已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Engineering blood exosomes for tumor-targeting efficient gene/chemo combination therapy

微泡 遗传增强 癌症研究 医学 基因 化学 小RNA 生物化学
作者
Qiang Zhan,Kaikai Yi,Hongzhao Qi,Sidi Li,Xueping Li,Qixue Wang,Yunfei Wang,Chaoyong Liu,Ming-zhe Qiu,Xubo Yuan,Jin Zhao,Xin Hou,Chunsheng Kang
出处
期刊:Theranostics [Ivyspring International Publisher]
卷期号:10 (17): 7889-7905 被引量:107
标识
DOI:10.7150/thno.45028
摘要

Rationale: Developing an effective nanoplatform to realize 'multi-in-one' is essential to broaden the therapeutic potential of combination therapy. Exosomes are ideal candidates since their intrinsic abilities of integrating multiple contents and functions. However, only limited efforts have been devoted to engineering exosomes to integrate the needed properties, also considering the safety and yield, for tumor-targeted and efficient gene/chemo combination therapy. Methods: Herein, by manipulating the exosome membrane, blood exosomes with high abundance and safety are engineered as a versatile combinatorial delivery system, where the doxorubicin (Dox) and cholesterol-modified miRNA21 inhibitor (miR-21i) are co-embedded into the lipid bilayer of exosomes, and the magnetic molecules and endosomolytic peptides L17E are bind to the exosome membrane through ligand-receptor coupling and electrostatic interactions, respectively. Results: It is proved that such engineering strategy not only preserves their intrinsic features, but also readily integrates multiple properties of tumor targeting, efficient transfection and gene/chemo combination therapy into blood exosomes. The lipid bilayer structure of exosomes allows them to co-load Dox and miR-21i with high-payloads. Moreover, profiting from the integration of magnetic molecules and L17E peptides, the engineered exosomes exhibit an enhanced tumor accumulation and an improved endosome escape ability, thereby specifically and efficiently delivering encapsulated cargos to tumor cells. As a result, a remarkable inhibition of tumor growth is observed in the tumor-bearing mice, and without noticeable side effects. Conclusions: This study demonstrates the potential of engineered blood exosomes as feasible co-delivery nanosystem for tumor-targeted and efficient combination therapy. Further development by replacing the drugs combined regimens can potentially make this engineered exosome become a general platform for the design of safe and effective combination therapy modality.

科研通智能强力驱动
Strongly Powered by AbleSci AI
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
科研通AI6.2应助孙笑川258采纳,获得10
1秒前
2秒前
意义发布了新的文献求助10
2秒前
123完成签到 ,获得积分10
4秒前
LA发布了新的文献求助30
8秒前
图图完成签到,获得积分10
8秒前
9秒前
9秒前
9秒前
熊猫海发布了新的文献求助10
10秒前
意义完成签到,获得积分10
10秒前
张亚妮完成签到,获得积分20
10秒前
Akim应助tcf采纳,获得10
10秒前
ding应助调皮的蓝天采纳,获得10
11秒前
11秒前
斯文败类应助星空采纳,获得10
13秒前
14秒前
Jane发布了新的文献求助10
15秒前
69完成签到,获得积分10
16秒前
77完成签到 ,获得积分10
17秒前
关G完成签到 ,获得积分10
18秒前
18秒前
kkk发布了新的文献求助10
18秒前
科研通AI6.3应助陈中航采纳,获得10
19秒前
维生素发布了新的文献求助10
20秒前
明年发布了新的文献求助10
23秒前
格格完成签到,获得积分10
23秒前
24秒前
Cancellerzz完成签到,获得积分10
25秒前
科研通AI6.4应助童话金采纳,获得10
27秒前
yuyu完成签到,获得积分10
28秒前
科研通AI6.4应助kkk采纳,获得10
29秒前
852应助LMX采纳,获得10
29秒前
30秒前
xmm完成签到,获得积分10
31秒前
31秒前
32秒前
32秒前
Rain发布了新的文献求助10
33秒前
Alex应助shunshun51213采纳,获得30
34秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(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
Molecular Mechanisms of Photosynthesis, 4th Edition 1000
Organic Reactions, Volume 116 1000
Matrix Methods in Data Mining and Pattern Recognition 510
Reading and Understanding Health Research 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7252185
求助须知:如何正确求助?哪些是违规求助? 8874579
关于积分的说明 18732879
捐赠科研通 6932240
什么是DOI,文献DOI怎么找? 3199651
关于科研通互助平台的介绍 2374362
邀请新用户注册赠送积分活动 2174251