van Hoogmoed Chris G, Busscher Henk J, de Vos Paul
Department of Biomedical Engineering, Section of Bioadhesion, University of Groningen, Antonius Deusinglaan 1, 9713 AV Groningen, The Netherlands.
J Biomed Mater Res A. 2003 Oct 1;67(1):172-8. doi: 10.1002/jbm.a.10086.
Microencapsulation of cells is a promising approach to prevention of rejection in the absence of immunosuppression. Clinical application, however, is hampered by insufficient insight into the factors that influence the biocompatibility of the capsules. Capsules prepared of alginates with a high guluronic (G) acid content proved to be more adequate for clinical application since they are more stable, but, unfortunately, they are less biocompatible than capsules prepared of intermediate-G alginate. In order to get some insight into the physicochemical factors that influence the biocompatibility of capsules for the encapsulation of living cells, the chemical compositions of alginate[bond]Ca beads and alginate[bond]PLL capsules were studied by Fourier transform infrared spectroscopy. We found that during the transition of the alginate[bond]Ca beads to alginate[bond]PLL capsules, Ca connecting the alginate molecules, disappeared at the surface of both high-G and intermediate-G alginate[bond]PLL capsules. At the same time, it turned out that high-G alginate[bond]PLL capsules contained more hydrogen bonding than did intermediate[bond]G alginate capsules. Thus the well-known higher stability of high-G alginate[bond]PLL compared to intermediate-G alginate[bond]PLL capsules is not caused by a higher degree of binding to Ca of the alginate molecules but rather by the presence of more hydrogen bonds. Another observation was that after the transition from bead to capsule, high-G alginate[bond]PLL capsules contained 20% more PLL than the intermediate-G alginate[bond]PLL capsules. Finally, we show that in both high-G and intermediate-G alginate[bond]PLL capsules, the PLL exists in the alpha-helix, in the antiparallel beta-sheet, and in the random coil conformation. This study shows that FT-IR allows for successful analyses of the chemical factors essential for understanding differences in the biocompatibility of alginate[bond]PLL capsules.
细胞微囊化是一种在不进行免疫抑制的情况下预防排斥反应的有前景的方法。然而,临床应用受到对影响微囊生物相容性因素了解不足的阻碍。由高古洛糖醛酸(G)含量的藻酸盐制备的微囊被证明更适合临床应用,因为它们更稳定,但不幸的是,它们的生物相容性比由中等G含量藻酸盐制备的微囊要差。为了深入了解影响用于封装活细胞的微囊生物相容性的物理化学因素,通过傅里叶变换红外光谱研究了藻酸盐-Ca珠和藻酸盐-PLL微囊的化学成分。我们发现,在藻酸盐-Ca珠转变为藻酸盐-PLL微囊的过程中,连接藻酸盐分子的Ca在高G和中等G藻酸盐-PLL微囊表面均消失。同时,结果表明高G藻酸盐-PLL微囊比中等G藻酸盐微囊含有更多的氢键。因此,与中等G藻酸盐-PLL微囊相比,高G藻酸盐-PLL微囊具有更高稳定性,并非是由于藻酸盐分子与Ca的结合程度更高,而是由于存在更多的氢键。另一个观察结果是,从珠子转变为微囊后,高G藻酸盐-PLL微囊所含的PLL比中等G藻酸盐-PLL微囊多20%。最后,我们表明在高G和中等G藻酸盐-PLL微囊中,PLL均以α-螺旋、反平行β-折叠和无规卷曲构象存在。这项研究表明,傅里叶变换红外光谱能够成功分析理解藻酸盐-PLL微囊生物相容性差异所必需的化学因素。