Author
Listed:
- Simona Bianco
(University of Glasgow)
- Muhammad Hasan
(University of Warwick)
- Ashfaq Ahmad
(University of Warwick
University of Warwick)
- Sarah-Jane Richards
(University of Warwick
University of Manchester)
- Bart Dietrich
(University of Glasgow)
- Matthew Wallace
(University of East Anglia, Norwich Research Park)
- Qiao Tang
(University of Warwick)
- Andrew J. Smith
(Diamond House, Harwell Science and Innovation Campus)
- Matthew I. Gibson
(University of Warwick
University of Warwick
University of Manchester
University of Manchester)
- Dave J. Adams
(University of Glasgow)
Abstract
A long-standing challenge is how to formulate proteins and vaccines to retain function during storage and transport and to remove the burdens of cold-chain management. Any solution must be practical to use, with the protein being released or applied using clinically relevant triggers. Advanced biologic therapies are distributed cold, using substantial energy, limiting equitable distribution in low-resource countries and placing responsibility on the user for correct storage and handling. Cold-chain management is the best solution at present for protein transport but requires substantial infrastructure and energy. For example, in research laboratories, a single freezer at −80 °C consumes as much energy per day as a small household1. Of biological (protein or cell) therapies and all vaccines, 75% require cold-chain management; the cost of cold-chain management in clinical trials has increased by about 20% since 2015, reflecting this complexity. Bespoke formulations and excipients are now required, with trehalose2, sucrose or polymers3 widely used, which stabilize proteins by replacing surface water molecules and thereby make denaturation thermodynamically less likely; this has enabled both freeze-dried proteins and frozen proteins. For example, the human papilloma virus vaccine requires aluminium salt adjuvants to function, but these render it unstable against freeze–thaw4, leading to a very complex and expensive supply chain. Other ideas involve ensilication5 and chemical modification of proteins6. In short, protein stabilization is a challenge with no universal solution7,8. Here we designed a stiff hydrogel that stabilizes proteins against thermal denaturation even at 50 °C, and that can, unlike present technologies, deliver pure, excipient-free protein by mechanically releasing it from a syringe. Macromolecules can be loaded at up to 10 wt% without affecting the mechanism of release. This unique stabilization and excipient-free release synergy offers a practical, scalable and versatile solution to enable the low-cost, cold-chain-free and equitable delivery of therapies worldwide.
Suggested Citation
Simona Bianco & Muhammad Hasan & Ashfaq Ahmad & Sarah-Jane Richards & Bart Dietrich & Matthew Wallace & Qiao Tang & Andrew J. Smith & Matthew I. Gibson & Dave J. Adams, 2024.
"Mechanical release of homogenous proteins from supramolecular gels,"
Nature, Nature, vol. 631(8021), pages 544-548, July.
Handle:
RePEc:nat:nature:v:631:y:2024:i:8021:d:10.1038_s41586-024-07580-0
DOI: 10.1038/s41586-024-07580-0
Download full text from publisher
As the access to this document is restricted, you may want to search for a different version of it.
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:631:y:2024:i:8021:d:10.1038_s41586-024-07580-0. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.