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首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >PREPARATION AND CHARACTERIZATION OF ARTESUNATE - NICOTINAMIDE COCRYSTAL BY SOLVENT EVAPORATION AND SLURRY METHOD
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PREPARATION AND CHARACTERIZATION OF ARTESUNATE - NICOTINAMIDE COCRYSTAL BY SOLVENT EVAPORATION AND SLURRY METHOD

机译:溶剂蒸发-淤浆法制备及表征青蒿琥酯-烟酰胺结晶。

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Objective : The present study aims to prepare and characterize cocrystals of artesunate (AR) - nicotinamide (NI) in order to improve bioavailability and efficacy of artesunate as an antimalarial drug. Methods : Cocrystals were prepared using solvent evaporation and slurry methods. Physicochemical characterizations were performed using Hot Stage Microscope (HSM), infrared spectroscopy (IR), thermal analysis DTA, X-Ray Powder Diffraction (PXRD) and Scanning Electron Microscope (SEM). Results : The study revealed that re-crystallization of AR, NI and a physical mixture of both compounds showed distinctive shapes as shown by HSM microscope. AR has a needle shape, whereas NI showed mosaic spherulite crystal. Furthermore, as the two compounds experienced a contact one another, new crystals i.e. fiber-like shape were observed, indicating formation of a cocrystal of AR-NI was successfully achieved. Two different molar ratios of AR-NI from the phase diagram (i.e. 50:50 and 60:40 percent) showed a decrease in the melting temperature i.e. 104.0°C and 104.7°C, respectively, in comparison with the melting point of the constituent materials (AR 133.6°C and NI 142.2°C). PXRD diffractogram showed that cocrystal of AR–NI exhibited new diffraction peaks at 2q = 5,8°; 17,4° and 17,8°, whereas no peaks were found for physical mixtures of AR - NI. Characterization with IR showed disappearance of transmission peaks at 2976 and 2639 cm -1 indicating a loss of NH 3+ bending bands. Furthermore, disappearance of C=O stretch at 1346 cm -1 and -OH bending at 1485 cm -1 indicated a formation of hydrogen bonding between AR and NI. This was due to the formation of cocrystals prepared by solvent evaporation method, since the cocrystals made by the slurry method only showed the loss of NH 3 + at 2639 cm -1 . SEM micrographs showed that co-crystals prepared by solvent method have a more homogeneous mixture of AR-NI compared to the cocrystal formed by slurry method. Conclusion: The study concludes that cocrystals of AR-NI were successfully formed using solvent evaporation and slurry methods. The formed co-crystals of AR - NI exhibited different physicochemical characteristics as compared to the constituent materials. The formed cocrystals prepared by solvent evaporation method have a lower melting point and relatively more homogeneous in terms of crystal composition.
机译:目的:本研究旨在制备和表征青蒿琥酯(AR)-烟酰胺(NI)的共晶体,以提高青蒿琥酯作为抗疟药的生物利用度和功效。方法:使用溶剂蒸发和淤浆法制备共晶。使用热台显微镜(HSM),红外光谱(IR),热分析DTA,X射线粉末衍射(PXRD)和扫描电子显微镜(SEM)进行理化表征。结果:研究表明,AR,NI和这两种化合物的物理混合物的重结晶显示出独特的形状,如HSM显微镜所示。 AR呈针状,而NI呈镶嵌球晶。此外,由于两种化合物彼此接触,因此观察到新的晶体,即纤维状形状,表明成功实现了AR-NI的共晶体的形成。相图中两种不同的AR-NI摩尔比(即50:50和60:40%)与成分的熔点相比,熔融温度分别降低了104.0°C和104.7°C材料(AR 133.6°C和NI 142.2°C)。 PXRD衍射图表明,AR–NI的共晶体在2q = 5,8°处出现新的衍射峰。 1,74°和17.8°,而AR-NI的物理混合物未发现峰。用IR表征显示在2976和2639cm -1的透射峰消失,表明NH 3+弯曲带的损失。此外,在1346cm -1处C = O拉伸消失和在1485cm -1处-OH弯曲消失表明AR和NI之间形成氢键。这是由于通过溶剂蒸发法形成的共晶体的形成,因为通过淤浆法制备的共晶体仅在2639cm -1处显示出NH 3 +的损失。 SEM显微照片显示,与通过淤浆法形成的共晶体相比,通过溶剂法制备的共晶体具有更均匀的AR-NI混合物。结论:研究得出结论,使用溶剂蒸发和淤浆法成功形成了AR-NI共晶。与组成材料相比,所形成的AR-NI共晶体表现出不同的理化特性。通过溶剂蒸发法制备的形成的共晶体具有较低的熔点,并且就晶体组成而言相对更均匀。

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