Thermo-controlled microfluidic generation of monodisperse alginate microspheres based on external gelation†

IF 3.9 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
RSC Advances Pub Date : 2024-10-10 DOI:10.1039/D4RA07049F
Saray Chen, Tal Shahar and Smadar Cohen
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引用次数: 0

Abstract

Droplet-based microfluidic systems have received much attention as promising tools for fabricating monodisperse microspheres of alginate solutions with high accuracy and reproducibility. The immediate and simple ionotropic gelation of alginate, its biocompatibility, and its tunability of mechanical properties make it a favorable hydrogel in the biomedical and tissue engineering fields. In these fields, micron-sized alginate hydrogel spheres have shown high potential as cell vehicles and drug delivery systems. Although on-chip microfluidic gelation of the produced alginate droplets is common, several challenges remain. Complicated chemical and microfabrication processes are required, and the risk of microchannel clogging is high. In the current study, we present an easy-to-use microfluidic external gelation process to produce highly spherical and monodisperse microspheres from very low-concentrated alginate-RGD solution [0.5% (w/v)]. To accomplish this, gelatin, a thermo-sensitive and inexpensive biomaterial, was incorporated into the alginate solution as a sacrificial biomaterial that mediates the off-chip external gelation of the alginate with Ca2+, and avoids droplet coalescence. Utilizing the methodology mentioned above, we successfully generated monodisperse alginate microspheres (AMs) with diameters ranging from 27 μm to 46 μm, with a coefficient of variation of 0.14, from a mixture of Arg-Gly-Asp (RGD)-modified very low viscosity alginate and gelatin. These RGD-AMs were used as microcarriers for human umbilical vein endothelial cells. The described easy-to-use and cost-effective microfluidic off-chip external gelation strategy exhibits comparable advantages to on-chip external gelation and demonstrates superiority over the latter since clogging is impossible.

Abstract Image

基于外部凝胶化的单分散藻酸盐微球的热控微流控生成技术†。
基于液滴的微流体系统作为制造单分散海藻酸溶液微球的理想工具,以其高精度和可重复性而备受关注。海藻酸具有直接而简单的离子凝胶化、生物相容性和机械性能可调性,使其成为生物医学和组织工程领域的理想水凝胶。在这些领域,微米大小的海藻酸盐水凝胶球已显示出作为细胞载体和药物输送系统的巨大潜力。虽然在芯片上对生产的海藻酸液滴进行微流体凝胶化很常见,但仍存在一些挑战。需要复杂的化学和微制造工艺,而且微通道堵塞的风险很高。在当前的研究中,我们提出了一种易于使用的微流体外部凝胶化工艺,利用浓度极低的海藻酸-RGD 溶液[0.5%(w/v)]生产高球形和单分散微球。为了实现这一目标,在藻酸盐溶液中加入了明胶(一种对热敏感且价格低廉的生物材料),作为一种牺牲生物材料,用 Ca2+ 介导藻酸盐的片外凝胶化,并避免液滴凝聚。利用上述方法,我们成功地从Arg-Gly-Asp(RGD)修饰的极低粘度藻酸盐和明胶的混合物中生成了直径在27微米到46微米之间的单分散藻酸盐微球(AMs),变异系数为0.14。这些 RGD-AMs 被用作人脐静脉内皮细胞的微载体。所描述的易于使用且经济高效的微流控芯片外凝胶化策略具有与芯片外凝胶化相当的优势,而且由于不可能发生堵塞,因此比芯片外凝胶化更具优越性。
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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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