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载硫辛酸的中空金纳米粒子设计用于骨质疏松治疗:制备、表征和评价。

α-Lipoic acid loaded hollow gold nanoparticles designed for osteoporosis treatment: preparation, characterization and evaluation.

机构信息

Department of Spine Surgery, Second Affiliated Hospital of Naval Medical University, Shanghai, China.

Department of Spine Surgery, the Second People's Hospital of Changshu, Changshu, China.

出版信息

Artif Cells Nanomed Biotechnol. 2023 Dec;51(1):131-138. doi: 10.1080/21691401.2022.2149542.

Abstract

Osteoporosis is a common disease among the ageing society. Oxidative stress caused by excessive accumulation of reactive oxygen species (ROS) is the aetiology of osteoporosis. α-Lipoic acid (ALA) is an antioxidant in the body, which can eliminate excess ROS in the body and inhibits levels of oxidative stress in cells. Herein, we designed PEGylated hollow gold nanoparticles (HGNPs) loaded with ALA (mPEG@HGNPs-ALA) to remove ROS in the treatment of osteoporosis. First, mPEG@HGNPs with a particle size of ∼63 nm has been successfully synthesized. By comparing the drug loading of mPEG@HGNPs, it was concluded that the optimal mass ratio of mPEG@HGNPs (calculated by the amount of gold) to ALA was ∼1:2. ABTS antioxidant assay showed that free radical removal ability. results revealed that the preparation had good biocompatibility. At the gold concentration of 1-150 μg/mL, the cell viability of mPEG@HGNPs was more than 100%, which indicated that it could promote the proliferation of osteoblasts. What's more, mPEG@HGNPs-ALA could effectively remove the ROS caused by HO injury and improve the cell viability. According to these results, it can be considered that mPEG@HGNPs-ALA has the potential to treat osteoporosis.

摘要

骨质疏松症是老龄化社会的一种常见疾病。活性氧(ROS)过度积累引起的氧化应激是骨质疏松症的病因。α-硫辛酸(ALA)是体内的一种抗氧化剂,它可以清除体内多余的 ROS,并抑制细胞内氧化应激水平。在此,我们设计了负载 ALA 的聚乙二醇化空心金纳米颗粒(mPEG@HGNPs-ALA),以消除 ROS,用于骨质疏松症的治疗。首先,成功合成了粒径约为 63nm 的 mPEG@HGNPs。通过比较 mPEG@HGNPs 的载药量,得出 mPEG@HGNPs(按金的量计算)与 ALA 的最佳质量比约为 1:2。ABTS 抗氧化测定结果表明,游离基清除能力。结果表明,该制剂具有良好的生物相容性。在金浓度为 1-150μg/mL 时,mPEG@HGNPs 的细胞活力超过 100%,这表明它可以促进成骨细胞的增殖。更重要的是,mPEG@HGNPs-ALA 可以有效清除 HO 损伤引起的 ROS,提高细胞活力。根据这些结果,可以认为 mPEG@HGNPs-ALA 有治疗骨质疏松症的潜力。

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