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Chemical stability, mass loss and hydrolysis mechanism of sterile and non- sterile lipid-core nanocapsules: The influence of the molar mass of the polymer wall

机译:无菌和非无菌脂质核纳米胶囊的化学稳定性,质量损失和水解机理:聚合物壁摩尔质量的影响

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The purpose of this study was to investigate the chemical stability and the mechanism of hydrolysis of the polyester wall of lipid-core nanocapsules (LNC) dispersed in water comparing sterile and non-sterile formulations. Sterile or non-sterile LNC formulations (LNCS and LNC, respectively) were prepared using poly(epsilon-capro-lactone) (PCL) with different molar masses (M-n 10 kg mol(-1), M-n 80 kg mol(-1) and a mixture (1:9, w/w) of both PCL). All formulations presented unimodal size distribution profile without significant changes (p .05) after 60 days. Molar weight changes, fraction of chain scissions and hydrolysis mechanism of LNC under storage (60 days; 5 degrees C) were determined by size exclusion chromatography (SEC). The highest PCL weight loss was observed for the non-sterile formulations (LNC 1-45%; LNC 2-32%; LNC 3-27%). In turn, the sterile formulations showed a lower weight loss, proving that biotic hydrolysis was responsible for accelerating hydrolysis of the LNC even when stored at low temperature (5 degrees C). In conclusion, the predominant hydrolysis mechanism was of the non-catalyzed type.
机译:这项研究的目的是比较无菌和非无菌制剂,研究分散在水中的脂质核心纳米胶囊(LNC)聚酯壁的化学稳定性和水解机理。使用具有不同摩尔质量(Mn 10 kg mol(-1),Mn 80 kg mol(-1)的聚(ε-己内酯)(PCL)制备无菌或非无菌LNC制剂(分别为LNCS和LNC)以及两种PCL的混合物(1:9,w / w)。所有制剂在60天后均呈现单峰尺寸分布,无明显变化(p> .05)。通过尺寸排阻色谱法(SEC)测定在储存(60天; 5℃)下LNC的摩尔重量变化,链切割分数和水解机理。对于非无菌制剂(LNC 1-45%; LNC 2-32%; LNC 3-27%),观察到最高的PCL重量损失。继而,无菌制剂显示出较低的重量损失,证明了即使在低温(5℃)下储存时,生物水解也可促进LNC的水解。总之,主要的水解机理是非催化类型。

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