材料科学
纳米颗粒
聚电解质
壳聚糖
胰岛素
化学工程
制作
水溶液
纳米技术
聚合物
药物输送
化学
复合材料
有机化学
替代医学
病理
内分泌学
工程类
医学
作者
Zhiyu He,José Luís Santos,Houkuan Tian,Huahua Huang,Yizong Hu,Lixin Liu,Kam W. Leong,Yongming Chen,Hai‐Quan Mao
出处
期刊:Biomaterials
[Elsevier]
日期:2017-03-22
卷期号:130: 28-41
被引量:209
标识
DOI:10.1016/j.biomaterials.2017.03.028
摘要
Controlled delivery of protein would find diverse therapeutic applications. Formulation of protein nanoparticles by polyelectrolyte complexation between the protein and a natural polymer such as chitosan (CS) is a popular approach. However, the current method of batch-mode mixing faces significant challenges in scaling up while maintaining size control, high uniformity, and high encapsulation efficiency. Here we report a new method, termed flash nanocomplexation (FNC), to fabricate insulin nanoparticles by infusing aqueous solutions of CS, tripolyphosphate (TPP), and insulin under rapid mixing condition (Re > 1600) in a multi-inlet vortex mixer. In comparison with the bulk-mixing method, the optimized FNC process produces CS/TPP/insulin nanoparticles with a smaller size (down to 45 nm) and narrower size distribution, higher encapsulation efficiency (up to 90%), and pH-dependent nanoparticle dissolution and insulin release. The CS/TPP/insulin nanoparticles can be lyophilized and reconstituted without loss of activity, and produced at a throughput of 5.1 g h−1 when a flow rate of 50 mL min−1 is used. Evaluated in a Type I diabetes rat model, the smaller nanoparticles (45 nm and 115 nm) control the blood glucose level through oral administration more effectively than the larger particles (240 nm). This efficient, reproducible and continuous FNC technique is amenable to scale-up in order to address the critical barrier of manufacturing for the translation of protein nanoparticles.
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