Clinical and Preclinical Methods of Heat-Stabilization of Human Vaccines.

Mol Pharm

Division of Pharmacoengineering & Molecular Pharmaceutics, Eshelman School of Pharmacy, UNC, Chapel Hill, North Carolina 27599, United States.

Published: March 2024

AI Article Synopsis

  • - Vaccines historically struggle with stability in areas without reliable cold chain systems, prompting exploration of techniques to enhance their thermostability for better storage and transportation.
  • - Lyophilization effectively converts liquid vaccines into a powdered form, but it can cause protein denaturation, leading to the investigation of alternatives like cryoprotectants (starch and sugar) and innovative methods like biomineralization for protection during freeze-drying.
  • - Despite limited clinical trials on these techniques, early indications show their potential, highlighting the necessity for heat-stable vaccines to improve global distribution and adaptability in varying storage conditions.

Article Abstract

Vaccines have historically faced challenges regarding stability, especially in regions lacking a robust cold chain infrastructure. This review delves into established and emergent techniques to improve the thermostability of vaccines. We discuss the widely practiced lyophilization method, effectively transforming liquid vaccine formulations into a solid powdered state, enhancing storage and transportation ability. However, potential protein denaturation during lyophilization necessitates alternative stabilization methods. Cryoprotectants, namely, starch and sugar molecules, have shown promise in protecting vaccine antigens and adjuvants from denaturation and augmenting the stability of biologics during freeze-drying. Biomineralization, a less studied yet innovative approach, utilizes inorganic or organic-inorganic hybrids to encapsulate biological components of vaccines with a particular emphasis on metal-organic coordination polymers. Encapsulation in organic matrices to form particles or microneedles have also been studied in the context of vaccine thermostability, showing some ability to store outside the cold-chain. Unfortunately, few of these techniques have advanced to clinical trials that evaluate differences in storage conditions. Nonetheless, early trials suggest that alternative storage techniques are viable and emphasize the need for more comprehensive studies. This review underscores the pressing need for heat-stable vaccines, especially in light of the increasing global distribution challenges. Combining traditional methods with novel approaches holds promise for the future adaptability of vaccine distribution and use.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11607726PMC
http://dx.doi.org/10.1021/acs.molpharmaceut.3c00844DOI Listing

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