journal article·2017-09-13

Selenylsulfide Bond-Launched Reduction-Responsive Superparamagnetic Nanogel Combined of Acid-Responsiveness for Achievement of Efficient Therapy with Low Side Effect

Yanan Xue, Xiaoyang Xia, Bo Yu, Lijun Tao, Qian Wang, Shi-Wen Huang, Faquan Yu

Publisher page

Abstract

With the objective to achieve in-between reduction-responsive drug release, selenylsulfide bond was first explored as a reduction cleavable linkage, compared with the most commonly employed disulfide and diselenide bonds. The reductive nanogel, with a combination of superparamagnetic and acid responsiveness, was fabricated. The expected release profiles were testified. Cytotoxicity assays illustrated the remarkable inhibition to the growth of HeLa cells, in contrast, high tolerance to L02 cells. In vivo investigation exhibited the obvious shrinkage in tumor but a healthy appearance. Hematoxylin-eosin staining and histological examination revealed the lower toxicity. The complex nanogels would have appeared highly promising in cancer therapy.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoplatforms for cancer theranostics · Nanoparticle-Based Drug Delivery · Sulfur Compounds in Biology

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

Affiliations

Key Laboratory for Green Chemical Process of Ministry of Education, Hubei Key Laboratory for Novel Reactor and Green Chemistry Technology, School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, Wuhan 430073, China

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China

Funding

Natural Science Foundation of Hubei Province · National Natural Science Foundation of China · Department of Education, Hubei Provincial

References (24)

Show source-provided references
1. 10.1039/C5PY01355K10.1039/C5PY01355K ↗
2. 10.1038/nmat377610.1038/nmat3776 ↗
3. 10.1039/C5TB01851J10.1039/C5TB01851J ↗
4. 10.1039/C5NR02878G10.1039/C5NR02878G ↗
5. 10.1016/j.biomaterials.2011.05.05010.1016/j.biomaterials.2011.05.050 ↗
6. 10.1039/c0cc04983b10.1039/c0cc04983b ↗
7. 10.1016/j.msec.2014.10.00310.1016/j.msec.2014.10.003 ↗
8. 10.1021/ja908124g10.1021/ja908124g ↗
9. 10.1039/C6BM00960C10.1039/C6BM00960C ↗
10. 10.1016/j.biomaterials.2016.06.04410.1016/j.biomaterials.2016.06.044 ↗
11. 10.1039/C6PY01423B10.1039/C6PY01423B ↗
12. 10.1016/j.biomaterials.2017.01.00210.1016/j.biomaterials.2017.01.002 ↗
13. 10.1016/j.actbio.2013.04.04710.1016/j.actbio.2013.04.047 ↗
14. 10.1016/j.jconrel.2013.05.02910.1016/j.jconrel.2013.05.029 ↗
15. 10.1007/s00330010090810.1007/s003300100908 ↗
16. 10.1021/am504624710.1021/am5046247 ↗
17. 10.1006/jssc.1993.124210.1006/jssc.1993.1242 ↗
18. 10.1007/s10853-014-8798-710.1007/s10853-014-8798-7 ↗
19. 10.1016/j.biomaterials.2009.05.00510.1016/j.biomaterials.2009.05.005 ↗
20. 10.1039/c3py00364g10.1039/c3py00364g ↗
21. 10.1016/j.biomaterials.2009.11.10210.1016/j.biomaterials.2009.11.102 ↗
22. 10.1039/c2sm27616j10.1039/c2sm27616j ↗
23. 10.1089/ars.2012.501310.1089/ars.2012.5013 ↗
24. 10.1021/jo101156910.1021/jo1011569 ↗