Samuel J. M. Hale MBChB, Raymond Kim PhD, Mark O'Carroll MBChB, Kristi Biswas PhD, Brett Wagner Mackenzie PhD, Richard G. Douglas MD
{"title":"作为一种抗生物膜剂,Maxitrol 在耳鼻咽喉头颈外科中具有潜在应用价值","authors":"Samuel J. M. Hale MBChB, Raymond Kim PhD, Mark O'Carroll MBChB, Kristi Biswas PhD, Brett Wagner Mackenzie PhD, Richard G. Douglas MD","doi":"10.1002/lio2.1245","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Objectives</h3>\n \n <p><i>Maxitrol</i> (Novartis) is a topical ophthalmic medication that contains polymyxin B, neomycin, and dexamethasone. If it possesses antibiofilm activity, it may be useful for treating diseases of the head and neck in which biofilms are implicated, including chronic rhinosinusitis, chronic suppurative otitis media and osteoradionecrosis. We investigated the <i>in vitro</i> efficacy of <i>Maxitrol</i> against <i>Staphylococcus aureus</i> and <i>Pseudomonas aeruginosa</i> biofilms.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Minimum biofilm eradication concentration (MBEC) assays were performed using biofilms of <i>P. aeruginosa</i> ATCC 27853 and <i>S. aureus</i> ATCC 6538 type strains, grown on 96-pin lids and treated in <i>Maxitrol</i> for 30 min, 1 h, or 6 h. Isolates of both species were collected from the middle meatuses of patients with cystic fibrosis. Biofilms of clinical isolates were grown and treated <i>in vitro</i> for 6 h with <i>Maxitrol</i>, both undiluted at full concentration and at the identified MBEC, then cultured to identify bacterial survival.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Neither type strain was eradicated at 30 min nor <i>S. aureus</i> at 1 h at any tested concentration. <i>P. aeruginosa</i> was eradicated by a median of 90% and 5.6% <i>Maxitrol</i> at 1 and 6 h, respectively, and <i>S. aureus</i> with 90% <i>Maxitrol</i> at 6 h. Undiluted <i>Maxitrol</i> reliably eradicated all clinical isolates of <i>P. aeruginosa</i> but only one of five <i>S. aureus</i> isolates.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p><i>Maxitrol</i> reliably eradicates <i>P. aeruginosa</i> biofilm but not <i>S. aureus</i> biofilm <i>in vitro</i><i>.</i> It may have a therapeutic role against biofilms in which <i>P. aeruginosa</i> is the dominant pathogen.</p>\n </section>\n \n <section>\n \n <h3> Level of Evidence</h3>\n \n <p>N/A.</p>\n </section>\n </div>","PeriodicalId":48529,"journal":{"name":"Laryngoscope Investigative Otolaryngology","volume":"9 3","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2024-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/lio2.1245","citationCount":"0","resultStr":"{\"title\":\"Maxitrol as an antibiofilm agent with potential applications in Otolaryngology-Head and Neck Surgery\",\"authors\":\"Samuel J. M. Hale MBChB, Raymond Kim PhD, Mark O'Carroll MBChB, Kristi Biswas PhD, Brett Wagner Mackenzie PhD, Richard G. Douglas MD\",\"doi\":\"10.1002/lio2.1245\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Objectives</h3>\\n \\n <p><i>Maxitrol</i> (Novartis) is a topical ophthalmic medication that contains polymyxin B, neomycin, and dexamethasone. If it possesses antibiofilm activity, it may be useful for treating diseases of the head and neck in which biofilms are implicated, including chronic rhinosinusitis, chronic suppurative otitis media and osteoradionecrosis. We investigated the <i>in vitro</i> efficacy of <i>Maxitrol</i> against <i>Staphylococcus aureus</i> and <i>Pseudomonas aeruginosa</i> biofilms.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Minimum biofilm eradication concentration (MBEC) assays were performed using biofilms of <i>P. aeruginosa</i> ATCC 27853 and <i>S. aureus</i> ATCC 6538 type strains, grown on 96-pin lids and treated in <i>Maxitrol</i> for 30 min, 1 h, or 6 h. Isolates of both species were collected from the middle meatuses of patients with cystic fibrosis. Biofilms of clinical isolates were grown and treated <i>in vitro</i> for 6 h with <i>Maxitrol</i>, both undiluted at full concentration and at the identified MBEC, then cultured to identify bacterial survival.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Neither type strain was eradicated at 30 min nor <i>S. aureus</i> at 1 h at any tested concentration. <i>P. aeruginosa</i> was eradicated by a median of 90% and 5.6% <i>Maxitrol</i> at 1 and 6 h, respectively, and <i>S. aureus</i> with 90% <i>Maxitrol</i> at 6 h. Undiluted <i>Maxitrol</i> reliably eradicated all clinical isolates of <i>P. aeruginosa</i> but only one of five <i>S. aureus</i> isolates.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p><i>Maxitrol</i> reliably eradicates <i>P. aeruginosa</i> biofilm but not <i>S. aureus</i> biofilm <i>in vitro</i><i>.</i> It may have a therapeutic role against biofilms in which <i>P. aeruginosa</i> is the dominant pathogen.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Level of Evidence</h3>\\n \\n <p>N/A.</p>\\n </section>\\n </div>\",\"PeriodicalId\":48529,\"journal\":{\"name\":\"Laryngoscope Investigative Otolaryngology\",\"volume\":\"9 3\",\"pages\":\"\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2024-05-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/lio2.1245\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Laryngoscope Investigative Otolaryngology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/lio2.1245\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"OTORHINOLARYNGOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laryngoscope Investigative Otolaryngology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/lio2.1245","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OTORHINOLARYNGOLOGY","Score":null,"Total":0}
Maxitrol as an antibiofilm agent with potential applications in Otolaryngology-Head and Neck Surgery
Objectives
Maxitrol (Novartis) is a topical ophthalmic medication that contains polymyxin B, neomycin, and dexamethasone. If it possesses antibiofilm activity, it may be useful for treating diseases of the head and neck in which biofilms are implicated, including chronic rhinosinusitis, chronic suppurative otitis media and osteoradionecrosis. We investigated the in vitro efficacy of Maxitrol against Staphylococcus aureus and Pseudomonas aeruginosa biofilms.
Methods
Minimum biofilm eradication concentration (MBEC) assays were performed using biofilms of P. aeruginosa ATCC 27853 and S. aureus ATCC 6538 type strains, grown on 96-pin lids and treated in Maxitrol for 30 min, 1 h, or 6 h. Isolates of both species were collected from the middle meatuses of patients with cystic fibrosis. Biofilms of clinical isolates were grown and treated in vitro for 6 h with Maxitrol, both undiluted at full concentration and at the identified MBEC, then cultured to identify bacterial survival.
Results
Neither type strain was eradicated at 30 min nor S. aureus at 1 h at any tested concentration. P. aeruginosa was eradicated by a median of 90% and 5.6% Maxitrol at 1 and 6 h, respectively, and S. aureus with 90% Maxitrol at 6 h. Undiluted Maxitrol reliably eradicated all clinical isolates of P. aeruginosa but only one of five S. aureus isolates.
Conclusions
Maxitrol reliably eradicates P. aeruginosa biofilm but not S. aureus biofilm in vitro. It may have a therapeutic role against biofilms in which P. aeruginosa is the dominant pathogen.