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Internal liquid crystal structures in nanocarriers containing drug hydrophobic ion pairs dictate drug release

机译:含有药物疏水离子对的纳米载体中的内部液晶结构决定了药物释放

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摘要

Hypothesis: Hydrophobic ion pairing (HIP), a solubility engineering technique in which ionic hydrophilic molecules are paired with a hydrophobic counterion, is an attractive strategy for encapsulating ionic water-soluble species into nanocarriers (NCs). Drug release from NCs containing HIP complexes is sensitive to ionic strength, pH, and drug:counterion charge ratio, but the exact mechanism for this was unknown, as was the underlying microstructure inside the NCs. We hypothesize that HIP complexes arrange into liquid crystalline structures in NC cores and that these structures are responsible for salt and pH-dependent release.
机译:假设:疏水离子配对(HIP)是一种溶解度工程技术,其中离子亲水分子与疏水反离子配对,是将离子水溶性物种封装到纳米载体(NCs)中的一种有吸引力的策略。含有HIP复合物的NCs的药物释放对离子强度、pH值和药物:反离子电荷比敏感,但其确切机制尚不清楚,NCs内部的潜在微观结构也不清楚。我们假设HIP复合物排列成NC核中的液晶结构,这些结构负责盐和pH依赖性释放。

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