Division of Pharmaceutics, Department of Pharmaceutical Tecnology, Kolkata-700032, W.B., India.
Division of Pharmaceutics, Department of Pharmaceutical Tecnology, Kolkata-700032, W.B., India.
Colloids Surf B Biointerfaces. 2014 Feb 1;114:36-44. doi: 10.1016/j.colsurfb.2013.09.045. Epub 2013 Sep 30.
In the present work, various aceclofenac-loaded chitosan-egg albumin nanoparticles were prepared through heat coagulation method. These aceclofenac-loaded nanoparticles were characterized by FE-SEM, FTIR, DSC and P-XRD analyses. The in vitro drug release from nanoparticles showed sustained drug release over 8h. Aceclofenac-loaded nanoparticles (prepared using 200mg chitosan, 500 mg egg albumin and 2% (w/v) NaTPP) showed highest drug entrapment (96.32±1.52%), 352.90 nm average particle diameter and -22.10 mV zeta potential, which was used for further preparation of Carbopol 940 gel for transdermal application. The prepared gel exhibited sustained ex vivo permeation of aceclofenac over 8h through excised mouse skin. The in vivo anti-inflammatory activity in carrageenean-induced rats demonstrated comparative higher inhibition of swelling of rat paw edema by the prepared gel compared with that of the marketed aceclofenac gel over 4 h.
在本工作中,通过热凝聚法制备了各种负载双氯芬酸的壳聚糖-卵清蛋白纳米粒子。通过 FE-SEM、FTIR、DSC 和 P-XRD 分析对这些负载双氯芬酸的纳米粒子进行了表征。纳米粒子的体外药物释放显示出 8 小时以上的持续药物释放。负载双氯芬酸的纳米粒子(使用 200mg 壳聚糖、500mg 卵清蛋白和 2%(w/v)NaTPP 制备)显示出最高的药物包封率(96.32±1.52%)、352.90nm 的平均粒径和-22.10mV 的 Zeta 电位,这被用于进一步制备卡波姆 940 凝胶用于透皮应用。所制备的凝胶通过离体小鼠皮肤显示出双氯芬酸的持续体外渗透,在卡拉胶诱导的大鼠中进行的体内抗炎活性研究表明,与市售的双氯芬酸钠凝胶相比,在 4 小时内,所制备的凝胶对大鼠足肿胀的抑制作用更高。
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