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纳米层状中空载体中非人类酶的可控药物释放。

Controllable drug release from nano-layered hollow carrier by non-human enzyme.

机构信息

Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul, 03722, Republic of Korea.

出版信息

Nanoscale. 2018 Oct 4;10(38):18228-18237. doi: 10.1039/c8nr05269g.

Abstract

Natural polymers are widely used in biomedical applications because of their numerous effects. Especially, plant-derived natural polymers extracted from cell walls, especially wood, which is abundant, inexpensive and nontoxic to cells, have high mechanical strength to retain their turgor pressure. Plant-derived polymers are also unaffected by enzymes present in the human body, having a strong possibility to create a polymeric structure that releases drugs only exactly where needed. Therefore, plant-derived polymers are suitable for use in drug delivery systems (DDS) as they have durability with few drug leakage issues in the body. Here, to improve drug incorporation and release efficiency, we prepared a multilayer nanofilm from tannic acid (TA) and lignin extracted from plants and wood. We used a strategy involving film degradation by tannase and laccase, which are not present in humans, to depolymerize TA and lignin, respectively. The TA and lignin film was highly stable for 7 days at pH 3-7 and was readily degraded after enzyme treatment. We also observed controllable drug release and anticancer effect from the TA and lignin hollow carriers depending on enzymatic activity. By taking advantage of plant-derived polymers and non-toxic enzymatic reactions, we have demonstrated the film growth and degradation mechanism in depth and explored their use in a smart DDS with easily controlled release kinetics, which is useful as a DDS platform.

摘要

天然聚合物因其多种功效而被广泛应用于生物医学领域。特别是从细胞壁中提取的植物源性天然聚合物,特别是木材,其来源丰富、价格低廉且对细胞无毒,具有较高的机械强度以保持其膨压。植物源性聚合物也不受人体中存在的酶的影响,具有很强的可能性来构建一种仅在需要的地方释放药物的聚合结构。因此,植物源性聚合物适合用作药物传递系统 (DDS),因为它们在体内具有耐用性,很少有药物泄漏问题。在这里,为了提高药物的包封和释放效率,我们从植物和木材中提取的单宁酸 (TA) 和木质素制备了多层纳米薄膜。我们使用了一种涉及单宁酶和漆酶降解薄膜的策略,分别将 TA 和木质素解聚。在 pH 值为 3-7 时,TA 和木质素薄膜在 7 天内高度稳定,并且在酶处理后很容易降解。我们还观察到 TA 和木质素空心载体具有可控的药物释放和抗癌作用,这取决于酶的活性。通过利用植物源性聚合物和无毒的酶反应,我们深入研究了薄膜的生长和降解机制,并探索了它们在具有易于控制的释放动力学的智能 DDS 中的应用,这作为一种 DDS 平台非常有用。

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