Nanocarrier-Mediated Cytosolic Delivery of Biopharmaceuticals

被引:135
|
作者
He, Wei [2 ]
Xing, Xuyang [2 ]
Wang, Xiaoling [3 ]
Wu, Debra [1 ,4 ]
Wu, Wei [5 ]
Guo, Junling [3 ,4 ]
Mitragotri, Samir [1 ,4 ]
机构
[1] Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[2] China Pharmaceut Univ, Sch Pharm, Dept Pharmaceut, Nanjing 210009, Peoples R China
[3] Sichuan Univ, Sch Biomass Sci & Engn, Chengdu 610065, Peoples R China
[4] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02115 USA
[5] Fudan Univ, Sch Pharm, Minist Educ China, Key Lab Smart Drug Delivery, Shanghai 201203, Peoples R China
关键词
biopharmaceuticals; cytosolic delivery; endosomal escape; intracellular delivery; nanocarriers; HIGH-DENSITY-LIPOPROTEIN; SUPPORTED LIPID-BILAYERS; IN-VIVO FATE; INTRACELLULAR DELIVERY; CELLULAR UPTAKE; DRUG-DELIVERY; PROTEIN DELIVERY; ANTIMICROBIAL PEPTIDES; ENDOSOMAL ESCAPE; SIRNA DELIVERY;
D O I
10.1002/adfm.201910566
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biopharmaceuticals have emerged to play a vital role in disease treatment and have shown promise in the rapidly expanding pharmaceutical market due to their high specificity and potency. However, the delivery of these biologics is hindered by various physiological barriers, owing primarily to the poor cell membrane permeability, low stability, and increased size of biologic agents. Since many biological drugs are intended to function by interacting with intracellular targets, their delivery to intracellular targets is of high relevance. In this review, the authors summarize and discuss the use of nanocarriers for intracellular delivery of biopharmaceuticals via endosomal escape and, especially, the routes of direct cytosolic delivery by means including the caveolae-mediated pathway, contact release, intermembrane transfer, membrane fusion, direct translocation, and membrane disruption. Strategies with high potential for translation are highlighted. Finally, the authors conclude with the clinical translation of promising carriers and future perspectives.
引用
收藏
页数:22
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