Complex investigation of the effect mechanism of polyvinylpyrrolidone in the additive-assisted crystallization of famotidine

Utilizing the positive impact of additives, including pharmaceutical excipients, to achieve favorable crystal morphology and polymorphism is a widely researched area. Despite the obvious benefits of additive-assisted crystallization, the quantification of process parameter influences on the effect mechanism of additives is usually discussed only from a nucleation inhibition point of view or focusing on technological feasibility. Accordingly, the relevant literature can be divided into technological and mechanism studies, but it lacks a complex combined approach. However, to develop robust crystallization procedures, the systematic analysis of process conditions is essential. Thus, understanding the molecular-scale effect mechanism is also crucial to designing these complex processes. Therefore, in this work, the effect of a pharmaceutical binder, poly(vinyl pyrrolidone) (PVP), and several process parameters were investigated on the nucleation of famotidine (FMT), an antihistamine, both experimentally and theoretically. To systematically investigate the effect of PVP concentration, temperature, and supersaturation, we applied the Design of Experiment (DoE) methodology combined with a camera-aided analytical set-up. Based on the experimental data, the nucleation rate of FMT was studied according to the Classical Nucleation Theory (CNT). Finally, molecular simulations were conducted, and a possible effect mechanism was suggested for the PVP-effected nucleation of FMT. This way, the complex DoE-based process parameter investigation and molecular scale interpretation of these effects is a novel approach of the subject. The experimental results revealed that the nucleation inhibiting effect of PVP is dependent on the set temperature, while increasing FMT concentration generally counterforces it. Based on the CNT calculations, PVP decreased the nucleation rate of FMT by orders of magnitude. Additionally, molecular modelling suggests the effect mechanism of PVP is manifested through H-bonding and steric hindrance.

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Publication Details

Journal
International Journal of Pharmaceutics
Published
2025-07-24
DOI
https://doi.org/10.1016/j.ijpharm.2025.125994
Primary Topic
Crystallization and Solubility Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Complex investigation of the effect mechanism of polyvinylpyrrolidone in the additive-assisted crystallization of famotidine

Éva Pusztai, György Marosi, Kornélia Tacsi, György Nimród Stoffán et al.
International Journal of Pharmaceutics
Crystallization and Solubility Studies
article

Complex investigation of the effect mechanism of polyvinylpyrrolidone in the additive-assisted crystallization of famotidine

Éva Pusztai, György Marosi, Kornélia Tacsi, György Nimród Stoffán, Tibor Höltzl, Hajnalka Pataki, Attila Farkas, Zsolt Lőrincz
article en

Abstract

Utilizing the positive impact of additives, including pharmaceutical excipients, to achieve favorable crystal morphology and polymorphism is a widely researched area. Despite the obvious benefits of additive-assisted crystallization, the quantification of process parameter influences on the effect mechanism of additives is usually discussed only from a nucleation inhibition point of view or focusing on technological feasibility. Accordingly, the relevant literature can be divided into technological and mechanism studies, but it lacks a complex combined approach. However, to develop robust crystallization procedures, the systematic analysis of process conditions is essential. Thus, understanding the molecular-scale effect mechanism is also crucial to designing these complex processes. Therefore, in this work, the effect of a pharmaceutical binder, poly(vinyl pyrrolidone) (PVP), and several process parameters were investigated on the nucleation of famotidine (FMT), an antihistamine, both experimentally and theoretically. To systematically investigate the effect of PVP concentration, temperature, and supersaturation, we applied the Design of Experiment (DoE) methodology combined with a camera-aided analytical set-up. Based on the experimental data, the nucleation rate of FMT was studied according to the Classical Nucleation Theory (CNT). Finally, molecular simulations were conducted, and a possible effect mechanism was suggested for the PVP-effected nucleation of FMT. This way, the complex DoE-based process parameter investigation and molecular scale interpretation of these effects is a novel approach of the subject. The experimental results revealed that the nucleation inhibiting effect of PVP is dependent on the set temperature, while increasing FMT concentration generally counterforces it. Based on the CNT calculations, PVP decreased the nucleation rate of FMT by orders of magnitude. Additionally, molecular modelling suggests the effect mechanism of PVP is manifested through H-bonding and steric hindrance.

International Journal of PharmaceuticsVol. 682
Budapest University of Technology and Economics (HU)
Nemzeti Kutatási, Fejlesztési és Innovaciós Alap
Openalex Percentile: Top 87%
Crystallization and Solubility Studies
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