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盐酸阿替卡因的平衡溶解度和油水分配系数的测定 被引量:5

Determination of equilibrium solubility and oil/water partition coefficient of articaine hydrochloride
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摘要 目的:测定盐酸阿替卡因在不同介质中的平衡溶解度和在正辛醇-水和正辛醇-缓冲液体系中表观油水分配系数并研究pH对其的影响.方法:采用HPLC法测定盐酸阿替卡因的浓度,用摇瓶法测定盐酸阿替卡因的表观油水分配系数.结果:盐酸阿替卡因易溶于生理盐水、蒸馏水和系列不同pH的磷酸盐缓冲液.盐酸阿替卡因在正辛醇-水中的分配系数P为0.31(lgP=-0.51).结论:盐酸阿替卡因为溶解度大的亲水性药物. Aim:To determine the equilibrium solubility of articaine hydrochloride in various media, its oil /water partition coefficients in n-octanol-water/buffer solution systems,and to investigate the effects of pH on the above parameters.Methods:High performance liquid chromatography was used to determine the concentration of articaine hydrochloride;the partition coefficients of articaine hydrochloride in n-octanol-water/buffer solution systems were determined by shaking flask method.Results:Articaine hydrochloride is freely soluble in normal saline,distilled water and buffer solutions with various pH values.The partition coefficients of articaine hydrochloride was 0.31 (lgP =-0.51 )in n-octanol-water system.Conclusion:Articaine hydrochloride is a drug with great solubility and hydrophilicity.
出处 《暨南大学学报(自然科学与医学版)》 CAS CSCD 北大核心 2016年第5期394-397,共4页 Journal of Jinan University(Natural Science & Medicine Edition)
基金 广东省自然科学基金项目(2014A030313320) 广东省科技计划项目(2013B021800152) 广州市科技计划项目(201510010120)
关键词 盐酸阿替卡因 平衡溶解度 油水分配系数 HPLC articaine hydrochloride equilibrium solubility oil-water partition coefficient HPLC
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  • 1张婷婷,徐文,胡生亮,何仲贵.水飞蓟宾在不同介质中平衡溶解度和表观油水分配系数的测定[J].中国药学杂志,2006,41(20):1569-1571. 被引量:48
  • 2蒋合众.苦参碱及氧化苦参碱药理作用和制备方法研究进展[J].实用中西医结合临床,2007,7(1):89-90. 被引量:50
  • 3ABRAHAM D J. Burger's Medicinal Chemistry and Drug Discovery. Vol 2: Drug Discover and Drug Development[M]. 6th ed, New Zealand: John Wiley & Sons Inc., 2003:249- 293.
  • 4DRESSMAN J B, AMIDON G L, REPPAS C, et al. Dissolution testing as a prognostic tool for oral drug absorption: Immediate release dosage forms[J]. Pharm Res, 1998, 15(1): 11-22.
  • 5LIPINSKI C A, LOMBARDO F, DOM1NY B W, et al. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings[J]. Adv Drug Deliv Rev, 1997, 23(1-3): 3-25.
  • 6SHAO F, WANG G J, XIE H T, et al. Pbarmacokinetic study of triptolide, a constituent of imlnunosuppressive Chinese herb medicine in rats[J]. Biol Pharm Bull, 2007 , 30(4): 702-707.
  • 7梁文权.生物药剂学与药物动力学[M].第一版.北京:人民卫生出版社,2004:26-27.
  • 8张敏.荆芥内酯聚乳酸乙醇酸纳米粒冻干粉末的药效学及药代动力学研究[D].江苏:南京中医药大学,2007.
  • 9Pliska V, Testa B, Van de H Walerbeemd. Lipophilicity in drug action and toxicology[J]. Pharm Acta Helv, 1998,5(72) :313.
  • 10Lai J P,He XW,Jiang Y,et al.Preparative separstion and detemination of matrine from the Chinese medicinal plant Sophora flavescens Ait by molecularly imprinted solid-phase extraction[J].Anal Bioanal Chem,2003,375 (2):264.

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