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用于喉癌细胞靶向治疗的荧光金属有机框架核碳酸钙-聚乙烯亚胺-叶酸壳层纳米粒子的设计与体外评价

Design and In Vitro Evaluation of Fluorescent MOF-Core CaCO₃-PEI-FA Shell Nanoparticles for Targeted Therapy of Laryngeal Cancer Cells.

作者信息

Zhu Hongmei, Yang Bo, Niu Yang, Huang Yongjiu

机构信息

Department of Otolaryngology, Taizhou People's Hospital Affiliated to Nanjing Medical University, Taizhou, Jiangsu, China.

出版信息

J Fluoresc. 2024 Oct 23. doi: 10.1007/s10895-024-04013-z.

Abstract

Laryngeal cancer, a common malignant respiratory tumor, is primarily treated through surgery. However, challenges such as recurrence, metastasis, and drug resistance persist. In recent years, multifunctional drug delivery systems (DDS) based on nanoparticles have shown great potential in improving drug loading and release. We developed a biocompatible core-shell nanoparticle system with a zinc-based metal-organic framework (MOF) as the core, named CP1. The shell, composed of polyethyleneimine (PEI), folic acid, and calcium carbonate, forms a composite called CaCO-PEI-FA. This system enhances biocompatibility and increases the efficacy of biomedical applications. Encapsulating CP1 within the CaCO-PEI-FA shell allows for the targeted delivery of the anticancer drug doxorubicin (DOX) to laryngeal cancer cells (Hep-2), resulting in the CaCO-PEI-FA@CP1@DOX system. The CaCO-PEI-FA composite exhibits strong fluorescence with a peak around 350 nm, confirming successful synthesis and demonstrating its potential as a bioimaging probe. Importantly, the nanoparticle system without DOX showed low toxicity to normal human skin fibroblasts (HSF). In vitro cytology experiments revealed a 38% inhibition rate of Hep-2 cells after 24 h, highlighting the nanocomposite's significant potential in inhibiting laryngeal cancer cell proliferation and inducing apoptosis, underscoring its promise in targeted laryngeal cancer therapy.

摘要

喉癌是一种常见的恶性呼吸道肿瘤,主要通过手术治疗。然而,复发、转移和耐药性等挑战依然存在。近年来,基于纳米颗粒的多功能药物递送系统(DDS)在提高药物负载和释放方面显示出巨大潜力。我们开发了一种以锌基金属有机框架(MOF)为核心的生物相容性核壳纳米颗粒系统,命名为CP1。外壳由聚乙烯亚胺(PEI)、叶酸和碳酸钙组成,形成一种名为CaCO-PEI-FA的复合材料。该系统增强了生物相容性,并提高了生物医学应用的功效。将CP1包裹在CaCO-PEI-FA外壳内可实现抗癌药物阿霉素(DOX)向喉癌细胞(Hep-2)的靶向递送,从而形成CaCO-PEI-FA@CP1@DOX系统。CaCO-PEI-FA复合材料在350 nm左右呈现出强荧光峰,证实了其成功合成,并展示了其作为生物成像探针的潜力。重要的是,不含DOX的纳米颗粒系统对正常人皮肤成纤维细胞(HSF)显示出低毒性。体外细胞学实验显示,24小时后Hep-2细胞的抑制率为38%,突出了该纳米复合材料在抑制喉癌细胞增殖和诱导凋亡方面的巨大潜力,强调了其在喉癌靶向治疗中的前景。

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