Precise Monitoring of Singlet Oxygen in Specific Endocytic Organelles by Super-pH-Resolved Nanosensors
Source abstract
Abstract
Singlet oxygen (1O2) plays a vital role in pathophysiological processes and is the dominant executor of photodynamic therapy (PDT). Several small molecular probes have been designed to detect singlet oxygen for the evaluation of PDT efficacy. However, little attention was paid to the precise visualization of the 1O2 signal at the subcellular organelle level in living biological systems. Herein, a super-pH-resolved (SPR) nanosensor was developed to specifically illuminate 1O2 in endocytic organelles through encoding the cell-impermeant singlet oxygen sensor green (SOSG) into pH-sensitive micelles. The acid-activatable SPR-SOSG achieved more than 10-fold amplification of the 1O2 signal, leading to extremely higher sensitivity of singlet oxygen detection in specific endocytic organelles of living cells and animals, as compared with the nonactivatable nanoprobe and the commercially available 2′,7′-dichlorofluorescein diacetate (DCFH-DA) probe. Hence, the SPR-SOSG nanoplatform provides a promising tool to evaluate the efficacy and mechanism of nanocarrier-based photodynamic therapy.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanoplatforms for cancer theranostics · Photodynamic Therapy Research Studies · Porphyrin and Phthalocyanine Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Natural and Biomimetic Drugs, Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery Systems, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China
Funding
Ministry of Science and Technology of the People's Republic of China · Natural Science Foundation of Beijing Municipality · China Postdoctoral Science Foundation · National Natural Science Foundation of China
References (39)
Show source-provided references
1. 10.1039/b926014p10.1039/b926014p ↗
2. 10.1021/acs.chemrev.8b0055410.1021/acs.chemrev.8b00554 ↗
3. 10.1016/j.addr.2009.01.00410.1016/j.addr.2009.01.004 ↗
4. 10.1016/j.addr.2013.05.01010.1016/j.addr.2013.05.010 ↗
5. 10.1158/1078-0432.CCR-09-096410.1158/1078-0432.CCR-09-0964 ↗
6. 10.1039/C6CS00271D10.1039/C6CS00271D ↗
7. 10.1038/nrc107110.1038/nrc1071 ↗
8. 10.1039/C7CS00594F10.1039/C7CS00594F ↗
9. 10.1002/smll.20150192310.1002/smll.201501923 ↗
10. 10.1021/cr500419810.1021/cr5004198 ↗
11. 10.1007/BF0276509910.1007/BF02765099 ↗
12. 10.1021/ja208356910.1021/ja2083569 ↗
13. 10.1007/s00216-019-01910-210.1007/s00216-019-01910-2 ↗
14. 10.1111/j.1751-1097.1978.tb06972.x10.1111/j.1751-1097.1978.tb06972.x ↗
15. 10.1021/ja070713i10.1021/ja070713i ↗
16. 10.3109/1071576950906402510.3109/10715769509064025 ↗
17. 10.1562/0031-8655(2002)0750382DNILDO2.0.CO210.1562/0031-8655(2002)0750382DNILDO2.0.CO2 ↗
18. 10.1562/2006-04-14-IR-87410.1562/2006-04-14-IR-874 ↗
19. 10.1016/S1572-1000(05)00030-X10.1016/S1572-1000(05)00030-X ↗
20. 10.1111/j.1751-1097.1999.tb08284.x10.1111/j.1751-1097.1999.tb08284.x ↗
21. 10.1080/15548627.2018.151560910.1080/15548627.2018.1515609 ↗
22. 10.1021/ja408286k10.1021/ja408286k ↗
23. 10.1021/acsnano.9b0982710.1021/acsnano.9b09827 ↗
24. 10.1038/ncomms978510.1038/ncomms9785 ↗
25. Probes/Invitrogen, M · 2004
26. 10.1111/j.1751-1097.2011.00900.x10.1111/j.1751-1097.2011.00900.x ↗
27. 10.1002/anie.20160905010.1002/anie.201609050 ↗
28. 10.1021/acs.analchem.8b0485910.1021/acs.analchem.8b04859 ↗
29. 10.1038/nmat381910.1038/nmat3819 ↗
30. 10.1038/s41551-016-000610.1038/s41551-016-0006 ↗
31. 10.1038/nnano.2017.5210.1038/nnano.2017.52 ↗
32. 10.1021/acs.nanolett.9b0166010.1021/acs.nanolett.9b01660 ↗
33. 10.1021/acs.nanolett.7b0157110.1021/acs.nanolett.7b01571 ↗
34. 10.1021/ja505315810.1021/ja5053158 ↗
35. 10.1002/adma.20160379410.1002/adma.201603794 ↗
36. 10.1002/anie.20110088410.1002/anie.201100884 ↗
37. 10.1002/advs.20200225310.1002/advs.202002253 ↗
38. 10.1038/nbt.283810.1038/nbt.2838 ↗
39. 10.1016/S0891-5849(98)00174-910.1016/S0891-5849(98)00174-9 ↗