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基于壳聚糖的静电或空间稳定的氧化铁纳米粒子水基悬浮液的制备、表征及生物相容性。

Water-Based Suspensions of Iron Oxide Nanoparticles with Electrostatic or Steric Stabilization by Chitosan: Fabrication, Characterization and Biocompatibility.

机构信息

Departamento de Electricidad y Electrónica and BCMaterials, Universidad del País Vasco UPV-EHU, 48080 Bilbao, Spain.

Institute of Natural Sciences and Mathematics, Ural Federal University, Ekaterinburg 620002, Russia.

出版信息

Sensors (Basel). 2017 Nov 13;17(11):2605. doi: 10.3390/s17112605.

Abstract

Present day biomedical applications, including magnetic biosensing, demand better understanding of the interactions between living systems and magnetic nanoparticles (MNPs). In this work spherical MNPs of maghemite were obtained by a highly productive laser target evaporation technique. XRD analysis confirmed the inverse spinel structure of the MNPs (space group Fd-3m). The ensemble obeyed a lognormal size distribution with the median value 26.8 nm and dispersion 0.362. Stabilized water-based suspensions were fabricated using electrostatic or steric stabilization by the natural polymer chitosan. The encapsulation of the MNPs by chitosan makes them resistant to the unfavorable factors for colloidal stability typically present in physiological conditions such as pH and high ionic force. Controlled amounts of suspensions were used for in vitro experiments with human blood mononuclear leukocytes (HBMLs) in order to study their morphofunctional response. For sake of comparison the results obtained in the present study were analyzed together with our previous results of the study of similar suspensions with human mesenchymal stem cells. Suspensions with and without chitosan enhanced the secretion of cytokines by a 24-h culture of HBMLs compared to a control without MNPs. At a dose of 2.3, the MTD of chitosan promotes the stimulating effect of MNPs on cells. In the dose range of MNPs 10-1000 MTD, chitosan "inhibits" cellular secretory activity compared to MNPs without chitosan. Both suspensions did not caused cell death by necrosis, hence, the secretion of cytokines is due to the enhancement of the functional activity of HBMLs. Increased accumulation of MNP with chitosan in the cell fraction at 100 MTD for 24 h exposure, may be due to fixation of chitosan on the outer membrane of HBMLs. The discussed results can be used for an addressed design of cell delivery/removal incorporating multiple activities because of cell capability to avoid phagocytosis by immune cells. They are also promising for the field of biosensor development for the detection of magnetic labels.

摘要

当今的生物医学应用,包括磁生物传感,需要更好地理解活系统与磁性纳米粒子(MNPs)之间的相互作用。在这项工作中,通过高效的激光靶蒸发技术获得了球形的磁赤铁矿 MNPs。XRD 分析证实了 MNPs 的反尖晶石结构(空间群 Fd-3m)。集合体遵循对数正态尺寸分布,中值为 26.8nm,分散度为 0.362。通过天然聚合物壳聚糖静电或空间稳定作用制备了稳定的水基悬浮液。MNPs 被壳聚糖包裹,使它们能够抵抗胶体稳定性的不利因素,这些因素通常存在于生理条件下,如 pH 值和高离子强度。控制一定量的悬浮液用于与人类单核白细胞(HBML)的体外实验,以研究其形态功能反应。为了进行比较,分析了本研究中获得的结果以及我们以前关于具有类似悬浮液的人类间充质干细胞的研究结果。与不含 MNPs 的对照组相比,含有和不含有壳聚糖的悬浮液均增强了 HBML 培养 24 小时后的细胞因子分泌。壳聚糖的 MTD 为 2.3 时,促进了 MNPs 对细胞的刺激作用。在 MNPs 的剂量范围 10-1000 MTD 内,壳聚糖“抑制”了细胞的分泌活性,与不含壳聚糖的 MNPs 相比。两种悬浮液都没有通过坏死引起细胞死亡,因此,细胞因子的分泌是由于 HBMLs 功能活性的增强。在 100 MTD 暴露 24 小时后,MNPs 与壳聚糖在细胞部分的积累增加,这可能是由于壳聚糖固定在 HBMLs 的外膜上。讨论的结果可用于设计具有多种活性的细胞输送/去除,因为细胞有能力避免被免疫细胞吞噬。它们也有望用于开发用于检测磁性标签的生物传感器领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d95a/5712992/e50ae9a51300/sensors-17-02605-g001.jpg

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