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核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

壳聚糖用于核酸递送。

Chitosans for delivery of nucleic acids.

机构信息

Dept. Chemical Engineering and Inst. Biomedical Engineering, Ecole Polytechnique, Montreal, QC, Canada.

出版信息

Adv Drug Deliv Rev. 2013 Aug;65(9):1234-70. doi: 10.1016/j.addr.2013.07.005. Epub 2013 Jul 18.


DOI:10.1016/j.addr.2013.07.005
PMID:23872012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7103275/
Abstract

Alternatives to efficient viral vectors in gene therapy are desired because of their poor safety profiles. Chitosan is a promising non-viral nucleotide delivery vector because of its biocompatibility, biodegradability, low immunogenicity and ease of manufacturing. Since the transfection efficiency of chitosan polyplexes is relatively low compared to viral counterparts, there is an impetus to gain a better understanding of the structure-performance relationship. Recent progress in preparation and characterisation has enabled coupling analysis of chitosans structural parameters that has led to increased TE by tailoring of chitosan's structure. In this review, we summarize the recent advances that have lead to a more rational design of chitosan polyplexes. We present an integrated review of all major areas of chitosan-based transfection, including preparation, chitosan and polyplexes physicochemical characterisation, in vitro and in vivo assessment. In each, we present the obstacles to efficient transfection and the strategies adopted over time to surmount these impediments.

摘要

由于其安全性不佳,人们希望在基因治疗中寻找替代高效病毒载体的方法。壳聚糖由于其生物相容性、可生物降解性、低免疫原性和易于制造,是一种很有前途的非病毒核苷酸递送载体。由于与病毒相比,壳聚糖多聚物的转染效率相对较低,因此人们有动力更好地了解结构-性能关系。最近在制备和表征方面的进展使得可以对壳聚糖结构参数进行耦合分析,从而通过壳聚糖结构的调整来提高 TE。在这篇综述中,我们总结了最近的进展,这些进展使得更合理地设计壳聚糖多聚物成为可能。我们综合回顾了基于壳聚糖的转染的所有主要领域,包括制备、壳聚糖和多聚物的理化特性、体外和体内评估。在每一部分中,我们都介绍了高效转染的障碍以及随着时间的推移采用的克服这些障碍的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0c/7103275/3397643c576d/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0c/7103275/33547d4d2972/fx1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0c/7103275/1ae06b401755/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0c/7103275/30d1e6648672/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0c/7103275/a94b3c2a841a/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0c/7103275/3397643c576d/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0c/7103275/33547d4d2972/fx1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0c/7103275/1ae06b401755/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0c/7103275/30d1e6648672/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0c/7103275/a94b3c2a841a/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0c/7103275/3397643c576d/gr4_lrg.jpg

相似文献

[1]
Chitosans for delivery of nucleic acids.

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[2]
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[6]
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[7]
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[8]
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[10]
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本文引用的文献

[1]
Water-soluble N-[(2-hydroxy-3-trimethylammonium)propyl]chitosan chloride as a nucleic acids vector for cell transfection.

Carbohydr Polym. 2012-4-1

[2]
Ionization behavior of chitosan and chitosan-DNA polyplexes indicate that chitosan has a similar capability to induce a proton-sponge effect as PEI.

Biomacromolecules. 2013-5-15

[3]
Gene-carried hepatoma targeting complex induced high gene transfection efficiency with low toxicity and significant antitumor activity.

Int J Nanomedicine. 2012-6-27

[4]
Enhancement of chitosan nanoparticle-facilitated gene transfection by ultrasound both in vitro and in vivo.

J Biomed Mater Res B Appl Biomater. 2012-7-18

[5]
An inhalable β₂-adrenoceptor ligand-directed guanidinylated chitosan carrier for targeted delivery of siRNA to lung.

J Control Release. 2012-6-12

[6]
Tumor-homing poly-siRNA/glycol chitosan self-cross-linked nanoparticles for systemic siRNA delivery in cancer treatment.

Angew Chem Int Ed Engl. 2012-6-13

[7]
The effect of nanoparticle size, shape, and surface chemistry on biological systems.

Annu Rev Biomed Eng. 2012-4-18

[8]
Chitosan-based drug nanocarriers: where do we stand?

J Control Release. 2012-3-23

[9]
Low molecular weight chitosan nanoparticulate system at low N:P ratio for nontoxic polynucleotide delivery.

Int J Nanomedicine. 2012-3-13

[10]
Clinical and biological relevance of enhancer of zeste homolog 2 in triple-negative breast cancer.

Hum Pathol. 2012-3-19

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