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采用脂质体过滤法对除菌级过滤膜进行基准测试。

Benchmarking of Sterilizing-Grade Filter Membranes with Liposome Filtration.

作者信息

Singh Bhuwan, Mundlamuri Ramesh, Friese Thomas, Mundrigi Ashok, Handt Sebastian, Loewe Thomas

机构信息

Sartorius Stedim India Pvt Ltd., Bangalore, India.

Panacea Biotech Limited, Punjab, India.

出版信息

PDA J Pharm Sci Technol. 2018 May-Jun;72(3):223-235. doi: 10.5731/pdajpst.2017.007757. Epub 2017 Dec 14.

Abstract

Cytotoxic drugs can be encapsulated in liposomes vesicles, which act as drug delivery vehicles and reduce the risk of exposure of drug to healthy cells. The sterility of such liposome solutions is typically ensured using 0.2 μm-rated sterilizing-grade membranes, but due to the high viscosity and low surface tension of these formulations, they can cause premature blocking and increased risk of bacterial penetration through a 0.2 μm sterilizing-grade membrane. The low surface tension of liposome solutions affects the contact angle with membrane and reduces bubble point, leading to bacterial penetration through the membrane. This poses a great challenge to select an appropriate sterilizing-grade membrane for a given process and for filter manufacturers to develop a sterilizing-grade membrane that specifically addresses these needs. In this study, the influence of different variables that could affect the total throughput and bacterial retention performance of different membrane types on processing of liposome solutions was evaluated. Based on the results, we conclude that the membrane properties, for example, surface porosity, surface tension, pore size, symmetry/asymmetry, hydrophilicity and liposome properties (e.g., composition, lipid size, and concentration) affect bacterial retention and total throughput capacity. Process parameters such as temperature, pressure, and flow should also be optimized to improve process efficiency. Cytotoxic drugs can be encapsulated in liposomes vesicles, which act as drug delivery vehicles and reduce the risk of exposure of drug to healthy cells. Liposome solution cause premature blocking and increased risk of bacterial penetration through a 0.2 μm sterilizing-grade membrane due to their high viscosity and low surface tension. In this study, we demonstrated the total throughput and bacterial retention performance of different sterilizing-grade membranes with liposome solution. Based on the results, we conclude that some sterilizing-grade membranes yield less throughput and bacterial retention compared to other membranes. This is due to liposome formulation and membrane properties. Therefore, it is important to identify the product formulation and membrane properties before selection of a suitable sterilizing-grade filter for a given process application to ensure expected throughput and bacterial retention.

摘要

细胞毒性药物可封装在脂质体囊泡中,脂质体囊泡作为药物递送载体,可降低药物暴露于健康细胞的风险。此类脂质体溶液的无菌性通常使用孔径为0.2μm的除菌级膜来确保,但由于这些制剂的高粘度和低表面张力,它们可能会导致过早堵塞,并增加细菌透过0.2μm除菌级膜的风险。脂质体溶液的低表面张力会影响与膜的接触角并降低泡点,从而导致细菌透过膜。这给为特定工艺选择合适的除菌级膜以及过滤器制造商开发专门满足这些需求的除菌级膜带来了巨大挑战。在本研究中,评估了不同变量对不同膜类型在脂质体溶液处理过程中的总通量和细菌截留性能的影响。基于这些结果,我们得出结论,膜的特性,例如表面孔隙率、表面张力、孔径、对称/不对称性、亲水性以及脂质体特性(例如组成、脂质大小和浓度)会影响细菌截留和总通量能力。还应优化温度、压力和流速等工艺参数以提高工艺效率。细胞毒性药物可封装在脂质体囊泡中,脂质体囊泡作为药物递送载体,可降低药物暴露于健康细胞的风险。脂质体溶液由于其高粘度和低表面张力,会导致过早堵塞并增加细菌透过0.2μm除菌级膜的风险。在本研究中,我们展示了不同除菌级膜对脂质体溶液的总通量和细菌截留性能。基于这些结果,我们得出结论,与其他膜相比,一些除菌级膜的通量和细菌截留率较低。这是由于脂质体制剂和膜的特性所致。因此,在为特定工艺应用选择合适的除菌级过滤器之前,识别产品制剂和膜的特性非常重要,以确保预期的通量和细菌截留率。

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