[在原料药物和坎波提取物中验证元素杂质和观察的程序]
Mizuki Tomiyasu1, Shota Yoshida1, Hongyan Zhang1
1Kampo Research Laboratories, Kracie Ltd.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan
|November 30, 2025
概括
日本药典中的日本药典.
科学领域:
- 药理学和毒理学 药理学和毒理学
- 分析化学 分析化学
背景情况:
- 日本药典第18版引入了基本杂质的一般测试2.66.
- 这种转变是从测色方法转向用于单个元素控制的仪器分析,同时考虑毒理风险.
研究的目的:
- 评估一般测试对原始药物和坎波提取物2.66的适用性.
- 为了进一步了解这些草药产品中元素杂质相关的风险.
主要方法:
- 基于2.66原则,对七种第1类和第2A类元素杂质 (Cd,Pb,As,Hg,Co,V,Ni) 的量化.
- 使用经过验证的分析方法分析了十种原始药物 (根和根茎) 和十二种坎波提取物.
主要成果:
- 一般测试中的分析程序 2.66适用于测试的草药和坎波提取物.
- 控制元素度达到允许的水平对于原始药物来说是具有挑战性的,这是由于药物输送途径.
结论:
- 草药和坎波提取物中的元素杂质可以使用日本药典的2.66方法进行评估.
- 建议对官方专著中的元素进行个别控制,考虑到测量含量,而不是对原始药物的固定允许度进行控制.
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