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一种用于细胞微囊化及其他生物材料应用的新方法:“串联”式热凝胶化和化学交联。

A new process for cell microencapsulation and other biomaterial applications: Thermal gelation and chemical cross-linking in "tandem".

作者信息

Cellesi F, Tirelli N

机构信息

School of Pharmacy & Molecular Materials Centre, University of Manchester, Manchester, M13 9PL, UK.

出版信息

J Mater Sci Mater Med. 2005 Jun;16(6):559-65. doi: 10.1007/s10856-005-0532-1.

Abstract

The very rapid gelation of a cell- or biomolecule-containing solution is at the basis of most processes employed in microencapsulation. Adequately quick ('instantaneous') gelation kinetics are provided by a number of phenomena based on physical association. On the other hand, physical gels are inherently reversible structures, which can be solubilized or disrupted in response to often poorly controllable phenomena in the environment of application, such as dilution, changes in temperature, ion strength and composition, pH, or other physical or chemical parameters. Chemically cross-linked hydrogels would have therefore significant advantages in terms of stability and end-properties; however, the time required for chemical reactions to produce a chemically cross-linked material is in a more general case hardly compatible with microencapsulation processes. In a recent study of our laboratory we have proposed a new approach for providing both quick gelation kinetics and good stability, by simply combining the rapid kinetics of a physical hardening phenomenon with a slower chemical curing; the former process is thus responsible of the morphogenesis of the material, while the latter develops its end-properties.

摘要

含有细胞或生物分子的溶液的快速凝胶化是大多数微囊化过程的基础。基于物理缔合的多种现象可提供足够快的(“瞬时”)凝胶化动力学。另一方面,物理凝胶本质上是可逆结构,在应用环境中,它们可能会因稀释、温度、离子强度和组成、pH值或其他物理或化学参数等通常难以控制的现象而溶解或破坏。因此,化学交联水凝胶在稳定性和最终性能方面具有显著优势;然而,在更一般的情况下,化学反应生成化学交联材料所需的时间与微囊化过程很难兼容。在我们实验室最近的一项研究中,我们提出了一种新方法,通过简单地将物理硬化现象的快速动力学与较慢的化学固化相结合,来同时提供快速凝胶化动力学和良好的稳定性;因此,前一过程负责材料的形态形成,而后一过程则发展其最终性能。

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