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1. 天津中医药大学实验教学部
2. 黑龙江中医药大学药学院
纸质出版日期:2011
移动端阅览
[1]曹颖,李永吉,吕邵娃,王艳宏.丁香苦苷解离常数及油水分配系数的测定[J].中国实验方剂学杂志,2011,17(23):65-67.
CAO Ying1, LI Yong-ji2, LV Shao-wa2, et al. Determination of Dissociation Constants and Apparent Oil/Water Partition Coefficient of Syringopicroside[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(23): 65-67.
[1]曹颖,李永吉,吕邵娃,王艳宏.丁香苦苷解离常数及油水分配系数的测定[J].中国实验方剂学杂志,2011,17(23):65-67. DOI: 10.13422/j.cnki.syfjx.2011.23.051.
CAO Ying1, LI Yong-ji2, LV Shao-wa2, et al. Determination of Dissociation Constants and Apparent Oil/Water Partition Coefficient of Syringopicroside[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(23): 65-67. DOI: 10.13422/j.cnki.syfjx.2011.23.051.
目的:测定丁香苦苷解离常数和油水分配系数。方法:采用紫外分光光度法
测得丁香苦苷解离常数
应用HPLC测定丁香苦苷的表观正辛醇/水分配系数。结果:丁香苦苷解离常数pKa为9.628 4±0.14。油水分配系数Papp为1.206 9(logPapp=0.0817)
当pH 4.5
5.5
6.5
7.5
8.5时
油水分配系数Papp分别为1.388 1
1.352 9
1.335 8
1.370 4
1.133 3
表明丁香苦苷的表观正辛醇/缓冲溶液分配系数受缓冲溶液pH的影响不大。结论:在生理pH下
丁香苦苷大部分以未解离的分子状态存在
但丁香苦苷水溶性好
脂溶性较差
可能会对丁香苦苷的吸收分布及设计药物剂型产生影响。
Objective:To determine the dissociation constants of syringopicroside and its partition coefficients for the n-octanol-water/buffer solution systems.Method: To determine the dissociation constants of syringopicroside were determined by UV-visible spectrophotometer
at the same time
the partition coefficients in the n-octanol-water /buffer solution systems of syringopicroside were determined by shaking flask method.Result: The pka value is 9.628 4±0.14
and the n-octanol/water partition coefficient Papp is 1.206 9(logPapp=0.081 7).When the pH is 4.5
5.5
6.5
7.5
8.5
the n-octanol/water partition coefficient Papp is 1.388 1
1.352 9
1.335 8
1.370 4
1.133 3 respectively
indicating that there is little effect on the n-octanol/water partition coefficient of syringopicroside in different pH values buffer solution.Conclusion: In the physiological environment
drugs most existed as most molecular state.The syringopicroside has good hydrophilicity
but poor liposolubility
it maybe affect the absorption
distribution of syringopicroside and the design of dosage forms.
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