Chandrasekhar Saradha, Topp Elizabeth M
Department of Industrial and Physical Pharmacy, Purdue University, West Lafayette, Indiana.
J Pharm Sci. 2015 Apr;104(4):1291-302. doi: 10.1002/jps.24370. Epub 2015 Jan 28.
Lyophilization (freeze-drying) is frequently used to stabilize protein therapeutics. However, covalent modifications such as thiol-disulfide exchange and disulfide scrambling can occur even in the solid state. The effects of lyophilization and storage of lyophilized powders on the mechanism and kinetics of thiol-disulfide exchange have not been elucidated and are explored here. Reaction kinetics was monitored in peptides corresponding to tryptic fragments of human growth hormone (T20 + T20-T21 or T20 + cT20-T21) during different stages of lyophilization and during storage of the lyophilized powders at 22°C and ambient RH. The concentrations of reactants and products were determined using RP-HPLC and product identity confirmed using liquid chromatography-mass spectrometry. Loss of native disulfide was observed for the reaction of T20 with both linear (T20-T21) and cyclic (cT20-T21) peptides during the primary drying step; however, the native disulfides were regenerated during secondary drying with no further change till the end of lyophilization. Deviations from Arrhenius parameters predicted from solution studies and the absence of buffer effects during lyophilization suggest that factors such as temperature, initial peptide concentration, buffer type, and concentration do not influence thiol-disulfide exchange during lyophilization. Results from a "cold finger" method used to study peptide adsorption to ice indicate that there is no preferential adsorption to the ice surface and that its presence may not influence disulfide reactivity during primary drying. Overall, reaction rates and product distribution differ for the reaction of T20 with T20-T21 or cT20-T21 in the solid state and aqueous solution, whereas the mechanism of thiol-disulfide remains unchanged. Increased reactivity of the cyclic peptide in the solid state suggests that peptide cyclization does not offer protection against lyophilization and that damage induced by a process stress further affects storage stability at 22°C and ambient RH.
冻干(冷冻干燥)常用于稳定蛋白质治疗剂。然而,即使在固态下也可能发生共价修饰,如硫醇-二硫键交换和二硫键重排。冻干及冻干粉末储存对硫醇-二硫键交换机制和动力学的影响尚未阐明,本文对此进行了探讨。在冻干的不同阶段以及冻干粉末在22°C和环境相对湿度下储存期间,监测了对应于人生长激素胰蛋白酶片段(T20 + T20-T21或T20 + cT20-T21)的肽中的反应动力学。使用反相高效液相色谱法测定反应物和产物的浓度,并使用液相色谱-质谱法确认产物的同一性。在一次干燥步骤中,观察到T20与线性(T20-T21)和环状(cT20-T21)肽反应时天然二硫键的损失;然而,在二次干燥期间天然二硫键得以再生,直至冻干结束都没有进一步变化。与溶液研究预测的阿伦尼乌斯参数存在偏差,且冻干过程中不存在缓冲效应,这表明温度、初始肽浓度、缓冲液类型和浓度等因素不会影响冻干过程中的硫醇-二硫键交换。用于研究肽在冰上吸附的“冷指”方法的结果表明,肽对冰表面没有优先吸附,并且其存在可能不会影响一次干燥期间的二硫键反应性。总体而言,T20与T20-T