间皮素介导的紫杉醇相移纳米给药系统用于卵巢癌的分子超声成像和靶向治疗。

Yujie Wan, Li Luo, Xinzhi Xu, Qihuan Fu, Ying Li, Kaifeng Huang, Hang Zhou, Fang Li
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引用次数: 0

摘要

背景:卵巢癌对妇女的健康和生命构成巨大风险,早期检测和治疗具有挑战性。靶向纳米给药系统被认为是提高卵巢癌治疗效果和超声波成像结果的一种有前途的方法:研究了一种负载紫杉醇(PTX)并进一步与阿维丁(Ab)共轭的相移纳米给药系统(NPs),旨在探讨靶向纳米给药策略对卵巢癌体外疗效和超声成像的影响。这项研究为未来利用这种方法进行体内治疗奠定了基础:方法:采用单一油包水(O/W)乳液溶剂蒸发法制备 PTX-NPs,并通过生物素-阿维蛋白亲和力实现阿维蛋白偶联。采用紫外分光光度法分析了 PTX 的包封效率和释放曲线。评价了 Ab-PTX-NPs 给药系统的相移特性,并评估了各种纳米给药系统的靶向效率、对 SKOV3 细胞的细胞毒性和体内生物安全性:结果:制备的纳米给药系统结构稳定均匀,粒度分布良好,在超声暴露下表现出良好的释放特性。体外实验显示,该纳米给药系统对SKOV3细胞具有良好的靶向性和细胞毒性作用,表明Ab-PTX-NPs给药系统具有卵巢癌靶向治疗的潜力。体内安全性研究表明所制备的纳米给药系统具有很高的生物安全性:结论:该研究开发了一种新型纳米给药系统,其实验结果为进一步研究体内超声分子成像技术提供了坚实的实验基础,为靶向超声分子成像和卵巢癌治疗提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mesothelin-Mediated Paclitaxel Phase-Shifted Nanodelivery System for Molecular Ultrasound Imaging and Targeted Therapy Potential in Ovarian Cancer.

Background: Ovarian cancer presents a substantial risk to women's health and lives, with early detection and treatment proving challenging. Targeted nanodelivery systems are viewed as a promising approach to enhance the effectiveness of ovarian cancer treatment and ultrasonic imaging outcomes.

Objective: A phase-shifted nanodelivery system (NPs) loaded with paclitaxel (PTX) and further conjugated with avidin (Ab) was studied, with the goal of investigating the effects of targeted nanodelivery strategies on the in vitro therapeutic efficacy and ultrasonic imaging of ovarian cancer. This study provides a foundation for future in vivo treatments utilizing this approach.

Methods: PTX-NPs were prepared using the single water-in-oil (O/W) emulsion solvent evaporation method, with avidin coupling achieved through biotin-avidin affinity. The encapsulation efficiency and release profile of PTX were analyzed using UV spectrophotometry. The phase-shift properties of the Ab-PTX-NPs delivery system were evaluated, and the targeting efficiency, cytotoxicity against SKOV3 cells, and in vivo biosafety of various nanodelivery systems were assessed.

Results: The prepared nanodelivery system showed a stable and uniform structure with a good particle size distribution and exhibited favorable release characteristics under ultrasound exposure. In vitro experiments revealed that the nanodelivery system displayed excellent targeting and cytotoxic effects against SKOV3 cells, indicating the potential of the Ab-PTX-NPs delivery system for targeted ovarian cancer therapy. In vivo safety studies demonstrated the high biosafety of the prepared nanodelivery system.

Conclusion: A novel nanodelivery system was developed, and the experimental results obtained provide a solid experimental basis for further research on in vivo ultrasound molecular imaging technology, offering new insights into targeted ultrasound molecular imaging and the treatment of ovarian cancer.

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