Development of "CLAN" Nanomedicine for Nucleic Acid Therapeutics

被引:44
|
作者
Xu, Cong-Fei [1 ,2 ,3 ,4 ,5 ]
Iqbal, Shoaib [6 ]
Shen, Song [7 ,8 ]
Luo, Ying-Li [1 ,2 ]
Yang, Xianzhu [7 ,8 ,9 ]
Wang, Jun [1 ,2 ,3 ,4 ,5 ,9 ]
机构
[1] South China Univ Technol, Sch Med, Guangzhou Peoples Hosp 1, Guangzhou 510006, Guangdong, Peoples R China
[2] South China Univ Technol, Sch Biomed Sci & Engn, Guangzhou Int Campus, Guangzhou 510006, Guangdong, Peoples R China
[3] South China Univ Technol, Natl Engn Res Ctr Tissue Restorat & Reconstruct, Guangzhou 510006, Guangdong, Peoples R China
[4] South China Univ Technol, Key Lab Biomed Engn Guangdong Prov, Guangzhou 510006, Guangdong, Peoples R China
[5] South China Univ Technol, Innovat Ctr Tissue Restorat & Reconstruct, Guangzhou 510006, Guangdong, Peoples R China
[6] Univ Sci & Technol China, Sch Life Sci, Hefei 230027, Anhui, Peoples R China
[7] South China Univ Technol, Sch Med, Inst Life Sci, Guangzhou 510006, Guangdong, Peoples R China
[8] South China Univ Technol, Key Lab Biomed Mat & Engn, Minist Educ, Guangzhou 510006, Guangdong, Peoples R China
[9] Guangzhou Regenerat Med & Hlth Guangdong Lab, Guangzhou 510005, Guangdong, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金; 国家重点研发计划;
关键词
cationic lipid assisted nanoparticles; gene editing; nanomedicine; nucleic acid therapeutics; siRNA delivery; PEG-PLA NANOPARTICLES; SIRNA DELIVERY; PLGA NANOPARTICLES; POLYMERIC NANOPARTICLES; DRUG-DELIVERY; CANCER; THERAPY; INHIBITION; OLIGONUCLEOTIDES; INFLAMMATION;
D O I
10.1002/smll.201900055
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nucleic acid-based macromolecules have paved new avenues for the development of therapeutic interventions against a spectrum of diseases; however, their clinical translation is limited by successful delivery to the target site and cells. Therefore, numerous systems have been developed to overcome delivery challenges to nucleic acids. From the viewpoint of clinical translation, it is highly desirable to develop systems with clinically validated materials and controllability in synthesis. With this in mind, a cationic lipid assisted PEG-b-PLA nanoparticle (CLAN) is designed that is capable of protecting nucleic acids via encapsulation inside the aqueous core, and delivers them to target cells, while maintaining or improving nucleic acid function. The system is formulated from clinically validated components (PEG-b-PLA and its derivatives) and can be scaled-up for large scale manufacturing, offering potential for its future use in clinical applications. Here, the development and working mechanisms of CLANs, the ways to improve its delivery efficacy, and its application in various disease treatments are summarized. Finally, a prospective for the further development of CLAN is also discussed.
引用
收藏
页数:15
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