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载姜黄素的聚乙二醇化介孔硅载药系统的光动力抗菌研究。

Photodynamic antibacterial research on hypericin-loaded PEGylated mesoporous silica delivery system.

机构信息

Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Key Laboratory of Fermentation Engineering (Ministry of Education), Hubei Key Laboratory of Industrial Microbiology, Hubei University of Technology, Wuhan, China.

Hubei Key Lab of Quality and Safety of Traditional Chinese Medicine & Health Food, Jing Brand Chizhengtang Pharmaceutical Co., Ltd, Huangshi, China.

出版信息

J Biomater Sci Polym Ed. 2024 Aug;35(12):1795-1818. doi: 10.1080/09205063.2024.2356961. Epub 2024 May 27.

DOI:10.1080/09205063.2024.2356961
PMID:38801735
Abstract

In this study, a novel drug delivery system (MSN-PEG-Hypericin) was successfully fabricated using tetraethyl orthosilicate and 3-aminopropyltriethoxysilane as raw materials, and the PEGylation of the prepared aminated mesoporous silica and grafting of hypericin onto the carrier were further conducted to obtain MSN-PEG-Hypericin. The successful preparation of MSN-PEG-Hypericin was characterized by several physical-chemical techniques. Furthermore, the MSN-PEG-Hypericin system increased the ability of hypericin to generate reactive oxygen species (ROS) . The cytotoxicity assay and hemolysis analysis showed that MSN-PEG-Hypericin had good biocompatibility. For antibacterial studies, the irradiation time and incubation time of photodynamic therapy (PDT) for and were respectively 8 min and 8 h, and the concentrations of hypericin were 2.5 and 5 μg/mL. The result of triphenyl tetrazolium chloride assay indicated that MSN-PEG-Hypericin had stronger photodynamic antibacterial activity than free hypericin, and was more sensitive to PDT than , which was related to their cell structural differences. The antibacterial mechanism study indicated that the generated ROS could destroy the bacterial structures and cause bacterial death due to the leakage of the contents. The MSN-PEG-Hypericin system prepared in this study had potential application prospects in the antibacterial field.

摘要

在这项研究中,使用正硅酸乙酯和 3-氨丙基三乙氧基硅烷作为原料,成功制备了一种新型药物传递系统(MSN-PEG-Hypericin),并对制备的氨基介孔硅进行了 PEG 化,将 Hypericin 接枝到载体上,得到 MSN-PEG-Hypericin。通过多种物理化学技术对 MSN-PEG-Hypericin 的成功制备进行了表征。此外,MSN-PEG-Hypericin 系统提高了 Hypericin 生成活性氧物种(ROS)的能力。细胞毒性试验和溶血分析表明,MSN-PEG-Hypericin 具有良好的生物相容性。对于抗菌研究,光动力疗法(PDT)的辐照时间和孵育时间分别为 8 min 和 8 h,Hypericin 的浓度分别为 2.5 和 5 μg/mL。三苯基四唑氯化物测定结果表明,MSN-PEG-Hypericin 具有比游离 Hypericin 更强的光动力抗菌活性,并且 比 对 PDT 更敏感,这与它们的细胞结构差异有关。抗菌机制研究表明,生成的 ROS 可以破坏细菌结构,并由于内容物的泄漏导致细菌死亡。本研究中制备的 MSN-PEG-Hypericin 系统在抗菌领域具有潜在的应用前景。

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