Wang Jiayu, Li Pan, Tian Rui, Hu Wenjing, Zhang Yuxia, Yuan Pei, Tang Yalan, Jia Yuntao, Zhang Liangke
J Biomed Nanotechnol. 2016 Mar;12(3):516-24. doi: 10.1166/jbn.2016.2181.
Drug-loaded microbubbles have shown attractive potential in disease treatment applications. The present work presents a unique ultrasound (US)-triggered system in which drug-loaded nanoparticles and perfluorocarbon gas are encapsulated within the internal space of microbubbles. The prepared curcumin-loaded albumin nanoparticle payload microbubbles (CcmANP-MB) exhibited a mean diameter of 4895.1 nm ± 421.2 nm and a drug-loading efficiency of 2.23% ± 0.08% (297% increase compared with the drug loading of common drug-loaded microbubbles). US allowed the release of the internal payload. In vitro US-triggered drug release experiments showed that the drug release of CcmANP-MB was delayed by lipid membranes and significantly increased after sonication. In vitro and in vivo US imaging experiments demonstrated that CcmANP-MB evidently enhances US imaging, which indicates that the microbubbles possess good acoustic properties even after encapsulation of nanoparticles. Tumor bearing mice were administered with CcmANP-MB through the tail vein and were then exposed to ultrasound, which resulted in an enhanced drug accumulation in tumor tissues and a significant increase in tumor growth inhibition rate (57.1%) compared with CcmANP-MB alone (28.8%) as well as curcumin-loaded albumin nanoparticle (26.2%). Therefore, the combination of lecithin microbubbles and albumin nanoparticles provides a platform for targeted drug delivery in clinical therapy and disease diagnosis.
载药微泡在疾病治疗应用中显示出诱人的潜力。目前的工作展示了一种独特的超声(US)触发系统,其中载药纳米颗粒和全氟碳气体被包裹在微泡的内部空间中。制备的载姜黄素白蛋白纳米颗粒有效载荷微泡(CcmANP-MB)的平均直径为4895.1 nm±421.2 nm,载药效率为2.23%±0.08%(与普通载药微泡的载药量相比增加了297%)。超声可使内部有效载荷释放。体外超声触发药物释放实验表明,CcmANP-MB的药物释放受到脂质膜的延迟,超声处理后显著增加。体外和体内超声成像实验表明,CcmANP-MB明显增强了超声成像,这表明即使在包裹纳米颗粒后,微泡仍具有良好的声学特性。给荷瘤小鼠尾静脉注射CcmANP-MB,然后进行超声照射,与单独使用CcmANP-MB(28.8%)以及载姜黄素白蛋白纳米颗粒(26.2%)相比,这导致肿瘤组织中的药物积累增加,肿瘤生长抑制率显著提高(57.1%)。因此,卵磷脂微泡和白蛋白纳米颗粒的组合为临床治疗和疾病诊断中的靶向药物递送提供了一个平台。