journal article·2018-10-24

PEGylated Multistimuli-Responsive Dendritic Prodrug-Based Nanoscale System for Enhanced Anticancer Activity

Zhenyu Duan, Hao Cai, Hu Zhang, Kai Chen, Ning Li, Zhuping Xu, Qiyong Gong, Kui Luo

ACS Applied Materials & Interfaces· Volume 10· Issue 42
Publisher page

Abstract

A PEGylated multistimuli-responsive dendritic copolymer-doxorubicin (DOX) prodrug-based nanoscale system was developed as a delivery model for hydrophobic drugs. In this system, PEGylation did not only prolong circulation of the nanoscale system in the body (average half-life of 14.6 h, four times longer than that of the free drug), but also allowed the system to aggregate into nanoparticles (NPs) because of interactions between hydrophilic (polyethylene glycol) and hydrophobic (dendritic prodrug) moieties for better uptake through endocytosis (around 150 nm of particle size with a neutrally charged surface for the PEGylated dendritic prodrug with 12.1 wt % of DOX). The dendritic structure was built by bridging poly[ N-(2-hydroxypropyl)methacrylamide] segments with enzyme-responsive GFLG (Gly-Phe-Leu-Gly tetrapeptide) linkers. DOX was released by hydrolyzing the hydrazone bond between DOX and the copolymer framework in the acidic endosomes/lysosomes. In vitro studies on DOX released from the NPs induced mitochondrial dysfunction during apoptosis. By imaging the main organs and tumor tissues from mice treated with the NPs, boosted accumulation of this nanoscale medicine was found in tumor tissues, leading to a decrease in toxicity and side effects to normal tissues and enhancement in drug tolerance. In the 4T1 breast cancer model, these NPs exhibited a superior antitumor efficacy confirmed by inhibiting angiogenesis, proliferation of tumor tissues, and inducing procedural apoptosis of tumor cells. The highest tumor growth inhibition value mediated by the NPs was up to 86.5%. Therefore, this PEGylated multistimuli-responsive dendritic copolymer-DOX prodrug-based nanoscale system may be further explored as an alternative to traditional chemotherapy for breast cancer treatment.
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Research context

OpenAlex topics: Nanoparticle-Based Drug Delivery · Nanoplatforms for cancer theranostics · Dendrimers and Hyperbranched Polymers

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

Affiliations

National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, China

Amgen Bioprocess Centre, Keck Graduate Institute, Claremont, California 91711, United States

Funding

Ministry of Science and Technology of the People's Republic of China · Ministry of Education of the People's Republic of China · National Natural Science Foundation of China · Sichuan Province · Chengdu City

References (55)

Show source-provided references
1. 10.1126/science.109583310.1126/science.1095833 ↗
2. 10.1038/nrc167010.1038/nrc1670 ↗
3. 10.1038/nrc.2016.10810.1038/nrc.2016.108 ↗
4. 10.1038/nbt.333010.1038/nbt.3330 ↗
5. 10.1016/j.biomaterials.2016.01.06110.1016/j.biomaterials.2016.01.061 ↗
6. 10.1021/acs.macromol.6b0139710.1021/acs.macromol.6b01397 ↗
7. 10.1016/j.addr.2012.01.02010.1016/j.addr.2012.01.020 ↗
8. 10.1038/nmat377610.1038/nmat3776 ↗
9. 10.1021/acsnano.6b0129610.1021/acsnano.6b01296 ↗
10. 10.1002/adma.20140297510.1002/adma.201402975 ↗
11. 10.1039/c3cs60094g10.1039/c3cs60094g ↗
12. 10.1002/adma.20160535710.1002/adma.201605357 ↗
13. 10.1002/adma.20170117010.1002/adma.201701170 ↗
14. 10.1002/adfm.20170033910.1002/adfm.201700339 ↗
15. 10.1002/adfm.20160175410.1002/adfm.201601754 ↗
16. 10.1021/acsami.5b0183310.1021/acsami.5b01833 ↗
17. 10.1016/j.reactfunctpolym.2010.10.00510.1016/j.reactfunctpolym.2010.10.005 ↗
18. 10.1016/j.jconrel.2012.06.02910.1016/j.jconrel.2012.06.029 ↗
19. 10.1021/acsami.6b0098010.1021/acsami.6b00980 ↗
20. 10.1016/j.jconrel.2011.06.01510.1016/j.jconrel.2011.06.015 ↗
21. 10.1021/bm101254e10.1021/bm101254e ↗
22. 10.1016/j.apmt.2018.02.00310.1016/j.apmt.2018.02.003 ↗
23. 10.1021/acsami.6b1523210.1021/acsami.6b15232 ↗
24. 10.1038/nrd103310.1038/nrd1033 ↗
25. 10.1166/jbn.2018.255610.1166/jbn.2018.2556 ↗
26. 10.1166/jbn.2018.253810.1166/jbn.2018.2538 ↗
27. 10.1016/j.biomaterials.2014.07.05910.1016/j.biomaterials.2014.07.059 ↗
28. 10.1002/mabi.20080001510.1002/mabi.200800015 ↗
29. 10.1016/j.jconrel.2011.01.01710.1016/j.jconrel.2011.01.017 ↗
30. 10.1016/j.jconrel.2013.07.02710.1016/j.jconrel.2013.07.027 ↗
31. 10.1016/j.jconrel.2005.09.01010.1016/j.jconrel.2005.09.010 ↗
32. Kuppusamy P. · Cancer Res. · 2002 · 62 · 307
33. 10.1039/b815918a10.1039/b815918a ↗
34. 10.1002/anie.20140303610.1002/anie.201403036 ↗
35. 10.1016/j.addr.2007.06.00810.1016/j.addr.2007.06.008 ↗
36. 10.1021/mp050065e10.1021/mp050065e ↗
37. 10.1007/978-1-60327-017-5_210.1007/978-1-60327-017-5_2 ↗
38. 10.1016/s0959-8049(00)00374-910.1016/s0959-8049(00)00374-9 ↗
39. 10.1016/j.jconrel.2012.12.00910.1016/j.jconrel.2012.12.009 ↗
40. 10.1021/la904437u10.1021/la904437u ↗
41. 10.1002/adma.20120229610.1002/adma.201202296 ↗
42. 10.1016/j.biomaterials.2010.01.06510.1016/j.biomaterials.2010.01.065 ↗
43. 10.3390/cancers301040810.3390/cancers3010408 ↗
44. 10.1039/c4cc05008h10.1039/c4cc05008h ↗
45. 10.1016/j.ejps.2014.02.01610.1016/j.ejps.2014.02.016 ↗
46. 10.1166/jbn.2017.246610.1166/jbn.2017.2466 ↗
47. 10.1021/nn301616210.1021/nn3016162 ↗
48. 10.1021/acsami.6b0200610.1021/acsami.6b02006 ↗
49. 10.1016/j.ijpharm.2007.04.03610.1016/j.ijpharm.2007.04.036 ↗
50. 10.1016/j.biomaterials.2012.11.00710.1016/j.biomaterials.2012.11.007 ↗
51. 10.1016/j.biomaterials.2013.07.03710.1016/j.biomaterials.2013.07.037 ↗
52. 10.1016/j.jconrel.2011.01.02110.1016/j.jconrel.2011.01.021 ↗
53. 10.1038/3502522010.1038/35025220 ↗
54. 10.1200/jco.2005.07.50110.1200/jco.2005.07.501 ↗
55. 10.1021/acsami.6b1550510.1021/acsami.6b15505 ↗