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基于钙的纳米颗粒可加速皮肤伤口愈合。

Calcium-based nanoparticles accelerate skin wound healing.

机构信息

Hagey Laboratory for Pediatric Regenerative Medicine, Stanford University School of Medicine, Stanford, California, United States of America.

出版信息

PLoS One. 2011;6(11):e27106. doi: 10.1371/journal.pone.0027106. Epub 2011 Nov 2.

Abstract

INTRODUCTION

Nanoparticles (NPs) are small entities that consist of a hydroxyapatite core, which can bind ions, proteins, and other organic molecules from the surrounding environment. These small conglomerations can influence environmental calcium levels and have the potential to modulate calcium homeostasis in vivo. Nanoparticles have been associated with various calcium-mediated disease processes, such as atherosclerosis and kidney stone formation. We hypothesized that nanoparticles could have an effect on other calcium-regulated processes, such as wound healing. In the present study, we synthesized pH-sensitive calcium-based nanoparticles and investigated their ability to enhance cutaneous wound repair.

METHODS

Different populations of nanoparticles were synthesized on collagen-coated plates under various growth conditions. Bilateral dorsal cutaneous wounds were made on 8-week-old female Balb/c mice. Nanoparticles were then either administered intravenously or applied topically to the wound bed. The rate of wound closure was quantified. Intravenously injected nanoparticles were tracked using a FLAG detection system. The effect of nanoparticles on fibroblast contraction and proliferation was assessed.

RESULTS

A population of pH-sensitive calcium-based nanoparticles was identified. When intravenously administered, these nanoparticles acutely increased the rate of wound healing. Intravenously administered nanoparticles were localized to the wound site, as evidenced by FLAG staining. Nanoparticles increased fibroblast calcium uptake in vitro and caused contracture of a fibroblast populated collagen lattice in a dose-dependent manner. Nanoparticles also increased the rate of fibroblast proliferation.

CONCLUSION

Intravenously administered, calcium-based nanoparticles can acutely decrease open wound size via contracture. We hypothesize that their contraction effect is mediated by the release of ionized calcium into the wound bed, which occurs when the pH-sensitive nanoparticles disintegrate in the acidic wound microenvironment. This is the first study to demonstrate that calcium-based nanoparticles can have a therapeutic benefit, which has important implications for the treatment of wounds.

摘要

简介

纳米粒子(NPs)是由羟磷灰石核心组成的小实体,可与周围环境中的离子、蛋白质和其他有机分子结合。这些小聚集体可以影响环境中的钙水平,并有可能调节体内的钙稳态。纳米粒子与多种钙介导的疾病过程有关,如动脉粥样硬化和肾结石形成。我们假设纳米粒子可能对其他钙调节过程有影响,如伤口愈合。在本研究中,我们合成了 pH 敏感的钙基纳米粒子,并研究了它们增强皮肤伤口修复的能力。

方法

在不同的生长条件下,在胶原蛋白涂层的平板上合成了不同群体的纳米粒子。在 8 周龄雌性 Balb/c 小鼠的双侧背部皮肤制造伤口。然后将纳米粒子经静脉内或局部施用于伤口床。量化伤口闭合率。使用 FLAG 检测系统跟踪静脉内注射的纳米粒子。评估纳米粒子对成纤维细胞收缩和增殖的影响。

结果

鉴定出一种 pH 敏感的钙基纳米粒子群体。当静脉内给药时,这些纳米粒子可急性增加伤口愈合速度。静脉内给予的纳米粒子被定位到伤口部位,如 FLAG 染色所示。纳米粒子在体外增加成纤维细胞钙摄取,并以剂量依赖的方式引起成纤维细胞填充的胶原格子的收缩。纳米粒子还增加了成纤维细胞的增殖速度。

结论

静脉内给予的钙基纳米粒子可通过收缩急性减小开放伤口的大小。我们假设它们的收缩作用是通过将离子化钙释放到伤口床中介导的,当 pH 敏感的纳米粒子在酸性伤口微环境中崩解时发生这种释放。这是第一项证明钙基纳米粒子具有治疗益处的研究,这对伤口治疗具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/869a/3206933/d02658c3e211/pone.0027106.g001.jpg

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