Polymer composites with enhanced electrochemical properties and their application in non-small cell lung cancer treatment

IF 4 2区 化学 Q2 CHEMISTRY, PHYSICAL
Yujun Wei , Zhiling Zhang , Tianrang Ao
{"title":"Polymer composites with enhanced electrochemical properties and their application in non-small cell lung cancer treatment","authors":"Yujun Wei ,&nbsp;Zhiling Zhang ,&nbsp;Tianrang Ao","doi":"10.1016/j.molstruc.2025.141813","DOIUrl":null,"url":null,"abstract":"<div><div>Cancer, particularly non-small cell lung cancer (NSCLC), remains a leading cause of cancer-related deaths, with a dismal 5-year survival rate of approximately 15 %. This underscores the urgent need for novel, safe, and effective targeted therapies. In this study, we synthesized compound 1 for lung cancer treatment, considering the challenges in drug delivery. A new three-dimensional (3D) La(III)-based coordination polymer with the chemical composition of {[La(L)(H<sub>2</sub>O)<sub>3</sub>]Cl·H<sub>2</sub>O}<sub>n</sub> (<strong>1</strong>) (H<sub>2</sub>L = (4-(pyridyl-N-oxide)methylphosphonic acid), was successfully self-assembled via diffusion method at room temperature and characterized by single-crystal X-ray diffraction, elemental analyses and FT-IR. Following this, we developed a composite drug delivery material, PCL-CB@CP1@1, and assessed its inhibitory effects on NSCLC cell proliferation. The results demonstrated that PCL-CB@CP1@1 effectively inhibited cell growth by modulating the Nrf2/HO-1/GPX4 signaling pathway. Additionally, molecular docking simulations indicated multiple binding interactions between the La(III) complex and receptor sites, further highlighting its significant biological activity. These findings suggest that PCL-CB@CP1@1 holds potential as a targeted therapeutic agent for lung cancer treatment, offering new possibilities for improving patient outcomes.</div></div>","PeriodicalId":16414,"journal":{"name":"Journal of Molecular Structure","volume":"1334 ","pages":"Article 141813"},"PeriodicalIF":4.0000,"publicationDate":"2025-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Structure","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022286025004995","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Cancer, particularly non-small cell lung cancer (NSCLC), remains a leading cause of cancer-related deaths, with a dismal 5-year survival rate of approximately 15 %. This underscores the urgent need for novel, safe, and effective targeted therapies. In this study, we synthesized compound 1 for lung cancer treatment, considering the challenges in drug delivery. A new three-dimensional (3D) La(III)-based coordination polymer with the chemical composition of {[La(L)(H2O)3]Cl·H2O}n (1) (H2L = (4-(pyridyl-N-oxide)methylphosphonic acid), was successfully self-assembled via diffusion method at room temperature and characterized by single-crystal X-ray diffraction, elemental analyses and FT-IR. Following this, we developed a composite drug delivery material, PCL-CB@CP1@1, and assessed its inhibitory effects on NSCLC cell proliferation. The results demonstrated that PCL-CB@CP1@1 effectively inhibited cell growth by modulating the Nrf2/HO-1/GPX4 signaling pathway. Additionally, molecular docking simulations indicated multiple binding interactions between the La(III) complex and receptor sites, further highlighting its significant biological activity. These findings suggest that PCL-CB@CP1@1 holds potential as a targeted therapeutic agent for lung cancer treatment, offering new possibilities for improving patient outcomes.
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Molecular Structure
Journal of Molecular Structure 化学-物理化学
CiteScore
7.10
自引率
15.80%
发文量
2384
审稿时长
45 days
期刊介绍: The Journal of Molecular Structure is dedicated to the publication of full-length articles and review papers, providing important new structural information on all types of chemical species including: • Stable and unstable molecules in all types of environments (vapour, molecular beam, liquid, solution, liquid crystal, solid state, matrix-isolated, surface-absorbed etc.) • Chemical intermediates • Molecules in excited states • Biological molecules • Polymers. The methods used may include any combination of spectroscopic and non-spectroscopic techniques, for example: • Infrared spectroscopy (mid, far, near) • Raman spectroscopy and non-linear Raman methods (CARS, etc.) • Electronic absorption spectroscopy • Optical rotatory dispersion and circular dichroism • Fluorescence and phosphorescence techniques • Electron spectroscopies (PES, XPS), EXAFS, etc. • Microwave spectroscopy • Electron diffraction • NMR and ESR spectroscopies • Mössbauer spectroscopy • X-ray crystallography • Charge Density Analyses • Computational Studies (supplementing experimental methods) We encourage publications combining theoretical and experimental approaches. The structural insights gained by the studies should be correlated with the properties, activity and/ or reactivity of the molecule under investigation and the relevance of this molecule and its implications should be discussed.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信