Suppr超能文献

超声介导的微泡破坏(UMMD)促进CA19-9靶向且负载紫杉醇的mPEG-PLGA-PLL纳米颗粒在胰腺癌中的递送。

Ultrasound-Mediated Microbubble Destruction (UMMD) Facilitates the Delivery of CA19-9 Targeted and Paclitaxel Loaded mPEG-PLGA-PLL Nanoparticles in Pancreatic Cancer.

作者信息

Xing Lingxi, Shi Qiusheng, Zheng Kailiang, Shen Ming, Ma Jing, Li Fan, Liu Yang, Lin Lizhou, Tu Wenzhi, Duan Yourong, Du Lianfang

机构信息

Department of Ultrasound, Shanghai General Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200080, P. R. China.

Engineering Department, Crop Science Division of Bayer, Institute, WV, 25112, USA.

出版信息

Theranostics. 2016 Jun 18;6(10):1573-87. doi: 10.7150/thno.15164. eCollection 2016.

Abstract

Pancreatic cancer, one of the most lethal human malignancies with dismal prognosis, is refractory to existing radio-chemotherapeutic treatment modalities. There is a critical unmet need to develop effective approaches, especially for targeted pancreatic cancer drug delivery. Targeted and drug-loaded nanoparticles (NPs) combined with ultrasound-mediated microbubble destruction (UMMD) have been shown to significantly increase the cellular uptake in vitro and drug retention in vivo, suggesting a promising strategy for cancer therapy. In this study, we synthesized pancreatic cancer-targeting organic NPs that were modified with anti CA19-9 antibody and encapsulated paclitaxol (PTX). The three-block copolymer methoxy polyethylene glycol-polylacticco-glycolic acid-polylysine (mPEG-PLGA-PLL) constituted the skeleton of the NPs. We speculated that the PTX-NPs-anti CA19-9 would circulate long-term in vivo, "actively target" pancreatic cancer cells, and sustainably release the loaded PTX while UMMD would "passively target" the irradiated tumor and effectively increase the permeability of cell membrane and capillary gaps. Our results demonstrated that the combination of PTX-NPs-anti CA19-9 with UMMD achieved a low IC50, significant cell cycle arrest, and cell apoptosis in vitro. In mouse pancreatic tumor xenografts, the combined application of PTX-NP-anti CA19-9 NPs with UMMD attained the highest tumor inhibition rate, promoted the pharmacokinetic profile by increasing AUC, t1/2, and mean residence time (MRT), and decreased clearance. Consequently, the survival of the tumor-bearing nude mice was prolonged without obvious toxicity. The dynamic change in cellular uptake, targeted real-time imaging, and the concentration of PTX in the plasma and tumor were all closely associated with the treatment efficacy both in vitro and in vivo. Our study suggests that PTX-NP-anti CA19-9 NPs combined with UMMD is a promising strategy for the treatment of pancreatic cancer.

摘要

胰腺癌是人类最致命的恶性肿瘤之一,预后极差,对现有的放化疗治疗方式具有耐药性。迫切需要开发有效的治疗方法,尤其是针对胰腺癌的靶向给药。靶向载药纳米颗粒(NPs)与超声介导的微泡破坏(UMMD)相结合,已被证明可显著提高体外细胞摄取率和体内药物保留率,这表明其是一种很有前景的癌症治疗策略。在本研究中,我们合成了用抗CA19-9抗体修饰并包裹紫杉醇(PTX)的靶向胰腺癌有机纳米颗粒。三嵌段共聚物甲氧基聚乙二醇-聚乳酸-乙醇酸-聚赖氨酸(mPEG-PLGA-PLL)构成了纳米颗粒的骨架。我们推测,PTX-NPs-抗CA19-9将在体内长期循环,“主动靶向”胰腺癌细胞,并持续释放负载的PTX,而UMMD将“被动靶向”受照射的肿瘤,有效增加细胞膜和毛细血管间隙的通透性。我们的结果表明,PTX-NPs-抗CA19-9与UMMD联合使用在体外实现了低IC50、显著的细胞周期阻滞和细胞凋亡。在小鼠胰腺肿瘤异种移植模型中,PTX-NP-抗CA19-9纳米颗粒与UMMD联合应用达到了最高的肿瘤抑制率,通过增加AUC、t1/2和平均驻留时间(MRT)改善了药代动力学特征,并降低了清除率。因此,荷瘤裸鼠的生存期延长,且无明显毒性。细胞摄取的动态变化、靶向实时成像以及血浆和肿瘤中PTX的浓度均与体内外治疗效果密切相关。我们的研究表明,PTX-NP-抗CA19-9纳米颗粒与UMMD联合使用是一种很有前景的胰腺癌治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a956/4955056/0feef3846e47/thnov06p1573g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验