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首页> 外文期刊>Open Pharmaceutical Sciences Journal >Improvement in Dissolution of Bosentan Monohydrate by Solid Dispersions Using Spray Drying Technique
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Improvement in Dissolution of Bosentan Monohydrate by Solid Dispersions Using Spray Drying Technique

机译:喷雾干燥技术通过固体分散体改善波生坦一水合物的溶解度

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Background:Bosentan monohydrate (BM), a dual endothelin receptor antagonist, is indicated for the treatment of patients with pulmonary arterial hypertension (PAH). It is poorly soluble in water, and having absolute bioavailability of 50%.Objective:The aim of the present work is to develop and evaluate the solid dispersions (SD) of a poorly water soluble drug bosentan monohydrate (BM).Method:Solid dispersions (SDs) systems of BM were prepared with Hydroxy propyle β-cyclodextrin (HPβ-CD) and Polyethylene glycol (PEG-4000) polymers using a spray drying technique.Result:The significant rise in a saturation solubility 174.23±1.36 mg/mL; and drug dissolution 95.11±1.22%; was observed with optimized formulation (SD 6). The solid state characterization of optimized formulation (SD 6) by SEM, DSC, and XRPD revealed the absence of crystalline nature of BM in solid dispersion. High dissolution rate of solid dispersion (SD 6) compared with pure drug indicated the increase in dissolution characteristics.Conclusion:In conclusion, our studies illustrated that spray drying technique could be useful large scale producing method to prepare the solid dispersion of bosentan with HP β-CD, which can improve the solubility as well as stability of the formulation.
机译:背景:波生坦一水合物(BM)是一种双重内皮素受体拮抗剂,适用于肺动脉高压(PAH)患者的治疗。它在水中难溶,具有50%的绝对生物利用度。目的:本工作的目的是开发和评估难溶于水的一水波生坦药物(BM)的固体分散体(SD)。方法:固体分散体采用喷雾干燥技术,用羟丙基β-环糊精(HPβ-CD)和聚乙二醇(PEG-4000)聚合物制备了BM(SDs)体系。结果:饱和溶解度显着提高174.23±1.36 mg / mL;药物溶出度95.11±1.22%;用优化配方(SD 6)观察到。通过SEM,DSC和XRPD对优化配方(SD 6)进行的固态表征表明,固体分散体中不存在BM的结晶性。固体分散体(SD 6)的溶出度高于纯药物,表明溶出度有所提高。结论:结论:我们的研究表明,喷雾干燥技术可能是大规模制备含有HPβ的波生坦固体分散体的有用方法。 -CD,其可以改善制剂的溶解度以及稳定性。

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