首页> 美国卫生研究院文献>Theranostics >GSH-sensitive Pt(IV) prodrug-loaded phase-transitional nanoparticles with a hybrid lipid-polymer shell for precise theranostics against ovarian cancer
【2h】

GSH-sensitive Pt(IV) prodrug-loaded phase-transitional nanoparticles with a hybrid lipid-polymer shell for precise theranostics against ovarian cancer

机译:GSH敏感的Pt(IV)前药负载的相变纳米粒子具有混合的脂类聚合物壳可用于精确治疗卵巢癌

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>Background: Platinum (II) (Pt(II))-based anticancer drugs dominate the chemotherapy field of ovarian cancer. However, the patient's quality of life has severely limited owing to dose-limiting toxicities and the advanced disease at the time of diagnosis. Multifunctional tumor-targeted nanosized ultrasound contrast agents (glutathione (GSH)-sensitive platinum (IV) (Pt(IV)) prodrug-loaded phase-transitional nanoparticles, Pt(IV) NP-cRGD) were developed for precise theranostics against ovarian cancer.>Methods: Pt(IV) NP-cRGD were composed of a perfluorohexane (PFH) liquid core, a hybrid lipid-polymer shell with PLGA12k-PEG2k and DSPE-PEG1k-Pt(IV), and an active targeting ligand, the cRGD peptide (PLGA: poly(lactic-co-glycolic acid), PEG: polyethylene glycol, DSPE: 1,2-distearoyl-sn-glycero-3-phosphoethanolamine, cRGD: cyclic Arg-Gly-Asp). Pt(IV), a popular alternative to Pt(II), was covalently attached to DSPE-PEG1k to form the prodrug, which fine-tuned lipophilicity and improved cellular uptake. The potential of Pt(IV) NP-cRGD as contrast agents for ultrasound (US) imaging was assessed in vitro and in vivo. Moreover, studies on the antitumor efficiency and antitumor mechanism of Pt(IV) NP-cRGD assisted by US were carried out.>Results: Pt(IV) NP-cRGD exhibited strong echogenic signals and excellent echo persistence under an US field. In addition, the GSH-sensitive and US-triggered drug delivery system maximized the therapeutic effect while reducing the toxicity of chemotherapy. The mechanistic studies confirmed that Pt(IV) NP-cRGD with US consumed GSH and enhanced reactive oxy gen species (ROS) levels, which further causes mitochondria-mediated apoptosis.>Conclusion: A multifunctional nanoplatform based on phase-transitional Pt(IV) NP-cRGD with US exhibited excellent echogenic signals, brilliant therapeutic efficacy and limited side effect, suggesting precise theranostics against ovarian cancer.
机译:>背景:基于铂(II)(Pt(II))的抗癌药物主导着卵巢癌的化学治疗领域。然而,由于剂量限制的毒性和诊断时疾病的进展,患者的生活质量受到严重限制。多功能肿瘤靶向纳米超声造影剂(谷胱甘肽(GSH)敏感铂(IV)(Pt(IV))前药加载的相变纳米粒子Pt(IV)NP-cRGD)被开发用于精确的卵巢癌治疗方法学。 >方法:Pt(IV)NP-cRGD由全氟己烷(PFH)液体核,具有PLGA12k-PEG2k和DSPE-PEG1k-Pt(IV)的混合脂质-聚合物壳组成靶向配体,cRGD肽(PLGA:聚乳酸-乙醇酸共聚物,PEG:聚乙二醇,DSPE:1,2-二硬脂酰基-sn-甘油-3-磷酸乙醇胺,cRGD:环状Arg-Gly-Asp)。 Pt(IV)是Pt(II)的一种流行替代物,共价附于DSPE-PEG1k以形成前药,该药物可微调亲脂性并改善细胞吸收。在体外和体内评估了Pt(IV)NP-cRGD作为超声(US)造影剂的潜力。此外,还进行了美国辅助Pt(IV)NP-cRGD的抗肿瘤效果和抗肿瘤机制的研究。>结果:Pt(IV)NP-cRGD在强烈的回声下表现出较强的回声信号和优异的回声持久性。美国领域。此外,对GSH敏感且由US触发的给药系统最大程度地提高了治疗效果,同时降低了化学疗法的毒性。机理研究证实,美国的Pt(IV)NP-cRGD消耗了GSH并增强了活性氧(ROS)水平,这进一步导致了线粒体介导的细胞凋亡。>结论:一种基于相的多功能纳米平台具有US的Pt(IV)过渡Pt(IV)NP-cRGD表现出优异的回声信号,出色的治疗功效和有限的副作用,表明对卵巢癌的精确治疗学意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号