Designing siRNA/chitosan-methacrylate complex nanolipogel for prolonged gene silencing effects

• Published in: Scientific reports Vol. 12; no. 1; pp. 3527 - 13
• Main Authors: Cao, Ye, Tan, Yang Fei, Wong, Yee Shan, Aminuddin, Muhammad, Ramya, Bhuthalingam, Liew, Melvin Wen Jie, Liu, Jiaxin, Venkatraman, Subbu S.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 03.03.2022; Nature Publishing Group; Nature Portfolio
• Subjects: 631/154; 639/925; Chitosan; Chitosan - metabolism; Clinical trials; Controlled release; Cytoplasm; Delayed-Action Preparations; Encapsulation; Endocytosis; Gene Silencing; Gene therapy; Humanities and Social Sciences; Lipids; Materials science; Methacrylates; multidisciplinary; Nanoparticles; Polymers; RNA, Small Interfering - genetics; RNA, Small Interfering - metabolism; Science; Science (multidisciplinary); Severe acute respiratory syndrome coronavirus 2; siRNA; Transfection
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-022-07554-0

Despite immense revolutionary therapeutics potential, sustaining release of active small interfering RNA (siRNA) remains an arduous challenge. The development of nanoparticles with siRNA sustained release capabilities provides an avenue to enhance the therapeutic efficacy of gene-based therapy. Herein, we present a new system based on the encapsulation of siRNA/chitosan-methacrylate (CMA) complexes into liposomes to form UV crosslinkable Nanolipogels (NLGs) with sustained siRNA-release properties in vitro. We demonstrated that the CMA nanogel in NLGs can enhance the encapsulation efficiency of siRNA and provide sustained release of siRNA up to 28 days. To understand the particle mechanism of cellular entry, multiple endocytic inhibitors have been used to investigate its endocytosis pathways. The study saw positively charged NLGs entering cells via multiple endocytosis pathways, facilitating endosomal escape and slowly releasing siRNA into the cytoplasm. Transfection experiments confirmed that the crosslinked NLG delivery system provides effective transfection and prolonged silencing effect up to 14 days in cell cultures. We expect that this sustained-release siRNA NLG platform would be of interest in both fundamental biological studies and in clinical applications to extend the use of siRNA-based therapies.