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冻干无定形盐酸伐地那非与糖类的组合作为提高溶解速率和渗透性的一种方法。

Combinations of Freeze-Dried Amorphous Vardenafil Hydrochloride with Saccharides as a Way to Enhance Dissolution Rate and Permeability.

作者信息

Wiergowska Gabriela, Ludowicz Dominika, Wdowiak Kamil, Miklaszewski Andrzej, Lewandowska Kornelia, Cielecka-Piontek Judyta

机构信息

Tarchomin Pharmaceutical Works "Polfa" S.A., A. Fleminga 2, 03-176 Warsaw, Poland.

Department of Pharmacognosy, Poznan University of Medical Sciences, Swiecickiego 4, 60-781 Poznan, Poland.

出版信息

Pharmaceuticals (Basel). 2021 May 11;14(5):453. doi: 10.3390/ph14050453.

Abstract

To improve physicochemical properties of vardenafil hydrochloride (VAR), its amorphous form and combinations with excipients-hydroxypropyl methylcellulose (HPMC) and β-cyclodextrin (β-CD)-were prepared. The impact of the modification on physicochemical properties was estimated by comparing amorphous mixtures of VAR to their crystalline form. The amorphous form of VAR was obtained as a result of the freeze-drying process. Confirmation of the identity of the amorphous dispersion of VAR was obtained through the use of comprehensive analysis techniques-X-ray powder diffraction (PXRD) and differential scanning calorimetry (DSC), supported by FT-IR (Fourier-transform infrared spectroscopy) coupled with density functional theory (DFT) calculations. The amorphous mixtures of VAR increased its apparent solubility compared to the crystalline form. Moreover, a nearly 1.3-fold increase of amorphous VAR permeability through membranes simulating gastrointestinal epithelium as a consequence of the changes of apparent solubility (P = 6.83 × 10 cm/s vs. P = 8.75 × 10 cm/s) was observed, especially for its combinations with β-CD in the ratio of 1:5-more than 1.5-fold increase (P = 8.75 × 10 cm/s vs. P = 13.43 × 10 cm/s). The stability of the amorphous VAR was confirmed for 7 months. The HPMC and β-CD are effective modifiers of its apparent solubility and permeation through membranes simulating gastrointestinal epithelium, suggesting a possibility of a stronger pharmacological effect.

摘要

为改善盐酸伐地那非(VAR)的理化性质,制备了其无定形形式以及与辅料羟丙基甲基纤维素(HPMC)和β-环糊精(β-CD)的组合物。通过比较VAR的无定形混合物与其结晶形式,评估了改性对理化性质的影响。VAR的无定形形式是冷冻干燥过程的结果。通过使用综合分析技术——X射线粉末衍射(PXRD)和差示扫描量热法(DSC),并辅以傅里叶变换红外光谱(FT-IR)结合密度泛函理论(DFT)计算,确认了VAR无定形分散体的特性。与结晶形式相比,VAR的无定形混合物提高了其表观溶解度。此外,由于表观溶解度的变化,观察到无定形VAR透过模拟胃肠道上皮的膜的渗透率增加了近1.3倍(P = 6.83×10 cm/s对P = 8.75×10 cm/s),特别是其与β-CD以1:5比例组合时——增加超过1.5倍(P = 8.75×10 cm/s对P = 13.43×10 cm/s)。无定形VAR的稳定性在7个月内得到证实。HPMC和β-CD是其表观溶解度和透过模拟胃肠道上皮的膜的渗透的有效改性剂,这表明可能具有更强的药理作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec9/8151567/8117962329b1/pharmaceuticals-14-00453-sch001.jpg

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