Controllable preparation of magnesium-hybridized PLA-PEG-PLA porous microspheres with anti-inflammatory function.

Xu Liu, Ziyang Yuan, Dong Zhou, Ziwei Tao, Mingpei Li, Lan Xiao, Jinzhong Zhao, Guomo Ruan, Yulin Li
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Abstract

Biodegradable polylactic acid-based microspheres have been widely used in biomedical applications such as drug delivery and tissue engineering, however, most of the microspheres typically possess simple surface structures, lacking bioactivity and the ability to promote cell adhesion. Our group previously synthesized poly (L-lactic acid) magnesium-doped microspheres (PMg) with immunomodulatory and osteogenic potential. However, several drawbacks of PMgs, such as high hydrophobicity, a narrow pore distribution and large average particle size, and limited sustainable Mg2+release, can affect cell adhesion and growth and thus restricting their biomedical applications. To address these limitations, in the current study, a poly (lactic acid)-poly (ethylene glycol)-poly (lactic acid) (PLEL) triblock copolymer was synthesized, and magnesium-incorporated PLEL porous microspheres (PEMg) were prepared through emulsion solvent evaporation combined with anin-situdoping method. Benefiting from hydrophilic PEG segments, PEMg displayed significantly improved surface wettability and structural stability. The optimized PEMg possessed nearly half of the average size of PMg. and an interconnected hierarchical larger pore structure (1-30 μm, average: 10 ± 1.4 μm), which effectively promoted cell adhesion and deep infiltration. Moreover, PEMg showed a sustained Mg2+release which is nearly 1.87-fold higher than PMg, capable of neutralizing acidic by-products and stabilizing the local microenvironment. The biocompatible PEMg could upregulate anti-inflammatory biomarkers (Arg-1, CD206) and inhibit pro-inflammatory factors (iNOS, TNF-α), achieving over 1.5 times anti-inflammatory capacity of PMg. In summary, the creatively developed PEMg microspheres integrate optimized structural features and enhanced biological performances. Compared with PMg, PEMg showed much better potential to satisfy the complex demands of tendon soft tissue repair and presents promising prospects for inflammatory microenvironment regulation and soft tissue regeneration.

具有抗炎功能的镁杂化PLA-PEG-PLA多孔微球的可控制备。
可生物降解聚乳酸微球已广泛应用于生物医学领域,如药物传递和组织工程,然而,大多数微球通常具有简单的表面结构,缺乏生物活性和促进细胞粘附的能力。本小组先前合成了具有免疫调节和成骨潜力的聚l -乳酸镁掺杂微球(PMg)。然而,pmg +的一些缺点,如高疏水性、狭窄的孔隙分布和大的平均粒径,以及有限的可持续Mg 2 +释放,会影响细胞的粘附和生长,从而限制了它们在生物医学上的应用。为了解决这些局限性,本研究合成了聚乳酸-聚乙二醇-聚乳酸(PLEL)三嵌段共聚物,并通过乳液溶剂蒸发结合原位掺杂法制备了镁掺杂的PLEL多孔微球(PEMg)。得益于亲水的PEG片段,pemm表现出显著改善的表面润湿性和结构稳定性。优化后的聚能电池的体积几乎是普通聚能电池的一半。具有相互连接的层次状大孔结构(1 ~ 30 μm,平均10±1.4 μm),有效促进细胞粘附和深度浸润。此外,pem2 +的持续释放量比PMg高近1.87倍,能够中和酸性副产物,稳定局部微环境。具有生物相容性的PMg可上调抗炎生物标志物(Arg-1、CD206),抑制促炎因子(iNOS、TNF-α),抗炎能力是PMg的1.5倍以上。总之,创造性开发的PEMg微球集成了优化的结构特征和增强的生物性能。与PMg相比,PEMg在满足肌腱软组织修复的复杂需求方面表现出更好的潜力,在炎症微环境调节和软组织再生方面具有广阔的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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