Controlling endosomal escape using nanoparticle composition: current progress and future perspectives

被引:76
作者
Cupic, Kristofer I. [1 ,2 ]
Rennick, Joshua J. [2 ]
Johnston, Angus P. R. [2 ,3 ]
Such, Georgina K. [1 ]
机构
[1] Univ Melbourne, Sch Chem, Melbourne, Vic 3010, Australia
[2] Monash Univ, Drug Delivery Disposit & Dynam, Monash Inst Pharmaceut Sci, Parkville, Vic 3052, Australia
[3] Monash Univ, ARC Ctr Excellence Convergent Bionano Sci & Techn, Parkville, Vic 3052, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
endosomal escape; membrane interaction; nanoparticles; pH-responsive polymers; proton sponge; therapeutic delivery; N-SUBSTITUTED POLYASPARTAMIDES; GENE DELIVERY; INTRACELLULAR DELIVERY; RADICAL POLYMERIZATION; CYTOSOLIC DELIVERY; SIDE-CHAIN; PH; POLYMERS; CELLS; MOLECULES;
D O I
10.2217/nnm-2018-0326
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Polymer nanoparticles offer significant benefits for improving delivery of biological therapeutics such as DNA and proteins, as they allow the cargo to be protected until it is delivered to a target cell. However, there are still challenges with achieving efficient delivery to the optimal cellular region. One significant roadblock is escape of nanoparticles from within the endosomal/lysosomal compartments into the cytosol. Here, we review the recent advances in understanding endosomal escape of polymer nanoparticles. We also discuss the current progress on investigating how nanoparticle structure can control endosomal escape. It is important to understand the fundamental biological processes that govern endosomal escape in order to design more effective therapeutic delivery systems.
引用
收藏
页码:215 / 223
页数:9
相关论文
共 50 条
[1]   Shrinkage of a rapidly growing tumor by drug-loaded polymersomes: pH-triggered release through copolymer degradation [J].
Ahmed, Fariyal ;
Pakunlu, Refika I. ;
Srinivas, Goundla ;
Brannan, Aaron ;
Bates, Frank ;
Klein, Michael L. ;
Minko, Tamara ;
Discher, Dennis E. .
MOLECULAR PHARMACEUTICS, 2006, 3 (03) :340-350
[2]   The Possible "Proton Sponge" Effect of Polyethylenimine (PEI) Does Not Include Change in Lysosomal pH [J].
Benjaminsen, Rikke V. ;
Mattebjerg, Maria A. ;
Henriksen, Jonas R. ;
Moghimi, S. Moein ;
Andresen, Thomas L. .
MOLECULAR THERAPY, 2013, 21 (01) :149-157
[3]   Intracellular Delivery System for Antibody-Peptide Drug Conjugates [J].
Berguig, Geoffrey Y. ;
Convertine, Anthony J. ;
Frayo, Shani ;
Kern, Hanna B. ;
Procko, Erik ;
Roy, Debashish ;
Srinivasan, Selvi ;
Margineantu, Daciana H. ;
Booth, Garrett ;
Palanca-Wessels, Maria Corinna ;
Baker, David ;
Hockenbery, David ;
Press, Oliver W. ;
Stayton, Patrick S. .
MOLECULAR THERAPY, 2015, 23 (05) :907-917
[4]   Intracellular route and transcriptional competence of polyethylenimine-DNA complexes [J].
Bieber, T ;
Meissner, W ;
Kostin, S ;
Niemann, A ;
Elsasser, HP .
JOURNAL OF CONTROLLED RELEASE, 2002, 82 (2-3) :441-454
[5]   PLGA-PEI nanoparticles for gene delivery to pulmonary epithelium [J].
Bivas-Benita, M ;
Romeijn, S ;
Junginger, HE ;
Borchard, G .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2004, 58 (01) :1-6
[6]   A VERSATILE VECTOR FOR GENE AND OLIGONUCLEOTIDE TRANSFER INTO CELLS IN CULTURE AND IN-VIVO - POLYETHYLENIMINE [J].
BOUSSIF, O ;
LEZOUALCH, F ;
ZANTA, MA ;
MERGNY, MD ;
SCHERMAN, D ;
DEMENEIX, B ;
BEHR, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7297-7301
[7]   Endocytosis at the nanoscale [J].
Canton, Irene ;
Battaglia, Giuseppe .
CHEMICAL SOCIETY REVIEWS, 2012, 41 (07) :2718-2739
[8]   Living free-radical polymerization by reversible addition-fragmentation chain transfer: The RAFT process [J].
Chiefari, J ;
Chong, YK ;
Ercole, F ;
Krstina, J ;
Jeffery, J ;
Le, TPT ;
Mayadunne, RTA ;
Meijs, GF ;
Moad, CL ;
Moad, G ;
Rizzardo, E ;
Thang, SH .
MACROMOLECULES, 1998, 31 (16) :5559-5562
[9]   Development of a novel endosomolytic diblock copolymer for siRNA delivery [J].
Convertine, Anthony J. ;
Benoit, Danielle S. W. ;
Duvall, Craig L. ;
Hoffman, Allan S. ;
Stayton, Patrick S. .
JOURNAL OF CONTROLLED RELEASE, 2009, 133 (03) :221-229
[10]   Endosomal escape of polymeric gene delivery complexes is not always enhanced by polymers buffering at low pH [J].
Funhoff, AM ;
van Nostrum, CF ;
Koning, GA ;
Schuurmans-Nieuwenbroek, NME ;
Crommelin, DJA ;
Hennink, WE .
BIOMACROMOLECULES, 2004, 5 (01) :32-39