利用热喷墨生物打印技术制造尺寸可调的细胞负载水凝胶微颗粒的简便方法

Droplet Pub Date : 2024-08-28 DOI:10.1002/dro2.144
Ratima Suntornnond, Wei Long Ng, Viktor Shkolnikov, Wai Yee Yeong
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引用次数: 0

摘要

本研究探讨了基于热喷墨(TIJ)的按需滴墨(DOD)生物打印系统在制造可调尺寸的细胞负载水凝胶微颗粒(HMPs)中的应用。TIJ 生物打印技术通过热能在打印室中形成气泡,将生物墨水小液滴喷射到基底上。这项研究采用了一种经过热处理的皂化明胶基生物墨水 HSP-GelMA。这种生物墨水通过甲基丙烯酸酐功能化改性,并经过后续的皂化和热处理过程。对矿物油中不同浓度的 SPAN 80 表面活性剂进行了评估,以评估它们对 HMP 尺寸和稳定性的影响。结果表明,SPAN 80 浓度越高,HMP 的尺寸越小,稳定性越好,两者之间存在直接的相关性。研究还进一步调查了喷射量对 HMP 尺寸分布的影响,结果表明,喷射量越大,HMP 尺寸越大,这归因于液滴凝聚。我们通过蒙特卡罗模拟进行的进一步研究证实了这一点,该模拟显示,液滴的平均直径与分配液滴的数量呈近似线性增长。此外,该研究还证明了 TIJ 生物打印系统在 HMP 内实现多材料封装的能力,用不同的细胞质膜染料对活细胞进行染色就是例证。所介绍的方法为细胞负载 HMP 的受控制造提供了见解,突出了 TIJ 生物打印系统在组织工程和药物输送领域潜在应用的多功能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A facile method to fabricate cell-laden hydrogel microparticles of tunable sizes using thermal inkjet bioprinting

A facile method to fabricate cell-laden hydrogel microparticles of tunable sizes using thermal inkjet bioprinting

This study investigates the application of a drop-on-demand (DOD) thermal inkjet (TIJ)-based bioprinting system for the fabrication of cell-laden hydrogel microparticles (HMPs) with tunable sizes. The TIJ bioprinting technique involves the formation of vapor bubbles within the print chamber through thermal energy, expelling small droplets of bio-ink onto a substrate. The study employs a heat-treated saponified gelatin-based bio-ink, HSP-GelMA. This bio-ink is modified through methacrylic anhydride functionalization and undergoes subsequent saponification and heat treatment processes. Various concentrations of SPAN 80 surfactant in mineral oil were evaluated to assess their influence on HMP size and stability. The results indicate a direct correlation, with higher SPAN 80 concentrations resulting in smaller and more stable HMPs. The study further investigates the influence of jetting volume on HMP size distribution, revealing that larger jetting volumes lead to increased HMP sizes, attributed to droplet coalescence. This is supported by our further study via a Monte Carlo simulation, which shows that the mean droplet diameter grows approximately linear with the number of dispensed droplets. In addition, the study demonstrates the capability of the TIJ bioprinting system to achieve multimaterial encapsulation within HMPs, exemplified by staining living cells with distinct cytoplasmic membrane dyes. The presented approach provides insights into the controlled fabrication of cell-laden HMPs, highlighting the versatility of the TIJ bioprinting system for potential applications in tissue engineering and drug delivery.

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