Size-dependent in vivo toxicity of PEG-coated gold nanoparticles

Xiao-Dong Zhang, Di Wu, Xiu Shen, Pei-Xun Liu, Na Yang, Bin Zhao, Hao Zhang, Yuan-Ming Sun, Liang-An Zhang, Fei-Yue FanInstitute of Radiation Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin Key Laboratory of Molecular Nuclear Medicine, Tianjin, People&...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Zhang XD, Wu D, Shen X, Liu PX, Yang N, Zhao B, Zhang H, Sun YM, Zhang LA, Fan FY
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2011
Materias:
Acceso en línea:https://doaj.org/article/587e6a4244564dda811694283f52bc20
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:587e6a4244564dda811694283f52bc20
record_format dspace
spelling oai:doaj.org-article:587e6a4244564dda811694283f52bc202021-12-02T05:09:59ZSize-dependent in vivo toxicity of PEG-coated gold nanoparticles1176-91141178-2013https://doaj.org/article/587e6a4244564dda811694283f52bc202011-09-01T00:00:00Zhttp://www.dovepress.com/size-dependent-in-vivo-toxicity-of-peg-coated-gold-nanoparticles-a8322https://doaj.org/toc/1176-9114https://doaj.org/toc/1178-2013Xiao-Dong Zhang, Di Wu, Xiu Shen, Pei-Xun Liu, Na Yang, Bin Zhao, Hao Zhang, Yuan-Ming Sun, Liang-An Zhang, Fei-Yue FanInstitute of Radiation Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin Key Laboratory of Molecular Nuclear Medicine, Tianjin, People’s Republic of ChinaBackground: Gold nanoparticle toxicity research is currently leading towards the in vivo experiment. Most toxicology data show that the surface chemistry and physical dimensions of gold nanoparticles play an important role in toxicity. Here, we present the in vivo toxicity of 5, 10, 30, and 60 nm PEG-coated gold nanoparticles in mice.Methods: Animal survival, weight, hematology, morphology, organ index, and biochemistry were characterized at a concentration of 4000 µg/kg over 28 days.Results: The PEG-coated gold particles did not cause an obvious decrease in body weight or appreciable toxicity even after their breakdown in vivo. Biodistribution results show that 5 nm and 10 nm particles accumulated in the liver and that 30 nm particles accumulated in the spleen, while the 60 nm particles did not accumulate to an appreciable extent in either organ. Transmission electron microscopic observations showed that the 5, 10, 30, and 60 nm particles located in the blood and bone marrow cells, and that the 5 and 60 nm particles aggregated preferentially in the blood cells. The increase in spleen index and thymus index shows that the immune system can be affected by these small nanoparticles. The 10 nm gold particles induced an increase in white blood cells, while the 5 nm and 30 nm particles induced a decrease in white blood cells and red blood cells. The biochemistry results show that the 10 nm and 60 nm PEG-coated gold nanoparticles caused a significant increase in alanine transaminase and aspartate transaminase levels, indicating slight damage to the liver.Conclusion: The toxicity of PEG-coated gold particles is complex, and it cannot be concluded that the smaller particles have greater toxicity. The toxicity of the 10 nm and 60 nm particles was obviously higher than that of the 5 nm and 30 nm particles. The metabolism of these particles and protection of the liver will be more important issues for medical applications of gold-based nanomaterials in future.Keywords: gold nanoparticles, in vivo, toxicity, sizeZhang XDWu DShen XLiu PXYang NZhao BZhang HSun YMZhang LAFan FYDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2011, Iss default, Pp 2071-2081 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Zhang XD
Wu D
Shen X
Liu PX
Yang N
Zhao B
Zhang H
Sun YM
Zhang LA
Fan FY
Size-dependent in vivo toxicity of PEG-coated gold nanoparticles
description Xiao-Dong Zhang, Di Wu, Xiu Shen, Pei-Xun Liu, Na Yang, Bin Zhao, Hao Zhang, Yuan-Ming Sun, Liang-An Zhang, Fei-Yue FanInstitute of Radiation Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin Key Laboratory of Molecular Nuclear Medicine, Tianjin, People’s Republic of ChinaBackground: Gold nanoparticle toxicity research is currently leading towards the in vivo experiment. Most toxicology data show that the surface chemistry and physical dimensions of gold nanoparticles play an important role in toxicity. Here, we present the in vivo toxicity of 5, 10, 30, and 60 nm PEG-coated gold nanoparticles in mice.Methods: Animal survival, weight, hematology, morphology, organ index, and biochemistry were characterized at a concentration of 4000 µg/kg over 28 days.Results: The PEG-coated gold particles did not cause an obvious decrease in body weight or appreciable toxicity even after their breakdown in vivo. Biodistribution results show that 5 nm and 10 nm particles accumulated in the liver and that 30 nm particles accumulated in the spleen, while the 60 nm particles did not accumulate to an appreciable extent in either organ. Transmission electron microscopic observations showed that the 5, 10, 30, and 60 nm particles located in the blood and bone marrow cells, and that the 5 and 60 nm particles aggregated preferentially in the blood cells. The increase in spleen index and thymus index shows that the immune system can be affected by these small nanoparticles. The 10 nm gold particles induced an increase in white blood cells, while the 5 nm and 30 nm particles induced a decrease in white blood cells and red blood cells. The biochemistry results show that the 10 nm and 60 nm PEG-coated gold nanoparticles caused a significant increase in alanine transaminase and aspartate transaminase levels, indicating slight damage to the liver.Conclusion: The toxicity of PEG-coated gold particles is complex, and it cannot be concluded that the smaller particles have greater toxicity. The toxicity of the 10 nm and 60 nm particles was obviously higher than that of the 5 nm and 30 nm particles. The metabolism of these particles and protection of the liver will be more important issues for medical applications of gold-based nanomaterials in future.Keywords: gold nanoparticles, in vivo, toxicity, size
format article
author Zhang XD
Wu D
Shen X
Liu PX
Yang N
Zhao B
Zhang H
Sun YM
Zhang LA
Fan FY
author_facet Zhang XD
Wu D
Shen X
Liu PX
Yang N
Zhao B
Zhang H
Sun YM
Zhang LA
Fan FY
author_sort Zhang XD
title Size-dependent in vivo toxicity of PEG-coated gold nanoparticles
title_short Size-dependent in vivo toxicity of PEG-coated gold nanoparticles
title_full Size-dependent in vivo toxicity of PEG-coated gold nanoparticles
title_fullStr Size-dependent in vivo toxicity of PEG-coated gold nanoparticles
title_full_unstemmed Size-dependent in vivo toxicity of PEG-coated gold nanoparticles
title_sort size-dependent in vivo toxicity of peg-coated gold nanoparticles
publisher Dove Medical Press
publishDate 2011
url https://doaj.org/article/587e6a4244564dda811694283f52bc20
work_keys_str_mv AT zhangxd sizedependentinvivotoxicityofpegcoatedgoldnanoparticles
AT wud sizedependentinvivotoxicityofpegcoatedgoldnanoparticles
AT shenx sizedependentinvivotoxicityofpegcoatedgoldnanoparticles
AT liupx sizedependentinvivotoxicityofpegcoatedgoldnanoparticles
AT yangn sizedependentinvivotoxicityofpegcoatedgoldnanoparticles
AT zhaob sizedependentinvivotoxicityofpegcoatedgoldnanoparticles
AT zhangh sizedependentinvivotoxicityofpegcoatedgoldnanoparticles
AT sunym sizedependentinvivotoxicityofpegcoatedgoldnanoparticles
AT zhangla sizedependentinvivotoxicityofpegcoatedgoldnanoparticles
AT fanfy sizedependentinvivotoxicityofpegcoatedgoldnanoparticles
_version_ 1718400530698469376