| Literature DB >> 30797106 |
Tingting Li1, Sixiang Shi2, Shreya Goel3, Xue Shen4, Xiaoxue Xie4, Zhongyuan Chen4, Hanxi Zhang4, Shun Li5, Xiang Qin5, Hong Yang5, Chunhui Wu5, Yiyao Liu6.
Abstract
Recently, drug delivery systems based on nanotechnology have received great attention in cancer therapeutics and diagnostics since they can not only improve the treatment efficacy but also reduce the side effects. Among them, mesoporous silica nanoparticles (MSNs) with large surface area, high pore volume, tunable pore size, abundant surface chemistry, and acceptable biocompatibility exhibit unique advantages and are considered as promising candidates for cancer diagnosis and therapy. In this review, we update the recent progress on MSN-based systems for cancer treatment purposes. We also discuss the drug loading mechanism of MSNs, stimuli-responsive drug release, and surface modification strategies for improving biocompatibility, and targeting functionalities. STATEMENT OF SIGNIFICANCE: The development of MSN-based delivery systems that can be used in both diagnosis and treatment of cancer has attracted tremendous interest in the past decade. MSN-based delivery systems can improve therapeutic efficacy and reduce cytotoxicity to normal tissue. To further improve the in vivo properties of MSNs and potential translation to the clinics, it is critical to design MSNs with appropriate surface engineering and desirable cancer targeting. This review is intended to provide the readers a comprehensive background of the vast literature till date on silica-based drug delivery systems, and to inspire further innovations in silica nanomedicine in the future.Entities:
Keywords: Biocompatibility; Combination therapy; Mesoporous silica nanoparticles (MSNs); Stimuli-responsive release
Mesh:
Substances:
Year: 2019 PMID: 30797106 DOI: 10.1016/j.actbio.2019.02.031
Source DB: PubMed Journal: Acta Biomater ISSN: 1742-7061 Impact factor: 8.947