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Spray-dried chitosan microspheres cross-linked with d, l-glyceraldehyde as a potential drug delivery system: preparation and characterization

机译:喷雾干燥的壳聚糖微球与d,l-甘油醛交联作为潜在的药物递送系统:制备和表征

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Chitosan microspheres of a small particle size and with good sphericity were prepared by a spray-drying method followed by treatment with a cross-linking agent. Owing to restrictions on the use of cross-linked chitosan microspheres in the pharmaceutical field, d,l-glyceraldehyde, a biocompatible reatant was used. The parameters studied affecting extent of cross-linking were cross-linking time and concentration of the cross-linking agent. Glutaraldehyde, the aldehyde most frequently employed as chemical cross-linking agent for proteins, was also used as a control. The cross-linked spray-dried chitosan microspheres were analyzed with respect to their morphological aspects, particle size, zeta potential and water uptake capacity. It was found that an increase either in d,l-glyceraldehyde concentration or in duration of cross-linking caused a decrease in both the swelling capacity and the zeta potential of the chitosan microspheres. Compared to glutaraldehyde, d,l-glyceraldehyde appears to be a good cross-linking agent for chitosan microspheres with the advantage that it is nontoxic.
机译:通过喷雾干燥法制备小粒径,球形度好的壳聚糖微球,然后用交联剂处理。由于在药物领域中使用交联的壳聚糖微球,d,1-甘油醛的限制,所以使用了生物相容性稀土。影响交联程度的研究参数是交联时间和交联剂的浓度。戊二醛,最常被用作蛋白质的化学交联剂的醛,也被用作对照。分析了交联的喷雾干燥的壳聚糖微球的形态,粒径,ζ电势和吸水能力。已发现,d,1-甘油醛浓度或交联持续时间的增加引起壳聚糖微球的溶胀能力和ζ电势均降低。与戊二醛相比,d,1-甘油醛似乎是壳聚糖微球的良好交联剂,其优点是无毒。

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