Engineering: Pharmacokinetics and Pharmaceutical Technology Area, Miguel Hernandez University, Spain.
Engineering: Pharmacokinetics and Pharmaceutical Technology Area, Miguel Hernandez University, Spain.
Eur J Pharm Biopharm. 2021 Jan;158:185-197. doi: 10.1016/j.ejpb.2020.11.009. Epub 2020 Nov 26.
Finding predictive dissolution tests and valid IVIVCs are essential activities in generic industry, as they can be used as substitutes of human bioequivalence studies. IVIVCs can be developed by two different strategies: a one-step approach or a two-step approach. The objectives of this work were to compare different deconvolution and convolution methods used in the development of two-step level A IVIVCs and to study if the relationship between the in vitro dissolution rate and the in vivo dissolution rate should guide the decision between using a two-step approach or a one-step approach during the development of a new IVIVC. When the in vitro and the in vivo dissolution rates had a linear relationship, valid and biopredictive two-step IVIVCs were obtained, although there was not a combination of deconvolution and convolution methods that could be named as the best one, as long as all the prediction errors for any combination were within the limits. It was not possible to obtain a valid two-step IVIVC when the relationship between dissolution rates was non-linear, but the one-step approach was able to overcome this fact and it gave valid IVIVCs regardless of whether the relationship between dissolution rates was linear or non-linear.
寻找预测性溶出度试验和有效的 IVIVC 是仿制药行业的重要活动,因为它们可以作为人体生物等效性研究的替代品。IVIVC 可以通过两种不同的策略开发:一步法或两步法。本工作的目的是比较在两步法 A 级 IVIVC 开发中使用的不同解卷积和卷积方法,并研究在开发新的 IVIVC 时,体外溶出度与体内溶出度之间的关系是否应指导在两步法和一步法之间做出选择。当体外和体内溶出度呈线性关系时,可获得有效且生物预测性的两步 IVIVC,尽管没有一种解卷积和卷积方法的组合可以被称为最佳组合,只要任何组合的预测误差都在限制范围内。当溶出度之间的关系是非线性时,无法获得有效的两步 IVIVC,但一步法能够克服这一事实,并且无论溶出度之间的关系是线性还是非线性,它都能给出有效的 IVIVC。