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可生物降解微粒药物释放的数学模型:γ 辐射的影响

Mathematical modeling of drug release from bioerodible microparticles: effect of gamma-irradiation.

作者信息

Faisant N, Siepmann J, Richard J, Benoit J P

机构信息

INSERM ERIT-M 0104, Université d'Angers, Angers, France.

出版信息

Eur J Pharm Biopharm. 2003 Sep;56(2):271-9. doi: 10.1016/s0939-6411(03)00104-8.

Abstract

Bioerodible polymers used in controlled drug delivery systems, such as poly(lactic-co-glycolic acid) (PLGA) undergo radiolytic degradation during gamma-irradiation. In spite of the considerable practical importance, yet only little knowledge is available on the consequences of this sterilization method on the resulting drug release patterns in a quantitative way. The major objectives of the present study were: (i) to monitor the effects of different gamma-irradiation doses on the physicochemical properties of drug-free and drug-loaded, PLGA-based microparticles; (ii) to analyze the obtained experimental results using adequate mathematical models; (iii) to get further insight into the occurring physical and chemical phenomena; and (iv) to relate the applied gamma-irradiation dose in a quantitative way to the resulting drug release rate. 5-Fluorouracil-loaded, PLGA-based microparticles were prepared with an oil-in-water solvent extraction method and exposed to gamma-irradiation doses ranging from 0 to 33 kGy. Size exclusion chromatography, differential scanning calorimetry, scanning electron microscopy, particle size analysis, determination of the actual drug loading and in vitro drug release kinetics were used to study the effects of the gamma-irradiation dose on the physicochemical properties of the microparticles. Two mathematical models-a simplified and a more comprehensive one-were used to analyze the experimental results. The simplified model considers drug diffusion based on Fick's second law for spherical geometry and a Higuchi-like pseudo-steady-state approach. The complex model combines Monte Carlo simulations (describing polymer erosion) with partial differential equations quantifying drug diffusion with time-, position- and direction-dependent diffusivities. Interestingly, exponential relationships between the gamma-irradiation dose and the initial drug diffusivity within the microparticles could be established. Based on this knowledge both models were used to predict the resulting drug release kinetics as a function of the gamma-irradiation dose. Importantly, the theoretical predictions were confirmed by experimental results.

摘要

用于控释给药系统的生物可蚀性聚合物,如聚乳酸 - 乙醇酸共聚物(PLGA),在伽马射线辐照过程中会发生辐射降解。尽管这一实际应用意义重大,但关于这种灭菌方法对最终药物释放模式的影响,目前仅有少量的定量研究。本研究的主要目的是:(i)监测不同伽马射线辐照剂量对不含药物和载药的PLGA基微粒物理化学性质的影响;(ii)使用适当的数学模型分析所获得的实验结果;(iii)进一步深入了解所发生的物理和化学现象;(iv)以定量方式将所施加的伽马射线辐照剂量与最终的药物释放速率联系起来。采用水包油溶剂萃取法制备了载有5 - 氟尿嘧啶的PLGA基微粒,并使其暴露于0至33 kGy的伽马射线辐照剂量下。使用尺寸排阻色谱法、差示扫描量热法、扫描电子显微镜、粒度分析、实际载药量测定和体外药物释放动力学来研究伽马射线辐照剂量对微粒物理化学性质的影响。使用了两个数学模型——一个简化模型和一个更全面的模型——来分析实验结果。简化模型基于菲克第二定律用于球形几何形状的药物扩散以及类似Higuchi的准稳态方法。复杂模型将蒙特卡罗模拟(描述聚合物侵蚀)与偏微分方程相结合,该方程用与时间、位置和方向相关的扩散系数来量化药物扩散。有趣的是,能够建立伽马射线辐照剂量与微粒内初始药物扩散率之间的指数关系。基于这一知识,两个模型都被用于预测作为伽马射线辐照剂量函数的最终药物释放动力学。重要的是,理论预测得到了实验结果的证实。

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