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Desalting Plasma Protein Solutions by Membrane Capacitive Deionization
Bharat Shrimant1, Tanmay Kulkarni1, Mahmudul Hasan1
1Department of Chemical Engineering, Pennsylvania State University, University Park, Pennsylvania 16802, United States.
Membrane capacitive deionization (MCDI) effectively removes salt ions from plasma protein solutions, offering a promising alternative to traditional methods in biopharmaceutical manufacturing with minimal protein loss.
Area of Science:
- Biopharmaceutical Manufacturing
- Separation Science
- Chemical Engineering
Background:
- Plasma protein therapies are vital for treating numerous diseases.
- Conventional salt ion removal methods like diafiltration and ion-exchange chromatography face challenges with protein fouling.
- Efficient ion removal is critical for the purity and efficacy of plasma protein products.
Purpose of the Study:
- To investigate membrane capacitive deionization (MCDI) as a novel method for salt ion removal from plasma protein solutions.
- To evaluate the efficacy of MCDI in reducing ion concentration with minimal protein loss.
- To explore the use of advanced ion exchange membranes (IEMs) for improved MCDI performance.
Main Methods:
- Applied membrane capacitive deionization (MCDI) to human serum albumin solutions.
- Utilized highly conductive poly(phenylene alkylene)-based ion exchange membranes (IEMs).
- Incorporated ionomer-coated nylon meshes in the spacer channel to reduce electrical resistance.
Main Results:
- Achieved a 28% reduction in salt ions (sodium, chloride, phosphate) from plasma protein solutions.
- Demonstrated less than 3% protein loss during the MCDI process.
- Enhanced energy efficiency in MCDI due to improved membrane conductivity and reduced Ohmic resistances.
Conclusions:
- MCDI is a viable and effective platform for deionizing plasma protein solutions in biopharmaceutical manufacturing.
- This technique offers a significant advantage over conventional methods by minimizing protein loss.
- MCDI presents a scalable solution for purifying pharmaceutical formulations without compromising active pharmaceutical ingredients.
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