作为纳米粒子配方筛选平台的合成粘液屏障阵列†。

Harry Zou, Allison Boboltz, Yahya Cheema, Daniel Song, Devorah Cahn and Gregg A. Duncan
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引用次数: 0

摘要

黏液凝胶层覆盖着全身组织的管腔表面,以保护它们免受感染性病原体和微粒的侵袭。因此,输送到这些部位的纳米颗粒给药系统可能会被粘液困住,随后在到达靶细胞之前被清除。因此,优化纳米颗粒给药载体的特性(如表面化学性质和尺寸)对于提高其穿透粘液屏障的能力至关重要。在之前的工作中,我们开发了一种基于粘蛋白的水凝胶,它具有与原生粘液类似的粘弹性,可进一步定制以模拟特定的粘膜组织和疾病状态。利用这种仿生水凝胶系统,我们创建了一个包含合成粘液屏障的三维打印阵列,该阵列与 96 孔板兼容,可用作纳米粒子药物递送应用的高通量筛选平台。为了验证该系统,我们评估了几个既定的设计参数,以确定它们对纳米粒子穿透合成粘液屏障的影响。与文献报道一致,我们发现尺寸较小并涂有 PEG 保护层的纳米粒子能更有效地穿透合成粘液屏障。此外,我们还评估了一种粘液溶解剂(三(2-羧乙基)膦,TCEP)作为粘膜给药渗透促进剂的使用情况。与 N-乙酰半胱氨酸(NAC)相比,我们发现 TCEP 能显著改善纳米颗粒在类似疾病的合成粘液屏障中的渗透性。总之,我们的研究结果建立了一种新的高通量筛选方法,利用合成粘液屏障阵列来确定向粘膜组织给药的有前景的纳米颗粒配方策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthetic mucus barrier arrays as a nanoparticle formulation screening platform†

Synthetic mucus barrier arrays as a nanoparticle formulation screening platform†

A mucus gel layer lines the luminal surface of tissues throughout the body to protect them from infectious agents and particulates. As a result, nanoparticle drug delivery systems delivered to these sites may become trapped in mucus and subsequently cleared before they can reach target cells. As such, optimizing the properties of nanoparticle delivery vehicles, such as their surface chemistry and size, is essential to improving their penetration through the mucus barrier. In previous work, we developed a mucin-based hydrogel that has viscoelastic properties like that of native mucus which can be further tailored to mimic specific mucosal tissues and disease states. Using this biomimetic hydrogel system, a 3D-printed array containing synthetic mucus barriers was created that is compatible with a 96-well plate enabling its use as a high-throughput screening platform for nanoparticle drug delivery applications. To validate this system, we evaluated several established design parameters to determine their impact on nanoparticle penetration through synthetic mucus barriers. Consistent with the literature, we found nanoparticles of smaller size and coated with a protective PEG layer more efficiently penetrated through synthetic mucus barriers. In addition, we evaluated a mucolytic (tris(2-carboxyethyl) phosphine, TCEP) for use as a permeation enhancer for mucosal drug delivery. In comparison to N-acetyl cysteine (NAC), we found TCEP significantly improved nanoparticle penetration through a disease-like synthetic mucus barrier. Overall, our results establish a new high-throughput screening approach using synthetic mucus barrier arrays to identify promising nanoparticle formulation strategies for drug delivery to mucosal tissues.

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