Eisner Devon Roshan, Hubbard Aaron, Eppler Kirk, Tegoulia Vassia, Maa Yuh-Fun
Pharmaceutical Processing and Technology Development, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080.
Pharmaceutical Processing and Technology Development, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080
PDA J Pharm Sci Technol. 2019 Sep-Oct;73(5):443-458. doi: 10.5731/pdajpst.2019.009928. Epub 2019 Apr 19.
In the vapor-phase hydrogen peroxide (VPHP)-sanitized environment, VPHP uptake by product-contacting components could eventually lead to undesired oxidation of biological drug products. Silicone tubing and primary packaging materials are prominent examples of such product-contacting surfaces that are typically processed/sterilized prior to use. This study investigated the VPHP-uptake tendency of these components and how their respective processing/sterilization methods affect the uptake behaviors. Silicone tubing that was sterilized via autoclave or gamma irradiation exhibited different VPHP uptake patterns-decreased uptake rates post autoclaving vs. increased uptake rates post gamma irradiation. The reduced uptake tendency of autoclaved tubing is maintained for 14 days after sterilization, whereas the uptake tendency of irradiated tubing was mostly reversed to normal levels 1 month after irradiation. Empty glass vials adsorbed hydrogen peroxide via the diffusion of VPHP into the vial with high vial-to-vial variability. Vial pretreatment (i.e., depyrogenation) and surface hydrophilicity/hydrophobicity impacted the uptake tendency. Stoppers and empty syringes also adsorbed hydrogen peroxide but at a relatively low level. The uptake behavior of these components appeared to correlate with water levels at the surface (i.e., hydrophilicity). This study provides process development scientists and engineers an in-depth understanding of the VPHP uptake by critical product-contacting surfaces so that they can mitigate the impact on drug product quality. This study investigated vapor-phase hydrogen peroxide (VPHP) absorption by biopharmaceutical drug products via VPHP uptake by critical product-contacting components during the aseptic manufacturing process with a focus on various pretreatments and processing of these components. Sterilization of silicone tubing by gamma irradiation or autoclaving resulted in different VPHP uptake profiles with different effect durations. Primary packaging components, such as vials, syringes, and stoppers, also showed different levels of VPHP uptake with surface hydrophilicity/hydrophobicity playing a critical role. These outcomes suggested that VPHP uptake is a complex phenomenon and should be carefully considered to minimize its impact on product quality. The approach and outcome of this study can benefit scientists and engineers who develop biological product manufacturing processes by providing an in-depth understanding of drug product process risks.
在气相过氧化氢(VPHP)消毒的环境中,与产品接触的组件对VPHP的吸收最终可能导致生物药品发生意外氧化。硅胶管和初级包装材料就是这类与产品接触表面的典型例子,它们通常在使用前进行处理/灭菌。本研究调查了这些组件对VPHP的吸收趋势,以及它们各自的处理/灭菌方法如何影响吸收行为。通过高压灭菌或伽马射线辐照灭菌的硅胶管表现出不同的VPHP吸收模式——高压灭菌后吸收率降低,而伽马射线辐照后吸收率增加。高压灭菌后的硅胶管在灭菌后14天内保持较低的吸收趋势,而辐照后的硅胶管在辐照后1个月其吸收趋势大多恢复到正常水平。空玻璃小瓶通过VPHP扩散到瓶内吸收过氧化氢,不同小瓶之间的吸收情况差异很大。小瓶预处理(即除热原)和表面亲水性/疏水性会影响吸收趋势。瓶塞和空注射器也会吸收过氧化氢,但吸收水平相对较低。这些组件的吸收行为似乎与表面的水分含量(即亲水性)相关。本研究为工艺开发科学家和工程师提供了对关键产品接触表面吸收VPHP的深入理解,以便他们能够减轻对药品质量的影响。本研究调查了在无菌生产过程中,生物制药产品通过关键产品接触组件对VPHP的吸收情况,重点关注这些组件的各种预处理和加工过程。通过伽马射线辐照或高压灭菌对硅胶管进行灭菌会导致不同的VPHP吸收情况,且影响持续时间不同。小瓶、注射器和瓶塞等初级包装组件也表现出不同程度的VPHP吸收,表面亲水性/疏水性起着关键作用。这些结果表明,VPHP吸收是一个复杂的现象,应仔细考虑以尽量减少其对产品质量的影响。本研究的方法和结果可为开发生物产品制造工艺的科学家和工程师提供帮助,使他们深入了解药品生产过程中的风险。