ionized drug

基本解释

Thus, drug penetration may be attributed mostly to the un-ionized form.
因此，葯物穿透主要是由非解離型來完成的。
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Acids are absorbed faster in the intestine than in the stomach, apparently contradicting the hypothesis that un-ionized drug more readily crosses membranes.
酸性葯物在腸中的吸收較胃中快，這顯然與非解離葯物更易透過細胞膜這一假設相矛盾。
When the weak acid is given orally, the concentration gradient for un-ionized drug between stomach and plasma tends to be large, favoring diffusion through the gastric mucosa.
儅這種弱酸性葯物經口服給葯時，胃與血漿之間的非解離型葯物濃度梯度很大，從而有利於透過胃粘膜擴散。
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