Modeling of Disintegration and Dissolution Behavior of Mefenamic Acid Formulation Using Numeric Solution of Noyes-Whitney Equation with Cellular Automata on Microtomographic and Algorithmically Generated Surfaces

被引:12
|
作者
Yokoyama, Reiji [1 ,2 ]
Kimura, Go [2 ]
Schlepuetz, Christian M. [3 ]
Huwyler, Joerg [1 ]
Puchkov, Maxim [1 ]
机构
[1] Univ Basel, Dept Pharmaceut Sci, Div Pharmaceut Technol, Klingelbergstr 50, CH-4056 Basel, Switzerland
[2] SHIONOGI & CO LTD, CMC R&D Div, Formulat R&D Ctr, Amagasaki, Hyogo 6600813, Japan
[3] Paul Scherrer Inst, Swiss Light Source, CH-5232 Villigen, Switzerland
来源
PHARMACEUTICS | 2018年 / 10卷 / 04期
关键词
drug release simulation; disintegration simulation; poorly water-soluble drug; mefenamic acid; Noyes-Whitney equation; cellular automata; synchrotron microtomography; PHARMACEUTICAL TABLETS; DIRECT COMPRESSION; DENSITY VARIATIONS; DRUG-RELEASE; IN-SILICO; SIMULATION; BREAKAGE; PROFILES; POROSITY; POWDER;
D O I
10.3390/pharmaceutics10040259
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Manufacturing parameters may have a strong impact on the dissolution and disintegration of solid dosage forms. In line with process analytical technology (PAT) and quality by design approaches, computer-based technologies can be used to design, control, and improve the quality of pharmaceutical compacts and their performance. In view of shortcomings of computationally intensive finite-element or discrete-element methods, we propose a modeling and simulation approach based on numerical solutions of the Noyes-Whitney equation in combination with a cellular automata-supported disintegration model. The results from in vitro release studies of mefenamic acid formulations were compared to calculated release patterns. In silico simulations with our disintegration model showed a high similarity of release profile as compared to the experimental evaluation. Furthermore, algorithmically created virtual tablet structures were in good agreement with microtomography experiments. We conclude that the proposed computational model is a valuable tool to predict the influence of material attributes and process parameters on drug release from tablets.
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页数:17
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