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Utilization of thin film method for preparation of celecoxib loaded liposomes

机译:薄膜法制备塞来昔布脂质体的制备

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Purpose:Celecoxib is nonsteroiddal anti-inflammatory drug that has been used extensively to treat patients with arthritis. The aim of the present study was to formulate and characterize liposomal vesicles loaded with celecoxib. Methods:Liposomes were prepared by thin film method using soya lecithin and cholesterol. The release of drug was determined using a dialysis membrane method. Liposomes were characterized by Differential Scanning Calorimetery (DSC), Transmission Electron Microscopy (TEM) and their particle size was also determined.Results:The results showed that the drug encapsulation efficiency was 67.34% and there was 67.16% release after 0.5, 1, 2, 3, 4, 5, 6, 7, 8 and 24 h. Results of particle size determination showed a mean size of 677nm and nanoparticles were spherical as shown by TEM. The DSC curve of lecithin, cholesterol and celecoxibwere different from celecoxib containing liposome.Conclusion:The results of characterization of the vesicles indicated the potential application of celecoxib loadedliposome as carrier system
机译:目的:塞来昔布是一种非甾体类抗炎药,已广泛用于治疗关节炎患者。本研究的目的是配制和表征载有塞来昔布的脂质体囊泡。方法:利用大豆卵磷脂和胆固醇通过薄膜法制备脂质体。使用透析膜方法确定药物的释放。用差示扫描量热法(DSC),透射电镜(TEM)对脂质体进行了表征,并测定了其粒径。结果:结果表明,包封率分别为67.34%和0.5、1、2、6、6%。 ,3、4、5、6、7、8和24小时。粒度测定结果显示平均粒径为677nm,纳米颗粒呈球形,如T​​EM所示。卵磷脂,胆固醇和塞来昔布的DSC曲线与塞来昔布含脂质体的DSC曲线不同。结论:囊泡的表征结果表明载有塞来昔布脂质体作为载体系统的潜在应用

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