Department of Pharmaceutical Science, Nanfang Hospital, Southern Medical University, No. 1838 Guangzhou Ave., Guangzhou, 510515, PR China.
Department of Pharmaceutics, School of Pharmacy, Ningxia Medical University, No. 1160 Shengli South Street, Yinchuan, 750004, PR China.
Int J Pharm. 2014 May 15;466(1-2):314-20. doi: 10.1016/j.ijpharm.2014.03.030. Epub 2014 Mar 20.
Recently, a new class of multifunctional nanodroplets that combine the properties of polymeric drug carriers, ultrasound imaging contrast agents, and enhancers of ultrasound-mediated drug delivery has been developed. We studied the formation mechanism of nanodroplets of a drug and its application in chemotherapy. Curcumin was loaded in polymeric micelles as a anti-cancer drug using polyethylene glycol block-poly(caprolactone) with encapsulation efficiency of 95.60%. At room temperature, the developed systems comprised perfluorocarbon nanodroplets stabilized by walls comprising biodegradable block copolymers. Upon heating to 37°C, the nanodroplets were converted to nano/microbubbles. Under ultrasound, nanobubbles cavitated and collapsed, resulting in release of the encapsulated drug. The percentage release of curcumin-loaded nanodroplets by insonation was 90.95%, showing enhancement compared with the non-ultrasound group. Nanodroplets strongly retained the loaded drugs in vivo yet, under ultrasound-mediated vaporization, they released the drugs, thereby implementing effective targeting into the tumor. The tumor inhibition of the group in which curcumin-loaded nanodroplets were combined with ultrasound was 71.30%, more than that of the group of curcumin-loaded nanodroplets (53.00%). Nanodroplets showed high enhancement of anti-cancer effects under ultrasound. Upon intravenous injection, a long-lasting, strong and selective ultrasound contrast was observed, suggesting their coalescence into larger, highly echogenic microbubbles. These multifunctional nanodroplets, which manifest excellent therapeutic and ultrasound properties, could be promising anti-cancer drug delivery systems.
最近,开发了一类新的多功能纳米液滴,它结合了聚合物药物载体、超声成像对比剂和超声介导药物递送增强剂的特性。我们研究了药物纳米液滴的形成机制及其在化疗中的应用。姜黄素被负载在聚合物胶束中作为抗癌药物,使用聚乙二醇嵌段-聚(己内酯),包封效率为 95.60%。在室温下,开发的系统由壁稳定的全氟碳纳米液滴组成,壁由可生物降解的嵌段共聚物组成。加热至 37°C 时,纳米液滴转化为纳米/微泡。在超声下,纳米气泡空化和破裂,导致封装药物的释放。载有姜黄素的纳米液滴的超声释放百分比为 90.95%,与非超声组相比表现出增强。纳米液滴在体内强烈保留负载的药物,但在超声介导的蒸发下,它们释放药物,从而实现对肿瘤的有效靶向。载有姜黄素的纳米液滴与超声结合的组的肿瘤抑制率为 71.30%,高于载有姜黄素的纳米液滴组(53.00%)。纳米液滴在超声下表现出对抗癌作用的高度增强。静脉注射后,观察到持续时间长、强度高且选择性强的超声对比,表明它们聚合并形成更大、高回声的微泡。这些具有多功能的纳米液滴表现出优异的治疗和超声特性,可能成为有前途的抗癌药物递送系统。