Pfizer Global Research and Development, Groton, Connecticut 06340, USA.
J Pharm Sci. 2012 Feb;101(2):610-5. doi: 10.1002/jps.22789. Epub 2011 Oct 12.
The chemical reaction rate for solid-state product formation in a pharmaceutical case study was monitored by equilibration with either a 75%, 21.5%, 75% relative humidity (RH) cycle ("high-low-high", HLH) or a 21.5%, 75%, 21.5% RH cycle ("low-high-low", LHL). For the HLH cycle, it was found that the degradant formation rate was reversible; that is, the rate at the final 75% RH step was equivalent to the rate at the initial 75% RH step. For samples equilibrated with the LHL cycle, a significantly higher rate of product formation was seen when the low RH condition was re-established than for the initial sample that had never been exposed to high RH. The observed hysteresis in degradant formation rate as a function of RH is not explained by hysteresis in the bulk moisture sorption isotherm, which is minimal in the case studied. It is suggested that high RH exposure impacts the solid-solid interface by either changing the amount of solid-solution present, by altering the mechanical properties of the material such that there is a greater mobility even when moisture is removed, or by altering the interfacial material to have a greater amount of moisture present even when dried.
在一项药物案例研究中,通过与 75%、21.5%、75%相对湿度(RH)循环(“高低高”,HLH)或 21.5%、75%、21.5% RH 循环(“低高低”,LHL)平衡来监测固态产物形成的化学反应速率。对于 HLH 循环,发现降解物形成速率是可逆的;也就是说,最终 75% RH 步骤的速率与初始 75% RH 步骤的速率相当。对于用 LHL 循环平衡的样品,当重新建立低 RH 条件时,产物形成的速率明显高于从未暴露于高 RH 的初始样品。RH 函数中降解物形成速率的观察到的滞后现象不能用吸湿等温线的滞后现象来解释,在研究的情况下,这种滞后现象很小。有人认为,高 RH 暴露通过改变固溶体的含量、改变材料的机械性能(即使去除水分时也具有更大的流动性)或者通过改变界面材料以使其在干燥时具有更多的水分来影响固-固界面。