Engineering Diffusion-Controlled Drug Delivery Systems to Achieve a Desired Drug Release Profile: Mathematical Modelling and Optimisation.

IF 4.1 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Pharmaceutical Research Pub Date : 2026-09-01 Epub Date: 2026-08-03 DOI:10.1007/s11095-026-04149-6
Daniele Peri, Elliot J Carr, Giuseppe Pontrelli, Sean McGinty
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引用次数: 0

Abstract

Objective: Drug delivery devices offer a promising strategy for the localized treatment of disease while minimising systemic side effects. However, designing diffusion-controlled systems to achieve a prescribed drug release profile remains a major challenge due to their inherently time-varying release rates. This study aims to develop a mathematical framework to enable the rational design of such systems to achieve desired therapeutic release profiles.

Methods: We develop a continuum-scale mathematical model describing diffusion-controlled drug release from a spherical microcapsule composed of a functionally graded polymer with spatially varying diffusivity and non-uniform initial drug distribution. These spatial design variables are parameterised using Bézier curves and identified via an inverse optimisation procedure based on a hybrid imperialist competitive algorithm. The framework is applied to two inverse design problems: (i) achieving near constant (zero-order) drug release over a specified time window, and (ii) reproducing prescribed release profiles defined by target checkpoints.

Results: The results show that a constant release rate can be achieved by tailoring the initial drug distribution while selecting an appropriate constant diffusivity. In contrast, more general release profiles require simultaneous optimisation of both spatially varying diffusivity and initial drug loading.

Conclusions: The proposed framework demonstrates how mathematical modelling and optimisation can enable the rational design of diffusion-controlled drug delivery systems capable of producing tailored therapeutic release behaviours.

工程扩散控制药物输送系统,以实现所需的药物释放概况:数学建模和优化。
目的:药物输送装置为局部治疗疾病提供了一种有希望的策略,同时将全身副作用降到最低。然而,由于其固有的时变释放速率,设计扩散控制系统以达到规定的药物释放特征仍然是一个主要挑战。本研究旨在建立一个数学框架,使这种系统的合理设计,以实现所需的治疗释放概况。方法:我们建立了一个连续尺度的数学模型来描述扩散控制药物从球形微胶囊中释放的过程,该球形微胶囊由具有空间变化扩散率和非均匀初始药物分布的功能梯度聚合物组成。这些空间设计变量使用bsamizier曲线进行参数化,并通过基于混合帝国主义竞争算法的逆优化程序进行识别。该框架应用于两个反设计问题:(i)在指定的时间窗口内实现接近恒定(零阶)的药物释放,以及(ii)再现由目标检查点定义的规定释放曲线。结果:通过调整初始药物分布,选择合适的恒定扩散系数,可获得恒定的释药速率。相比之下,更一般的释放曲线需要同时优化空间变化的扩散率和初始药物负载。结论:提出的框架证明了数学建模和优化如何能够合理设计扩散控制的药物传递系统,从而产生量身定制的治疗释放行为。
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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来源期刊
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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