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负载紫杉醇和孟加拉玫瑰红的微泡用于胰腺癌的超声靶向化学-声动力治疗

Paclitaxel and rose bengal loaded microbubbles for the ultrasound targeted chemo-sonodynamic therapy of pancreatic cancer.

作者信息

Wright Jack, Logan Keiran, McKaig Thomas, Kamila Sukanta, McClenaghan Chloe, Nesbitt Heather, Taylor Mark A, Love Mark, Stride Eleanor, Ruan Jia-Ling, McHale Anthony P, Callan John F

机构信息

Biomedical Sciences Research Institute, University of Ulster, Coleraine, Northern Ireland, UK.

Department of HPB Surgery, Mater Hospital, Belfast BT14 6AB Northern Ireland, UK.

出版信息

Eur J Pharm Biopharm. 2026 Jan;218:114937. doi: 10.1016/j.ejpb.2025.114937. Epub 2025 Nov 19.

Abstract

Despite significant advances in cancer treatment over the past five decades, survival outcomes for pancreatic cancer have remained largely unchanged. The effectiveness of chemotherapy as a treatment for pancreatic cancer is limited by the dense, protective tumour stroma, which impedes drug delivery. Ultrasound-targeted microbubble destruction (UTMD) has emerged as a promising strategy for enhancing the delivery of chemotherapy agents to solid tumours. In this study, we report the development and evaluation of a novel microbubble (MB) formulation, ST-001, which incorporates paclitaxel chemotherapy and a Rose Bengal sonosensitiser for targeted chemo-sonodynamic therapy of pancreatic cancer. The principle of UTMD using ST-001 was demonstrated in a murine model of pancreatic cancer, where B-mode ultrasound imaging was used to visualize MB accumulation within the tumour and its subsequent clearance following the application of therapeutic ultrasound. Preclinical efficacy studies demonstrated a significant survival advantage in ST-001 treated mice, which survived more than twice as long as those treated with standard Taxol, despite receiving only 14% of the paclitaxel dose. Additionally, a preclinical toxicology study in healthy mice demonstrated an excellent safety profile for ST-001, with no adverse effects observed in key hematological and blood biochemical markers, or in the histology of the spleen, liver, and kidneys.

摘要

尽管在过去五十年中癌症治疗取得了重大进展,但胰腺癌的生存结果在很大程度上仍未改变。化疗作为胰腺癌治疗方法的有效性受到致密、保护性肿瘤基质的限制,这种基质阻碍了药物递送。超声靶向微泡破坏(UTMD)已成为一种有前景的策略,可增强化疗药物向实体瘤的递送。在本研究中,我们报告了一种新型微泡(MB)制剂ST-001的开发和评估,该制剂结合了紫杉醇化疗药物和孟加拉玫瑰红超声敏化剂,用于胰腺癌的靶向化学-声动力治疗。在胰腺癌小鼠模型中证明了使用ST-001进行UTMD的原理,其中B型超声成像用于可视化微泡在肿瘤内的积聚及其在应用治疗性超声后的后续清除。临床前疗效研究表明,接受ST-001治疗的小鼠具有显著的生存优势,尽管仅接受了紫杉醇剂量的14%,但其存活时间是接受标准紫杉醇治疗小鼠的两倍多。此外,在健康小鼠中进行的临床前毒理学研究表明,ST-001具有出色的安全性,在关键血液学和血液生化指标以及脾脏、肝脏和肾脏的组织学检查中均未观察到不良反应。

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