中国药学(英文版)
中國藥學(英文版)
중국약학(영문판)
JOURNAL OF CHINESE PHARMACEUTICAL SCIENCES
2006年
2期
69-75
,共7页
杨照罡%古丽斯坦·阿吾提%曹轶%朱静%伍博深%王坚成%吕万良%张烜%张强
楊照罡%古麗斯坦·阿吾提%曹軼%硃靜%伍博深%王堅成%呂萬良%張烜%張彊
양조강%고려사탄·아오제%조질%주정%오박심%왕견성%려만량%장훤%장강
槲皮素%羟丙基-β-环糊精%包合物%包合常数%物相鉴定
槲皮素%羥丙基-β-環糊精%包閤物%包閤常數%物相鑒定
곡피소%간병기-β-배호정%포합물%포합상수%물상감정
quercetin%hydroxypropyl-β-cyclodextrin%inclusion complex%inclusion constant%Phase behavior
目的用研磨法制备槲皮素-羟丙基-β-环糊精包合物,测定包合常数及包合过程热力学参数,并对物相进行鉴定.方法采用研磨法制备包合物,对其包合常数进行测定,利用差热分析(DSC)、红外光谱分析(IR)、粉末X衍射(X-ray)、扫描电镜(SEM)等方法对其进行物相鉴定,以溶解度和溶出实验考察其溶解性质.结果所制备的包合物溶解度较槲皮素纯品增加约37倍,5分钟的溶出百分率较槲皮素纯品提高近10倍.DSC结果表明包合物中槲皮素吸热峰位前移;IR图谱槲皮素羰基吸收峰产生位移;X-衍射图谱包合物中槲皮素吸收峰消失;电镜扫描照片包合物中未见槲皮素晶体,说明形成新物相.结论研磨可使槲皮素与羟丙基β环糊精形成包合物,改善槲皮素的溶解性.
目的用研磨法製備槲皮素-羥丙基-β-環糊精包閤物,測定包閤常數及包閤過程熱力學參數,併對物相進行鑒定.方法採用研磨法製備包閤物,對其包閤常數進行測定,利用差熱分析(DSC)、紅外光譜分析(IR)、粉末X衍射(X-ray)、掃描電鏡(SEM)等方法對其進行物相鑒定,以溶解度和溶齣實驗攷察其溶解性質.結果所製備的包閤物溶解度較槲皮素純品增加約37倍,5分鐘的溶齣百分率較槲皮素純品提高近10倍.DSC結果錶明包閤物中槲皮素吸熱峰位前移;IR圖譜槲皮素羰基吸收峰產生位移;X-衍射圖譜包閤物中槲皮素吸收峰消失;電鏡掃描照片包閤物中未見槲皮素晶體,說明形成新物相.結論研磨可使槲皮素與羥丙基β環糊精形成包閤物,改善槲皮素的溶解性.
목적용연마법제비곡피소-간병기-β-배호정포합물,측정포합상수급포합과정열역학삼수,병대물상진행감정.방법채용연마법제비포합물,대기포합상수진행측정,이용차열분석(DSC)、홍외광보분석(IR)、분말X연사(X-ray)、소묘전경(SEM)등방법대기진행물상감정,이용해도화용출실험고찰기용해성질.결과소제비적포합물용해도교곡피소순품증가약37배,5분종적용출백분솔교곡피소순품제고근10배.DSC결과표명포합물중곡피소흡열봉위전이;IR도보곡피소탄기흡수봉산생위이;X-연사도보포합물중곡피소흡수봉소실;전경소묘조편포합물중미견곡피소정체,설명형성신물상.결론연마가사곡피소여간병기β배호정형성포합물,개선곡피소적용해성.
Aim To prepare and characterize the QURC-HP-β-CD inclusion complexes and investigate the thermodynamic parameters of the process. Methods QURC-HP-β-CD inclusion complexes were prepared by the grinding method. The equilibrium inclusion constants and thermodynamic parameters were determinated by phase solubility analysis. Dissolution tests were performed to study the dissolution rate of inclusion complexes. The formation of inclusion complexes was confirmed by differential scanning calorimetry ( DSC), infrared spectroscopy ( IR), powder X-ray diffractometry (PXRD) and scanning electron microscopy (SEM). Results The aqueous solubility of quercetin was greatly increased ( about 37 folds) by inclusion technique, and the initial dissolution rate was markedly improved (10 folds) in the first 5 min. The results of DSC and SEM photographs showed that quercetin crystal disappeared in inclusion complexes, which indicated the formation of new phase. FT-IR spectra showed that the carbonyl absorption band of quercetin was shifted. PXRD showed that the diffraction peak of quercetin crystal disappeared. Conclusion QURC-HP-β-CD inclusion complexes are produced by the grinding method. The solubility of quercetin is improved by the inclusion technique.