Matrix Mediated Viral Gene Delivery: A Review

被引:10
|
作者
Steinhaufft, Douglas [1 ,3 ]
Ghandehari, Hamidreza [1 ,2 ,3 ]
机构
[1] Univ Utah, Dept Biomed Engn, 36 South Wasatch Dr, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, 36 South Wasatch Dr, Salt Lake City, UT 84112 USA
[3] Nano Inst Utah, Utah Ctr Nanomed, 36 South Wasatch Dr, Salt Lake City, UT 84112 USA
基金
美国国家卫生研究院;
关键词
ELASTINLIKE PROTEIN POLYMER; MESENCHYMAL STEM-CELLS; IN-VIVO EVALUATION; ADENOASSOCIATED VIRUS SEROTYPE-2; LOCALIZED LENTIVIRUS DELIVERY; BONE MORPHOGENETIC PROTEIN-7; MATURE VACCINIA VIRUS; CONTROLLED-RELEASE; RECOMBINANT ADENOVIRUS; FIBRIN SCAFFOLD;
D O I
10.1021/acs.bioconjchem.8b00853
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Polymeric matrices inherently protect viral vectors from preexisting immune conditions, limit dissemination to off-target sites, and can sustain vector release. Advancing methodologies in development of particulate based vehicles have led to improved encapsulation of viral vectors. Polymeric delivery systems have contributed to increasing cellular transduction, responsive release mechanisms, cellular infiltration, and cellular signaling. Synthetic polymers are easily customizable, and are capable of balancing matrix retention with cellular infiltration. Natural polymers contain inherent biorecognizable motifs adding therapeutic efficacy to the incorporated viral vector. Recombinant polymers use highly conserved motifs to carefully engineer matrices, allowing for precise design including elements of vector retention and responsive release mechanisms. Composite polymer systems provide opportunities to create matrices with unique properties. Carefully designed matrices can control spatiotemporal release patterns that synergize with approaches in regenerative medicine and antitumor therapies.
引用
收藏
页码:384 / 399
页数:16
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