journal article·2016-08-03

Multifunctions of Excited Gold Nanoparticles Decorated Artificial Kidney with Efficient Hemodialysis and Therapeutic Potential

Hsiao-Chien Chen, Chung-Yi Cheng, Hsiu-Chen Lin, Hsi-Hsien Chen, Cheng-Hsien Chen, Chih-Ping Yang, Kai-Huei Yang, Chun-Mao Lin, Tsung-Yao Lin, Chwen-Ming Shih, Yu-Chuan Liu

Publisher page

Abstract

Chronic kidney disease (CKD) is inflammation-related. Patients with chronic renal failure who undergo hemodialysis (HD) have some acute adverse effects caused by dialysis-induced oxidative stress, protein adsorption, platelet adhesion, and activation of coagulation and inflammation. Here, resonantly illuminated gold nanoparticles-modified artificial kidney (AuNPs@AK) for achieving high efficiency accompanying therapeutic strategy for CKD during HD is proposed. The efficiency in removing uremic toxins increased obviously, especially in the presence of protein (closer to the real blood). The excited AuNPs@AK expressed negatively charged surface reduced some acute adverse effects caused by dialysis-induced protein adsorption, platelet adhesion, and activation of coagulation, thus avoiding thrombosis during HD. Unlike to traditional HD which provides only one function of removing uremic toxins, the solution collected from the outlet of the sample channel of excited AuNPs@AK showed an efficient free radical scavenger that could decrease dialysis-induced oxidative stress. In the CKD mouse model, this antioxidative solution from excited AuNPs@AK further decreased fibronectin expression and attenuated renal fibrosis, suggesting a reduced inflammatory response. These successful in vitro and in vivo approaches suggest that resonantly illuminated AuNPs@AK in HD take multiadvantages in shortening treatment time and reducing risk of adverse effects, which promise trailblazing therapeutic strategies for CKD.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Dialysis and Renal Disease Management · Hydrogen's biological and therapeutic effects

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

Affiliations

Department of Biochemistry and Molecular Cell Biology, School of Medicine, College of Medicine, Taipei Medical University, No. 250, Wuxing Street., Taipei 11031, Taiwan

Division of Nephrology, Department of Internal Medicine, Taipei Medical University Wan Fang Hospital, 111 Hsing-Long Road, Section 3, Taipei 11696, Taiwan

Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, No. 250, Wuxing Street, Taipei 11031, Taiwan

Department of Laboratory Medicine, Taipei Medical University Hospital, No. 252, Wuxing Street, Taipei 11031, Taiwan

Department of Pediatrics, School of Medicine, College of Medicine, Taipei Medical University, No. 250, Wuxing Street, Taipei 11031, Taiwan

Division of Nephrology, Department of Internal Medicine, Taipei Medical University Hospital, No. 252, Wuxing Street, Taipei 11031, Taiwan

Graduate Institute of Medical Science, College of Medicine, Taipei Medical University, No. 250, Wuxing Street, Taipei 11031, Taiwan

Funding

Taipei Medical University · Ministry of Science and Technology, Taiwan · Taipei Municipal Wanfang Hospital

References (34)

Show source-provided references
1. 10.1111/j.1492-7535.2005.01116.x10.1111/j.1492-7535.2005.01116.x ↗
2. 10.1046/j.1525-1594.2003.07170.x10.1046/j.1525-1594.2003.07170.x ↗
3. 10.1038/ki.2009.13810.1038/ki.2009.138 ↗
4. 10.1038/ki.2012.13010.1038/ki.2012.130 ↗
5. 10.1038/nrneph.2012.10010.1038/nrneph.2012.100 ↗
6. 10.1053/j.ajkd.2006.01.01810.1053/j.ajkd.2006.01.018 ↗
7. 10.1021/acsami.5b0395110.1021/acsami.5b03951 ↗
8. 10.1016/j.biomaterials.2007.11.01910.1016/j.biomaterials.2007.11.019 ↗
9. 10.1016/j.biomaterials.2010.09.00510.1016/j.biomaterials.2010.09.005 ↗
10. 10.1159/00035083710.1159/000350837 ↗
11. 10.1039/C3TB21388A10.1039/C3TB21388A ↗
12. 10.1016/j.biomaterials.2011.08.03010.1016/j.biomaterials.2011.08.030 ↗
13. 10.1681/ASN.201305054510.1681/ASN.2013050545 ↗
14. 10.1016/j.memsci.2014.12.02510.1016/j.memsci.2014.12.025 ↗
15. 10.1007/s10856-013-4870-010.1007/s10856-013-4870-0 ↗
16. 10.1002/jbm.a.3542510.1002/jbm.a.35425 ↗
17. 10.1038/nm.381410.1038/nm.3814 ↗
18. 10.1038/ki.2014.30610.1038/ki.2014.306 ↗
19. 10.1111/j.1523-1755.2005.09801.x10.1111/j.1523-1755.2005.09801.x ↗
20. 10.1007/s00467-008-1046-010.1007/s00467-008-1046-0 ↗
21. 10.1021/nn406403c10.1021/nn406403c ↗
22. 10.1021/ac503943410.1021/ac5039434 ↗
23. 10.1002/jrs.276410.1002/jrs.2764 ↗
24. 10.1038/nm157710.1038/nm1577 ↗
25. 10.1126/science.123275110.1126/science.1232751 ↗
26. 10.1681/ASN.200912131110.1681/ASN.2009121311 ↗
27. 10.1007/s10570-013-0045-x10.1007/s10570-013-0045-x ↗
28. 10.1021/nn500685h10.1021/nn500685h ↗
29. 10.3324/haematol.2008.00317810.3324/haematol.2008.003178 ↗
30. 10.1038/ki.2011.47710.1038/ki.2011.477 ↗
31. 10.1038/nature1428210.1038/nature14282 ↗
32. 10.1016/j.cell.2015.01.00410.1016/j.cell.2015.01.004 ↗
33. 10.1038/ncomms770210.1038/ncomms7702 ↗
34. 10.1016/j.cell.2014.10.02810.1016/j.cell.2014.10.028 ↗