In situ generation of Copper sulfide within Poly(lactic-co-glycolic acid): A strategy for Safer photothermal therapy in Triple-Negative breast cancer

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics Pub Date : 2025-01-26 DOI:10.1016/j.ijpharm.2025.125287
Zhenzhen Chen , Lingyan Hu , Bingbing Xu , Zhihong Liu , Lingjun Zeng , Minxin Zhang , Haihong Tian , Hongtao Song
{"title":"In situ generation of Copper sulfide within Poly(lactic-co-glycolic acid): A strategy for Safer photothermal therapy in Triple-Negative breast cancer","authors":"Zhenzhen Chen ,&nbsp;Lingyan Hu ,&nbsp;Bingbing Xu ,&nbsp;Zhihong Liu ,&nbsp;Lingjun Zeng ,&nbsp;Minxin Zhang ,&nbsp;Haihong Tian ,&nbsp;Hongtao Song","doi":"10.1016/j.ijpharm.2025.125287","DOIUrl":null,"url":null,"abstract":"<div><div>Copper sulfide nanoparticles (CuS NPs) have garnered significant attention in photothermal therapy (PTT) owing to their facile synthesis, biodegradability, stability, and excellent photothermal conversion efficiency. Nonetheless, their potential toxic effects have restricted their application. This research focuses on the encapsulation of CuS NPs with the biocompatible polymer poly(lactic-co-glycolic acid) (PLGA) to enhance their biocompatibility, thereby improving the efficacy and safety of PTT in the treatment of triple-negative breast cancer (TNBC). Three distinct methods, namely aqueous phase loading method, oil phase loading method, and “<em>in situ</em> reduction” method were employed to synthesize PLGA-coated CuS (CuS@PLGA) NPs to optimize the encapsulation rate of CuS. Among these, the CuS@PLGA NPs fabricated <em>via</em> the “<em>in situ</em> reduction” method demonstrated the highest encapsulation efficiency for CuS, achieving a rate of (90.4 ± 3.3)%. The resulting CuS@PLGA NPs exhibited high stability, excellent photothermal effect, and good tumor-targeting ability. Moreover, CuS@PLGA NPs demonstrated enhanced anti-tumor efficacy and biocompatibility compared to CuS NPs in both <em>in vitro</em> and <em>in vivo</em> experiments. Consequently, this study offers an effective and safety strategy for PTT treatment of TNBC.</div></div>","PeriodicalId":14187,"journal":{"name":"International Journal of Pharmaceutics","volume":"671 ","pages":"Article 125287"},"PeriodicalIF":5.2000,"publicationDate":"2025-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Pharmaceutics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378517325001231","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Copper sulfide nanoparticles (CuS NPs) have garnered significant attention in photothermal therapy (PTT) owing to their facile synthesis, biodegradability, stability, and excellent photothermal conversion efficiency. Nonetheless, their potential toxic effects have restricted their application. This research focuses on the encapsulation of CuS NPs with the biocompatible polymer poly(lactic-co-glycolic acid) (PLGA) to enhance their biocompatibility, thereby improving the efficacy and safety of PTT in the treatment of triple-negative breast cancer (TNBC). Three distinct methods, namely aqueous phase loading method, oil phase loading method, and “in situ reduction” method were employed to synthesize PLGA-coated CuS (CuS@PLGA) NPs to optimize the encapsulation rate of CuS. Among these, the CuS@PLGA NPs fabricated via the “in situ reduction” method demonstrated the highest encapsulation efficiency for CuS, achieving a rate of (90.4 ± 3.3)%. The resulting CuS@PLGA NPs exhibited high stability, excellent photothermal effect, and good tumor-targeting ability. Moreover, CuS@PLGA NPs demonstrated enhanced anti-tumor efficacy and biocompatibility compared to CuS NPs in both in vitro and in vivo experiments. Consequently, this study offers an effective and safety strategy for PTT treatment of TNBC.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
聚乳酸-羟基乙酸中硫化铜的原位生成:一种更安全的三阴性乳腺癌光热治疗策略。
硫化铜纳米颗粒(cu NPs)由于其易于合成、可生物降解、稳定性和优异的光热转换效率,在光热治疗(PTT)领域引起了广泛的关注。然而,它们潜在的毒性作用限制了它们的应用。本研究主要研究生物相容性聚合物聚乳酸-羟基乙酸(PLGA)对CuS NPs进行包封,增强其生物相容性,从而提高PTT治疗三阴性乳腺癌(TNBC)的疗效和安全性。采用水相负载法、油相负载法和原位还原法三种不同的方法合成了plga包被CuS (CuS@PLGA) NPs,以优化CuS的包封率。其中,原位还原法制备的CuS@PLGA NPs对cu的包封效率最高,包封率为(90.4 ± 3.3)%。所得CuS@PLGA NPs具有高稳定性、优异的光热效应和良好的肿瘤靶向能力。此外,与CuS NPs相比,CuS@PLGA NPs在体外和体内实验中均表现出更强的抗肿瘤功效和生物相容性。因此,本研究为PTT治疗TNBC提供了一种有效且安全的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
文献相关原料
公司名称
产品信息
阿拉丁
Sodium sulfide nonahydrate
阿拉丁
Copper chloride dihydrate
来源期刊
CiteScore
10.70
自引率
8.60%
发文量
951
审稿时长
72 days
期刊介绍: The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
期刊最新文献
"Hot spring"-mimetic microneedle patches delivering probiotics to accelerate infected wound healing via antibacterial, anti-inflammatory, and angiogenesis. Polysaccharides from Adansonia digitata combined with whey protein and alginate enhance the viscosity, swelling, controlled release, and mucoadhesion properties of hydrogels for oral drug delivery. Narrow-width surface acoustic wave device-driven olfactory epithelium-targeted intranasal atomization. Unlocking the potential of lipid-based nanoparticles for intranasal drug delivery in Parkinson's disease. An integrated framework streamlining the manufacturing of high drug loading pharmaceutical tablets.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1