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使用先进的核磁共振成像技术并以Cu(2+)作为造影剂测定藻酸盐凝胶的交联特性。

Cross-linking properties of alginate gels determined by using advanced NMR imaging and Cu(2+) as contrast agent.

作者信息

Manz B, Hillgärtner M, Zimmermann H, Zimmermann D, Volke F, Zimmermann U

机构信息

Arbeitsgruppe Magnetische Resonanz, Fraunhofer-Institut für Biomedizinische Technik (IBMT), 66386, St Ingbert, Germany.

出版信息

Eur Biophys J. 2004 Feb;33(1):50-8. doi: 10.1007/s00249-003-0341-8. Epub 2003 Sep 16.

DOI:10.1007/s00249-003-0341-8
PMID:13680210
Abstract

The entrapment of enzymes, drugs, cells or tissue fragments in alginates cross-linked with Ca(2+) or Ba(2+) has great potential in basic research, biotechnology and medicine. The swelling properties and, in turn, the mechanical stability are key factors in designing an optimally cross-linked hydrogel matrix. These parameters depend critically on the cross-linking process and seemingly minor modifications in manufacture have a large impact. Thus, sensitive and non-invasive tools are required to determine the spatial homogeneity and efficacy of the cross-linking process. Here, we show for alginate microcapsules (between 400 microm and 600 microm in diameter) that advanced (1)H NMR imaging, along with paramagnetic Cu(2+) as contrast agent, can be used to validate the cross-linking process. Two- and three-dimensional images and maps of the spin-lattice relaxation time T(1) of Ba(2+) cross-linked microcapsules exposed to external Cu(2+) yielded qualitative as well as quantitative information about the accumulation of Cu(2+) within and removal from microcapsules upon washing with Cu(2+) free saline solution. The use of Cu(2+) (having a slightly higher affinity constant to alginate than Ba(2+)) for gelling gave a complementary insight into the spatial homogeneity of the cross-linking process together with information about the mechanical stability of the microcapsules. The potential of this technique was demonstrated for alginates extracted from two different algal sources and cross-linked either externally by the conventional air-jet dropping method or internally by the "crystal gun" method.

摘要

将酶、药物、细胞或组织片段包裹于与Ca(2+)或Ba(2+)交联的藻酸盐中,在基础研究、生物技术和医学领域具有巨大潜力。溶胀特性以及由此产生的机械稳定性是设计最佳交联水凝胶基质的关键因素。这些参数严重依赖于交联过程,而且生产过程中看似微小的改变都会产生很大影响。因此,需要灵敏且非侵入性的工具来确定交联过程的空间均匀性和效果。在此,我们表明,对于直径在400微米至600微米之间的藻酸盐微胶囊,先进的(1)H NMR成像技术,结合顺磁性Cu(2+)作为造影剂,可用于验证交联过程。二维和三维图像以及暴露于外部Cu(2+)的Ba(2+)交联微胶囊的自旋晶格弛豫时间T(1)图谱,提供了关于用无Cu(2+)盐溶液洗涤后Cu(2+)在微胶囊内的积累和去除的定性及定量信息。使用对藻酸盐亲和力常数略高于Ba(2+)的Cu(2+)进行凝胶化,能对交联过程的空间均匀性以及微胶囊的机械稳定性信息提供补充性见解。该技术的潜力在从两种不同藻类来源提取的藻酸盐中得到了证明,这些藻酸盐通过传统的空气喷射滴加法在外部交联,或通过“晶体枪”法在内部交联。

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