<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Tran KTM</submitter><pubmed_abstract>The necessity for multiple injections and cold-chain storage has contributed to suboptimal vaccine utilization, especially in pandemic situations. Thermally-stable and single-administration vaccines hold a great potential to revolutionize the global immunization process. Here, a new approach to thermally stabilize protein-based antigens is presented and a new high-throughput antigen-loading process is devised to create a single-administration, pulsatile-release microneedle (MN) patch which can deliver a recombinant SARS-CoV-2 S1-RBD protein-a model for the COVID-19 vaccine. Nearly 100% of the protein antigen could be stabilized at temperatures up to 100 °C for at least 1 h and at an average human body temperature (37 °C) for up to 4 months. Arrays of the stabilized S1-RBD formulations can be loaded into the MN shells via a single-alignment assembly step. The fabricated MNs are administered at a single time into the skin of rats and induce antibody response which could neutralize authentic SARS-CoV-2 viruses, providing similar immunogenic effect to that induced by multiple bolus injections of the same antigen stored in conventional cold-chain conditions. The MN system presented herein could offer the key solution to global immunization campaigns by avoiding low patient compliance, the requirement for cold-chain storage, and the need for multiple booster injections.</pubmed_abstract><journal>Advanced materials technologies</journal><pagination>2200905</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9874724</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Single-Administration Microneedle Skin Patch for Multi-Burst Release of Vaccine against SARS-CoV-2.</pubmed_title><pmcid>PMC9874724</pmcid><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Graichen A</pubmed_authors><pubmed_authors>Nguyen TD</pubmed_authors><pubmed_authors>Tran KTM</pubmed_authors><pubmed_authors>Gavitt TD</pubmed_authors><pubmed_authors>Szczepanek SM</pubmed_authors><pubmed_authors>Tulman ER</pubmed_authors><pubmed_authors>Lin F</pubmed_authors><pubmed_authors>Le TT</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Single-Administration Microneedle Skin Patch for Multi-Burst Release of Vaccine against SARS-CoV-2.</name><description>The necessity for multiple injections and cold-chain storage has contributed to suboptimal vaccine utilization, especially in pandemic situations. Thermally-stable and single-administration vaccines hold a great potential to revolutionize the global immunization process. Here, a new approach to thermally stabilize protein-based antigens is presented and a new high-throughput antigen-loading process is devised to create a single-administration, pulsatile-release microneedle (MN) patch which can deliver a recombinant SARS-CoV-2 S1-RBD protein-a model for the COVID-19 vaccine. Nearly 100% of the protein antigen could be stabilized at temperatures up to 100 °C for at least 1 h and at an average human body temperature (37 °C) for up to 4 months. Arrays of the stabilized S1-RBD formulations can be loaded into the MN shells via a single-alignment assembly step. The fabricated MNs are administered at a single time into the skin of rats and induce antibody response which could neutralize authentic SARS-CoV-2 viruses, providing similar immunogenic effect to that induced by multiple bolus injections of the same antigen stored in conventional cold-chain conditions. The MN system presented herein could offer the key solution to global immunization campaigns by avoiding low patient compliance, the requirement for cold-chain storage, and the need for multiple booster injections.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-03-27T16:49:08.182Z</modification><creation>2025-04-06T14:12:45.331Z</creation></dates><accession>S-EPMC9874724</accession><cross_references><pubmed>36714215</pubmed><doi>10.1002/admt.202200905</doi></cross_references></HashMap>