Pharmacokinetics Analysis of Controlled Insulin Delivery from Biodegradable Polymer Matrix

Ruojia Li
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Abstract

Diabetes is a group of metabolic disorders in which there are high blood sugar levels over a prolonged period. As of 2015, an estimated 415 million people had diabetes worldwide. Insulin is the most effective and safe medicines needed to stable the blood sugar level and so treat diabetes. Current insulin administration requires daily subcutaneous injection, which is not a favorable choice of patients and physicians. Biodegradable polymer delivery systems have been developed and demonstrate enormous potentials for therapeutics, including those within insulin. However, there is no well-developed pharmacokinetic model to analyze and predict the insulin release from polymer delivery system. In this presented work, we have developed a pharmacokinetic compartment model to describe insulin delivery from polymer matrix. PLGA degradation model was incorporated into the compartment model, which enables quantitative comparison between PLGA insulin controlled release and conventional insulin injection. Further, this model revealed that PLGA chemical properties significantly influence the insulin controlled release in pharmacokinetics. This novel model overcomes drawbacks of the conventional compartment models developed so far and provides insight into insulin controlled drug delivery system designing for more patient-friendly and personal diabetic treatment.
可生物降解聚合物基质控制胰岛素递送的药代动力学分析
糖尿病是一种代谢紊乱,患者长期处于高血糖状态。截至2015年,全球估计有4.15亿人患有糖尿病。胰岛素是稳定血糖水平、治疗糖尿病最有效、最安全的药物。目前的胰岛素给药需要每日皮下注射,这对患者和医生来说都不是一个有利的选择。可生物降解的聚合物输送系统已经开发出来,并显示出巨大的治疗潜力,包括胰岛素内的治疗。然而,目前还没有完善的药代动力学模型来分析和预测胰岛素在聚合物给药系统中的释放。在这项工作中,我们已经开发了一个药代动力学室模型来描述胰岛素从聚合物基质输送。将PLGA降解模型纳入室模型,定量比较PLGA胰岛素控释与常规胰岛素注射之间的差异。此外,该模型还揭示了PLGA的化学性质在药代动力学上显著影响胰岛素的控释。该模型克服了目前开发的传统隔室模型的缺点,为胰岛素控制给药系统的设计提供了新的思路,使糖尿病治疗更加人性化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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