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介孔SBA - 15二氧化硅负载槲皮素的纳米制剂:一种可能的肺癌放射增敏剂。

Mesoporous SBA-15 Silica-Loaded Nano-formulation of Quercetin: A Probable Radio-Sensitizer for Lung Carcinoma.

作者信息

Alkahtani Saad, Alarifi Saud, Aljarba Nada H, Alghamdi Hamzah A, Alkahtane Abdullah A

机构信息

Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.

Department of Biology, College of Sciences, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.

出版信息

Dose Response. 2022 Jan 18;20(1):15593258211050532. doi: 10.1177/15593258211050532. eCollection 2022 Jan-Mar.

Abstract

Lung cancer is considered as one of the most serious disease worldwide. The progress of drug carriers based on nonmaterial, which selectively hold chemotherapeutic agents to cancer cells, has become a major focus in biomedical research. This study aimed to evaluate the growth inhibition and apoptosis induction of the human lung cancer cells (A-549) by Q-loaded SBA-15 conjugate system. Mesoporous silica nanoparticles (SBA-15) as host materials for transporting therapeutics medicaments were fabricated for targeted drug delivery toward lung cancer. With the objective of increasing bioavailability and aqueous solubility of flavonoids, SBA-15 was successfully loaded with the quercetin (Q)-a major flavonoid and characterized with the help of Fourier-transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). The biological investigation on A549 cell line confirmed that the efficacy of Q-SBA-15 is much higher than only Q. Moreover, the apoptotic pathway of synthesized Q-SBA-15 NPs examined that the Q-SBA-15-mediated apoptosis PI3K/AKT/mTOR signaling pathway. Thus, the newly conjugated Q-SBA-15 system improved the apoptotic fate through caspase-mediated apoptosis PI3K/AKT/mTOR signaling pathway and hence, it can be potentially employed as an anticancer agent for lung cancer.

摘要

肺癌被认为是全球最严重的疾病之一。基于非物质的药物载体的进展,即选择性地将化疗药物递送至癌细胞,已成为生物医学研究的一个主要焦点。本研究旨在评估负载槲皮素的SBA-15共轭体系对人肺癌细胞(A-549)的生长抑制和凋亡诱导作用。制备了介孔二氧化硅纳米颗粒(SBA-15)作为运输治疗药物的主体材料,用于肺癌的靶向给药。为了提高黄酮类化合物的生物利用度和水溶性,SBA-15成功负载了主要黄酮类化合物槲皮素(Q),并借助傅里叶变换红外光谱(FTIR)和透射电子显微镜(TEM)对其进行了表征。对A549细胞系的生物学研究证实,Q-SBA-15的疗效远高于单独的Q。此外,对合成的Q-SBA-15纳米颗粒的凋亡途径研究表明,Q-SBA-15介导的凋亡通过PI3K/AKT/mTOR信号通路。因此,新的共轭Q-SBA-15体系通过半胱天冬酶介导的凋亡PI3K/AKT/mTOR信号通路改善了凋亡命运,因此,它有可能被用作肺癌的抗癌药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c2e/8777362/89d85f10d2ab/10.1177_15593258211050532-fig1.jpg

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