<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(8)</volume><submitter>Jitsuhiro A</submitter><pubmed_abstract>Contact-killing antibacterial materials are attracting attention owing to their ability for sustained antibacterial activity. However, contact-killing antibacterial polystyrene (PS) has not been extensively studied because its chemically stable structure impedes chemical modification. In this study, we developed an antibacterial PS sheet with a contact-killing surface using PS synthesized from 2,2'-azobis-[2-(1,3-dimethyl-4,5-dihydro-1&lt;i>H&lt;/i>-imidazol-3-ium-2-yl)]propane triflate (ADIP) as a radical initiator with cationic moieties. The PS sheet synthesized with ADIP (ADIP-PS) exhibited antibacterial activity in contrast to PS synthesized with other azo radical initiators. Surface ζ-potential measurements revealed that only ADIP-PS had a cationic surface, which contributed to its contact-killing antibacterial activity. The ADIP-PS sheets also exhibited antibacterial activity after washing. In contrast, PS sheets containing silver, a typical leachable antibacterial agent, lost all antibacterial activity after the same washing treatment. The antibacterial ADIP-PS sheet demonstrated strong broad-spectrum activity against both Gram-positive and Gram-negative bacteria, including drug-resistant bacteria. Cytotoxicity tests using L929 cells showed that the ADIP-PS sheets were noncytotoxic. This contact-killing antibacterial PS synthesized with ADIP thus demonstrated good prospects as an easily producible antimicrobial material.</pubmed_abstract><journal>ACS omega</journal><pagination>9803-9812</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10905582</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Contact-Killing Antibacterial Polystyrene Polymerized Using a Quaternized Cationic Initiator.</pubmed_title><pmcid>PMC10905582</pmcid><pubmed_authors>Kitagawa M</pubmed_authors><pubmed_authors>Endo F</pubmed_authors><pubmed_authors>Konoeda Y</pubmed_authors><pubmed_authors>Tsuji T</pubmed_authors><pubmed_authors>Maruyama H</pubmed_authors><pubmed_authors>Jitsuhiro A</pubmed_authors><pubmed_authors>Maeda T</pubmed_authors><pubmed_authors>Yamada S</pubmed_authors><pubmed_authors>Hotta A</pubmed_authors><pubmed_authors>Ogawa A</pubmed_authors><pubmed_authors>Tanimoto K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Contact-Killing Antibacterial Polystyrene Polymerized Using a Quaternized Cationic Initiator.</name><description>Contact-killing antibacterial materials are attracting attention owing to their ability for sustained antibacterial activity. However, contact-killing antibacterial polystyrene (PS) has not been extensively studied because its chemically stable structure impedes chemical modification. In this study, we developed an antibacterial PS sheet with a contact-killing surface using PS synthesized from 2,2'-azobis-[2-(1,3-dimethyl-4,5-dihydro-1&lt;i>H&lt;/i>-imidazol-3-ium-2-yl)]propane triflate (ADIP) as a radical initiator with cationic moieties. The PS sheet synthesized with ADIP (ADIP-PS) exhibited antibacterial activity in contrast to PS synthesized with other azo radical initiators. Surface ζ-potential measurements revealed that only ADIP-PS had a cationic surface, which contributed to its contact-killing antibacterial activity. The ADIP-PS sheets also exhibited antibacterial activity after washing. In contrast, PS sheets containing silver, a typical leachable antibacterial agent, lost all antibacterial activity after the same washing treatment. The antibacterial ADIP-PS sheet demonstrated strong broad-spectrum activity against both Gram-positive and Gram-negative bacteria, including drug-resistant bacteria. Cytotoxicity tests using L929 cells showed that the ADIP-PS sheets were noncytotoxic. This contact-killing antibacterial PS synthesized with ADIP thus demonstrated good prospects as an easily producible antimicrobial material.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2025-04-18T17:16:25.193Z</modification><creation>2025-04-07T04:50:42.915Z</creation></dates><accession>S-EPMC10905582</accession><cross_references><pubmed>38434858</pubmed><doi>10.1021/acsomega.3c10233</doi></cross_references></HashMap>