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Fentanyl Initiated Polymers Prepared by ATRP for Targeted Delivery.
Cohen-Karni, Devora; Kovaliov, Marina; Li, Shaohua; Jaffee, Stephen; Tomycz, Nestor D; Averick, Saadyah.
Afiliação
  • Cohen-Karni D; Neuroscience Disruptive Research Lab, Allegheny Health Network Research Institute, Allegheny General Hospital , Pittsburgh, Pennsylvania 15212, United States.
  • Kovaliov M; Neuroscience Institute, Allegheny Health Network, Allegheny General Hospital , Pittsburgh, Pennsylvania 15212, United States.
  • Li S; Neuroscience Disruptive Research Lab, Allegheny Health Network Research Institute, Allegheny General Hospital , Pittsburgh, Pennsylvania 15212, United States.
  • Jaffee S; Neuroscience Institute, Allegheny Health Network, Allegheny General Hospital , Pittsburgh, Pennsylvania 15212, United States.
  • Tomycz ND; Neuroscience Disruptive Research Lab, Allegheny Health Network Research Institute, Allegheny General Hospital , Pittsburgh, Pennsylvania 15212, United States.
  • Averick S; Neuroscience Institute, Allegheny Health Network, Allegheny General Hospital , Pittsburgh, Pennsylvania 15212, United States.
Bioconjug Chem ; 28(4): 1251-1259, 2017 04 19.
Article em En | MEDLINE | ID: mdl-28328199
ABSTRACT
The targeted delivery of polymers to neurons is a challenging yet important goal for polymer based drug delivery. We prepared a fentanyl based atom transfer radical polymerization (ATRP) initiator to target the Mu opioid receptor (MOR) for neuronal targeting. We incorporated our recently discovered rigid acrylate linking group into the initiator to retain a high degree of binding to the MOR and grafted random or block copolymers of poly(oligo(ethylene oxide) methacrylate)-block-(glycidyl methacrylate). Trifluoroethanol promoted amine ring opening of the glycidyl methacrylate was used for post-polymerization modification of the fentanyl initiated polymers to attach a near-infrared fluorescent dye (ADS790WS) or to build a targeted siRNA delivery system via modification with secondary amines. We examined the biocompatibility, cellular internalization, and siRNA binding properties of our polymer library in a green fluorescent protein expressing SY SH5Y neuroblastoma cell-line.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polímeros / Sistemas de Liberação de Medicamentos / RNA Interferente Pequeno Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polímeros / Sistemas de Liberação de Medicamentos / RNA Interferente Pequeno Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article