<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Guo H</submitter><funding>Fundamental Research Funds for the Central Universities</funding><funding>NICHD NIH HHS</funding><funding>National Natural Science Foundation of China</funding><funding>Liaoning Revitalization Talents Program</funding><funding>National Science Foundation</funding><pagination>2102724</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9521812</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(29)</volume><pubmed_abstract>Injured peripheral nerves typically exhibit unsatisfactory and incomplete functional outcomes, and there are no clinically approved therapies for improving regeneration. Post-operative electrical stimulation (ES) increases axon regrowth, but practical challenges from the cost of extended operating room time to the risks and pitfalls associated with transcutaneous wire placement have prevented broad clinical adoption. This study presents a possible solution in the form of advanced bioresorbable materials for thin, flexible, wireless implant that provides precisely controlled ES of the injured nerve for a brief time in the immediate post-operative period. Afterward, rapid, complete and safe modes of bioresorption naturally and quickly eliminate all of the constituent materials in their entir</pubmed_abstract><journal>Advanced functional materials</journal><pubmed_title>Advanced Materials in Wireless, Implantable Electrical Stimulators That Offer Rapid Rates of Bioresorption for Peripheral Axon Regeneration.</pubmed_title><pmcid>PMC9521812</pmcid><funding_grant_id>12072057</funding_grant_id><funding_grant_id>R03 HD101090</funding_grant_id><funding_grant_id>DUT20RC(3)032</funding_grant_id><funding_grant_id>XLYC1807126</funding_grant_id><funding_grant_id>12022209</funding_grant_id><funding_grant_id>CMMI1635443</funding_grant_id><funding_grant_id>11972103</funding_grant_id><funding_grant_id>DMR‐1720139</funding_grant_id><pubmed_authors>Koo J</pubmed_authors><pubmed_authors>Franz CK</pubmed_authors><pubmed_authors>Meda R</pubmed_authors><pubmed_authors>Xie Z</pubmed_authors><pubmed_authors>Murthy NK</pubmed_authors><pubmed_authors>Li R</pubmed_authors><pubmed_authors>Qiao Z</pubmed_authors><pubmed_authors>Bai W</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Guo H</pubmed_authors><pubmed_authors>Janes LE</pubmed_authors><pubmed_authors>D'Andrea D</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors><pubmed_authors>Song Z</pubmed_authors><pubmed_authors>Choi YS</pubmed_authors><pubmed_authors>Jordan SW</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors><pubmed_authors>Rogers JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Advanced Materials in Wireless, Implantable Electrical Stimulators That Offer Rapid Rates of Bioresorption for Peripheral Axon Regeneration.</name><description>Injured peripheral nerves typically exhibit unsatisfactory and incomplete functional outcomes, and there are no clinically approved therapies for improving regeneration. Post-operative electrical stimulation (ES) increases axon regrowth, but practical challenges from the cost of extended operating room time to the risks and pitfalls associated with transcutaneous wire placement have prevented broad clinical adoption. This study presents a possible solution in the form of advanced bioresorbable materials for thin, flexible, wireless implant that provides precisely controlled ES of the injured nerve for a brief time in the immediate post-operative period. Afterward, rapid, complete and safe modes of bioresorption naturally and quickly eliminate all of the constituent materials in their entir</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2025-04-26T15:32:46.58Z</modification><creation>2024-11-12T21:06:57.974Z</creation></dates><accession>S-EPMC9521812</accession><cross_references><pubmed>36189172</pubmed><doi>10.1002/adfm.202102724</doi></cross_references></HashMap>