首页> 外文期刊>Journal of Drug Delivery and Therapeutics >DESIGN AND IN VITRO EVALUATION OF MULTIPARTICULATE SYSTEM FOR THE CHRONOMODULATED DELIVERY OF LORNOXICAM Shrishailgouda
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DESIGN AND IN VITRO EVALUATION OF MULTIPARTICULATE SYSTEM FOR THE CHRONOMODULATED DELIVERY OF LORNOXICAM Shrishailgouda

机译:洛诺昔康Shrishailgouda慢性调节多药配送系统的设计和体外评价

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In view of chronobiological considerations of rheumatoid arthritis, the present study deals with the design and evaluation of multiparticulate system for the chronomodulated delivery of lornoxicam. The basic design is based on the Pulsincap technology and consisted of formaldehyde treated insoluble hard gelatin capsule body filled with tripolyphosphate cross-linked chitosan microspheres of lornoxicam and sealed with a hydrogel tablet plug. The entire device was enteric coated, so as to prevent the variable gastric emptying time. The microspheres were found to be discrete, nearly spherical with rough surface characteristics. Particle size, encapsulation efficiency and release rate of lornoxicam from the microspheres are dependent on the fabrication conditions of the microencapsulation. FT-IR, DSC and XRD studies revealed the compatibility of the drug with the excipients used. The exposure of hard gelatine capsule bodies with formaldehyde for a period of 12 hrs was found to be optimum in maintaining the intactness of the capsule bodies in the simulated GI fluids. The lag time of the designed delivery system varied from 4-8 hrs and depended on the nature and concentration of the plugging material. The ejection of the plug was delayed with increase in the polymer concentration. Among the two polymers studied as plugging materials, guar gum exhibited better control in maintaining the lag time compared to xanthan gum. From the study it can be concluded that, the lag time be efficiently tailored by varying the concentrations of the polymers in the hydrogel plug for the chronomodulated delivery of lornoxicam. Key Words: Rheumatoid arthritis; Lornoxicam; Microspheres; Chronomodulated delivery systems; Hydrogel plug; Lag time;
机译:鉴于类风湿关节炎的时间生物学考虑,本研究涉及氯诺昔康的计时输送多颗粒系统的设计和评估。基本设计基于Pulsincap技术,由甲醛处理的不溶性硬明胶胶囊体组成,其中填充了氯诺昔康的三聚磷酸交联壳聚糖微球,并用水凝胶片剂塞密封。整个装置是肠溶衣的,以防止可变的胃排空时间。发现微球是离散的,接近球形,具有粗糙的表面特征。氯诺昔康从微球的粒径,包封效率和释放速率取决于微囊的制备条件。 FT-IR,DSC和XRD研究表明该药物与所用赋形剂具有相容性。发现硬明胶胶囊体与甲醛接触12小时对于保持模拟GI液中胶囊体的完整性是最佳的。设计的输送系统的滞后时间为4-8小时不等,这取决于堵塞材料的性质和浓度。随着聚合物浓度的增加,塞子的排出被延迟。与黄原胶相比,在作为堵塞材料的两种聚合物中,瓜尔胶表现出更好的控制滞后时间的作用。从研究中可以得出结论,可以通过改变水凝胶塞中聚合物的浓度来有效地调整滞后时间,以实现氯诺昔康的定时调制递送。关键词:类风湿关节炎氯诺昔康;微球;定时输送系统;水凝胶塞;时差;

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