Wang Shuyan, Duan Yaou, Zhang Qiangzhe, Komarla Anvita, Gong Hua, Gao Weiwei, Zhang Liangfang
Departments of NanoEngineering, Chemical Engineering Program, and Moores Cancer Center, University of California San Diego, La Jolla, CA 92093, USA.
Small Struct. 2020 Oct;1(1). doi: 10.1002/sstr.202000018. Epub 2020 Sep 9.
Platelets possess distinct surface moieties responsible for modulating their adhesion to various disease-relevant substrates involving vascular damage, immune evasion, and pathogen interactions. Such broad biointerfacing capabilities of platelets have inspired the development of platelet-mimicking drug carriers that preferentially target drug payloads to disease sites for enhanced therapeutic efficacy. Among these carriers, platelet membrane-coated nanoparticles (denoted 'PNPs') made by cloaking synthetic substrates with the plasma membrane of platelets have emerged recently. Their 'top-down' design combines the functionalities of natural platelet membrane and the engineering flexibility of synthetic nanomaterials, which together create synergy for effective drug delivery and novel therapeutics. Herein, we review the recent progress of engineering PNPs with different structures for targeted drug delivery, focusing on three areas, including targeting injured blood vessels to treat vascular diseases, targeting cancer cells for cancer treatment and detection, and targeting drug-resistant bacteria to treat infectious diseases. Overall, current studies have established PNPs as versatile nanotherapeutics for drug targeting with strong potentials to improve the treatment of various diseases.
血小板具有独特的表面部分,这些部分负责调节其与各种与疾病相关的底物的粘附,这些底物涉及血管损伤、免疫逃逸和病原体相互作用。血小板如此广泛的生物界面能力激发了模仿血小板的药物载体的开发,这些载体优先将药物负载靶向疾病部位以提高治疗效果。在这些载体中,通过用血小板的质膜包裹合成底物制成的血小板膜包被纳米颗粒(称为“PNPs”)最近出现了。它们的“自上而下”设计结合了天然血小板膜的功能和合成纳米材料的工程灵活性,共同为有效的药物递送和新型治疗创造协同作用。在此,我们综述了工程化具有不同结构的PNPs用于靶向药物递送的最新进展,重点关注三个领域,包括靶向受损血管治疗血管疾病、靶向癌细胞进行癌症治疗和检测,以及靶向耐药细菌治疗传染病。总体而言,目前的研究已将PNPs确立为用于药物靶向的多功能纳米治疗剂,具有改善各种疾病治疗的强大潜力。