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The Port Delivery System with ranibizumab: a new paradigm for long-acting retinal drug delivery.
Ranade, Shrirang V; Wieland, Mark R; Tam, Tammy; Rea, Jennifer C; Horvath, Judit; Hieb, Aaron R; Jia, Weitao; Grace, Lori; Barteselli, Giulio; Stewart, Jay M.
Afiliação
  • Ranade SV; Genentech, Inc, South San Francisco, CA, USA.
  • Wieland MR; Northern California Retina Vitreous Associates, San Jose, CA, USA.
  • Tam T; Genentech, Inc, South San Francisco, CA, USA.
  • Rea JC; Genentech, Inc, South San Francisco, CA, USA.
  • Horvath J; Genentech, Inc, South San Francisco, CA, USA.
  • Hieb AR; Genentech, Inc, South San Francisco, CA, USA.
  • Jia W; Genentech, Inc, South San Francisco, CA, USA.
  • Grace L; Genentech, Inc, South San Francisco, CA, USA.
  • Barteselli G; Genentech, Inc, South San Francisco, CA, USA.
  • Stewart JM; Department of Ophthalmology, University of California, San Francisco, CA, USA.
Drug Deliv ; 29(1): 1326-1334, 2022 Dec.
Article em En | MEDLINE | ID: mdl-35499315
ABSTRACT
The Port Delivery System with ranibizumab (PDS) is an innovative intraocular drug delivery system designed for the continuous delivery of ranibizumab into the vitreous for 6 months and beyond. The PDS includes an ocular implant, a customized formulation of ranibizumab, and four dedicated ancillary devices for initial fill, surgical implantation, refill-exchange, and explantation, if clinically indicated. Ranibizumab is an ideal candidate for the PDS on account of its unique physicochemical stability and high solubility. Controlled release is achieved via passive diffusion through the porous release control element, which is tuned to specific drug characteristics to accomplish a therapeutic level of ranibizumab in the vitreous. To characterize drug release from the implant, release rate was measured in vitro with starting concentrations of ranibizumab 10, 40, and 100 mg/mL, with release of ranibizumab 40 and 100 mg/mL found to remain quantifiable after 6 months. Using a starting concentration of 100 mg/mL, active release rate at approximately 6 months was consistent after the initial fill and first, second, and third refills, demonstrating reproducibility between implants and between multiple refill-exchanges of the same implant. A refill-exchange performed with a single 100-µL stroke using the refill needle was shown to replace over 95% of the implant contents with fresh drug. In vitro data support the use of the PDS with fixed refill-exchange intervals of at least 6 months in clinical trials.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retina / Ranibizumab Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retina / Ranibizumab Idioma: En Ano de publicação: 2022 Tipo de documento: Article