共结晶提高姜黄素的溶解度和抗炎活性

Q2 Pharmacology, Toxicology and Pharmaceutics Science and Technology Indonesia Pub Date : 2023-07-06 DOI:10.26554/sti.2023.8.3.501-508
Yudi Wicaksono, Kuni Zu’aimah Barikah, Amanda Della Yudatama, Havidhatul Maulia, N. Nuri, D. Setyawan
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引用次数: 0

摘要

姜黄素(CUR)是一种多酚类化合物,具有强大的抗炎活性。然而,在口服给药过程中,只有少量的CUR被吸收,这是因为CUR很难溶解在水中。本研究的目的是通过溶剂蒸发使用异烟酰胺共形成剂(INIC)的共结晶技术来提高CUR的溶解度。使用粉末X射线衍射仪(PXRD)、差示扫描量热计(DSC)、傅里叶变换红外光谱仪(FTIR)和扫描电子显微镜(SEM)进行共晶表征。使用摇动法评估溶解度,而使用卡拉胶诱导的小鼠腿部水肿法进行抗炎活性测试。得到的CUR-INIC(1:1)共晶在15.00、16.22和22.89处具有新的衍射峰2θ的衍射图◦ 与CUR和INIC的单独衍射图相比。在共晶中,CUR和INIC形成氢键的分子间相互作用,形成熔点为160.1的新固相◦C.CUR-INIC共晶在水中的溶解度为73.1±0.23 ug/mL,与初始CUR的溶解度相比增加了14倍,初始CUR仅为5.05±0.07 ug/mL。CUR-INIC共结晶在小鼠中显示出比初始CUR高130%的水肿抑制百分比(5小时)。因此,CUR-INIC共晶可以用来提高CUR的溶解度,以获得更优异的抗炎效果。
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Increasing the Solubility and Anti-Inflammatory Activity of Curcumin by Cocrystallization
Curcumin (CUR) is a polyphenolic compound that exhibits potent anti-inflammatory activity. However, only a tiny amount of CUR is absorbed during oral administration, which is because CUR is difficult to dissolve in water. The aim of the research was to increase the solubility of CUR through the cocrystallization technique using isonicotinamide coformer (INIC) by solvent evaporation. Cocrystal characterization was carried out using a powder X-ray diffractometer (PXRD), a differential scanning calorimeter (DSC), a Fourier transform infrared spectrometer (FTIR), and a scanning electron microscope (SEM). Solubility was evaluated using the shaking method, while the anti-inflammatory activity test was carried out using the carrageenan induced mouse leg edema method. The resulting CUR-INIC (1:1) cocrystal has a diffractogram with new diffraction peaks of 2theta at 15.00, 16.22, and 22.89◦ compared to the individual diffractograms of CUR and INIC. In the cocrystal, CUR and INIC form intermolecular interactions of hydrogen bonds, resulting in a new solid phase with a melting point of 160.1◦C. The solubility of the CUR-INIC cocrystal in water was 73.1±0.23 ug/mL, which increased 14 times compared to the solubility of initial CUR, which was only 5.05±0.07 ug/mL. The CUR-INIC cocrystal showed a percentage of edema inhibition in mice (5 hours) 130% more potent than that of initial CUR. Therefore, CUR-INIC cocrystals can be used to improve CUR solubility to obtain more excellent anti-inflammatory effects.
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来源期刊
Science and Technology Indonesia
Science and Technology Indonesia Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
1.80
自引率
0.00%
发文量
72
审稿时长
8 weeks
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