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钙磷酸盐包覆核壳结构蛋白纳米载体:姜黄素递送的稳定、控释和增强抗癌活性。

Calcium phosphate coated core-shell protein nanocarriers: Robust stability, controlled release and enhanced anticancer activity for curcumin delivery.

机构信息

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, PR China.

Department of Food Technology and Innovation, Harper Adams University, Newport TF10 8NB, Shropshire, United Kingdom.

出版信息

Mater Sci Eng C Mater Biol Appl. 2020 Oct;115:111094. doi: 10.1016/j.msec.2020.111094. Epub 2020 May 19.

Abstract

Composite protein and inorganic nanodelivery systems can realise a pH-responsive release and effectively improve the stability and anti-cancer proliferative activity of hydrophobic molecules. In this study, a novel core-shell structure of NaCas (Sodium Caseinate)@CaP (Calcium Phosphate) as a nanodelivery system with NaCas as the core for increasing solubility and CaP as the shell for enhanced stability was built. By using Cur (Curcumin) as a model bioactive molecule, (Cur@NaCas)@CaP nanoparticles (NPs) demonstrated a uniform size distribution of 150-200 nm with a distinct nano-composite structure. After exposure to 80 °C for 2 h, the NaCas@CaP loaded Cur still retained 80% stability while under the same conditions only 12% of free Cur remained intact. UV-light stability was remarkably enhanced 8.56 fold by the protection of the core-shell structure. More importantly, pH-responsive release was achieved owing to the CaP surface coating. The encapsulated Cur by NaCas@CaP NPs exhibited an enhanced cellular anti-oxidant activity (CAA) based on MGC-803 cell monolayer models. The confocal laser-scanning microscopy (CLSM) images and cancer-cell-proliferation assay illustrated that (Cur@NaCas)@CaP NPs showed significantly improvements of cellular uptake and anti-cancer activity against A549 cancer cells than free Cur. These novels core-shell NaCas@CaP NPs are very promising for intensifying the stability and bioactivity of hydrophobic compounds in drug delivery and cancer treatment.

摘要

复合蛋白和无机纳米递药系统可以实现 pH 响应释放,并有效提高疏水分子的稳定性和抗癌增殖活性。在这项研究中,构建了一种新型的 NaCas(酪蛋白酸钠)@CaP(磷酸钙)核壳结构纳米递药系统,以 NaCas 为核增加溶解度,以 CaP 为壳增加稳定性。以 Cur(姜黄素)为模型生物活性分子,(Cur@NaCas)@CaP 纳米粒(NPs)表现出 150-200nm 的均匀粒径分布,具有明显的纳米复合材料结构。在 80°C 下暴露 2 小时后,负载 Cur 的 NaCas@CaP 仍保持 80%的稳定性,而在相同条件下,只有 12%的游离 Cur 保持完整。由于核壳结构的保护,紫外光稳定性显著增强了 8.56 倍。更重要的是,由于 CaP 表面涂层实现了 pH 响应释放。NaCas@CaP NPs 包封的 Cur 基于 MGC-803 细胞单层模型显示出增强的细胞抗氧化活性(CAA)。共聚焦激光扫描显微镜(CLSM)图像和癌细胞增殖实验表明,(Cur@NaCas)@CaP NPs 对 A549 癌细胞的细胞摄取和抗癌活性均明显优于游离 Cur。这些新型核壳 NaCas@CaP NPs 非常有前途,可以在药物输送和癌症治疗中增强疏水性化合物的稳定性和生物活性。

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