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Combined sonodynamic and antimetabolite therapy for the improved treatment of pancreatic cancer using oxygen loaded microbubbles as a delivery vehicle

机译:超声动力学和抗代谢药物联合治疗,以载氧微泡为载体,改善胰腺癌的治疗

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In this manuscript we describe the preparation of an oxygen-loaded microbubble (O2MB) platform for the targeted treatment of pancreatic cancer using both sonodynamic therapy (SDT) and antimetabolite therapy. O2MB were prepared with either the sensitiser Rose Bengal (O2MB-RB) or the antimetabolite 5-fluorouracil (O2MB-5FU) attached to the microbubble (MB) surface. The MB were characterised with respect to size, physical stability and oxygen retention. A statistically significant reduction in cell viability was observed when three different pancreatic cancer cell lines (BxPc-3, MIA PaCa-2 and PANC-1), cultured in an anaerobic cabinet, were treated with both SDT and antimetabolite therapy compared to either therapy alone. In addition, a statistically significant reduction in tumour growth was also observed when ectopic human xenograft BxPC-3 tumours in SCID mice were treated with the combined therapy compared to treatment with either therapy alone. These results illustrate not only the potential of combined SDT/antimetabolite therapy as a stand alone treatment option in pancreatic cancer, but also the capability of O-2-loaded MBs to deliver O-2 to the tumour microenvironment in order to enhance the efficacy of therapies that depend on O-2 to mediate their therapeutic effect. Furthermore, the use of MBs to facilitate delivery of O-2 as well as the sensitiser/antimetabolite, combined with the possibility to activate the sensitiser using externally applied ultrasound, provides a more targeted approach with improved efficacy and reduced side effects when compared with conventional systemic administration of antimetabolite drugs alone. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在本手稿中,我们描述了使用声动力学治疗(SDT)和抗代谢药物治疗针对胰腺癌进行靶向治疗的载氧微泡(O2MB)平台的制备。 O2MB的制备方法是将敏化剂Rose Bengal(O2MB-RB)或抗代谢物5-氟尿嘧啶(O2MB-5FU)连接到微泡(MB)表面。 MB的尺寸,物理稳定性和氧气保留率得到了表征。与单独使用任一疗法相比,当在厌氧柜中培养的三种不同的胰腺癌细胞系(BxPc-3,MIA PaCa-2和PANC-1)同时接受SDT和抗代谢药物治疗时,观察到细胞活力的统计学显着降低。 。另外,与单独使用任一疗法相比,当用联合疗法治疗SCID小鼠中异位人异种移植物BxPC-3肿瘤时,还观察到肿瘤生长的统计学显着降低。这些结果不仅说明了SDT /抗代谢药物联合治疗在胰腺癌中作为单独治疗方案的潜力,而且还表明了装载O-2-的MBs将O-2递送至肿瘤微环境的能力,从而增强了肿瘤的微​​环境。 O-2介导其治疗效果的疗法。此外,与常规方法相比,使用MB促进O-2以及敏化剂/抗代谢物的传递,再加上使用外部施加的超声波激活敏化剂的可能性,提供了一种更有针对性的方法,具有更高的疗效和更低的副作用仅抗代谢药物的全身性给药。 (C)2015 Elsevier Ltd.保留所有权利。

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