世界科学技术-中医药现代化
世界科學技術-中醫藥現代化
세계과학기술-중의약현대화
WORLD SCIENCE AND TECHNOLOGY-MODERNIZATION OF TRADITIONAL CHINESE MEDICINE
2014年
4期
821-824
,共4页
甘林建%刘静%余泉毅%孙彩霞%尹蓉莉%苏建春%赵俊霞
甘林建%劉靜%餘泉毅%孫綵霞%尹蓉莉%囌建春%趙俊霞
감림건%류정%여천의%손채하%윤용리%소건춘%조준하
刺五加叶总黄酮%载体材料%固体分散体%溶出度
刺五加葉總黃酮%載體材料%固體分散體%溶齣度
자오가협총황동%재체재료%고체분산체%용출도
Acanthopanax leaves total flavonoids%carrier material%solid dispersion%dissolution
目的:通过制备刺五加叶总黄酮固体分散体,提高其生物利用度。方法:以 PEG4000、PEG6000、F68、PVPK30为载体材料制备4种不同的固体分散体,筛选最优载体材料,并考察载体用量对溶出度的影响。以芦丁为对照品,亚硝酸钠-硝酸铝-氢氧化钠为显色体系,用紫外分光光度计在500 nm处测定吸光度,考察各比例固体分散体的体外溶出特性。结果:与原料药相比,以PVPK30为载体材料制得的固体分散体体外释放速率明显提高,并且累积释放度也明显增加。结论:固体分散体能显著提高药物在水中的体外释放度。
目的:通過製備刺五加葉總黃酮固體分散體,提高其生物利用度。方法:以 PEG4000、PEG6000、F68、PVPK30為載體材料製備4種不同的固體分散體,篩選最優載體材料,併攷察載體用量對溶齣度的影響。以蘆丁為對照品,亞硝痠鈉-硝痠鋁-氫氧化鈉為顯色體繫,用紫外分光光度計在500 nm處測定吸光度,攷察各比例固體分散體的體外溶齣特性。結果:與原料藥相比,以PVPK30為載體材料製得的固體分散體體外釋放速率明顯提高,併且纍積釋放度也明顯增加。結論:固體分散體能顯著提高藥物在水中的體外釋放度。
목적:통과제비자오가협총황동고체분산체,제고기생물이용도。방법:이 PEG4000、PEG6000、F68、PVPK30위재체재료제비4충불동적고체분산체,사선최우재체재료,병고찰재체용량대용출도적영향。이호정위대조품,아초산납-초산려-경양화납위현색체계,용자외분광광도계재500 nm처측정흡광도,고찰각비례고체분산체적체외용출특성。결과:여원료약상비,이PVPK30위재체재료제득적고체분산체체외석방속솔명현제고,병차루적석방도야명현증가。결론:고체분산체능현저제고약물재수중적체외석방도。
This study was aimed to prepare solid dispersions of Acanthopanax leaves total flavonoids in order to im-prove its bioavailability. PEG4000, PEG6000, F68, PVPK30 were used as carrier materials in the preparation of four different types of solid dispersion to screen the best type of carrier material and evaluate the amount of carrier mate-rial and its influence on the drug dissolution. Rutin was used as reference substance. NaNO2-Al(NO3)3-NaOH was used as the color system, with a UV spectrophotometer measured absorbance at 500 nm. The dissolution characteris-tics of different proportions of solid dispersions were examined in vitro. The results showed that compared with raw material, the in vitro drug release rate with PVPK30 as carrier material in the obtained solid dispersion of the pro-portion of the raw material was significantly improved, and the cumulative release rate was also increased significant-ly. It was concluded that the solid dispersion prepared by solvent method significantly improved in vitro drug release in water.