Department of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, 144 College Street, Toronto, Ontario M5S 3M2, Canada.
Int J Pharm. 2011 Oct 10;418(1):18-27. doi: 10.1016/j.ijpharm.2011.01.019. Epub 2011 Jan 18.
The purpose of this review is to provide an overview of approximate analytical solutions to the general moving boundary diffusion problems encountered during the release of a dispersed drug from matrix systems. Starting from the theoretical basis of the Higuchi equation and its subsequent improvement and refinement, available approximate analytical solutions for the more complicated cases involving heterogeneous matrix, boundary layer effect, finite release medium, surface erosion, and finite dissolution rate are also discussed. Among various modeling approaches, the pseudo-steady state assumption employed in deriving the Higuchi equation and related approximate analytical solutions appears to yield reasonably accurate results in describing the early stage release of a dispersed drug from matrices of different geometries whenever the initial drug loading (A) is much larger than the drug solubility (C(s)) in the matrix (or A≫C(s)). However, when the drug loading is not in great excess of the drug solubility (i.e. low A/C(s) values) or when the drug loading approaches the drug solubility (A→C(s)) which occurs often with drugs of high aqueous solubility, approximate analytical solutions based on the pseudo-steady state assumption tend to fail, with the Higuchi equation for planar geometry exhibiting a 11.38% error as compared with the exact solution. In contrast, approximate analytical solutions to this problem without making the pseudo-steady state assumption, based on either the double-integration refinement of the heat balance integral method or the direct simplification of available exact analytical solutions, show close agreement with the exact solutions in different geometries, particularly in the case of low A/C(s) values or drug loading approaching the drug solubility (A→C(s)). However, the double-integration heat balance integral approach is generally more useful in obtaining approximate analytical solutions especially when exact solutions are not available.
本综述的目的是提供从基质系统中释放分散药物时遇到的一般移动边界扩散问题的近似解析解概述。从 Higuchi 方程的理论基础及其随后的改进和完善出发,还讨论了涉及非均相基质、边界层效应、有限释放介质、表面侵蚀和有限溶解速率等更复杂情况的可用近似解析解。在各种建模方法中,在推导出 Higuchi 方程和相关近似解析解时采用的伪稳态假设,在描述不同几何形状的基质中分散药物的早期释放时,似乎可以得出相当准确的结果,只要初始药物负载(A)远大于药物在基质中的溶解度(C(s))(即 A≫C(s))。然而,当药物负载没有大大超过药物溶解度(即低 A/C(s) 值)或当药物负载接近药物溶解度(A→C(s))时,这在高水溶性药物中经常发生,基于伪稳态假设的近似解析解往往会失败,与平面几何形状的 Higuchi 方程相比,其误差为 11.38%。相比之下,在不进行伪稳态假设的情况下,基于热平衡积分法的双重积分细化或可用精确解析解的直接简化,对这个问题的近似解析解与不同几何形状的精确解之间具有很好的一致性,特别是在低 A/C(s) 值或药物负载接近药物溶解度(A→C(s))的情况下。然而,双重积分热平衡积分法通常更适用于获得近似解析解,特别是在没有精确解的情况下。