Biodistribution of colloidal gold nanoparticles after intravenous injection: Effects of PEGylation at the same particle size
Source abstract
Abstract
Background: Recently, polyethylene glycol (PEG) modified gold nanoparticles have been studied to maintaining long-term stability in biological fluids. Its biodistribution was also reported, however, comparison of bare gold nanoparticles and PEGylated gold nanoparticles with equal particle size is not sufficient. Objective: We prepared bare gold nanoparticles and PEGylated gold nanoparticles with diameters of 20-30-nm or 50-nm to avoid the influence of particle diameter, and studied their biodistribution in the mouse. Methods: Gold concentrations in brain, heart, lungs, liver, stomach, pancreas, spleen, kidneys, blood, urine, and feces were measured at 0.5, 1, 2, 3, 6, 12, 18, 24, and 48 h after administration of gold nanoparticles using inductively coupled plasma atomic emission spectrometry. Results: At 48 h after intravenous administration, accumulation in the liver and spleen was significantly reduced by PEGylation, and the gold amounts of PEGylated gold nanoparticles with diameters of 20-30 nm and 50-nm in the brain were 3.6 times and 2.7 times higher than those of bare gold nanoparticles, respectively. Conclusions: These results indicated that the usefulness of PEGylated gold nanoparticles with small particle size for a drug carrier.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Nanoparticles: synthesis and applications · Nanoparticle-Based Drug Delivery · Gold and Silver Nanoparticles Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Tokyo University of Science
References (30)
Show source-provided references
1. 10.1039/b806051g10.1039/b806051g ↗
2. ChenH. PaholakH. ItoM. SansanaphongprichaK. QianW. CheY. and SunD. ‘Living’ PEGylation on gold nanoparticles to optimize cancer cell uptake by controlling targeting ligand and charge densities Nanotechnology 24 (2013) 355101.10.1088/0957-4484/24/35/355101 ↗
3. 10.1021/ja064968s10.1021/ja064968s ↗
4. 10.1002/anie.20090435910.1002/anie.200904359 ↗
5. 10.1124/pr.57.2.410.1124/pr.57.2.4 ↗
6. 10.1016/j.saa.2004.10.03510.1016/j.saa.2004.10.035 ↗
7. 10.2147/IJN.S4436310.2147/IJN.S44363 ↗
8. 10.1007/s11468-007-9031-110.1007/s11468-007-9031-1 ↗
9. 10.1021/ie060672j10.1021/ie060672j ↗
10. 10.1016/j.bbrc.2010.02.04610.1016/j.bbrc.2010.02.046 ↗
11. 10.1016/j.biomaterials.2010.05.00910.1016/j.biomaterials.2010.05.009 ↗
12. 10.1021/ac061578f10.1021/ac061578f ↗
13. 10.1007/s13404-011-0015-810.1007/s13404-011-0015-8 ↗
14. 10.1016/j.ijpharm.2005.10.01010.1016/j.ijpharm.2005.10.010 ↗
15. 10.1002/smll.20070037810.1002/smll.200700378 ↗
16. 10.3390/ijms1504585210.3390/ijms15045852 ↗
17. 10.1039/C3RA22739A10.1039/C3RA22739A ↗
18. 10.1039/b713631p10.1039/b713631p ↗
19. 10.1016/S1359-6446(03)02903-910.1016/S1359-6446(03)02903-9 ↗
20. 10.1016/j.colsurfb.2008.07.00410.1016/j.colsurfb.2008.07.004 ↗
21. 10.1016/j.colsurfb.2008.02.01310.1016/j.colsurfb.2008.02.013 ↗
22. 10.1039/b712170a10.1039/b712170a ↗
23. 10.3233/BME-16160110.3233/BME-161601 ↗
24. 10.3233/BME-17167710.3233/BME-171677 ↗
25. 10.1016/j.colsurfa.2017.02.05410.1016/j.colsurfa.2017.02.054 ↗
26. 10.1007/s00396-016-3925-410.1007/s00396-016-3925-4 ↗
27. 10.1021/jp025744910.1021/jp0257449 ↗
28. 10.1016/j.bmc.2010.03.05010.1016/j.bmc.2010.03.050 ↗
29. 10.1146/annurev.physchem.58.032806.10460710.1146/annurev.physchem.58.032806.104607 ↗
30. 10.1016/j.biomaterials.2008.12.03810.1016/j.biomaterials.2008.12.038 ↗