羧酸酯酶
化学
聚山梨酯
固体脂质纳米粒
纳米颗粒
聚乙二醇化
胶束
色谱法
PEG比率
水解
酶水解
粒径
酯酶
酶
化学工程
肺表面活性物质
有机化学
纳米技术
生物化学
水溶液
材料科学
聚乙二醇
物理化学
财务
工程类
经济
作者
Melissa D. Howard,Xiuling Lü,John J. Rinehart,Michael Jay,Thomas D. Dziubla
出处
期刊:Langmuir
[American Chemical Society]
日期:2012-07-25
卷期号:28 (33): 12030-12037
被引量:8
摘要
Despite the importance of PEGylation in achieving long nanoparticle circulation times, many nanoparticles are coated with PEGylating agents susceptible to enzymatic degradation. In this study, solid lipid nanoparticles (SLNs) prepared with ester-containing compounds were evaluated for their stability in the presence of carboxylesterase. SLN suspensions became turbid within 30 min of enzymatic exposure, indicating possible disassociation of a portion of the nanoparticles. The particle size of SLNs incubated with the enzyme was smaller than the size of controls, although their morphologies appeared similar in transmission electron microscopy images. Although SLNs offered some protection over micelles, PEG6000 monostearate was rapidly degraded within 15 min. Hydrolysis of polysorbate 60 was much slower, reaching only 36% in 2 h. These studies reveal the importance of confirming the stability of PEG surface coatings prior to undertaking in vivo experiments in small animal models, which can have considerably higher plasma esterase activity than humans.
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