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Evaluation of Acetaminophen Release from Biodegradable Poly (Vinyl Alcohol) (PVA) and Nanocellulose Films Using a Multiphase Release Mechanism

机译:使用多相释放机理评估可生物降解的聚乙烯醇(PVA)和纳米纤维素膜中对乙酰氨基酚的释放

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摘要

Biodegradable polymers hold great therapeutic value, especially through the addition of additives for controlled drug release. Nanocellulose has shown promise in drug delivery, yet usually requires chemical crosslinking with harsh acids and solvents. Nanocellulose fibrils (NFCs) and 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO)-mediated oxidized nanocellulose fibrils (TNFCs) with poly (vinyl alcohol) (PVA) could be aqueously formulated to control the release of model drug acetaminophen over 144 h. The release was evaluated with a multiphase release mechanism to determine which mechanism(s) contribute to the overall release and to what degree. Doing so indicated that the TNFCs in PVA control the release of acetaminophen more than NFCs in PVA. Modeling showed that this release was mostly due to burst release—drug coming off the immediate surface, rather than diffusing out of the matrix.
机译:可生物降解的聚合物具有巨大的治疗价值,尤其是通过添加添加剂来控制药物释放。纳米纤维素在药物输送中已显示出希望,但通常需要与强酸和溶剂进行化学交联。可以配制含聚乙烯醇(PVA)的纳米纤维素原纤维(NFC)和2,2,6,6-四甲基哌啶-N-氧基(TEMPO)介导的氧化纳米纤维素原纤维(TNFC)以控制模型药物的释放对乙酰氨基酚144小时以上。使用多阶段释放机制评估释放,以确定哪些机制有助于总体释放以及达到何种程度。这样做表明,PVA中的TNFC比PVA中的NFC更能控制对乙酰氨基酚的释放。模型表明,这种释放主要是由于突发释放所致,即药物从直接表面上逸出,而不是从基质中扩散出来。

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