• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[静脉注射改性磁铁矿纳米颗粒后大鼠肝脏、肺脏、肾脏和脾脏中的巨噬细胞]

[Liver, lung, kidney and spleen macrophages in rats after intravenous administration of the modified magnetite nanoparticles].

作者信息

Mil'to I V

出版信息

Morfologiia. 2014;146(5):40-5.

PMID:25823288
Abstract

Using the immunohistochemical method, mononuclear phagocytes (MNPs) were detected in the liver, lung, kidneys and spleen of rats after a single intravenous injection of a suspension of magnetoliposomes and magnetic microspheres prepared on the basis of nanoscale magnetite particles of (NMPs). The dynamics of the of the number and topography of CD68(+)- and CD163(+)-cells in liver, lung and kidneys was characterized during 120 days after the intravenous injection of the suspension of modified NMPs. It was shown that NMPs surface modification reduced the degree and duration of macrophage activation. Signs of MNPs activation after the infusion of nanomaterial decreased in the following series: unmodified NMPs, magnetoliposomes, magnetic microspheres.

摘要

采用免疫组织化学方法,在大鼠单次静脉注射基于纳米级磁铁矿颗粒(NMPs)制备的磁脂质体和磁性微球悬浮液后,检测其肝脏、肺、肾脏和脾脏中的单核吞噬细胞(MNP)。在静脉注射修饰后的NMPs悬浮液后的120天内,对肝脏、肺和肾脏中CD68(+)和CD163(+)细胞的数量和分布动态进行了表征。结果表明,NMPs表面修饰降低了巨噬细胞激活的程度和持续时间。纳米材料注入后MNP激活的迹象在以下序列中减少:未修饰的NMPs、磁脂质体、磁性微球。

相似文献

1
[Liver, lung, kidney and spleen macrophages in rats after intravenous administration of the modified magnetite nanoparticles].[静脉注射改性磁铁矿纳米颗粒后大鼠肝脏、肺脏、肾脏和脾脏中的巨噬细胞]
Morfologiia. 2014;146(5):40-5.
2
[Structural changes of some organs in rats after a single intravenous injection of magnetite nanoparticles].[单次静脉注射磁铁矿纳米颗粒后大鼠某些器官的结构变化]
Morfologiia. 2012;141(2):49-53.
3
Paeoniflorin regulates macrophage activation in dimethylnitrosamine-induced liver fibrosis in rats.芍药苷调节二甲基亚硝胺诱导的大鼠肝纤维化中巨噬细胞的激活。
BMC Complement Altern Med. 2012 Dec 13;12:254. doi: 10.1186/1472-6882-12-254.
4
[Liver, lung, kidney, heart and spleen structure of rats after multiple intravenous injections of magnetite nanosuspension].[多次静脉注射磁铁矿纳米悬浮液后大鼠的肝脏、肺、肾脏、心脏和脾脏结构]
Vestn Ross Akad Med Nauk. 2012(3):75-9.
5
[Prooxidant and antioxidant activity of blood plasma and histology of internal organs of rats after intravenous administration of magnetite nanoparticles].[静脉注射磁铁矿纳米颗粒后大鼠血浆的促氧化和抗氧化活性及内脏组织学]
Biomed Khim. 2013 May-Jun;59(3):330-8.
6
[Cells of mononuclear phagocytes system of liver and lung in rats after intravenous application of magnetite nanoparticles].[静脉注射磁铁矿纳米颗粒后大鼠肝脏和肺脏单核吞噬细胞系统的细胞]
Tsitologiia. 2012;54(7):566-72.
7
Classically or alternatively activated bovine monocyte-derived macrophages in vitro do not resemble CD163/Calprotectin biased macrophage populations in the teat.体外经典或替代激活的牛单核细胞衍生巨噬细胞与乳房产道中偏向 CD163/钙卫蛋白的巨噬细胞群体不同。
Innate Immun. 2012 Dec;18(6):886-96. doi: 10.1177/1753425912446954. Epub 2012 May 23.
8
Iron metabolism after application of modified magnetite nanoparticles in rats.大鼠应用改性磁铁矿纳米颗粒后的铁代谢
Biochemistry (Mosc). 2014 Nov;79(11):1245-54. doi: 10.1134/S0006297914110121.
9
Heme carrier protein (HCP-1) spatially interacts with the CD163 hemoglobin uptake pathway and is a target of inflammatory macrophage activation.血红素载体蛋白(HCP-1)在空间上与CD163血红蛋白摄取途径相互作用,是炎症性巨噬细胞活化的一个靶点。
J Leukoc Biol. 2008 Feb;83(2):325-33. doi: 10.1189/jlb.0407226. Epub 2007 Oct 18.
10
Altered monocyte and macrophage numbers in blood and organs of chickens injected i.v. with lipopolysaccharide.静脉注射脂多糖的鸡的血液和器官中单核细胞和巨噬细胞数量的改变。
Vet Immunol Immunopathol. 2009 Oct 15;131(3-4):200-10. doi: 10.1016/j.vetimm.2009.04.010. Epub 2009 Apr 19.

引用本文的文献

1
Targeting and Therapy of Glioblastoma in a Mouse Model Using Exosomes Derived From Natural Killer Cells.利用自然杀伤细胞衍生的外泌体在小鼠模型中靶向和治疗神经胶质瘤。
Front Immunol. 2018 Apr 23;9:824. doi: 10.3389/fimmu.2018.00824. eCollection 2018.