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2
Electrophoretic Deposition of Dexamethasone-Loaded Mesoporous Silica Nanoparticles onto Poly(L-Lactic Acid)/Poly(ε-Caprolactone) Composite Scaffold for Bone Tissue Engineering.载地塞米松介孔硅纳米粒子的电泳沉积到聚(L-乳酸)/聚(ε-己内酯)复合支架用于骨组织工程。
ACS Appl Mater Interfaces. 2016 Feb 17;8(6):4137-48. doi: 10.1021/acsami.5b11879. Epub 2016 Feb 5.
3
Gold nanoparticles with different charge and moiety induce differential cell response on mesenchymal stem cell osteogenesis.带不同电荷和部分的金纳米粒子诱导间充质干细胞成骨分化的差异细胞反应。
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4
A Dual Gold Nanoparticle System for Mesenchymal Stem Cell Tracking.用于间充质干细胞追踪的双金纳米颗粒系统
J Mater Chem B. 2014 Dec 14;2(46):8220-8230. doi: 10.1039/C4TB00975D.
5
RGD peptide-modified dendrimer-entrapped gold nanoparticles enable highly efficient and specific gene delivery to stem cells.RGD 肽修饰的树突状聚合物包裹的金纳米粒子能够高效、特异地将基因递送至干细胞。
ACS Appl Mater Interfaces. 2015 Mar 4;7(8):4833-43. doi: 10.1021/am508760w. Epub 2015 Feb 19.
6
Biocompatibility of tungsten disulfide inorganic nanotubes and fullerene-like nanoparticles with salivary gland cells.二硫化钨无机纳米管和类富勒烯纳米颗粒与唾液腺细胞的生物相容性。
Tissue Eng Part A. 2015 Mar;21(5-6):1013-23. doi: 10.1089/ten.TEA.2014.0163. Epub 2014 Dec 19.
7
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8
Imaging strategies for tissue engineering applications.用于组织工程应用的成像策略。
Tissue Eng Part B Rev. 2015 Feb;21(1):88-102. doi: 10.1089/ten.TEB.2014.0180. Epub 2014 Aug 19.
9
Magnetic resonance functional nano-hydroxyapatite incorporated poly(caprolactone) composite scaffolds for in situ monitoring of bone tissue regeneration by MRI.用于通过磁共振成像原位监测骨组织再生的磁性共振功能化纳米羟基磷灰石复合聚己内酯支架
Tissue Eng Part A. 2014 Oct;20(19-20):2783-94. doi: 10.1089/ten.TEA.2014.0161. Epub 2014 Aug 20.
10
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Acta Biomater. 2014 Jan;10(1):439-49. doi: 10.1016/j.actbio.2013.09.037. Epub 2013 Oct 3.

载金超顺磁氧化铁核壳纳米粒子促进 MC3T3-E1 细胞成骨分化的浓度依赖性研究。

SPIO-Au core-shell nanoparticles for promoting osteogenic differentiation of MC3T3-E1 cells: Concentration-dependence study.

机构信息

Heavy Engineering 133, Department of Mechanical Engineering, State University of New York at Stony Brook, Stony Brook, New York, 11794-2300.

LE 153, Department of Mechanical Engineering, State University of New York at Stony Brook, Stony Brook, New York, 11794-2300.

出版信息

J Biomed Mater Res A. 2017 Dec;105(12):3350-3359. doi: 10.1002/jbm.a.36200. Epub 2017 Sep 19.

DOI:10.1002/jbm.a.36200
PMID:28869707
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5761339/
Abstract

This work aims to explore the concentration-dependence of SPIO-Au core-shell nanoscale particles (NPs) (17.3 ± 1.2 nm in diameter) on biocompatibility and osteogenic differentiation of preosteoblast MC3T3-E1 cells. The stability of NPs was first investigated by UV-vis absorption spectra and zeta potential measurement. Then concentration effects of NPs (1-80 μg/mL) were evaluated on viability, morphology, proliferation, cellular uptake, and alkaline phosphate (ALP) activity levels. Results have shown strong stability and no acute toxicity (viability > 93%) or morphological difference at all concentration levels of NPs. The proliferation results indicated that the concentration of NPs below 40 μg/mL does not affect the cell proliferation for 7 days of incubation. Transmission electron microscopy images revealed the successful internalization of NPs into MC3T3-E1 cells and the dose-dependent accumulation of NPs inside the cytoplasm. The ALP level of MC3T3-E1 cells was improved by 49% (of control) after treated with NPs at 10 μg/mL for 10 days, indicating their positive effect on early osteogenic differentiation. This study confirmed the excellent biocompatibility of SPIO-Au NPs and their great potential for promoting osteogenic differentiation and promised the future application for these NPs in bone engineering including drug delivery, cell labeling, and activity tracking within scaffolds. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 3350-3359, 2017.

摘要

本研究旨在探索超顺磁性氧化铁-金(SPIO-Au)核壳纳米粒子(NPs)(直径为 17.3±1.2nm)的浓度依赖性对前成骨细胞 MC3T3-E1 细胞的生物相容性和成骨分化的影响。首先通过紫外-可见吸收光谱和 Zeta 电位测量来研究 NPs 的稳定性。然后评估了 NPs(1-80μg/mL)浓度对细胞活力、形态、增殖、细胞摄取和碱性磷酸酶(ALP)活性水平的影响。结果表明,NPs 具有很强的稳定性,且在所有浓度水平下均无急性毒性(活力>93%)或形态差异。增殖结果表明,NPs 浓度低于 40μg/mL 时,在孵育 7 天内不会影响细胞增殖。透射电子显微镜图像显示 NPs 成功地被内化到 MC3T3-E1 细胞内,并且 NPs 在细胞质内呈剂量依赖性积累。用 10μg/mL 的 NPs 处理 10 天后,MC3T3-E1 细胞的 ALP 水平提高了 49%(与对照相比),表明其对早期成骨分化具有积极作用。本研究证实了 SPIO-Au NPs 的优异生物相容性及其在促进成骨分化方面的巨大潜力,并为这些 NPs 在骨工程中的未来应用(包括药物输送、细胞标记和支架内活性跟踪)提供了保证。© 2017 Wiley Periodicals, Inc. J 生物材料 Res 部分 A:105A:3350-3359,2017。