Approach of design for air mass balance in an aseptic processing area for cell-based products

IF 3.4 3区 环境科学与生态学 Q3 CELL & TISSUE ENGINEERING Regenerative Therapy Pub Date : 2024-11-28 DOI:10.1016/j.reth.2024.11.009
Shunpei Furomitsu , Manabu Mizutani , Masahiro Kino-oka
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Abstract

Introduction

The manufacture of cell-based products requires assuring sterility through all processes, with aseptic processing in a cleanroom. The environment consists of a critical processing zone (CPZ) that can ensure a level of cleanliness that allows cell culture containers to be opened, and a support zone (SZ) adjacent to it and accessed by an operator. In this study, an environment for cell manufacturing was proposed by designing an air mass balance in an aseptic processing area (APA).

Methods

We considered the distribution of particle concentration related to the airflow of clean air passing through a high efficiency particulate air (HEPA) filter and the location of the particle emission sources and set up a model dividing the SZ into two zones vertically: the upper and lower zones in a cleanroom, considering three cases practically. Both the air inlet and outlet were located outside the cleanroom and were connected to the CPZ directly by air ducts (Case 1). The inlets of the CPZ were located in the lower or upper zones of the SZ inside the cleanroom, and the outlets were located in the upper zone (Case 2 or Case 3, respectively). We analyzed how the cleanliness of the APA was affected by different locations of the inlet and outlet of the CPZ by varying the particle emission rate or air change rate.

Results

In Case 1, changes in the particle emission rate or air change rate within the SZ did not affect the particle concentration in the CPZ. In Case 2, an increase in the particle emission rate led to an increase in the particle concentration of the CPZ. In Case 3, the particle concentration of the CPZ was not affected by the particle emission rate. Cases 2 and 3 showed differences in particle concentrations between the CPZ and SZ, indicating that the location of the air inlet of the CPZ had an impact on the cleanliness of both zones. The partial circulation of air between the SZ and CPZ exhibited an additional air cleaning effect, leading to a reduction in the particle concentration in the SZ in Cases 2 and 3.

Conclusions

These results suggest that the appropriate location of the air inlet and outlet can construct the cleanliness of the APA, which reduces the risk of microbial contamination. In addition, we consider that this approach can realize an APA design policy, which eliminates the need for air ducts between the outside of the cleanroom and the equipment for the CPZ, reduces the requirements for gowning, thereby reducing the required air change rate.
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细胞类产品无菌加工区的空气质量平衡设计方法
导言细胞产品的生产需要在洁净室中进行无菌处理,以确保所有流程的无菌性。该环境由一个关键处理区(CPZ)和一个辅助区(SZ)组成,前者可确保达到允许打开细胞培养容器的洁净度水平,后者毗邻关键处理区,操作人员可进入辅助区。我们考虑了与通过高效微粒空气过滤器(HEPA)的洁净空气气流有关的微粒浓度分布以及微粒排放源的位置,并建立了一个模型,将 SZ 垂直分为两个区域:洁净室中的上区和下区,并实际考虑了三种情况。进风口和出风口都位于洁净室外部,通过风管直接与 CPZ 相连(情况 1)。CPZ 的进气口位于洁净室内 SZ 的下区或上区,出气口位于上区(分别为情况 2 或情况 3)。我们通过改变粒子排放率或换气率,分析了不同位置的 CPZ 入口和出口对 APA 清洁度的影响。结果在案例 1 中,SZ 内粒子排放率或换气率的变化不会影响 CPZ 中的粒子浓度。在案例 2 中,颗粒排放率的增加导致了 CPZ 中颗粒浓度的增加。在案例 3 中,CPZ 的颗粒浓度不受颗粒排放率的影响。案例 2 和案例 3 显示了 CPZ 和 SZ 之间的颗粒浓度差异,这表明 CPZ 的进气口位置对两个区域的清洁度都有影响。SZ 和 CPZ 之间的部分空气循环具有额外的空气净化效果,导致案例 2 和 3 中 SZ 的颗粒浓度降低。此外,我们认为这种方法可以实现 APA 的设计策略,即无需在洁净室外部和 CPZ 设备之间铺设风管,减少对穿袍的要求,从而降低所需的换气率。
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来源期刊
Regenerative Therapy
Regenerative Therapy Engineering-Biomedical Engineering
CiteScore
6.00
自引率
2.30%
发文量
106
审稿时长
49 days
期刊介绍: Regenerative Therapy is the official peer-reviewed online journal of the Japanese Society for Regenerative Medicine. Regenerative Therapy is a multidisciplinary journal that publishes original articles and reviews of basic research, clinical translation, industrial development, and regulatory issues focusing on stem cell biology, tissue engineering, and regenerative medicine.
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