Synthetic Approaches for Nucleic Acid Delivery: Choosing the Right Carriers

被引:52
作者
Ni, Rong [1 ,2 ]
Feng, Ruilu [1 ]
Chau, Ying [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Chem & Biol Engn, Kowloon, Clear Water Bay, Hong Kong 999077, Peoples R China
[2] Hong Kong Univ Sci & Technol, Inst Adv Study, Kowloon, Clear Water Bay, Hong Kong 999077, Peoples R China
来源
LIFE-BASEL | 2019年 / 9卷 / 03期
关键词
synthetic approach; nucleic acid delivery; intracellular barriers; endosomal escape; nuclear trafficking; synthetic carrier; artificial virus; CELL-PENETRATING PEPTIDE; LIPOSOME-DNA COMPLEXES; VIRUS-LIKE PARTICLES; GENE DELIVERY; INTRACELLULAR TRAFFICKING; SIRNA DELIVERY; MESSENGER-RNA; PLASMID DNA; TRANSFECTION EFFICIENCY; IN-VIVO;
D O I
10.3390/life9030059
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The discovery of the genetic roots of various human diseases has motivated the exploration of different exogenous nucleic acids as therapeutic agents to treat these genetic disorders (inherited or acquired). However, the physicochemical properties of nucleic acids render them liable to degradation and also restrict their cellular entrance and gene translation/inhibition at the correct cellular location. Therefore, gene condensation/protection and guided intracellular trafficking are necessary for exogenous nucleic acids to function inside cells. Diversified cationic formulation materials, including natural and synthetic lipids, polymers, and proteins/peptides, have been developed to facilitate the intracellular transportation of exogenous nucleic acids. The chemical properties of different formulation materials determine their special features for nucleic acid delivery, so understanding the property-function correlation of the formulation materials will inspire the development of next-generation gene delivery carriers. Therefore, in this review, we focus on the chemical properties of different types of formulation materials and discuss how these formulation materials function as protectors and cellular pathfinders for nucleic acids, bringing them to their destination by overcoming different cellular barriers.
引用
收藏
页数:28
相关论文
共 176 条
[31]   A Targeted and Stable Polymeric Nanoformulation Enhances Systemic Delivery of mRNA to Tumors [J].
Chen, Qixian ;
Qi, Ruogu ;
Chen, Xiyi ;
Yang, Xi ;
Wu, Sudong ;
Xiao, Haihua ;
Dong, Wenfei .
MOLECULAR THERAPY, 2017, 25 (01) :92-101
[32]   Fabrication of dual responsive co-delivery system based on three-armed peptides for tumor therapy [J].
Chen, Si ;
Lei, Qi ;
Li, Shi-Ying ;
Qin, Si-Yong ;
Jia, Hui-Zhen ;
Cheng, Yin-Jia ;
Zhang, Xian-Zheng .
BIOMATERIALS, 2016, 92 :25-35
[33]   Cell surface nucleolin serves as receptor for DNA nanoparticles composed of pegylated polylysine and DNA [J].
Chen, Xuguang ;
Kube, Dianne M. ;
Cooper, Mark J. ;
Davis, Pamela B. .
MOLECULAR THERAPY, 2008, 16 (02) :333-342
[34]   The role of helper lipids in lipid nanoparticles (LNPs) designed for oligonucleotide delivery [J].
Cheng, Xinwei ;
Lee, Robert J. .
ADVANCED DRUG DELIVERY REVIEWS, 2016, 99 :129-137
[35]   Self-aggregating 1.8 kDa polyethylenimines with dissolution switch at endosomal acidic pH are delivery carriers for plasmid DNA, mRNA, siRNA and exon-skipping oligonucleotides [J].
Chiper, Manuela ;
Tounsi, Nassera ;
Kole, Ryszard ;
Kichler, Antoine ;
Zuber, Guy .
JOURNAL OF CONTROLLED RELEASE, 2017, 246 :60-70
[36]   Quantification of plasmid DNA copies in the nucleus after lipoplex and polyplex transfection [J].
Cohen, Richard N. ;
van der Aa, Marieke A. E. M. ;
Macaraeg, Nichole ;
Lee, Ai Ping ;
Szoka, Francis C., Jr. .
JOURNAL OF CONTROLLED RELEASE, 2009, 135 (02) :166-174
[37]   Gene transfection efficiency of tracheal epithelial cells by DC-Chol-DOPE/DNA complexes [J].
Colosimo, A ;
Serafino, A ;
Sangiuolo, F ;
Di Sario, S ;
Bruscia, E ;
Amicucci, P ;
Novelli, G ;
Dallapiccola, B ;
Mossa, G .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1999, 1419 (02) :186-194
[38]   Intracellular trafficking of cationic liposome-DNA complexes in living cells [J].
Coppola, Stefano ;
Estrada, Laura C. ;
Digman, Michelle A. ;
Pozzi, Daniela ;
Cardarelli, Francesco ;
Gratton, Enrico ;
Caracciolo, Giulio .
SOFT MATTER, 2012, 8 (30) :7919-7927
[39]   Targeting cyclin B1 through peptide-based delivery of siRNA prevents tumour growth [J].
Crombez, Laurence ;
Morris, May Catherine ;
Dufort, Sandrine ;
Aldrian-Herrada, Gudrun ;
Nguyen, Quan ;
Mc Master, Gary ;
Coll, Jean-Luc ;
Heitz, Frederic ;
Divita, Gilles .
NUCLEIC ACIDS RESEARCH, 2009, 37 (14) :4559-4569
[40]   A New Potent Secondary Amphipathic Cell-penetrating Peptide for siRNA Delivery Into Mammalian Cells [J].
Crombez, Laurence ;
Aldrian-Herrada, Gudrun ;
Konate, Karidia ;
Nguyen, Quan N. ;
McMaster, Gary K. ;
Brasseur, Robert ;
Heitz, Frederic ;
Divita, Gilles .
MOLECULAR THERAPY, 2009, 17 (01) :95-103