Mixed Mode Chromatography Resin Market Backed by Antibody Production Boom and Multimodal Purification Demand
Mixed mode chromatography resins market is valued at USD 172 million in 2025 and is projected to grow at a CAGR of 15.7%, reaching USD 743 million by 2035. These resins use multimodal ligands, enabling protein binding through ionic, hydrogen bonding, and hydrophobic interactions, offering improved selectivity, resolution, and capacity compared to single-mode systems. This growth is driven by the increasing demand for sophisticated purification methods in biologics and biosimilar manufacturing, with a focus on process efficiency, scalability, and regulatory compliance in pharmaceutical and biopharmaceutical companies.
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The surge in monoclonal antibody and gene therapy production further fuels
adoption, as mixed mode resins provide high binding capacity and flexibility
for complex separations.
Market Segmentation and Trends:
The mixed mode chromatography resins market is segmented by type, application,
and region, providing a detailed understanding of its dynamics. Types include
ion exchange-hydrophobic type, hydroxyapatite type, and others. The ion
exchange-hydrophobic type is expected to be the most profitable segment, with a
CAGR of 17.1% from 2025 to 2035, due to its high binding capacity, flexibility,
and selectivity, essential for biologics and biosimilars production,
particularly in monoclonal antibody and gene therapy applications.
Applications encompass antibodies production, vaccine production, non-antibody
proteins, antibody-drug conjugate, and separation of low molecular weight
impurities. Antibodies production is set to be the most profitable application,
with a CAGR of 18.4% from 2025 to 2035, driven by the growth of monoclonal
antibody drugs and biosimilars, demanding high accuracy and scalability in
purification, especially for managing high titers and eliminating host cell
proteins.
Regionally, North America leads due to strong R&D, while Asia Pacific,
particularly China at a 16.5% CAGR, is emerging rapidly with policy initiatives
like "Healthy China 2030." Trends include advancements in
high-performance resins and increased investment in biomanufacturing.
Driving Factors Behind Market Growth:
The mixed mode chromatography resins market is propelled by several key
drivers. The growing demand for biologics and biosimilars, particularly
monoclonal antibodies, requires advanced purification techniques to achieve
high purity and yield. Increased R&D investments in cell and gene therapies
boost the need for resins with superior selectivity and capacity. Regulatory
compliance and quality standards in biopharmaceuticals push for efficient,
scalable processes, where mixed mode resins excel in removing impurities like
host cell proteins.
The expansion of contract development and manufacturing organizations (CDMOs)
supports market growth by providing specialized purification services.
Environmental and sustainability concerns favor resins that reduce solvent use
and waste. Additionally, the rise in vaccine production, accelerated by global
health challenges, demands robust separation technologies. These factors,
combined with technological innovations in ligand design, position the market
for sustained expansion, addressing the complexities of modern bioprocessing.
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Recent Developments and Key Players:
The mixed mode chromatography resins market is moderately concentrated, with
recent developments highlighting innovation and capacity expansions. In 2024,
Merck KGaA expanded its chromatography resin manufacturing capacity to meet
demand for resins used in monoclonal antibodies and other biologic products. In
2024, Bio-Rad Laboratories launched a new series of high-performance ion-exchange
chromatography resins for the biopharmaceutical sector, offering improved
capacity and selectivity for protein purification.
Key players include Thermo Fisher Scientific (25-30% market share), Cytiva
(Danaher) (20-25%), Merck KGaA (MilliporeSigma) (15-20%), Agilent Technologies
(10-15%), Bio-Rad Laboratories (8-12%), Tosoh Corporation (5-10%), GE
Healthcare (now part of Cytiva in chromatography), Purolite Corporation,
Avantor, JSR Micro Inc., Kaneka Corporation, Sepragen Corporation, Repligen
Corporation, Bio-Works Technologies, Mitsubishi Chemical Corporation, Hitachi
Chemical (now part of Showa Denko), Sartorius AG, and Waters Corporation.
Competitor analysis reveals a focus on R&D for next-generation resins with
increased selectivity and binding capacity.
Thermo Fisher and Cytiva lead through comprehensive portfolios and global
reach, while Merck emphasizes bioprocessing solutions. Strategic acquisitions
and collaborations enhance offerings, targeting high-value biologics and
biosimilars to capture market share in a competitive landscape.
Regional Insights and Opportunities:
North America dominates the mixed mode chromatography resins market, driven by
a robust R&D environment and biologics manufacturers, with the United
States focusing on cell and gene therapy and biosimilars. Europe follows, with
Germany at a 15.8% CAGR supported by precision biomanufacturing and EMA norms.
The Asia Pacific region is the fastest-growing, led by China at 16.5% CAGR,
fueled by public and private R&D investments and initiatives like
"Healthy China 2030," emphasizing biosimilars and monoclonal
antibodies. India grows at 16.2% CAGR, benefiting from cost-effective
manufacturing and "Make in India" policies.
South Korea at 16.4% CAGR is driven by investments from Samsung Biologics and
Celltrion. The United Kingdom (15.3% CAGR), France (15.6%), Italy (15.4%), and
Australia-New Zealand (15.2%) offer opportunities through biotech startups and
personalized medicine. Latin America and the Middle East & Africa present
potential via expanding biomanufacturing. Emerging markets offer growth through
strategic investments in R&D and collaborations for technology transfer.
Challenges and Future Outlook:
The mixed mode chromatography resins market faces challenges, including high
development costs for advanced ligands and scalability issues in bioprocessing.
Regulatory compliance and quality assurance pose hurdles, particularly for
biosimilars. However, the market's future is optimistic, with opportunities in
next-generation resin technologies and expanding biomanufacturing in emerging
economies.
As demand for monoclonal antibodies and gene therapies rises, innovations in
ion-exchange and hydroxyapatite types will drive growth. The market is
well-positioned to more than quadruple by 2035, revolutionizing biologics
purification through efficient, selective solutions.
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