Characterization of Solid Binary Systems of Efavirenz and Hydroxypropyl-β-Cyclodextrin

Bharati Arali, Y AnandKumar, C MallikarjunaSetty
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Abstract

http://dx.doi.org/10.21276/IJRDPL.22780238.2019.8(1).15-20 ABSTRACT: Efavirenz is a widely prescribed anti-retroviral drug that belongs to BCS class II and exhibit low and variable oral bioavailability due to its poor aqueous solubility and it requires enhancement in solubility and dissolution rate for increasing its oral bioavailability. The aim of this study was to increase the solubility of Efavirenz (EFA) by complexing it with Hydroxypropyl-β-cyclodextrin (HPβCD). Solid binary systems were prepared by co-grinding and microwave irradiation methods. The interaction of EFA with HPβCD was evaluated by Phase solubility studies, in vitro dissolution studies and different analytical techniques including Fourier Transform Infrared Spectroscopy (FTIR) and Differential Scanning Calorimetry (DSC). The apparent stability constant revealed EFA with HPβCD produces 1:1 M stoichiometric complex. The host guest interactions studied by FTIR and DSC confirmed true inclusion of EFA with HPβCD at 1:2 M. The Dissolution rates of EFAHPβCD binary systems were faster when compared to physical mixture and pure drug. Overall the rank order of improvement in dissolution properties of Efavirenz with ratios is 1:2M > 1:1M and methods MW > CG > PM > Pure drug. One-way ANOVA suggest the DP60 and DE60 values were significantly higher (P<0.05) in solid binary systems prepared by microwave irradiation method when compared to co-grinding and its corresponding physical mixtures and pure drug.
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依非韦伦与羟丙基-β-环糊精固体二元体系的表征
http://dx.doi.org/10.21276/IJRDPL.22780238.2019.8(1).15-20摘要:依非韦伦(Efavirenz)是一种广泛使用的抗逆转录病毒药物,属于BCS II类药物,由于其水溶性较差,口服生物利用度低且多变,需要提高其溶解度和溶出速度以提高其口服生物利用度。本研究的目的是通过与羟丙基-β-环糊精(HPβCD)络合来提高依非韦伦(EFA)的溶解度。采用共磨法和微波辐照法制备了固体二元体系。通过相溶解度研究、体外溶出度研究和不同的分析技术,包括傅里叶变换红外光谱(FTIR)和差示扫描量热法(DSC)来评估EFA与HPβCD的相互作用。表观稳定常数表明,EFA与hp - β - cd形成1:1 M的化学计量络合物。FTIR和DSC研究的主-客体相互作用证实了在1:2 m时EFA与hp - β - cd的真实包涵,efahp - β - cd二元体系的溶出速度比物理混合物和纯药物更快。依非韦伦溶出度的改善顺序为:1:2M > 1:1M,方法为:分子量> CG > PM >纯药物。单因素方差分析表明,微波辐照法制备的固体二元体系的DP60和DE60值显著高于共磨及其相应的物理混合物和纯药物(P<0.05)。
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