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Preparation and characterization of drop pills of effective part from safflower for anti-Parkinson's disease 被引量:2
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作者 Shixuan Cheng Yingcong Ma +10 位作者 Yujie Liu Ning Pang Ji Li Meng Sha Rutong Ren Nuramatjan Ablat Jing Cao Yi Sun Xiaoping Pu Min Ye Xianrong Qi 《Journal of Chinese Pharmaceutical Sciences》 CAS CSCD 2019年第1期27-39,共13页
Parkinson’s disease(PD) is a common degenerative disease of the central nervous system, and the pathologic features are mainly degeneration of substantianigra and dopamine neurons. Studies have shown that safflower f... Parkinson’s disease(PD) is a common degenerative disease of the central nervous system, and the pathologic features are mainly degeneration of substantianigra and dopamine neurons. Studies have shown that safflower flavonoid extract(SAFE) exhibits the neuroprotective effect. In this study, the safflower flavonoid extract drop pills(SAFE-DPs) for anti-PD were prepared by the heating and melting method using SAFE and matrix PEG6000. The performances of the pills were evaluated with powder X-ray diffraction(PXRD), differential scanning calorimetry(DSC), Fourier transform infrared spectroscopy(FT-IR), scanning electron microscopy(SEM) and dissolution testing. The analysis results demonstrated an amorphous state for SAFE dispersion in the matrix PEG6000 without any chemical reaction. The SAFE-DPs demonstrated acceptable chemical and physical stability irrespective of the manufacturing process and the storage period. Dissolution testing in three dissolution media(pH 1.0, pH 6.8 and pH 7.5) indicated that SAFE-DPs had excellent dissolution property. The transport of Kaempferol-3-rutinoside(K3 R) on the Caco-2 monolayer and the absorption of K3 R in situ intestinal perfusion revealed that the principal component of SAFE had a good transport and absorption capacity. Therefore, the drop pills had better release and absorption in the gastrointestinal tract, corresponding with the pharmacological and pharmacodynamic results for PD in vivo. 展开更多
关键词 safflower flavonoid extract Parkinson’s disease solid dispersion drop pills Kaempferol-3-O-rutinoside CHARACTERIZATIONs
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生姜速效滴丸的制备及其质量控制 被引量:4
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作者 许玲玲 李群力 +1 位作者 麻佳蕾 汪妍 《中国医药导报》 CAS 2012年第9期45-47,共3页
目的制备并测定生姜速效滴丸中总姜酚的含量,以控制其有效成分姜酚类物质。方法以PEG 4000和PEG6000为(1∶2)基质,液体石蜡为冷凝液,将从鲜姜中提取纯化后的姜辣素制备成滴丸;以6-姜酚为对照品,采用铁氰化钾-三氯化铁比色法测定总姜酚,... 目的制备并测定生姜速效滴丸中总姜酚的含量,以控制其有效成分姜酚类物质。方法以PEG 4000和PEG6000为(1∶2)基质,液体石蜡为冷凝液,将从鲜姜中提取纯化后的姜辣素制备成滴丸;以6-姜酚为对照品,采用铁氰化钾-三氯化铁比色法测定总姜酚,测定波长为680 nm。结果滴丸圆整度、硬度好,重量差异和溶散时限均符合规定。6-姜酚溶液浓度在25.6~320.0μg/mL浓度范围内,线性关系良好。总姜酚平均含量为2.22 mg/粒。结论本制备方法简便可行,可用于测定鲜姜滴丸中的总姜酚含量。 展开更多
关键词 生姜速效滴丸 制备 总姜酚 含量测定 比色法
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