Development and optimization of venlafaxine hydrochloride floating microspheres using response surface plots

Sachin Kumar, R. Mazumder
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引用次数: 2

Abstract

The current study deals with the development of floating microspheres of venlafaxine hydrochloride. This drug is known as a serotonin-norepinephrine reuptake inhibitor and used to treat depression. Due to the short elimination half life of 4-5 h, the drug has to be administred 2-3 times in a day to maintain the plasma concentration. Thus an attempt was made to decrease the dosing frequency. The microspheres were prepared by non-aqueous solvent evaporation method. The microspheres were evaluated for particle size and morphology using a photomicroscope and scanning electron microscopy, respectively. The incorporation efficiency of microspheres of batch F2 and F6 showed entrapment of 60.6% and 57.2%, respectively. The mean diameters of particles for all batches were found in the range of 226.15 ± 24.37 to 283.37 ± 21.56 μm. The Fourier transform infrared spectroscopy revealed absence of any drug polymer interactions. The microsphers remained buoyant for more than 12 h. The drug release from developed microspheres followed Fickian diffusion with swelling. The results suggested that the developed floating microspheres containing venlafaxine hydrochloride could enhance drug entrapment efficiency, reduce the initial burst release and modulate the drug release.
利用响应面法开发和优化盐酸文拉法辛漂浮微球
本文研究了盐酸文拉法辛漂浮微球的研制。这种药物被称为血清素-去甲肾上腺素再摄取抑制剂,用于治疗抑郁症。由于消除半衰期短,4-5小时,因此必须每天给药2-3次以维持血药浓度。因此,进行了降低给药频率的尝试。采用非水溶剂蒸发法制备微球。用显微显微镜和扫描电子显微镜分别对微球的粒径和形貌进行了评价。F2和F6批次微球的混染率分别为60.6%和57.2%。各批次的平均粒径范围为226.15±24.37 ~ 283.37±21.56 μm。傅里叶变换红外光谱显示没有任何药物-聚合物相互作用。微球保持浮力12 h以上。发育后的微球以菲克氏扩散伴溶胀释放药物。结果表明,制备的盐酸文拉法辛漂浮微球能提高药物包封效率,降低初始爆发释放,调节药物释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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