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Controlled release of ciprofloxacin and ceftriaxone from a single ototopical administration of antibiotic-loaded polymer microspheres and thermoresponsive gel.
Bruk, Liza A; Dunkelberger, Katherine E; Khampang, Pawjai; Hong, Wenzhou; Sadagopan, Srivatsun; Alper, Cuneyt M; Fedorchak, Morgan V.
Afiliação
  • Bruk LA; Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States of America.
  • Dunkelberger KE; Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States of America.
  • Khampang P; Department of Otolaryngology and Communication Sciences, Medical College of Wisconsin, Milwaukee, WI, United States of America.
  • Hong W; Department of Otolaryngology and Communication Sciences, Medical College of Wisconsin, Milwaukee, WI, United States of America.
  • Sadagopan S; Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States of America.
  • Alper CM; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, United States of America.
  • Fedorchak MV; Department of Otolaryngology, University of Pittsburgh, Pittsburgh, PA, United States of America.
PLoS One ; 15(10): e0240535, 2020.
Article em En | MEDLINE | ID: mdl-33045028
ABSTRACT
Acute otitis media (AOM) is the main indication for pediatric antibiotic prescriptions, accounting for 25% of prescriptions. While the use of topical drops can minimize the administered dose of antibiotic and adverse systemic effects compared to oral antibiotics, their use has limitations, partially due to low patient compliance, high dosing frequency, and difficulty of administration. Lack of proper treatment can lead to development of chronic OM, which may require invasive interventions. Previous studies have shown that gel-based drug delivery to the ear is possible with intratympanic injection or chemical permeation enhancers (CPEs). However, many patients are reluctant to accept invasive treatments and CPEs have demonstrated toxicity to the tympanic membrane (TM). We developed a novel method of delivering therapeutics to the TM and middle ear using a topical, thermoresponsive gel depot containing antibiotic-loaded poly(lactic-co-glycolic acid) microspheres. Our in vitro and ex vivo results suggest that the sustained presentation can safely allow therapeutically relevant drug concentrations to penetrate the TM to the middle ear for up to 14 days. Animal results indicate sufficient antibiotic released for treatment from topical administration 24h after bacterial inoculation. However, animals treated 72h after inoculation, a more clinically relevant treatment practice, displayed spontaneous clearance of infection as is also often observed in the clinic. Despite this variability in the disease model, data suggest the system can safely treat bacterial infection, with future studies necessary to optimize microsphere formulations for scaled up dosage of antibiotic as well as further investigation of the influence of spontaneous bacterial clearance and of biofilm formation on effectiveness of treatment. To our knowledge, this study represents the first truly topical drug delivery system to the middle ear without the use of CPEs.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Otite Média / Portadores de Fármacos / Administração Tópica / Antibacterianos Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Otite Média / Portadores de Fármacos / Administração Tópica / Antibacterianos Idioma: En Ano de publicação: 2020 Tipo de documento: Article