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姜黄素-赖氨酸共晶在无水乙醇中的热力学研究 被引量:3

Thermodynamics of Curcumin-lysine Cocrystal in Anhydrous Ethanol
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摘要 目的考察在三元体系中各条件下的平衡状态,计算姜黄素共晶的相关热力学常数,探讨无水乙醇作为特异性溶剂的合理性。方法采用溶液法分别测定姜黄素在不同温度下、不同浓度赖氨酸的无水乙醇中的溶解度,通过数学推导,得出姜黄素共晶的热力学常数。结果绘制了姜黄素-赖氨酸-无水乙醇的三元相图,并求得了K_(sp)、K_(ll)、△G°、△H及△S等热力学参数。结论无水乙醇可以作为特异性溶剂用于提取姜黄素共晶中混杂的姜黄素单体。 OBJECTIVE To calculate the thermodynamic constant of a ternary systerm made up with curcumin, lysine and anhydrous ethanol at different temperatures with different ratio. Moreover, to discuss the rationality of anhydrous ethanol as a specific solvent. METHODS Determine the solubility of curcumin in different concentration of lysine solutions at different temperature, and get the thermodynamic constants by calculating. RESULTS The ternary phase diagrams were graphed; K_(sp), K_(ll), △G°, △H and △S were calculated. CONCLUSION Anhydrous ethanol could be used as a specific solvent to extract curcumin monomer mixed in curcumin-lysine cocrystal.
作者 陈晓红 迟宗良 秦昆明 蔡宝昌 CHEN Xiaohong CHI Zongliang QIN Kunming CAI Baochang(Hangzhou Xiaoshan First People's Hospital, Hangzhou 311200, China Zhejiang Chinese Medical University, Hangzhou 310053, China Nanjing Haichang Chinese Medicine Group Co, Ltd., Nanjing 210044, China Jiangsu Key Laboratory of Chinese Medicine Processing, Nanjing 210049, China)
出处 《中国现代应用药学》 CAS CSCD 2017年第6期871-875,共5页 Chinese Journal of Modern Applied Pharmacy
基金 江苏省自然科学基金(BK20141094)
关键词 姜黄素-赖氨酸共晶 无水乙醇 热力学 特异性溶剂 curcumin-lysine cocrystal anhydrous ethanol thermodynamics specific solvent
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  • 1高振珅,王兰.姜黄素-羟丙基-β-环糊精包合物的制备及其理化性质研究[J].中国药房,2007,18(13):999-1000. 被引量:17
  • 2韩刚,霍文,李秋影,孙广利,段离潼.姜黄素的稳定性研究[J].中成药,2007,29(2):291-293. 被引量:43
  • 3Miroshnyk I,Mirza S,Sandler N.Pharmaceutical co-crystals-an opportunity for drug product enhancement[J].Expert Opin Drug Deliv,2009,6(4):333-341.
  • 4Starrett JE, Tortolani DR, Russell J, et al. Synthesis, oral bioavail- ability determination, and in vitro evaluation of prodrugs of the antiviral agent 9-[ 2-( phosphonomethoxy ) ethyl ] adenine (PMEA) [J]. J Med Chem, 1994,37(12) :1857 - 1864.
  • 5Gao Y,Zu H,Zhang JJ.Enhanced dissolution and stability of adefovir dipivoxil by cocrystal formation[J].J Pharm Pharmacol,2011,63(4):483-490.
  • 6Gao Y,Gao J,Liu ZL,et al.Coformer selection based on degradation pathway of drugs:a case study of adefovir dipivoxil-saccharin and adefovir dipivoxil-nicotinamide cocrystals[J].Int J Pharm,2012,438(1):327-335.
  • 7Ma K, Zhang Y, Kan HL, et al.Thermodynamic and kinetic investigation on the crucial factors affecting adefovir dipivoxil-saccharin cocrystallization[J].Pharm Res,2014,31(7):1766-1778.
  • 8Myerson A.Handbook of Industrial Crystallization[M].Boston:Butterworth-Heinemann,1993:65-87.
  • 9Lee MK,Lee H,Kim I,et al.Novel polymorphic form of adefovir dipivoxil derived from polymer-directed crystallization[J].Pharmazie,2011,66(10):766-770.
  • 10Jung S,Ha JM,Kim IW.Phase Transformation of adefovir dipivoxil/succinic acid cocrystals regulated by polymeric additives[J].Polymers,2013,6(1):1-11.

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