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淀粉/环糊精生物粘附微球的制备与表征:作为甲磺酸加贝酯(福怡)鼻腔给药治疗变应性鼻炎的平台

Preparation and characterization of starch/cyclodextrin bioadhesive microspheres as platform for nasal administration of Gabexate Mesylate (Foy) in allergic rhinitis treatment.

作者信息

Fundueanu Gheorghe, Constantin Marieta, Dalpiaz Alessandro, Bortolotti Fabrizio, Cortesi Rita, Ascenzi Paolo, Menegatti Enea

机构信息

Department of Pharmaceutical Sciences, University of Ferrara, Via Fossato di Mortara, 17-19, I-44100, Ferrara, Italy.

出版信息

Biomaterials. 2004 Jan;25(1):159-70. doi: 10.1016/s0142-9612(03)00477-0.

Abstract

Bioadhesive and biodegradable microspheres were obtained by chemical cross-linking with epichlorohydrin of an alkaline solution of a mixture of starch and alpha-, beta-, or gamma-cyclodextrin (CyD). Microspheres were characterized by scanning electron microscopy, swelling degree, and water retention. The percentage of the effective CyD in microspheres was estimated by measuring the amount of iodine and typical organic compounds (TOCs) retained in the hydrophobic cavity of CyD. Gabexate Mesylate (trade name Foy); GM), an antiallergic drug, was included in microspheres by soaking in an aqueous solution containing the drug, followed by solvent evaporation or lyophilization. UV, IR, and DSC data indicated that despite the fact that GM is a hydrophilic drug, its hydrophobic moiety close to the benzene ring is able to penetrate the CyD cavity and to form stable inclusion complexes. Values of the association equilibrium constant for GM binding to CyD, obtained by UV differential spectroscopy, indicated that the affinity of the drug for alpha- and gamma-CyD is higher than that for beta-CyD. In vitro, GM was gradually released during 1h. Even if the release rate of the drug is relatively fast, the microspheres might actually provide the best platform since the material adheres to the nasal mucosa which was proved by adhesion tests. The GM integrity was checked by comparing its anti-trypsin activity before and after release.

摘要

通过用环氧氯丙烷对淀粉与α-、β-或γ-环糊精(CyD)混合物的碱性溶液进行化学交联,制备了生物粘附性和可生物降解的微球。通过扫描电子显微镜、溶胀度和保水性对微球进行了表征。通过测量保留在CyD疏水腔内的碘和典型有机化合物(TOC)的量,估算了微球中有效CyD的百分比。将抗过敏药物甲磺酸加贝酯(商品名Foy;GM)浸泡在含有该药物的水溶液中,然后通过溶剂蒸发或冻干将其包封在微球中。紫外、红外和差示扫描量热数据表明,尽管GM是一种亲水性药物,但其靠近苯环的疏水部分能够穿透CyD腔并形成稳定的包合物。通过紫外差示光谱法获得的GM与CyD结合的缔合平衡常数表明,该药物对α-和γ-CyD的亲和力高于对β-CyD的亲和力。在体外,GM在1小时内逐渐释放。即使药物的释放速率相对较快,但微球实际上可能提供了最佳平台,因为粘附试验证明该材料可粘附于鼻黏膜。通过比较GM释放前后的抗胰蛋白酶活性来检查其完整性。

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