Remmele R L, Stushnoff C, Carpenter J F
Analytical Chemistry and Formulation, Immunex Corporation, Seattle, Washington 98101, USA.
Pharm Res. 1997 Nov;14(11):1548-55. doi: 10.1023/a:1012170116311.
First, to investigate the role of sucrose in stabilizing protein structure (as measured by changes in the amide I band of lysozyme) caused by dehydration encountered during lyophilization. Second, to demonstrate the utility of internal reflection spectroscopy as a tool for conducting controlled lyophilization experiments.
A custom-built internal reflection FTIR accessory was used to follow the entire freeze-drying process of solutions consisting of 49.4 mg/mL lysozyme in the presence and absence of 10% sucrose in real-time. Studies were carried out using D2O as a transparent medium in the infrared region of the protein amide bands. Potential self-association of the protein in the presence of sucrose was investigated using dynamic light scattering. Hydration levels were determined using a multiple regression equation. Differential scanning calorimetry (DSC) permitted characterization of the final lyophilized product. Moisture content was determined using Karl Fischer titration.
Throughout freezing and drying, minimal changes were observed both in frequency (1647 +/- 1 cm-1) and bandwidth (46 +/- 1 cm-1) of the amide I band in the presence of sucrose. In contrast, greater changes in frequency and band width were seen in the absence of sucrose. A successfully lyophilized cake was obtained which had properties of a glass as measured by DSC, with a Tg of 50 degree C. The lyophilized product containing sucrose had 4% moisture by weight. Three distinct rates of water desorption were discovered during drying under vacuum (50 mg/hr within the sample temperature range from -35 degrees to -25 degrees C; 30 mg/hr from -10 degrees to 25 degrees C; 1.2 mg/hr from 27 degrees to 38 degrees C).
The inclusion of sucrose served to minimize perturbations of protein structure caused by freezing and dehydration stresses encountered during lyophilization (compared to studies conducted in absence of sucrose). The results support the water replacement hypothesis and underscore the role of the sugar in preserving a native structure in the dried state. This investigation demonstrates the usefulness of infrared spectroscopy in evaluating lyophilization process parameters and formulation design.
第一,研究蔗糖在稳定冻干过程中因脱水导致的蛋白质结构(通过溶菌酶酰胺I带的变化来衡量)方面的作用。第二,证明内反射光谱法作为进行可控冻干实验工具的实用性。
使用定制的内反射傅里叶变换红外附件实时跟踪由49.4 mg/mL溶菌酶组成的溶液在有和没有10%蔗糖存在下的整个冻干过程。研究在蛋白质酰胺带的红外区域使用重水作为透明介质进行。使用动态光散射研究蔗糖存在下蛋白质的潜在自缔合。使用多元回归方程确定水合水平。差示扫描量热法(DSC)用于表征最终的冻干产品。使用卡尔费休滴定法测定水分含量。
在整个冷冻和干燥过程中,在有蔗糖存在的情况下,酰胺I带的频率(1647±1 cm-1)和带宽(46±1 cm-1)变化最小。相比之下,在没有蔗糖的情况下,频率和带宽变化更大。获得了一个成功冻干的饼状物,通过DSC测量其具有玻璃的性质,玻璃化转变温度为50℃。含有蔗糖的冻干产品的水分含量为4%(重量)。在真空干燥过程中发现了三种不同的水脱附速率(在样品温度范围从-35℃到-25℃时为50 mg/hr;从-10℃到25℃时为30 mg/hr;从27℃到38℃时为1.2 mg/hr)。
与在没有蔗糖的情况下进行的研究相比,加入蔗糖有助于使冻干过程中因冷冻和脱水应力导致的蛋白质结构扰动最小化。结果支持水替代假说,并强调了糖在保持干燥状态下天然结构方面的作用。本研究证明了红外光谱法在评估冻干工艺参数和配方设计方面的有用性。