Shalini Sundar, Allison Koopman, Thomas J. Manzoni, Weiran Xie, Qurat-Ul-Ain Bhatti, Chun-Yuan Lo, Vidhika S. Damani, Ai Nin Yang, Darrin Pochan, Justin Parreno, Julie B. Engiles, Laure V. Kayser and Charles Dhong*,
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引用次数: 0
摘要
组织水合作用使关节软骨具有动态粘弹性特性。早期骨关节炎(OA)的特征是蛋白聚糖和糖胺聚糖(GAG)的流失、固定电荷密度降低以及组织渗透功能受损。最常见的 GAG 替代品--硫酸软骨素(CS)未能显示出其有效性。在这里,我们研究了一种合成聚电解质--聚(苯乙烯磺酸盐)(PSS),它既是研究软骨中聚电解质运输的模型化合物,也是恢复软骨中 GAG 丢失后的固定电荷密度的潜在候选物质。通过牛外植体和组织学研究,我们测定了三种不同分子量的 PSS 的带状有效扩散系数。在静态和压缩解吸实验中,与 CS 相比,PSS 在缺失 GAG 的软骨中保留的时间更长。通过小角 X 射线散射,我们发现 PSS 的形态更紧凑,电荷密度更高,因此溶质性能更强。这项研究可能会改善 GAG 模拟分子的设计,从而修复 OA 软骨的渗透功能。
Kinetics and Retention of Polystyrenesulfonate for Proteoglycan Replacement in Cartilage
Tissue hydration provides articular cartilage with dynamic viscoelastic properties. Early stage osteoarthritis (OA) is marked by loss of proteoglycans and glycosaminoglycans (GAG), lowering fixed charge density, and impairing tissue osmotic function. The most common GAG replacement, chondroitin sulfate (CS), has failed to show effectiveness. Here, we investigated a synthetic polyelectrolyte, poly(styrenesulfonate) (PSS), both as a model compound to investigate polyelectrolyte transport in cartilage, and as a potential candidate to restore bulk fixed charge density in cartilage with GAG loss. Through bovine explants and histology, we determined zonal-based effective diffusion coefficients for three different molecular weights of PSS. Compared to CS, PSS was retained longer in GAG-depleted cartilage in static and compression-based desorption experiments. We explained enhanced solute performance of PSS by its more compact morphology and higher charge density by small-angle X-ray scattering. This study may improve design of GAG mimetic molecules for repairing osmotic function in OA cartilage.
期刊介绍:
Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine.
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