Department of Chemical Engineering, American University of Sharjah, Sharjah, United Arab Emirates.
Department of Chemical Engineering, University of Virginia, Charlottesville, VA, United States.
Recent Pat Anticancer Drug Discov. 2021;16(4):498-520. doi: 10.2174/1574892816666210706155110.
Existing cancer treatment methods have many undesirable side effects that greatly reduce the quality of life of cancer patients.
This review will focus on the use of ultrasound-responsive liposomes and polymeric micelles in cancer therapy.
This review presents a survey of the literature regarding ultrasound-triggered micelles and liposomes using articles recently published in various journals, as well as some new patents in this field.
Nanoparticles have proven promising as cancer theranostic tools. Nanoparticles are selective in nature, have reduced toxicity, and controllable drug release patterns making them ideal carriers for anticancer drugs. Numerous nanocarriers have been designed to combat malignancies, including liposomes, micelles, dendrimers, solid nanoparticles, quantum dots, gold nanoparticles, and, more recently, metal-organic frameworks. The temporal and spatial release of therapeutic agents from these nanostructures can be controlled using internal and external triggers, including pH, enzymes, redox, temperature, magnetic and electromagnetic waves, and ultrasound. Ultrasound is an attractive modality because it is non-invasive, can be focused on the diseased site, and has a synergistic effect with anticancer drugs.
The functionalization of micellar and liposomal surfaces with targeting moieties and the use of ultrasound as a triggering mechanism can help improve the selectivity and enable the spatiotemporal control of drug release from nanocarriers.
现有的癌症治疗方法有许多不良副作用,极大地降低了癌症患者的生活质量。
本综述将重点介绍超声响应脂质体和聚合物胶束在癌症治疗中的应用。
本综述通过查阅最近在各种期刊上发表的关于超声触发胶束和脂质体的文献,以及该领域的一些新专利,对文献进行了调查。
纳米颗粒已被证明是有前途的癌症治疗诊断工具。纳米颗粒具有选择性、毒性降低和可控的药物释放模式,使其成为抗癌药物的理想载体。已经设计了许多纳米载体来对抗恶性肿瘤,包括脂质体、胶束、树枝状大分子、固体纳米颗粒、量子点、金纳米颗粒,以及最近的金属有机骨架。可以使用内部和外部触发因素(包括 pH 值、酶、氧化还原、温度、磁场和电磁波以及超声)来控制这些纳米结构中治疗剂的时间和空间释放。超声是一种有吸引力的模式,因为它是非侵入性的,可以聚焦在患病部位,并与抗癌药物具有协同作用。
通过靶向基团对胶束和脂质体表面进行功能化,并将超声用作触发机制,可以帮助提高选择性,并实现纳米载体药物释放的时空控制。