Das Malay Kumar, Rao Kalakuntala Rama
Department of Pharmaceutical Sciences, Dibrugarh University, Dibrugarh-786004, Assam, India.
Acta Pol Pharm. 2006 Mar-Apr;63(2):141-8.
The preparation of zidovudine-loaded ethylcellulose microspheres by w/o/o double emulsion solvent diffusion method with high entrapment capacity and sustained release is described. A mixed solvent system (MSS) consisting of acetonitrile and dichloromethane in a 1:1 ratio and light liquid paraffin was selected as primary and secondary oil phases, respectively. Span 80 was used as the secondary surfactant for stabilizing the external oil phase. Spherical free flowing microspheres were obtained. The prepared microspheres were characterized by entrapment efficiency, in vitro release behavior, differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). The drug-loaded microspheres showed 32 - 55% entrapment capacity. The in vitro release profile could be altered significantly by changing various processing and formulation parameters to give sustained release of drug from the microspheres. The DSC thermograms confirmed the absence of any drug-polymer interaction. SEM studies showed that the microspheres were spherical and porous in nature. The in vitro release profiles from microspheres of different polymer-drug ratios were best fitted to Higuchi model with high correlation coefficient and the n value obtained from Korsmeyer-Peppas model was ranged between 0.23 - 0.54. The drug release was found to be diffusion controlled mechanism.
描述了通过w/o/o双乳液溶剂扩散法制备具有高包封率和缓释性能的齐多夫定负载乙基纤维素微球。分别选择由1:1比例的乙腈和二氯甲烷组成的混合溶剂体系(MSS)和轻质液体石蜡作为初级和次级油相。使用Span 80作为次级表面活性剂来稳定外部油相。获得了球形自由流动的微球。通过包封率、体外释放行为、差示扫描量热法(DSC)和扫描电子显微镜(SEM)对制备的微球进行了表征。载药微球的包封率为32 - 55%。通过改变各种加工和配方参数,可以显著改变体外释放曲线,使药物从微球中持续释放。DSC热谱图证实不存在任何药物 - 聚合物相互作用。SEM研究表明,微球呈球形且具有多孔结构。不同聚合物 - 药物比例的微球体外释放曲线最符合Higuchi模型,相关系数高,从Korsmeyer - Peppas模型获得的n值在0.23 - 0.54之间。发现药物释放为扩散控制机制。