Science Translational MedicineBioengineeringPeer-reviewed journal article
Glassy Surfactants Enable Ultra-High Concentration Biologic Therapeutics
Carolyn K. JonsiD, Alexander N. ProssnitziD, Noah EckmaniD, Changxin DongiD, Ashley UtziD, Eric Andrew AppeliD
Abstract
Protein therapeutics, like peptides and antibodies, have become critical to healthcare. Despite their exceptional potency and specificity, biopharmaceuticals are prone to aggregation, often necessitating low formulation concentrations as well as cold storage and distribution to maintain stability. Yet, high doses are required to treat many diseases. To achieve these doses, most approved protein drug products are administered intravenously, imposing excessive burdens on patients and the healthcare system. New approaches are needed to formulate proteins at high concentrations to enable less burdensome subcutaneous injection, preferably in an autoinjector format. To address this challenge, we report a subcutaneously injectable biotherapeutic delivery platform composed of spray-dried protein microparticles suspended in a non-solvent liquid carrier. These microparticles contain only active biopharmaceutical agent and a high glass transition temperature polyacrylamide-derived copolymer excipient affording several key benefits over traditional excipients, including: (i) improved stabilization of biopharmaceuticals through the spray drying process, and (ii) improved morphology and properties of the spray-dried particles, enhancing suspension injectability. Experiments with albumin and antibodies demonstrate that this technology enables ultra-high-concentration protein formulations (exceeding 500 mg/mL) that are injectable through standard needles with clinically relevant injection forces. Additionally, experiments in mice with two clinically relevant antibody drugs show these ultra-high- concentration formulations reduce required injection volumes without altering pharmacokinetics or efficacy. This approach could nearly triple the number of commercial protein drugs amenable to subcutaneous administration, dramatically reducing burden and improving access to these critical biopharmaceuticals. One Sentence SummaryHere we leverage a unique copolymer excipient to enable ultra-high concentration protein formulations with improved stability and amenable to subcutaneous injection that can reduce patient burden, lower costs, and improve access to critical drugs.
- organism: mouse
- assay: protein structure
- research focus: drug response / drug discovery
- approach: experimental assay
- Citations
- 19
- FWCI
- 4.72
- Field percentile
- top 3%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Stable High-Concentration Monoclonal Antibody Formulations Enabled by an Amphiphilic Copolymer Excipient
J. H. Klich, C. M. Kasse, … E. Appel·bioRxiv·May 25, 2022
- Defining Structure-Function Relationships of Amphiphilic Excipients Enables Rational Design of Ultra-Stable Biopharmaceuticals
Alexander N. Prossnitz, Leslee T. Nguyen, … Eric Andrew Appel·Advanced SciencePeer-reviewed·Jan 7, 2025
- Subcutaneous delivery of an antibody against SARS-CoV-2 from a supramolecular hydrogel depot
C. M. Kasse, A. C. Yu, … E. A. Appel·bioRxiv·May 24, 2022
- Multi-dimensional protein solubility optimization with an ultra-high-throughput microfluidic platform
N. A. Erkamp, M. Oeller, … T. Knowles·bioRxiv·Oct 21, 2022
- Patient-Centric Development of a Low-Volume, Low-Viscosity, Once Every 4 Weeks (Q4W) Autoinjector Combination Product for Povetacicept
Joanie Lucas, J Alaina Floyd, … Gabriel C. Graffius·bioRxiv·Oct 21, 2026
- Versatile Tissue-Injectable Hydrogels with Extended Hydrolytic Release of Bioactive Protein Therapeutics
E. S. Nealy, S. J. Reed, … J. M. Olson·bioRxiv·Sep 1, 2023