Encapsulation of honokiol-loaded nanoparticles in lecithin microbubbles for targeted tumor therapy

被引:2
|
作者
Li, Zhen [1 ]
Hao, Lan [2 ]
Yuan, Pei [1 ]
Hu, Wenjing [3 ]
Zhang, Liangke [1 ]
机构
[1] Chongqing Med Univ, Chongqing Res Ctr Pharmaceut Engn, Chongqing Key Lab Biochem & Mol Pharmacol, Sch Pharm, Chongqing 400016, Peoples R China
[2] Chongqing Med Univ, Inst Ultrasound Imaging, Chongqing Key Lab Ultrasound Mol Imaging, Chongqing 400016, Peoples R China
[3] Chongqingshi Shapingba Dist Peoples Hosp, Chongqing 400030, Peoples R China
来源
RSC ADVANCES | 2016年 / 6卷 / 60期
基金
新加坡国家研究基金会;
关键词
CONJUGATED ALBUMIN NANOPARTICLES; BLOOD-BRAIN-BARRIER; SERUM-ALBUMIN; ULTRASOUND; PERMEABILITY; THERANOSTICS; DELIVERY; MODEL;
D O I
10.1039/c6ra10047c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study aimed to develop a new drug delivery system that combines honokiol-loaded albumin nanoparticles (HKNs) with perfluorocarbon-filled microbubbles (MBs) to improve the target delivery of honokiol (HK). The HKNs were prepared through a desolvation method. The MBs were prepared by mechanical shaking and used to encapsulate the HKNs and perfluorocarbon gas (HKN-MBs). The prepared HKN-MBs displayed a mean diameter of 1447.0 +/- 182.4 nm and a drug-loading efficiency of 3.48% +/- 0.20%. The HKN-MBs demonstrated good acoustic properties in in vitro and in vivo ultrasound (US) imaging experiments, in which no significant difference to traditional MBs was found. The HKN-MBs had high drug encapsulation and loading efficiency while maintaining the acoustic properties as an US contrast agent. C57BL/6 mice with Lewis lung carcinoma tumor were treated with HKN-MBs through the tail vein and then exposed to an US destruction pulse, resulting in an improved curative effect on the tumor tissues. The experimental group administered with HKN-MBs and exposed to US showed an obvious increase in the rate of tumor growth inhibition (48.78%) compared with those of HKN-MBs (32.85%) and HKNs (29.94%). Encapsulation of HKNs in MBs is expected to improve the therapeutic efficacy of HK and provide a feasible technique for targeted tumor therapy.
引用
收藏
页码:54830 / 54835
页数:6
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