<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mousa AH</submitter><funding>European Research Council</funding><funding>Stiftelsen f?r?Strategisk Forskning</funding><funding>Vetenskapsr?det</funding><pagination>2752-2763</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8944941</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>34(6)</volume><pubmed_abstract>Injectable bioelectronics could become an alternative or a complement to traditional drug treatments. To this end, a new self-doped p-type conducting PEDOT-S copolymer (&lt;b>A5&lt;/b>) was synthesized. This copolymer formed highly water-dispersed nanoparticles and aggregated into a mixed ion-electron conducting hydrogel when injected into a tissue model. First, we synthetically repeated most of the published methods for PEDOT-S at the lab scale. Surprisingly, analysis using high-resolution matrix-assisted laser desorption ionization-mass spectroscopy showed that almost all the methods generated PEDOT-S derivatives with the same polymer lengths (i.e., oligomers, seven to eight monomers in average); thus, the polymer length cannot account for the differences in the conductivities reported earlier. The main difference, however, was that some methods generated an unintentional copolymer P(EDOT-S/EDOT-OH) that is more prone to aggregate and display higher conductivities in general than the PEDOT-S homopolymer. Based on this, we synthesized the PEDOT-S derivative &lt;b>A5&lt;/b>, that displayed the highest film conductivity (33 S cm&lt;sup>-1&lt;/sup>) among all PEDOT-S derivatives synthesized. Injecting &lt;b>A5&lt;/b> nanoparticles into the agarose gel cast with a physiological buffer generated a stable and highly conductive hydrogel (1-5 S cm&lt;sup>-1&lt;/sup>), where no conductive structures were seen in agarose with the other PEDOT-S derivatives. Furthermore, the ion-treated &lt;b>A5&lt;/b> hydrogel remained stable and maintained initial conductivities for 7 months (the longest period tested) in pure water, and &lt;b>A5&lt;/b> mixed with Fe&lt;sub>3&lt;/sub>O&lt;sub>4&lt;/sub> nanoparticles generated a magnetoconductive relay device in water. Thus, we have successfully synthesized a water-processable, syringe-injectable, and self-doped PEDOT-S polymer capable of forming a conductive hydrogel in tissue mimics, thereby paving a way for future applications within in vivo electronics.</pubmed_abstract><journal>Chemistry of materials : a publication of the American Chemical Society</journal><pubmed_title>Method Matters: Exploring Alkoxysulfonate-Functionalized Poly(3,4-ethylenedioxythiophene) and Its Unintentional Self-Aggregating Copolymer toward Injectable Bioelectronics.</pubmed_title><pmcid>PMC8944941</pmcid><funding_grant_id>RMX18-0083</funding_grant_id><funding_grant_id>2018-05258</funding_grant_id><funding_grant_id>2018-06197</funding_grant_id><funding_grant_id>834677</funding_grant_id><pubmed_authors>Mousa AH</pubmed_authors><pubmed_authors>Ekstrom P</pubmed_authors><pubmed_authors>Marko-Varga G</pubmed_authors><pubmed_authors>Bliman D</pubmed_authors><pubmed_authors>Strakosas X</pubmed_authors><pubmed_authors>Berggren M</pubmed_authors><pubmed_authors>Hellman K</pubmed_authors><pubmed_authors>Hjort M</pubmed_authors><pubmed_authors>Savvakis M</pubmed_authors><pubmed_authors>Ek F</pubmed_authors><pubmed_authors>Olsson R</pubmed_authors><pubmed_authors>Hiram Betancourt L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Method Matters: Exploring Alkoxysulfonate-Functionalized Poly(3,4-ethylenedioxythiophene) and Its Unintentional Self-Aggregating Copolymer toward Injectable Bioelectronics.</name><description>Injectable bioelectronics could become an alternative or a complement to traditional drug treatments. To this end, a new self-doped p-type conducting PEDOT-S copolymer (&lt;b>A5&lt;/b>) was synthesized. This copolymer formed highly water-dispersed nanoparticles and aggregated into a mixed ion-electron conducting hydrogel when injected into a tissue model. First, we synthetically repeated most of the published methods for PEDOT-S at the lab scale. Surprisingly, analysis using high-resolution matrix-assisted laser desorption ionization-mass spectroscopy showed that almost all the methods generated PEDOT-S derivatives with the same polymer lengths (i.e., oligomers, seven to eight monomers in average); thus, the polymer length cannot account for the differences in the conductivities reported earlier. The main difference, however, was that some methods generated an unintentional copolymer P(EDOT-S/EDOT-OH) that is more prone to aggregate and display higher conductivities in general than the PEDOT-S homopolymer. Based on this, we synthesized the PEDOT-S derivative &lt;b>A5&lt;/b>, that displayed the highest film conductivity (33 S cm&lt;sup>-1&lt;/sup>) among all PEDOT-S derivatives synthesized. Injecting &lt;b>A5&lt;/b> nanoparticles into the agarose gel cast with a physiological buffer generated a stable and highly conductive hydrogel (1-5 S cm&lt;sup>-1&lt;/sup>), where no conductive structures were seen in agarose with the other PEDOT-S derivatives. Furthermore, the ion-treated &lt;b>A5&lt;/b> hydrogel remained stable and maintained initial conductivities for 7 months (the longest period tested) in pure water, and &lt;b>A5&lt;/b> mixed with Fe&lt;sub>3&lt;/sub>O&lt;sub>4&lt;/sub> nanoparticles generated a magnetoconductive relay device in water. Thus, we have successfully synthesized a water-processable, syringe-injectable, and self-doped PEDOT-S polymer capable of forming a conductive hydrogel in tissue mimics, thereby paving a way for future applications within in vivo electronics.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-05T15:59:53.14Z</modification><creation>2025-04-05T15:59:53.14Z</creation></dates><accession>S-EPMC8944941</accession><cross_references><pubmed>35360437</pubmed><doi>10.1021/acs.chemmater.1c04342</doi></cross_references></HashMap>