Clerkin Shane, Singh Krutika, Winning Danielle, Krupa Ivan, Crean John, Brougham Dermot F, Wychowaniec Jacek K
Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin 4, Ireland.
School of Chemistry, University College Dublin, Belfield, Dublin 4, Ireland.
J Mater Chem B. 2025 Aug 6;13(31):9351-9376. doi: 10.1039/d5tb00588d.
Thermoresponsive biomaterials have the potential to improve the complexity of models, to generate dynamically controlled extracellular microenvironments and act as forming drug delivery systems. Due to its known biocompatibility and ease of use, poloxamer 407 (P407), also known as pluronic F127, has attracted significant attention as a component for next-generation cell culture and biomedical applications. P407 display rapid gelation into hydrogels with facile ease-of-handling, and which possess good shear-thinning properties that enable 3D printability with high fidelity. Although P407 has been extensively used as a support matrix for cell proliferation, differentiation and the on-demand release of biomolecules and drugs, significant issues relating to mechanical stability under physiological conditions limit its application. Multiple protocols report the use of P407 'hydrogel' for a variety of applications but often do not emphasise its inherent limitations at the concentrations described. Here we emphasise the disparity between written protocols and what specifically constitutes a hydrogel, showing selected examples from the literature and suggesting clarifications in the language used in describing P407 supports. We describe progress in the field, which is accelerating in part due to development of multi-network hydrogels that include P407 as a stabiliser, for shear-thinning and as a sacrificial component aiding 3D printing. We also contrast P407 to a panel of other promising thermoresponsive systems that have emerged as alternative biomaterials. Finally, we briefly discuss challenges and new opportunities in the field. This includes evaluation of the relative merits of current thermoresponsive polymer systems as they are formulated for use, also by advanced manufacturing, in next-generation 4D-responsive functional hydrogel networks for cell culture automation and as components in responsive-release devices.
热响应性生物材料有潜力提高模型的复杂性,生成动态可控的细胞外微环境,并用作成型药物递送系统。由于其已知的生物相容性和易用性,泊洛沙姆407(P407),也称为普朗尼克F127,作为下一代细胞培养和生物医学应用的一种成分引起了广泛关注。P407能快速凝胶化成水凝胶,易于操作,并且具有良好的剪切变稀特性,能够实现高保真的3D打印。尽管P407已被广泛用作细胞增殖、分化以及生物分子和药物按需释放的支撑基质,但在生理条件下与机械稳定性相关的重大问题限制了其应用。多个方案报告了使用P407“水凝胶”用于各种应用,但往往没有强调其在所描述浓度下的固有局限性。在这里,我们强调书面方案与具体构成水凝胶之间的差异,展示文献中的选定示例,并建议在描述P407支撑物时所用语言上进行澄清。我们描述了该领域的进展,这在一定程度上由于多网络水凝胶的发展而加速,这些多网络水凝胶将P407用作稳定剂以实现剪切变稀,并作为辅助3D打印的牺牲成分。我们还将P407与其他一些已成为替代生物材料的有前景的热响应系统进行了对比。最后,我们简要讨论了该领域的挑战和新机遇。这包括评估当前热响应性聚合物系统在其配方用于下一代用于细胞培养自动化的4D响应性功能水凝胶网络以及作为响应释放装置中的组件时的相对优点,同时也包括通过先进制造进行评估。