Upconversion superballs for programmable photoactivation of therapeutics

Zhen Zhang, Muthu Kumara Gnanasammandhan Jayakumar, Xiang Zheng, Swati Shikha, Yi Zhang, Akshaya Bansal, Dennis J. J. Poon, Pek Lim Chu, Eugenia L. L. Yeo, Melvin L. K. Chua, Soo Khee Chee, Yong Zhang*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

128 Citations (Scopus)
22 Downloads (CityUHK Scholars)

Abstract

Upconversion nanoparticles (UCNPs) are the preferred choice for deep-tissue photoactivation, owing to their unique capability of converting deep tissue-penetrating near-infrared light to UV/visible light for photoactivation. Programmed photoactivation of multiple molecules is critical for controlling many biological processes. However, syntheses of such UCNPs require epitaxial growth of multiple shells on the core nanocrystals and are highly complex/time-consuming. To overcome this bottleneck, we have modularly assembled two distinct UCNPs which can individually be excited by 980/808 nm light, but not both. These orthogonal photoactivable UCNPs superballs are used for programmed photoactivation of multiple therapeutic processes for enhanced efficacy. These include sequential activation of endosomal escape through photochemical-internalization for enhanced cellular uptake, followed by photocontrolled gene knockdown of superoxide dismutase-1 to increase sensitivity to reactive oxygen species and finally, photodynamic therapy under these favorable conditions. Such programmed activation translated to significantly higher therapeutic efficacy in vitro and in vivo in comparison to conventional, non-programmed activation. © 2019, The Author(s).
Original languageEnglish
Article number4586
JournalNature Communications
Volume10
Online published8 Oct 2019
DOIs
Publication statusPublished - 1 Dec 2019
Externally publishedYes

Funding

We acknowledge financial support from the Ministry of Education of Singapore (MOE 2016-T3-1-004, R-397-000-274-112, R-397-000-270-114), National Research Foundation (NRF) Competitive Research Program (NRF-CRP17-2017-05) and National University of Singapore. We also thank Selvarajan.J for technical support in preparing the schematic illustration and Sangeetha.K for support with flow cytometry studies.

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

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