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介孔氧化石墨烯纳米复合材料有效联合化疗/光疗治疗非小细胞肺癌。

Mesoporous Graphene Oxide Nanocomposite Effective for Combined Chemo/Photo Therapy Against Non-Small Cell Lung Cancer.

机构信息

Department of Medical Chemistry, School of Basic Medical Science, Shanxi Medical University, Taiyuan, Shanxi, 030000, People's Republic of China.

Department of Cardiothoracic Surgery, People's Hospital of Lvliang, Lvliang, Shanxi, 033099, People's Republic of China.

出版信息

Int J Nanomedicine. 2024 Jul 24;19:7493-7508. doi: 10.2147/IJN.S460767. eCollection 2024.

Abstract

INTRODUCTION

Lung cancer is the most common cancer worldwide, among which non-small cell lung cancer (NSCLC) accounts for about 80% of all lung cancers. Chemotherapy, a mainstay modality for NSCLC, has demonstrated restricted effectiveness due to the emergence of chemo-resistance and systemic side effects. Studies have indicated that combining chemotherapy with phototherapy, such as photodynamic therapy (PDT) and photothermal therapy (PTT), can enhance efficacy of therapy. In this work, an aminated mesoporous graphene oxide (rPGO)-protoporphyrin IX (PPIX)-hyaluronic acid (HA)@Osimertinib (AZD) nanodrug delivery system (rPPH@AZD) was successfully developed for combined chemotherapy/phototherapy for NSCLC.

METHODS

A pH/hyaluronidase-responsive nanodrug delivery system (rPPH@AZD) was prepared using mesoporous graphene oxide. Its morphology, elemental composition, surface functional groups, optical properties, in vitro drug release ability, photothermal properties, reactive oxygen species production, cellular uptake and cell viability were evaluated. In addition, the in vivo therapeutic effect, biocompatibility, and imaging capabilities of rPPH@AZD were verified by a tumor-bearing mouse model.

RESULTS

Aminated mesoporous graphene oxide (rPGO) plays a role as a drug delivery vehicle owing to its large specific surface area and ease of surface functionalization. rPGO exhibits excellent photothermal conversion properties under laser irradiation, while PPIX acts as a photosensitizer to generate singlet oxygen. AZD acts as a small molecule targeted drug in chemotherapy. In essence, rPPH@AZD shows excellent photothermal and fluorescence imaging effects in tumor-bearing mice. More importantly, in vitro and in vivo results indicate that rPPH@AZD can achieve hyaluronidase/pH dual response as well as combined chemotherapy/PTT/PDT anti-NSCLC treatment.

CONCLUSION

The newly prepared rPPH@AZD can serve as a promising pH/hyaluronidase-responsive nanodrug delivery system that integrates photothermal/fluorescence imaging and chemo/photo combined therapy for efficient therapy against NSCLC.

摘要

简介

肺癌是全球最常见的癌症,其中非小细胞肺癌(NSCLC)约占所有肺癌的 80%。化疗是 NSCLC 的主要治疗方式,但由于化疗耐药和全身副作用的出现,其疗效受到限制。研究表明,将化疗与光疗(如光动力疗法(PDT)和光热疗法(PTT))相结合可以提高治疗效果。在这项工作中,成功开发了一种胺化介孔氧化石墨烯(rPGO)-原卟啉 IX(PPIX)-透明质酸(HA)@奥希替尼(AZD)纳米药物递送系统(rPPH@AZD),用于 NSCLC 的联合化疗/光疗。

方法

采用介孔氧化石墨烯制备了一种 pH/透明质酸酶响应型纳米药物递送系统(rPPH@AZD)。对其形态、元素组成、表面官能团、光学性质、体外药物释放能力、光热性能、活性氧产生、细胞摄取和细胞活力进行了评价。此外,通过荷瘤小鼠模型验证了 rPPH@AZD 的体内治疗效果、生物相容性和成像能力。

结果

胺化介孔氧化石墨烯(rPGO)具有较大的比表面积和易于表面功能化的特点,可作为药物载体。rPGO 在激光照射下表现出优异的光热转换性能,而 PPIX 则作为光敏剂产生单线态氧。AZD 作为化疗的小分子靶向药物。本质上,rPPH@AZD 在荷瘤小鼠中表现出优异的光热和荧光成像效果。更重要的是,体外和体内结果表明,rPPH@AZD 可以实现透明质酸酶/pH 双重响应以及联合化疗/PTT/PDT 抗 NSCLC 治疗。

结论

新制备的 rPPH@AZD 可以作为一种有前途的 pH/透明质酸酶响应型纳米药物递送系统,集光热/荧光成像和化疗/光疗联合治疗于一体,高效治疗 NSCLC。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5173/11287468/ac27bf5f45da/IJN-19-7493-g0001.jpg

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