journal article·2019-05-29

Self-Strengthened Oxidation-Responsive Bioactivating Prodrug Nanosystem with Sequential and Synergistically Facilitated Drug Release for Treatment of Breast Cancer

Kaiyuan Wang, Bin Yang, Hao Ye, Xuanbo Zhang, Hang Song, Xia Wang, Na Li, Lin Wei, Yu Wang, Haotian Zhang, Qiming Kan, Zhonggui He, Dun Wang, Jin Sun

ACS Applied Materials & Interfaces· Volume 11· Issue 21
Publisher page

Abstract

Although environment-sensitive prodrug-based nanoparticles (NPs) have developed rapidly, lots of prodrug NPs still show poor selectivity and efficiency of parent drug bioactivation because of tumor heterogeneity. Herein, self-strengthened bioactivating prodrug-based NPs are fabricated via co-encapsulation of oxidation-responsive thioether-linked linoleic acid-paclitaxel conjugates (PTX-S-LA) and β-lapachone (LPC) into polymeric micelles (PMs). Following cellular uptake, PMs first release LPC to significantly elevate the reactive oxidative species (ROS) level through NAD(P)H: quinone oxidoreductase-1 (NQO1) catalysis. Then, NQO1-generated ROS in combination with endogenous high ROS levels in tumor cells could synergistically facilitate PTX-S-LA to release the active cytotoxic agent PTX. Such a novel prodrug nanosystem exhibits self-strengthened prodrug bioactivation, ultraselective release, and cytotoxicity between cancer and normal cells, prolonged circulation time, and enhanced tumor accumulation, leading to high antitumor efficiency and superior biosafety. Our findings pave the new way for the rational design of oxidation-responsive prodrug NPs for high-efficacy cancer chemotherapy.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoplatforms for cancer theranostics · Bioactive Compounds and Antitumor Agents · Nanoparticle-Based Drug Delivery

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Key Laboratory of Microbiology, School of Life Science, Heilongjiang University, Harbin 150080, P. R. China

Funding

National Natural Science Foundation of China

References (24)

Show source-provided references
1. 10.1016/j.tips.2017.10.00910.1016/j.tips.2017.10.009 ↗
2. 10.1002/smll.20160159710.1002/smll.201601597 ↗
3. 10.1021/acs.nanolett.8b0073710.1021/acs.nanolett.8b00737 ↗
4. 10.1016/j.jconrel.2018.07.01010.1016/j.jconrel.2018.07.010 ↗
5. 10.1039/c5nr06734k10.1039/c5nr06734k ↗
6. 10.1039/c8bm00548f10.1039/c8bm00548f ↗
7. 10.1016/j.apsb.2018.08.00810.1016/j.apsb.2018.08.008 ↗
8. 10.1016/j.biomaterials.2018.04.01510.1016/j.biomaterials.2018.04.015 ↗
9. 10.1016/j.jconrel.2016.10.02910.1016/j.jconrel.2016.10.029 ↗
10. 10.1039/c8nr02358a10.1039/c8nr02358a ↗
11. 10.1039/c8bm00899j10.1039/c8bm00899j ↗
12. 10.3109/1061186x.2015.107329610.3109/1061186x.2015.1073296 ↗
13. 10.1021/acs.jmedchem.8b0012410.1021/acs.jmedchem.8b00124 ↗
14. 10.1016/j.jconrel.2007.04.01410.1016/j.jconrel.2007.04.014 ↗
15. 10.1158/0008-5472.can-09-399510.1158/0008-5472.can-09-3995 ↗
16. 10.1016/j.jconrel.2009.11.01210.1016/j.jconrel.2009.11.012 ↗
17. 10.1002/adma.20170234210.1002/adma.201702342 ↗
18. 10.1021/acs.nanolett.6b0163210.1021/acs.nanolett.6b01632 ↗
19. 10.1021/acsami.8b1042110.1021/acsami.8b10421 ↗
20. 10.1021/acs.molpharmaceut.5b0044810.1021/acs.molpharmaceut.5b00448 ↗
21. 10.1021/acs.molpharmaceut.7b0059110.1021/acs.molpharmaceut.7b00591 ↗
22. 10.1080/10717544.2017.138120110.1080/10717544.2017.1381201 ↗
23. 10.1002/adma.20160662810.1002/adma.201606628 ↗
24. 10.1016/j.jconrel.2017.04.04310.1016/j.jconrel.2017.04.043 ↗