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Polycaprolactone thin films for retinal tissue engineering and drug delivery.

机译:聚己内酯薄膜,用于视网膜组织工程和药物输送。

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摘要

This dissertation focuses on the development of polycaprolactone thin films for retinal tissue engineering and drug delivery. We combined these thin films with techniques such as micro and nanofabrication to develop treatments for age-related macular degeneration (AMD), a disease that leads to the death of rod and cone photoreceptors. Current treatments are only able to slow or limit the progression of the disease, and photoreceptors cannot be regenerated or replaced by the body once lost.;The first experiments presented focus on a potential treatment for AMD after photoreceptor death has occurred. We developed a polymer thin film scaffold technology to deliver retinal progenitor cells (RPCs) to the affected area of the eye. Earlier research showed that RPCs destined to become photoreceptors are capable of incorporating into a degenerated retina. In our experiments, we showed that RPC attachment to a micro-welled polycaprolactone (PCL) thin film surface enhanced the differentiation of these cells toward a photoreceptor fate.;We then used our PCL thin films to develop a drug delivery device capable of sustained therapeutic release over a multi-month period that would maintain an effective concentration of the drug in the eye and eliminate the need for repeated intraocular injections. We first investigated the biocompatibility of PCL in the rabbit eye. We injected PCL thin films into the anterior chamber or vitreous cavity of rabbit eyes and monitored the animals for up to 6 months. We found that PCL thin films were well tolerated in the rabbit eye, showing no signs of chronic inflammation due to the implant. We then developed a multilayered thin film device containing a microporous membrane. We loaded these devices with lyophilized proteins and quantified drug elution for 10 weeks, finding that both bovine serum albumin and immunoglobulin G elute from these devices with zero order release kinetics.;These experiments demonstrate that PCL is an extremely useful biomaterial that may be used to treat AMD in multiple ways. Through both tissue engineering and drug delivery techniques we have established that PCL thin films have the potential to revolutionize the treatment of AMD.
机译:本文主要研究用于视网膜组织工程和药物输送的聚己内酯薄膜的开发。我们将这些薄膜与微细加工和纳米加工等技术相结合,以开发针对年龄相关性黄斑变性(AMD)的治疗方法,这种疾病导致杆状和锥状感光细胞死亡。目前的治疗方法只能减慢或限制疾病的进展,一旦失去光感受器,便无法再生或替换为光感受器。第一个实验着重于光感受器死亡后对AMD的潜在治疗。我们开发了一种聚合物薄膜支架技术,可将视网膜祖细胞(RPC)输送到眼睛的受影响区域。早期的研究表明,注定要成为感光器的RPC能够整合到退化的视网膜中。在我们的实验中,我们表明RPC与微孔聚己内酯(PCL)薄膜表面的附着增强了这些细胞向感光受体命运的分化;然后我们使用PCL薄膜开发了一种能够持续治疗的药物输送装置在一个多月的时间内释放,将保持药物在眼中的有效浓度,消除了重复眼内注射的需要。我们首先研究了PCL在兔眼中的生物相容性。我们将PCL薄膜注射到兔眼的前房或玻璃体腔中,并监测动物长达6个月。我们发现兔眼对PCL薄膜的耐受性良好,没有由于植入物引起的慢性炎症迹象。然后,我们开发了一种包含微孔膜的多层薄膜设备。我们将这些冻干蛋白装填到这些设备中并进行了10周的定量药物洗脱,发现牛血清白蛋白和免疫球蛋白G均以零级释放动力学从这些设备中洗脱出来;这些实验表明PCL是一种非常有用的生物材料,可用于以多种方式对待AMD。通过组织工程和药物输送技术,我们已经确定PCL薄膜具有彻底改变AMD治疗的潜力。

著录项

  • 作者

    Steedman, Mark Rory.;

  • 作者单位

    University of California, San Francisco with the University of California, Berkeley.;

  • 授予单位 University of California, San Francisco with the University of California, Berkeley.;
  • 学科 Engineering Biomedical.;Health Sciences Pharmacy.;Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 142 p.
  • 总页数 142
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 社会学;
  • 关键词

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