Physiological function and inflamed-brain migration of mouse monocyte-derived macrophages following cellular uptake of superparamagnetic iron oxide nanoparticles-Implication of macrophage-based drug delivery into-the central nervous system

doi:10.1016/j.ijpharm.2016.03.028

IOCAS-IR > 实验海洋生物学重点实验室

	Physiological function and inflamed-brain migration of mouse monocyte-derived macrophages following cellular uptake of superparamagnetic iron oxide nanoparticles-Implication of macrophage-based drug delivery into-the central nervous system
	Tong, Hsin-I 1,2; Kang, Wen 1,3; Shi, Yingli1,4 ; Zhou, Guangzhou 1,5; Lu, Yuanan 1
	2016-05-30
发表期刊	INTERNATIONAL JOURNAL OF PHARMACEUTICS
卷号	505 期号:1-2 页码:271-282
文章类型	Article
摘要	This study was designed to use superparamagnetic iron oxide nanoparticles (SPIONs) as evaluating tools to study monocyte-derived macrophages (MDM)-mediated delivery of small molecular agents into the diseased brains. MDM were tested with different-configured SPIONs at selected concentrations for their impacts on carrier cells' physiological and migratory properties, which were found to depend largely on particle size, coating, and treatment concentrations. SHP30, a SPION of 30-nm core size with oleic acids plus amphiphilic polymer coating, was identified to have high cellular uptake efficiency and cause little cytotoxic effects on MDM. At lower incubation dose (25 mu g/mL), few alteration was observed in carrier cells' physiological and in vivo migratory functions, as tested in a lipopolysaccharide-induced acute neuroinflammation mouse model. Nevertheless, significant increase in monocyte-to-macrophage differentiation, and decrease in in vivo carrier MDM inflamed-brain homing ability were found in groups treated with a higher dose of SHP30 at 100 mu g/mL. Overall, our results have identified MDM treatment at 25 mu g/mL SHP30 resulted in little functional changes, provided valuable parameters for using SPIONs as evaluating tools to study MDM-mediated therapeutics carriage and delivery, and supported the concepts of using monocytes-macrophages as cellular vehicles to transport small molecular agents to the brain. (C) 2016 Elsevier B.V. All rights reserved.
关键词	Nanoparticle Surface Coating Nanoparticle Size Monocyte-macrophage Drug Delivery Monocyte-macrophage Brain Migration Spions Neuroinflammation
DOI	10.1016/j.ijpharm.2016.03.028
收录类别	SCI
语种	英语
WOS记录号	WOS:000376695900031
引用统计	被引频次：27[WOS] [WOS记录] [WOS相关记录]
文献类型	期刊论文
条目标识符	http://ir.qdio.ac.cn/handle/337002/126225
专题	实验海洋生物学重点实验室
作者单位	1.Univ Hawaii Manoa, Off Publ Hlth Studies, Honolulu, HI 96822 USA 2.Univ Hawaii Manoa, Dept Microbiol, Honolulu, HI 96822 USA 3.Fourth Mil Med Univ, Tangdu Hosp, Dept Infect Dis, Xian 710032, Shaanxi, Peoples R China 4.Chinese Acad Sci, Inst Oceanol, Qingdao, Shandong, Peoples R China 5.Henan Univ Technol, Coll Bioengn, Zhengzhou 450000, Henan, Peoples R China
推荐引用方式 GB/T 7714	Tong, Hsin-I,Kang, Wen,Shi, Yingli,et al. Physiological function and inflamed-brain migration of mouse monocyte-derived macrophages following cellular uptake of superparamagnetic iron oxide nanoparticles-Implication of macrophage-based drug delivery into-the central nervous system[J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS,2016,505(1-2):271-282.
APA	Tong, Hsin-I,Kang, Wen,Shi, Yingli,Zhou, Guangzhou,&Lu, Yuanan.(2016).Physiological function and inflamed-brain migration of mouse monocyte-derived macrophages following cellular uptake of superparamagnetic iron oxide nanoparticles-Implication of macrophage-based drug delivery into-the central nervous system.INTERNATIONAL JOURNAL OF PHARMACEUTICS,505(1-2),271-282.
MLA	Tong, Hsin-I,et al."Physiological function and inflamed-brain migration of mouse monocyte-derived macrophages following cellular uptake of superparamagnetic iron oxide nanoparticles-Implication of macrophage-based drug delivery into-the central nervous system".INTERNATIONAL JOURNAL OF PHARMACEUTICS 505.1-2(2016):271-282.

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