Effect of Physicochemical Properties on the Basic Drug-Acid-Polymer Interactions and Miscibility in PVA Based Orodispersible Films.

IF 5 3区 医学 Q1 PHARMACOLOGY & PHARMACY AAPS Journal Pub Date : 2024-07-15 DOI:10.1208/s12248-024-00949-z
Jie Liu, Yongguo Zhang, Chao Liu, Liang Fang
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Abstract

Salts of weakly basic drugs can partially dissociate in formulations, to give basic drugs and counter acids. The aim of the present study was to clarify the effect of physicochemical properties on the basic drug-acid-polymer interactions and salt-polymer miscibility, and to explain the influence mechanism at the molecular level. Six maleate salts with different physicochemical properties were selected and PVA was used as the film forming material. The relationship between the physicochemical properties and the miscibility was presented with multiple linear regression analysis. The existence state of salts in formulations were determined by XRD and Raman imaging. The stability of salts was characterized by NMR and XPS. The intermolecular interactions were investigated by FTIR and NMR. The results showed that the salt-PVA miscibility was related to polar surface area of salts and Tg of free bases, which represented hydrogen bond interaction and solubility potential. The basic drug-acid-PVA intermolecular interactions determined the existence state and bonding pattern of the three molecules. Meanwhile, the decrease of the stability after formulation increased the number of free bases in orodispersible films, which in turn affected the miscibility with PVA. The study provided references for the rational design of PVA based orodispersible films.

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理化特性对基于 PVA 的可分散薄膜中基本药物-酸-聚合物相互作用和混溶性的影响
弱碱性药物的盐在制剂中会发生部分离解,生成碱性药物和反酸。本研究旨在阐明理化性质对碱性药物-酸-聚合物相互作用和盐-聚合物混溶性的影响,并从分子水平解释其影响机制。研究选取了六种不同理化性质的马来酸盐,并以 PVA 为成膜材料。通过多元线性回归分析,得出了理化性质与混溶性之间的关系。通过 XRD 和拉曼成像测定了配方中盐类的存在状态。通过核磁共振和 XPS 分析了盐的稳定性。傅立叶变换红外光谱和核磁共振对分子间相互作用进行了研究。结果表明,盐-PVA 的混溶性与盐的极性表面积和游离碱的 Tg 有关,它们代表了氢键相互作用和溶解潜力。碱性药物-酸-PVA 分子间的相互作用决定了三种分子的存在状态和成键模式。同时,配制后稳定性的降低增加了口崩膜中游离碱的数量,进而影响了与 PVA 的混溶性。该研究为合理设计基于 PVA 的口崩膜提供了参考。
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来源期刊
AAPS Journal
AAPS Journal 医学-药学
CiteScore
7.80
自引率
4.40%
发文量
109
审稿时长
1 months
期刊介绍: The AAPS Journal, an official journal of the American Association of Pharmaceutical Scientists (AAPS), publishes novel and significant findings in the various areas of pharmaceutical sciences impacting human and veterinary therapeutics, including: · Drug Design and Discovery · Pharmaceutical Biotechnology · Biopharmaceutics, Formulation, and Drug Delivery · Metabolism and Transport · Pharmacokinetics, Pharmacodynamics, and Pharmacometrics · Translational Research · Clinical Evaluations and Therapeutic Outcomes · Regulatory Science We invite submissions under the following article types: · Original Research Articles · Reviews and Mini-reviews · White Papers, Commentaries, and Editorials · Meeting Reports · Brief/Technical Reports and Rapid Communications · Regulatory Notes · Tutorials · Protocols in the Pharmaceutical Sciences In addition, The AAPS Journal publishes themes, organized by guest editors, which are focused on particular areas of current interest to our field.
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