Department of Biomedical Engineering, Duke University, 136 Hudson Hall, Box 90281, Durham, NC 27708, USA.
Ann Biomed Eng. 2010 Mar;38(3):935-44. doi: 10.1007/s10439-010-9947-z. Epub 2010 Feb 6.
Topical application of drugs for treatment of intraocular diseases is often limited by inadequate transport and induced toxicity in corneal tissues. To improve the drug delivery, a mathematical model was developed to numerically simulate the transport process of ethacrynic acid (ECA), a potential drug for glaucoma treatment, in the anterior segment of a typical human eye. The model considered diffusion of ECA in all tissues and the aqueous humor (AH) as well as convection of ECA in the AH. The simulation results showed that ECA concentration in the eye depended on the rate of AH production, the half-life of ECA in the precorneal tear film, and the transport parameters in the model. In addition, the main pathway for ECA clearance from the eye was the trabecular meshwork (TM) and the rate of clearance was approximately proportional to the AH production rate. The model predicted that the most effective approach to improving topical drug delivery was to prolong its half-life in the precorneal tear film. These simulation results and model prediction, which could be verified experimentally, might be useful for improving delivery of ECA and other therapeutic agents to the TM as well as other tissues in the anterior segment of the eye.
局部应用药物治疗眼内疾病常常受到角膜组织中药物传输不足和诱导毒性的限制。为了改善药物传递,我们建立了一个数学模型,以数值模拟乙磺酸(ECA)在典型人眼前段的传输过程。该模型考虑了 ECA 在所有组织和房水中的扩散以及 ECA 在房水中的对流。模拟结果表明,眼内 ECA 浓度取决于房水产生率、ECA 在角膜前泪膜中的半衰期以及模型中的传输参数。此外,ECA 从眼睛清除的主要途径是小梁网(TM),清除速率与房水产生率大致成正比。该模型预测,提高局部药物传递的最有效方法是延长其在角膜前泪膜中的半衰期。这些模拟结果和模型预测可以通过实验验证,对于改善 ECA 和其他治疗剂向 TM 以及眼睛前段其他组织的传递可能是有用的。