journal article·2014-08-13Open access

Glutathione-Coated Luminescent Gold Nanoparticles: A Surface Ligand for Minimizing Serum Protein Adsorption

Rodrigo D. Vinluan, Jinbin Liu, Chen Zhou, Mengxiao Yu, Shengyang Yang, Amit Kumar, Shasha Sun, Andrew Dean, Xiankai Sun, Jie Zheng

Abstract

Ultrasmall glutathione-coated luminescent gold nanoparticles (GS-AuNPs) are known for their high resistance to serum protein adsorption. Our studies show that these NPs can serve as surface ligands to significantly enhance the physiological stability and lower the serum protein adsorption of superparamagnetic iron oxide nanoparticles (SPIONs), in addition to rendering the NPs the luminescence property. After the incorporation of GS-AuNPs onto the surface of SPIONs to form the hybrid nanoparticles (HBNPs), these SPIONs' protein adsorption was about 10-fold lower than those of the pure glutathione-coated SPIONs suggesting that GS-AuNPs are capable of providing a stealth effect against serum proteins.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanocluster Synthesis and Applications · Gold and Silver Nanoparticles Synthesis and Applications · Nanoparticle-Based Drug Delivery

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

Affiliations

Department of Chemistry, The University of Texas at Dallas, Richardson, Texas 75080, United States

Department of Radiology, The University of Texas Southwestern Medical Center, Dallas, Texas 75390 United States

Funding

National Institutes of Health

References (35)

Show source-provided references
1. Soo Choi H. · Nat. Biotechnol. · 2007 · 25 · 116510.1038/nbt1340 ↗
2. Liu J. · J. Am. Chem. Soc. · 2013 · 135 · 497810.1021/ja401612x ↗
3. Zhou C. · Angew. Chem., Int. Ed. · 2011 · 50 · 316810.1002/anie.201007321 ↗
4. Kim J. · Angew. Chem., Int. Ed. · 2008 · 47 · 843810.1002/anie.200802469 ↗
5. Larsen E. K. U. · ACS Nano · 2009 · 3 · 194710.1021/nn900330m ↗
6. Wang Y. · ACS Nano · 2012 · 6 · 588010.1021/nn300464r ↗
7. Liu J. · Angew. Chem., Int. Ed. · 2013 · 52 · 1257210.1002/anie.201304465 ↗
8. Matsumura Y. · Cancer Res. · 1986 · 46 · 6387
9. Yongdong J. · Nat. Commun. · 2010 · 1 · 4110.1038/ncomms1042 ↗
10. Kim J. · Angew. Chem. · 2006 · 118 · 791810.1002/ange.200602471 ↗
11. Wang F. · J. Mater. Chem. · 2011 · 21 · 1124410.1039/c1jm10329f ↗
12. Wang M. · J. Am. Chem. Soc. · 2013 · 135 · 1530210.1021/ja408289b ↗
13. Yu H. · Nano Lett. · 2005 · 5 · 37910.1021/nl047955q ↗
14. Bhana S. · Nanoscale · 2012 · 4 · 493910.1039/c2nr31291c ↗
15. Durgadas C. V. · Nanoscale · 2011 · 3 · 478010.1039/c1nr10900f ↗
16. Xu Y. · Langmuir · 2012 · 28 · 876710.1021/la301200g ↗
17. Leung K. C.-F. · Chem. Rev. · 2012 · 41 · 1911
18. Yu M. · J. Am. Chem. Soc. · 2011 · 133 · 1101410.1021/ja201930p ↗
19. Kang Y. S. · Chem. Mater. · 1996 · 8 · 220910.1021/cm960157j ↗
20. Laurent S. · Chem. Rev. · 2008 · 108 · 206410.1021/cr068445e ↗
21. Déry J.-P. · Chem. Mater. · 2008 · 20 · 642010.1021/cm801075u ↗
22. Xu Y. · Langmuir · 2011 · 27 · 899010.1021/la201652h ↗
23. Karaagac O. · IEEE Trans. Magn. · 2010 · 46 · 397810.1109/TMAG.2010.2076824 ↗
24. Magde D. · Photochem. Photobiol. · 2002 · 75 · 32710.1562/0031-8655(2002)075<0327:FQYATR>2.0.CO;2 ↗
25. Chekina N. · J. Mater. Chem. · 2011 · 21 · 763010.1039/c1jm10621j ↗
26. Fabbrizzi L. · Chem.—Eur. J. · 1996 · 2 · 7510.1002/chem.19960020114 ↗
27. Jares-Erijman E. A. J. · Nat. Biotechnol. · 2003 · 21 · 138710.1038/nbt896 ↗
28. Mori K. · Chem. Mater. · 2007 · 19 · 124910.1021/cm061388l ↗
29. Zhang Y. · J. Mater. Chem. · 2009 · 19 · 369610.1039/b817159a ↗
30. Jun Y.-w. · Acc. Chem. Res. · 2008 · 41 · 17910.1021/ar700121f ↗
31. Lee N. · Chem. Soc. Rev. · 2012 · 41 · 257510.1039/C1CS15248C ↗
32. Tong S. · Nano Lett. · 2010 · 10 · 460710.1021/nl102623x ↗
33. Choi J.-s. · J. Am. Chem. Soc. · 2010 · 132 · 1101510.1021/ja104503g ↗
34. Jahnen-Dechent W. · Clin. Kidney J. · 2012 · 5 · i310.1093/ndtplus/sfr163 ↗
35. Izak-Nau E. · Part. Fibre Toxicol. · 2013 · 10 · 110.1186/1743-8977-10-56 ↗