journal article·2018-12-10

Glutathione Triggered Near Infrared Fluorescence Imaging-Guided Chemotherapy by Cyanine Conjugated Polypeptide

Zheng Ruan, Pan Yuan, Tuanwei Li, Youliang Tian, Quan Cheng, Lifeng Yan

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Abstract

Precise detection of the tumor environment for cancer diagnosis has been strongly demanded for further therapies. Here, a redox-responsive fluorescence switch off/on system PCQ was designed and synthesized conjugated with near-infrared (NIR) cyanine dyes (Cy5.5) and relevant quencher (FQ) in mixed polymeric micelles (PCy and PFQ). The mixed PCQ micelles were prepared with two kinds of polymers with poly(oligo (ethylene glycol) methacrylate) (POEGMA) as the hydrophilic shell, in which fluorescence emission was quenched by fluorescence resonance energy transfer (FRET) effect. The FQ was conjugated with POEGMA by disulfide linkage, which could be broken with a redox environment such as high glutathione (GSH) concentration in tumor cells. After the PCQ micelles got into tumor cells, PFQ blocks in PCQ would be disassembled to recompose PCy micelles. During that process, drugs like doxorubicin (DOX) could be loaded inside and formed PCQ@DOX nanoparticles and then released for accurate NIR bioimaging and drug delivery instantly.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoplatforms for cancer theranostics · Luminescence and Fluorescent Materials · Advanced biosensing and bioanalysis techniques

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

Affiliations

CAS Key Laboratory of Soft Matter Chemistry, Hefei National Laboratory for Physical Sciences at the Microscale, and Department of Chemical Physics, iCHEM, University of Science and Technology of China, Jinzai Road 96, Hefei 230026, Anhui, China

Funding

National Natural Science Foundation of China

References (42)

Show source-provided references
1. 10.1016/j.molonc.2008.04.00110.1016/j.molonc.2008.04.001 ↗
2. 10.1162/1535350020030314210.1162/15353500200303142 ↗
3. 10.1039/C0CS00058B10.1039/C0CS00058B ↗
4. 10.1021/cr200410310.1021/cr2004103 ↗
5. 10.1016/j.cbpa.2003.08.00710.1016/j.cbpa.2003.08.007 ↗
6. 10.1016/j.cbpa.2009.09.02910.1016/j.cbpa.2009.09.029 ↗
7. 10.1016/j.cbpa.2009.10.02210.1016/j.cbpa.2009.10.022 ↗
8. 10.1039/C3CS60271K10.1039/C3CS60271K ↗
9. 10.1039/C2CS35313J10.1039/C2CS35313J ↗
10. 10.1038/nmeth.198810.1038/nmeth.1988 ↗
11. 10.1021/acsami.8b0262110.1021/acsami.8b02621 ↗
12. 10.1007/s13233-018-6034-z10.1007/s13233-018-6034-z ↗
13. 10.1016/j.biomaterials.2015.05.01610.1016/j.biomaterials.2015.05.016 ↗
14. 10.1021/acsnano.7b0094410.1021/acsnano.7b00944 ↗
15. 10.1002/adfm.20170037110.1002/adfm.201700371 ↗
16. 10.1021/cr990402t10.1021/cr990402t ↗
17. 10.1016/j.biomaterials.2011.06.02410.1016/j.biomaterials.2011.06.024 ↗
18. 10.1039/C6RA05657A10.1039/C6RA05657A ↗
19. 10.1021/am301600u10.1021/am301600u ↗
20. 10.1016/j.jconrel.2016.11.01510.1016/j.jconrel.2016.11.015 ↗
21. 10.1016/j.addr.2011.09.00910.1016/j.addr.2011.09.009 ↗
22. 10.1016/j.addr.2010.04.00910.1016/j.addr.2010.04.009 ↗
23. 10.1038/nnano.2007.38710.1038/nnano.2007.387 ↗
24. 10.1039/c3pp50118c10.1039/c3pp50118c ↗
25. 10.1039/C6DT03141B10.1039/C6DT03141B ↗
26. 10.1038/nmat281110.1038/nmat2811 ↗
27. 10.1021/ja807337410.1021/ja8073374 ↗
28. 10.1021/ac302806810.1021/ac3028068 ↗
29. 10.1021/ja809721j10.1021/ja809721j ↗
30. 10.1021/ja025678o10.1021/ja025678o ↗
31. 10.1021/cb900089j10.1021/cb900089j ↗
32. 10.1126/science.210616110.1126/science.2106161 ↗
33. 10.1039/C6PY00799F10.1039/C6PY00799F ↗
34. 10.1093/jnci/djm13510.1093/jnci/djm135 ↗
35. Kuppusamy P. · Cancer Res. · 2002 · 62 · 307
36. 10.1002/adma.20110160910.1002/adma.201101609 ↗
37. 10.1039/C5PY01629K10.1039/C5PY01629K ↗
38. 10.1039/C6PY01818A10.1039/C6PY01818A ↗
39. 10.1016/j.ab.2009.02.02410.1016/j.ab.2009.02.024 ↗
40. 10.1039/C3PY01192E10.1039/C3PY01192E ↗
41. 10.1039/C6BM00581K10.1039/C6BM00581K ↗
42. 10.1039/C6BM00787B10.1039/C6BM00787B ↗