Microemulsion-Confined Assembly of Magnetic Nanoclusters for pH/H2O2 Dual-Responsive T2–T1 Switchable MRI
Source abstract
Abstract
In this work, a T2–T1 switchable superparamagnetic iron oxide nanoprobe with a pH/H2O2 dual response was obtained using a microemulsion method. This novel method for the controllable assembly of small iron clusters followed by their independent modification was reported, which could not be prepared by common synthetic methods. The size of the assembled nanoprobe was uniform and controllable, with a stable T2 magnetic resonance imaging (MRI) signal under a single condition. When the nanoprobe was exposed to the tumor environment, the higher H+ and H2O2 concentrations at the tumor site could dissociate the nanoprobe and redisperse into small iron clusters. When this occurred, the T2 MRI signal was converted into a T1 MRI signal, achieving specific detection of tumors by a pH/H2O2 dual-response T2–T1 MRI.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Lanthanide and Transition Metal Complexes · Nanocluster Synthesis and Applications · Nanoparticle-Based Drug Delivery
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Chemo/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China
Institute of Applied Chemistry, School of Science, Central South University of Forestry and Technology, Changsha 410004, P. R. China
Funding
National Natural Science Foundation of China · Changsha Municipal Natural Science Foundation · Hunan Provincial Science and Technology Foundation
References (35)
Show source-provided references
1. 10.1021/acsbiomaterials.0c0154710.1021/acsbiomaterials.0c01547 ↗
2. 10.1021/acsnano.0c0553010.1021/acsnano.0c05530 ↗
3. 10.1021/acs.chemrev.8b0036310.1021/acs.chemrev.8b00363 ↗
4. 10.1021/am301301f10.1021/am301301f ↗
5. 10.1021/nn900761s10.1021/nn900761s ↗
6. 10.1038/nnano.2016.7210.1038/nnano.2016.72 ↗
7. 10.1021/cr200259610.1021/cr2002596 ↗
8. 10.1021/acs.molpharmaceut.6b0083910.1021/acs.molpharmaceut.6b00839 ↗
9. 10.1021/acs.bioconjchem.9b0049910.1021/acs.bioconjchem.9b00499 ↗
10. 10.1021/acsnano.5b0578310.1021/acsnano.5b05783 ↗
11. 10.1021/nn304605510.1021/nn3046055 ↗
12. 10.1021/acsbiomaterials.9b0119810.1021/acsbiomaterials.9b01198 ↗
13. 10.1021/ja203340u10.1021/ja203340u ↗
14. 10.1039/c8cc08943d10.1039/c8cc08943d ↗
15. 10.1039/d0nr08039j10.1039/d0nr08039j ↗
16. 10.1021/jacs.8b0416910.1021/jacs.8b04169 ↗
17. 10.1002/anie.20201434810.1002/anie.202014348 ↗
18. 10.1021/acs.nanolett.6b0033110.1021/acs.nanolett.6b00331 ↗
19. 10.1021/acs.nanolett.8b0441110.1021/acs.nanolett.8b04411 ↗
20. 10.1021/acsabm.0c0095810.1021/acsabm.0c00958 ↗
21. 10.1021/acsabm.1c0015010.1021/acsabm.1c00150 ↗
22. 10.1021/acs.jmedchem.0c0035410.1021/acs.jmedchem.0c00354 ↗
23. 10.1021/acsami.1c0853210.1021/acsami.1c08532 ↗
24. 10.1021/acs.analchem.8b0491210.1021/acs.analchem.8b04912 ↗
25. 10.1021/acs.bioconjchem.0c0013510.1021/acs.bioconjchem.0c00135 ↗
26. 10.1021/acsnano.8b0589310.1021/acsnano.8b05893 ↗
27. 10.1021/acs.bioconjchem.9b0044810.1021/acs.bioconjchem.9b00448 ↗
28. 10.1021/acsnano.8b0145610.1021/acsnano.8b01456 ↗
29. 10.1021/acs.analchem.1c0312810.1021/acs.analchem.1c03128 ↗
30. 10.1021/acs.analchem.0c0464410.1021/acs.analchem.0c04644 ↗
31. 10.1126/science.123726510.1126/science.1237265 ↗
32. 10.1021/acs.langmuir.7b0077310.1021/acs.langmuir.7b00773 ↗
33. 10.1007/s40820-019-0347-010.1007/s40820-019-0347-0 ↗
34. 10.1016/j.dyepig.2018.03.03810.1016/j.dyepig.2018.03.038 ↗
35. 10.1039/c6cs00636a10.1039/c6cs00636a ↗