High-concentration protein formulations: How high is high?
Abstract
High-concentration protein formulation (HCPF) is a term that is used to describe protein formulations, mostly monoclonal antibody (mAb) drugs, at high protein concentration. The concentration is rarely defined, with typical ranges varying between 50 and 150mg/ml for mAbs. The term HCPF is meant to include and express specific solution properties of formulations that are prone to appear at high protein concentrations such as high viscosity, high opalescence, phase separation, gel formation or the increased propensity for protein particle formation. Thus the term HCPF can be understood as a descriptor of protein formulations, usually at high protein (monoclonal antibody) concentrations, which have specific solution, stability and colloidal properties that differ from formulations at low protein concentration (e.g. at 10mg/ml). The current paper highlights in brief the development challenges that might occur for high-concentration protein/monoclonal antibody formulations. In particular, the maximum concentration regimes achievable in HCPF remained unclear. Based on geometrical considerations involving packing of monoclonal antibodies in a lattice we map out a maximum concentration range that might be theoretically achievable. Different geometrical assumptions and packing models are compared and their relevance is critically discussed, in particular concerning the influence of the physicochemical properties of the monoclonal antibodies on their solubility, which is neglected in the simple geometrical model. According to our estimates, monoclonal antibody concentration above 500mg/ml will be very challenging to achieve. Our results have implications for setting up realistic drug product development strategies and for preparing convincing drug target product profiles for development.
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Significant progress has been made towards the development of high-concentration formulations to reduce the overall volume of a subcutaneous medication.
“Significant progress has been made towards the development of high-concentration formulations [17] to reduce the overall volume of a subcutaneous medication.”
From Subcutaneous Administration of Biotherapeutics: An Overview of Current Challenges and Opportunities (2018) · cites this paper as [17]
The development of high-concentration dosing solutions remains a challenge due to high viscosities, limitations in protein solubility, protein degradation and aggregation, protein stability in long-term storage, and difficulty of achieving mAb concentrations > 500 mg/ml.
“However, the development of such high-concentration dosing solutions remains a challenge for many reasons, including the high viscosities involved, limitations in protein solubility, protein degradation and aggregation, protein stability in long-term storage, and the difficulty of achieving mAb concentrations > 500 mg/ml [17].”
From Subcutaneous Administration of Biotherapeutics: An Overview of Current Challenges and Opportunities (2018) · cites this paper as [17]
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References 72 · Cited by 187
- Authors
- Garidel, P., Kuhn, A. B., Schäfer, L. V., Karow-Zwick, A. R., & Blech, M.
- Affiliations
- Boehringer Ingelheim (Germany) (DE)
- Ruhr University Bochum (DE)
- Corresponding author
- Garidel, Patrick
- Venue
- European Journal of Pharmaceutics and Biopharmaceutics
- Publisher
- Elsevier BV
- Published
- 2017-10
- Volume
- 119
- Pages
- 353-360
- ISSN
- 0939-6411 (ISSN-L)
- OpenAlex
- W2730013470
- Cited by
- 187
- References
- 72
- Citations by year
- 2026: 22 · 2025: 26 · 2024: 20 · 2023: 26 · 2022: 17 · 2021: 23 · 2020: 25 · 2019: 14 · 2018: 10 · 2017: 2
- FWCI
- 5.69
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Journal of Pharmaceutics and Biopharmaceutics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Cluster of Excellence RESOLV (EXC1069)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein purification and stability
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Life Sciences › Immunology and Microbiology › Immunology › Biosimilars and Bioanalytical Methods
- Keywords
- monoclonal antibodies, solubility, colloidal stability, viscosity, opalescence, phase separation, pharmaceutical product development, target product profile
- MeSH terms
- Antibodies, Monoclonal, Chemistry, Pharmaceutical, Hydrogen-Ion Concentration, Proteins, Solubility, Viscosity
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