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Mucoadhesive microspheres for nasal administration of cyclodextrins.

机译:用于环糊精鼻腔给药的粘膜粘附微球。

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The aim of this study was to examine the in vitro capacity of cyclodextrins to interfere on the beta-amyloid fibril formation; then, mucoadhesive microspheres containing cyclodextrins were prepared and characterised as nasal delivery system for brain targeting. Eight batches of microspheres containing chitosan or alginate loaded with beta-cyclodextrin or hydroxypropyl-beta-cyclodextrin in two different cyclodextrin to polymer ratios were produced by spray drying. The results show that none of the tested CDs has direct cellular toxicity and they protect the cell viability from beta-peptide. The microspheres prepared are characterised by small particle sizes, ability to absorb water and to delay the in vitro dissolution rate of the CDs; good ex vivo mucoadhesive properties of the formulations are assessed. The microsphere properties are influenced by the kind of polymer, of cyclodextrin and by cyclodextrin to polymer ratio used. In particular, the alginate formulation containing the higher cyclodextrin content shows the best performance.
机译:这项研究的目的是检查环糊精在体外干扰β-淀粉样蛋白原纤维形成的能力。然后,制备含有环糊精的粘膜粘附性微球,并将其表征为用于脑靶向的鼻腔输送系统。通过喷雾干燥制得八批含有负载有β-环糊精或羟丙基-β-环糊精的壳聚糖或藻酸盐的微球,所述两种不同的环糊精与聚合物的比例。结果表明,所有测试的CD都没有直接的细胞毒性,并且它们保护细胞免受β肽的生存。制备的微球的特点是粒径小,能够吸收水并延缓CD的体外溶解速度。评估了制剂的良好的体外粘膜粘附特性​​。微球性质受聚合物种类,环糊精和所用环糊精与聚合物之比的影响。特别地,含有较高环糊精含量的藻酸盐制剂显示出最佳性能。

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