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作为纳米颗粒制剂筛选平台的合成黏液屏障阵列

Synthetic mucus barrier arrays as a nanoparticle formulation screening platform.

作者信息

Zou Harry, Boboltz Allison, Cheema Yahya, Song Daniel, Cahn Devorah, Duncan Gregg A

机构信息

Fischell Department of Bioengineering, University of Maryland College Park MD 20742 USA

出版信息

RSC Pharm. 2024 Apr 18;1(2):218-226. doi: 10.1039/d3pm00057e. eCollection 2024 Jun 18.

Abstract

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 -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.

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因子和颗粒物的侵害。因此,递送至这些部位的纳米颗粒药物递送系统可能会被困在黏液中,并在到达靶细胞之前被清除。因此,优化纳米颗粒递送载体的性质,如它们的表面化学性质和尺寸,对于提高它们穿透黏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黏蛋白的水凝胶,其具有与天然黏液类似的黏弹性,可进一步定制以模拟特定的黏膜组织和疾病状态。利用这种仿生水凝胶系统,创建了一个包含合成黏液屏障的3D打印阵列,该阵列与96孔板兼容,使其能够用作纳米颗粒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,以确定它们对纳米颗粒穿透合成黏液屏障的影响。与文献一致,我们发现尺寸较小且涂有保护性聚乙二醇(PEG)层的纳米颗粒能更有效地穿透合成黏液屏障。此外,我们评估了一种黏液溶解剂(三(2-羧乙基)膦,TCEP)作为黏膜药物递送的渗透增强剂。与N-乙酰半胱氨酸(NAC)相比,我们发现TCEP显著提高了纳米颗粒通过类似疾病的合成黏液屏障的穿透能力。总体而言,我们的结果建立了一种新的高通量筛选方法,即使用合成黏液屏障阵列来识别有前景的纳米颗粒制剂策略,用于向黏膜组织递送药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c628/11185047/0a0d0cbb8da7/d3pm00057e-f1.jpg

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