journal article·2022-03-08

Influence of Linkers within Stimuli-Responsive Prodrugs on Cancer Therapy: A Case of Five Doxorubicin Dimer-Based Nanoparticles

Qiang Wang, Chong Wang, Shiyou Li, Yuxuan Xiong, Huimin Wang, Zheng Li, Jiangling Wan, Xiangliang Yang, Zifu Li

Chemistry of Materials· Volume 34· Issue 5
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Abstract

Stimuli-responsive prodrugs are promising candidates for effective cancer therapy, while the linker is one of the indispensable components in prodrugs. However, with so many endogenous stimuli to compete with in the tumor microenvironment (TME) and intertumoral heterogeneity of chemical species, we must mull over the properties of the linker to guarantee efficient drug release. Here, we prepared five kinds of stimuli-responsive doxorubicin (DOX) dimeric prodrug self-assembled nanoparticles (NPs) and compared their antitumor effects against triple-negative breast cancer (TNBC) and hepatocellular carcinoma (HCC) tumors. These prodrugs were linked with stable carbon chain, trace amide disulfide and traceless carbamate disulfide, borate ester, and dimethylmaleamide linkers and could self-assemble into NPs without any carrier. With these self-assembled NPs, we demonstrated that the traceless carbamate disulfide linker exhibited superiority than the noncleavable carbon chain and trace amide disulfide linkers. However, no prodrug NPs exhibited superior antitumor efficacy and cleavage rates in the tumors of TNBC and HCC. We further revealed that different cancer cells exhibited distinctive capacities to maintain endogenous chemical species, while intertumoral heterogeneity hampered the availability of prodrug NPs with broad-spectrum superiority. Our results suggest that a precise and traceless linker should be pursued for the construction of potent prodrugs, providing significant implications for the development of efficient stimuli-responsive prodrugs.
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Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · Dendrimers and Hyperbranched Polymers · Nanoplatforms for cancer theranostics

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

Affiliations

National Engineering Research Center for Nanomedicine, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, P. R. China

Key Laboratory of Molecular Biophysics of Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, P. R. China

Hubei Key Laboratory of Bioinorganic Chemistry and Materia Medical, Huazhong University of Science and Technology, Wuhan 430074, P. R. China

GBA Research Innovation Institute for Nanotechnology, Guangdong 510530, P. R. China

Hubei Engineering Research Center for Biomaterials and Medical Protective Materials, Huazhong University of Science and Technology, Wuhan 430074, P. R. China

Wuhan Institute of Biotechnology, High Tech Road 666, East Lake high tech Zone, Wuhan 430040, P. R. China

Funding

Ministry of Science and Technology of the People's Republic of China · Huazhong University of Science and Technology · National Natural Science Foundation of China

References (48)

Show source-provided references
1. 10.1038/nrd.2018.4610.1038/nrd.2018.46 ↗
2. 10.1039/D0NJ04134C10.1039/D0NJ04134C ↗
3. 10.1016/j.ejmech.2018.12.03510.1016/j.ejmech.2018.12.035 ↗
4. 10.1016/j.addr.2016.06.01510.1016/j.addr.2016.06.015 ↗
5. 10.1038/s41573-018-0005-010.1038/s41573-018-0005-0 ↗
6. 10.1039/C8CS00676H10.1039/C8CS00676H ↗
7. 10.3390/ph1309024510.3390/ph13090245 ↗
8. 10.1038/s41551-021-00698-w10.1038/s41551-021-00698-w ↗
9. 10.1039/C7CS00557A10.1039/C7CS00557A ↗
10. 10.1208/s12249-018-1262-210.1208/s12249-018-1262-2 ↗
11. 10.1016/S0140-6736(19)31774-X10.1016/S0140-6736(19)31774-X ↗
12. 10.1038/s41570-017-006310.1038/s41570-017-0063 ↗
13. 10.1007/s13238-016-0323-010.1007/s13238-016-0323-0 ↗
14. 10.1002/adtp.20180003010.1002/adtp.201800030 ↗
15. 10.1016/j.ajps.2017.11.00210.1016/j.ajps.2017.11.002 ↗
16. 10.1039/D0CS01061H10.1039/D0CS01061H ↗
17. 10.1021/acsmacrolett.0c0048810.1021/acsmacrolett.0c00488 ↗
18. 10.1038/nature1262610.1038/nature12626 ↗
19. 10.1152/physrev.00015.201610.1152/physrev.00015.2016 ↗
20. 10.1038/s41565-021-00910-710.1038/s41565-021-00910-7 ↗
21. 10.1021/acs.nanolett.9b0276910.1021/acs.nanolett.9b02769 ↗
22. 10.1016/j.biomaterials.2021.12095510.1016/j.biomaterials.2021.120955 ↗
23. 10.2147/DDDT.S14063810.2147/DDDT.S140638 ↗
24. 10.1039/D0RA04155F10.1039/D0RA04155F ↗
25. 10.1039/D0SC00929F10.1039/D0SC00929F ↗
26. 10.1038/s41467-019-11193-x10.1038/s41467-019-11193-x ↗
27. 10.1021/acs.chemmater.0c0408010.1021/acs.chemmater.0c04080 ↗
28. 10.1126/sciadv.abc172510.1126/sciadv.abc1725 ↗
29. 10.1002/adma.20190756810.1002/adma.201907568 ↗
30. 10.31635/ccschem.020.20200012410.31635/ccschem.020.202000124 ↗
31. 10.1126/scitranslmed.aan368210.1126/scitranslmed.aan3682 ↗
32. 10.1002/anie.20200873210.1002/anie.202008732 ↗
33. 10.1002/adma.20170014110.1002/adma.201700141 ↗
34. 10.1016/j.nantod.2020.10103010.1016/j.nantod.2020.101030 ↗
35. 10.1038/s41551-017-0115-810.1038/s41551-017-0115-8 ↗
36. 10.1021/acsami.6b1193210.1021/acsami.6b11932 ↗
37. 10.1016/j.jconrel.2018.04.01910.1016/j.jconrel.2018.04.019 ↗
38. 10.1021/jacs.1c0301310.1021/jacs.1c03013 ↗
39. 10.1038/srep0136510.1038/srep01365 ↗
40. 10.1039/b815918a10.1039/b815918a ↗
41. 10.1002/advs.20210023310.1002/advs.202100233 ↗
42. 10.3390/cancers1209243710.3390/cancers12092437 ↗
43. 10.1038/s41580-019-0185-410.1038/s41580-019-0185-4 ↗
44. 10.1002/anie.20200710410.1002/anie.202007104 ↗
45. 10.1016/j.canlet.2019.03.02010.1016/j.canlet.2019.03.020 ↗
46. 10.1016/j.redox.2016.12.03510.1016/j.redox.2016.12.035 ↗
47. 10.1038/nmeth.121210.1038/nmeth.1212 ↗
48. 10.1038/nchem.264810.1038/nchem.2648 ↗