amin Amani,Toraj Kabiri,Samira Shafiee,A. A. Hamidi
出处
期刊:PubMed 卷期号:18 (1): 125-141 被引量:8
链接
标识
摘要

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.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
大模型应助小萝卜采纳,获得10
刚刚
晒鱼干的大喵完成签到,获得积分10
刚刚
繁荣的又亦完成签到 ,获得积分10
刚刚
sun发布了新的文献求助10
刚刚
Jasper应助坚强的笑天采纳,获得30
1秒前
辛勤的诗柳应助无脸男采纳,获得10
1秒前
1秒前
1秒前
2秒前
andy完成签到,获得积分10
2秒前
Qiancheni完成签到,获得积分10
3秒前
赘婿应助猫儿采纳,获得10
3秒前
3秒前
浮游应助小谢采纳,获得10
3秒前
4秒前
Shaineli发布了新的文献求助30
4秒前
maz123456发布了新的文献求助10
4秒前
4秒前
4秒前
林深见鹿发布了新的文献求助10
4秒前
深情秋刀鱼完成签到,获得积分10
5秒前
5秒前
量子星尘发布了新的文献求助10
5秒前
6秒前
研友_pLw6o8发布了新的文献求助10
6秒前
CipherSage应助墨然然采纳,获得10
7秒前
7秒前
ding应助rubo采纳,获得10
7秒前
7秒前
我要留学应助Katyusha采纳,获得10
7秒前
凛冰给凛冰的求助进行了留言
7秒前
蓝天完成签到,获得积分10
8秒前
小蘑菇应助chf102采纳,获得10
9秒前
wbhou完成签到 ,获得积分10
9秒前
123完成签到,获得积分10
10秒前
frl发布了新的文献求助10
10秒前
孤独丹秋发布了新的文献求助10
11秒前
11秒前
ikki发布了新的文献求助10
11秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Разработка технологических основ обеспечения качества сборки высокоточных узлов газотурбинных двигателей,2000 1000
Vertebrate Palaeontology, 5th Edition 510
碳捕捉技术能效评价方法 500
Optimization and Learning via Stochastic Gradient Search 500
Nuclear Fuel Behaviour under RIA Conditions 500
Why America Can't Retrench (And How it Might) 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 催化作用 遗传学 冶金 电极 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 4690190
求助须知:如何正确求助?哪些是违规求助? 4062316
关于积分的说明 12560350
捐赠科研通 3759943
什么是DOI,文献DOI怎么找? 2076535
邀请新用户注册赠送积分活动 1105263
科研通“疑难数据库(出版商)”最低求助积分说明 984007