Your browser doesn't support javascript.
loading
Design of Hollow Hyaluronic Acid Cylinders for Sustained Intravitreal Protein Delivery.
Van Kampen, Erik; Vandervelden, Craig; Fakhari, Amir; Qian, Jian; Berkland, Cory; Gehrke, Stevin H.
Afiliação
  • Van Kampen E; Department of Chemical and Petroleum Engineering, University of Kansas, Lawrence, Kansas 66045.
  • Vandervelden C; Department of Chemical and Petroleum Engineering, University of Kansas, Lawrence, Kansas 66045.
  • Fakhari A; Bioengineering Program, University of Kansas, Lawrence, Kansas 66045.
  • Qian J; Department of Pharmaceutical Chemistry, University of Kansas, Lawrence, Kansas 66045.
  • Berkland C; Department of Chemical and Petroleum Engineering, University of Kansas, Lawrence, Kansas 66045; Department of Pharmaceutical Chemistry, University of Kansas, Lawrence, Kansas 66045.
  • Gehrke SH; Department of Chemical and Petroleum Engineering, University of Kansas, Lawrence, Kansas 66045; Bioengineering Program, University of Kansas, Lawrence, Kansas 66045. Electronic address: shgehrke@ku.edu.
J Pharm Sci ; 107(9): 2354-2365, 2018 09.
Article em En | MEDLINE | ID: mdl-29729900
A hollow cylinder intravitreal implant was developed to achieve sustained release of protein to the retina for the treatment of retinal diseases. Hollow cylinders were fabricated by molding and cross-linking hyaluronic acid, the major component of the vitreous humor. Hollow cylinders were filled with a concentrated protein solution, and the properties of the cylinder walls were tested. Cross-linked hyaluronic acid hydrogels with swelling degrees as low as 2.7 were achieved as a means to extend the release of protein. Hollow cylinders were capable of releasing an antigen-binding fragment for over 4 months at a maximum release rate of 4 µg per day. Protein release from hollow cylinders was modeled using COMSOL Multiphysics® software, and diffusion coefficients between 1.0 × 10-11 and 3.0 × 10-11 cm2/s yielded therapeutically effective levels of protein. Cylinders with a 1 mm outer radius were capable of loading >1 mg of protein while releasing at least 2.5 µg a day for over 4.5 months. Although smaller cylinders facilitate intravitreal placement, decreasing the cylinder radius severely limited drug loading. Design of hollow cylinder intravitreal implants must balance high drug loading to reduce device size with control of the diffusion coefficient to sustain protein release.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Portadores de Fármacos / Desenho de Fármacos / Implantes Absorvíveis / Ácido Hialurônico Idioma: En Revista: J Pharm Sci Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Portadores de Fármacos / Desenho de Fármacos / Implantes Absorvíveis / Ácido Hialurônico Idioma: En Revista: J Pharm Sci Ano de publicação: 2018 Tipo de documento: Article