| Literature DB >> 30884095 |
Cong-Fei Xu1,2,3,4, Shoaib Iqbal5, Song Shen6,7, Ying-Li Luo1,2, Xianzhu Yang6,7,8, Jun Wang1,2,3,4,8.
Abstract
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.Entities:
Keywords: cationic lipid assisted nanoparticles; gene editing; nanomedicine; nucleic acid therapeutics; siRNA delivery
Year: 2019 PMID: 30884095 DOI: 10.1002/smll.201900055
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281