| Literature DB >> 26816249 |
Hao Wang1, Ren-lu Han1, Li-ming Yang2, Jun-hui Shi1, Zong-jun Liu1,3, Yu Hu1, You Wang1, Shu-juan Liu1, Yang Gan3.
Abstract
Novel core-shell-shell structured nanoparticles 75 nm in diameter with all-in-one "smart" functional capabilities for simultaneous photoresponsive drug release, photodynamic therapy, and cell imaging are designed and prepared. These nanoparticles consist of an upconversion (UC) emission core, a photosensitizer-embodied silica sandwich shell, and a β-cyclodextrin (β-CD) gated mesoporous silica outmost shell with drugs (Rhodamine B as a model) loaded inside. We show in this proof-of-concept demonstration that, under 980 nm near-infrared irradiation, UC 540 nm green light emissions were emitted for cell imaging, and 660 nm red light emissions were excited for activating photosensitizers to generate singlet oxygen, which could be exploited directly to kill cancer cells and simultaneously dissociate β-CD gatekeeper to release drugs. The preliminary results reported here will shed new light on the future design and applications of multifunctional platforms for cancer therapy and diagnostic.Entities:
Keywords: cell imaging; drug delivery; near-infrared light; photodynamic therapy; upconversion nanoparticles
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Year: 2016 PMID: 26816249 DOI: 10.1021/acsami.5b11197
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229