β -环糊精包合物的铣削络合

N. A. Adhage, P. Vavia
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引用次数: 22

摘要

研究了尼美舒利与β-环糊精(β-CyD)的络合反应。尼美舒利与β-CyD按重量比1:1、1:2、1:3、1:4混合。每种混合物在球磨机中以50转/分钟- 1的速度研磨6、12、24和48小时。样品进行溶解研究、差示扫描量热法和x射线衍射研究,并评估其抗炎和镇痛活性。与尼美舒利、球磨尼美舒利和冻干配合物相比,含有1:4比例的样品研磨6和12 h的T90值较低。将研磨时间增加到24或48小时,进一步提高了T90(90%的药物溶解所需的时间)值。尼美舒利的溶出速率常数随β-CyD浓度的增加而增大。研磨样品(1:4比例研磨6和12 h)也显示出显著的抗炎和镇痛活性。结果表明,与β-CyD包合形成的药物提高了尼美舒利的吸收率,从而提高了生物利用度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
β‐Cyclodextrin Inclusion Complexation by Milling
The study involved the complexation of nimesulide with β-cyclodextrin (β-CyD) by milling. Nimesulide and β-CyD were mixed in the ratios 1:1, 1:2, 1:3 and 1:4 by weight. Each mixture was ground in a ball mill at 50 rev min−1 for 6, 12, 24 and 48 h. The samples were subjected to dissolution studies, differential scanning calorimetry and X-ray diffraction studies and were also evaluated for anti-inflammatory and analgesic activity. The sample containing the 1:4 ratio milled for 6 and 12 h exhibited a lower T90 value compared with nimesulide, ball-milled nimesulide and the freeze-dried complex. Increasing the milling time to 24 or 48 h further increased the T90 (time required for 90% of the drug to dissolve) value. The dissolution rate constant for nimesulide increased with an increase in β-CyD concentration. Milled samples (1:4 ratio milled for 6 and 12 h) also showed significant anti-inflammatory and analgesic activity. The results showed an improved rate of nimesulide absorption and hence better bioavailability by inclusion complex formation of the drug with β-CyD.
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