Self-Quenched Polysaccharide Nanoparticles with a Reactive Oxygen Species-Sensitive Cascade for Enhanced Photodynamic Therapy
Source abstract
Abstract
Tumor microenvironment (TME)-responsive nanocarrier systems that keep the photosensitizer (PS) inactive during systemic circulation and then efficiently release or activate the PS in response to unique TME conditions have attracted much attention. Herein, we report novel TME-responsive, self-quenched polysaccharide nanoparticles (NPs) with a reactive oxygen species (ROS)-sensitive cascade. The PS, pheophorbide A (PhA), was conjugated to a water-soluble glycol chitosan (GC) through an ROS-sensitive thioketal (TK) linker. The amphiphilic GC-TK-PhA conjugates could arrange themselves into NPs and remain photoinactive due to their self-quenching effects. Upon reaching the ROS-rich hypoxic core of the tumor tissue, the NPs release the PS in a photoactive form by efficient, ROS-sensitive TK bond cleavage, thus generating potent phototoxic effects. Following near-infrared irradiation, the increase in locoregional ROS levels further accelerates the release and activation of PS. These cascade reactions caused a significant reduction in the tumor volume, demonstrating good antitumor potential.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanoplatforms for cancer theranostics · Photodynamic Therapy Research Studies · Cancer, Hypoxia, and Metabolism
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Polymer Science and Engineering, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon 34134, Republic of Korea
Department of Biomedical Science, BK21 PLUS Center for Creative Biomedical Scientists, Chonnam National University Medical School, 160 Baekseo-ro, Gwangju 61469, Republic of Korea
Funding
National Research Foundation of Korea · Ministry of Trade, Industry and Energy
References (34)
Show source-provided references
1. 10.1021/acs.chemmater.7b0475110.1021/acs.chemmater.7b04751 ↗
2. 10.1021/acsami.9b1262010.1021/acsami.9b12620 ↗
3. 10.1016/j.biomaterials.2019.119330I10.1016/j.biomaterials.2019.119330I ↗
4. 10.1016/j.colsurfa.2019.04.06010.1016/j.colsurfa.2019.04.060 ↗
5. 10.1021/acs.biomac.9b0058110.1021/acs.biomac.9b00581 ↗
6. 10.1016/j.reactfunctpolym.2018.10.01210.1016/j.reactfunctpolym.2018.10.012 ↗
7. 10.1016/j.biomaterials.2018.10.01010.1016/j.biomaterials.2018.10.010 ↗
8. 10.1002/cyto.a.23864I10.1002/cyto.a.23864I ↗
9. 10.1016/j.ejmech.2019.02.03110.1016/j.ejmech.2019.02.031 ↗
10. 10.1016/j.jmmm.2018.10.02010.1016/j.jmmm.2018.10.020 ↗
11. 10.3390/nano9010014I10.3390/nano9010014I ↗
12. 10.7150/thno.3107910.7150/thno.31079 ↗
13. 10.1021/acsami.9b1160710.1021/acsami.9b11607 ↗
14. 10.1021/acsami.9b1264110.1021/acsami.9b12641 ↗
15. 10.1021/acsami.9b1068510.1021/acsami.9b10685 ↗
16. 10.1002/adma.201901893I10.1002/adma.201901893I ↗
17. 10.1039/C9BM00333A10.1039/C9BM00333A ↗
18. 10.1002/anie.20190271410.1002/anie.201902714 ↗
19. 10.1016/j.jconrel.2019.03.01910.1016/j.jconrel.2019.03.019 ↗
20. 10.1002/advs.20197013610.1002/advs.201970136 ↗
21. 10.1039/C9BM00634F10.1039/C9BM00634F ↗
22. 10.1186/2055-7124-18-1910.1186/2055-7124-18-19 ↗
23. 10.1021/bm500361910.1021/bm5003619 ↗
24. 10.1080/00914037.2014.100213110.1080/00914037.2014.1002131 ↗
25. 10.1021/acsami.8b0649110.1021/acsami.8b06491 ↗
26. 10.1016/j.biomaterials.2013.05.01710.1016/j.biomaterials.2013.05.017 ↗
27. 10.1016/j.jconrel.2013.07.002I10.1016/j.jconrel.2013.07.002I ↗
28. 10.1186/s40824-018-0132-zI10.1186/s40824-018-0132-zI ↗
29. 10.1002/adma.201702342I10.1002/adma.201702342I ↗
30. 10.1177/117727191875539110.1177/1177271918755391 ↗
31. 10.7150/thno.1543310.7150/thno.15433 ↗
32. 10.1016/j.carbpol.2011.05.01110.1016/j.carbpol.2011.05.011 ↗
33. 10.7150/thno.1543310.7150/thno.15433 ↗
34. 10.1038/srep0687810.1038/srep06878 ↗