Characterisation of colloidal structures and their solubilising potential for BCS class II drugs in fasted state simulated intestinal fluid

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics Pub Date : 2024-09-22 DOI:10.1016/j.ijpharm.2024.124733
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Abstract

A suite of fasted state simulated intestinal fluid (SIF), based on variability observed in a range of fasted state human intestinal fluid (HIF) samples was used to study the solubility of eight poorly soluble drugs (three acidic drugs (naproxen, indomethacin and phenytoin), two basic drugs (carvedilol and tadalafil) and three neutral drugs (felodipine, fenofibrate, griseofulvin)). Particle size of the colloidal structures formed in these SIF in the presence and absence of drugs was measured using dynamic light scattering and nanoparticle tracking analysis.
Results indicate that drug solubility tends to increase with increasing total amphiphile concentration (TAC) in SIF with acidic drugs proving to be more soluble than basic or neutral drug in the media evaluated. Dynamic light scattering showed that as the amphiphile concentration increased, the hydrodynamic diameters of the structures decreased. The scattering distribution confirmed the polydispersity of the simulated intestinal fluids compared to the monodisperse distribution observed for FaSSIF v1). There was a large difference in the size of the structures found based on the composition of the SIF, for example, the diameter of the structures measured in felodipine in the minimum TAC media was measured to be 170 ± 5 nm which decreased to 5.1 ± 0.2 nm in the maximum TAC media point. The size measured of the colloidal structures of felodipine in the FaSSIF v1 was 86 ± 1 nm. However, there was no simple correlation between solubility and colloidal size.
Nanoparticle tracking analysis was used for the first time to characterise colloidal structures within SIF and the results were compared to those obtained by dynamic light scattering. The particle size measured by dynamic light scattering was generally greater in media with a lower concentration of amphiphiles and smaller in media of a higher concentration of amphiphiles, compared to that of the data yielded by nanoparticle tracking analysis.
This work shows that the colloidal structures formed vary depending on the composition of SIF which affects the solubility. Work is ongoing to determine the relationship between colloidal structure and solubility.

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空腹状态模拟肠液中 BCS II 类药物胶体结构及其增溶潜力的特征。
根据在一系列空腹状态人体肠液(HIF)样本中观察到的变异性,我们使用了一套空腹状态模拟肠液(SIF)来研究八种溶解性较差的药物(三种酸性药物(萘普生、吲哚美辛和苯妥英)、两种碱性药物(卡维地洛和他达拉非)和三种中性药物(非洛地平、非诺贝特和格列齐特))的溶解性。使用动态光散射和纳米粒子跟踪分析法测量了药物存在和不存在时在这些 SIF 中形成的胶体结构的粒度。结果表明,药物溶解度随着 SIF 中两性化合物总浓度(TAC)的增加而增加,在所评估的介质中,酸性药物的溶解度高于碱性或中性药物。动态光散射显示,随着双亲化合物浓度的增加,结构的流体力学直径减小。散射分布证实了模拟肠液的多分散性,而在 FaSSIF v1) 中观察到的是单分散分布。根据 SIF 的组成,所发现的结构大小差异很大,例如,在最小 TAC 介质中测得的非洛地平结构直径为 170 ± 5 nm,而在最大 TAC 介质点中则降至 5.1 ± 0.2 nm。在 FaSSIF v1 中测得的非洛地平胶体结构尺寸为 86 ± 1 nm。然而,溶解度和胶体大小之间并没有简单的相关性。我们首次使用纳米粒子跟踪分析法对 SIF 中的胶体结构进行了表征,并将结果与动态光散射法得出的结果进行了比较。与纳米粒子跟踪分析得出的数据相比,动态光散射法测得的粒径通常在两亲化合物浓度较低的介质中较大,而在两亲化合物浓度较高的介质中较小。这项工作表明,形成的胶体结构因 SIF 的成分而异,而 SIF 的成分会影响溶解度。确定胶体结构与溶解度之间关系的工作正在进行中。
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来源期刊
CiteScore
10.70
自引率
8.60%
发文量
951
审稿时长
72 days
期刊介绍: The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
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