磁力攪拌條件下溶解于10mL雙蒸水中,待固體物質完全溶解,放置冷卻至室溫。將50mg的4-羥甲基苯硼酸頻哪醇酯修飾γ-環糊精衍生物和5mg的2,2,6,6-四甲基哌啶氧化物溶解于5mL甲醇/ 二甲基乙酰胺中。然后在攪拌條件下,將有機相緩慢滴加于水相之中(lmL/min)。滴加完成后,60°C繼續攪拌6h以揮發去除有機溶劑。通過離心分離,用去離子水洗滌,冷凍干燥后即可得到本發明所述的納米藥物。
[0063]實施例15
[0064]首先將4mg卵磷脂和6mg聚乙二醇-二硬脂酰磷脂酰乙醇胺(其中聚乙烯醇的分子量為2000Da)在65°C恒溫磁力攪拌條件下溶解于10mL雙蒸水中,待固體物質完全溶解,放置冷卻至室溫。將50mg的4-羥甲基苯硼酸頻哪醇酯修飾α -環糊精衍生物和5mg的2,2,6,6-四甲基哌啶氧化物溶解于5mL甲醇/N-甲基吡咯烷酮中。然后在攪拌條件下,將有機相緩慢滴加于水相之中(lmL/min)。滴加完成后,60°C繼續攪拌8h以揮發去除有機溶劑。通過離心分離,用去離子水洗滌,冷凍干燥后即可得到本發明所述的納米藥物。
[0065]本發明所述的自由基清除藥物是對炎癥性腸病發揮治療作用的一大類活性物質。在上述實施例中,所采用的藥物為哌啶類氮氧自由基。但是這些氮氧自由基并不限制本發明的保護范圍,本領域普通技術人員可選擇合適的自由基清除藥物。
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