Planar microdevices enhance transport of large molecular weight molecules across retinal pigment epithelial cells

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• 作者：Jennifer S. Wade (1)
  Tejal A. Desai (1)
  
• 关键词：Retinal pigment epithelium ; Ocular drug delivery ; PEGDMA ; Microdevices ; Biologics
• 刊名：Biomedical Microdevices
• 出版年：2014
• 出版时间：August 2014
• 年：2014
• 卷：16
• 期：4
• 页码：629-638
• 全文大小：736 KB
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• 作者单位：Jennifer S. Wade (1)
  Tejal A. Desai (1)
  
  1. Department of Bioengineering and Therapeutic Sciences, University of California, 1700 4th Street, Byers Hall 204, Box 2520, San Francisco, CA, 94158, USA
  
• ISSN：1572-8781

文摘

Large molecular weight drug delivery to the posterior eye is challenging due to cellular barriers that hinder drug transport. Understanding how to enhance transport across the retinal barrier is important for the design of new drug delivery systems. A novel mechanism to enhance drug transport is the use of geometric properties, which has not been extensively explored in the retina. Planar SU-8/Poly(ethyleneglycol)dimethacrylate microdevices were constructed using photolithography to deliver FITC dextran across an in vitro retinal model. The model consists of retinal pigment epithelial (RPE) cells grown to confluence on transwell inserts, which provides an environment to investigate the influence of geometry on paracellular and transcellular delivery of encapsulated large molecules. Planar microdevices enhanced transport of large molecular weight dextrans across different models of RPE in a size dependent fashion. Increased drug permeation across the RPE was observed with the addition of microdevices as compared to a traditional bolus of FITC dextran. This phenomena was initiated by a non-toxic interaction between the microdevices and the retinal tight junction proteins. Suggesting that increased drug transport occurs via a paracellular pathway. These experiments provide evidence to support the future use of planar unidirectional microdevices for delivery of biologics in ocular applications.