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首页> 外文期刊>American Journal of PharmTech Research >Span 60 Niosomes of Silver Sulfadiazine: A Localized Sustained Release System for Burn Treatment
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Span 60 Niosomes of Silver Sulfadiazine: A Localized Sustained Release System for Burn Treatment

机译:磺胺嘧啶银跨度60尼索:用于烧伤治疗的局部缓释系统

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ABSTRACT This investigation deals with the formulation of sustained release niosome based system of silver sulfadiazine for the treatment of burn and thereby decreasing the dosing frequency which is really important for severe burn patient as every reapplication is very painful to them. In this investigation, the effect of different processing variables on entrapment efficiency of drug was evaluated. The vesicle size, photomicroscopy, in vitro release, scanning electron microscopy, stability and in vitro antimicrobial activity of niosomal vesicles formed were also characterized. Niosomes were developed from span 60 and cholesterol in different molar ratio by ether injection, thin film hydration and non solvent methods. Results indicated that the niosomes manufactured with span 60 and cholesterol in 50:50 molar ratio using 100mg of drug by thin film hydration method gives highest entrapment of 92.11%. The method of preparation and contents of cholesterol as well as drug were found to affect the entrapment. The optimized niosomal formulation exhibited significantly retarded in vitro release of 98.04% over 28 hours by a higuchi controlled mechanism. The in vitro antimicrobial study using Staphylococcus aureus revealed that niosomal formulation of silver sulfadiazine shows better zone of inhibition (18mm) in comparison to conventional dosage form (17mm). In conclusion this study showed that the niosomal formulation can be used as promising sustained release approach for the topical delivery of silver sulfadiazine in the treatment of burn. Keywords: Silver sulfadiazine; Antimicrobial study; Burn; Entrapment efficiency; Span 60
机译:摘要这项研究涉及用于治疗烧伤的持续释放基于脂质体的磺胺嘧啶银系统的配方,从而降低了给药频率,这对于重度烧伤患者而言确实非常重要,因为每次重新使用都使他们非常痛苦。在这项研究中,评估了不同加工变量对药物包封效率的影响。还表征了所形成的脂质体囊泡的囊泡大小,显微镜,体外释放,扫描电子显微镜,稳定性和体外抗菌活性。通过醚注入,薄膜水化和非溶剂方法,从60跨度和不同摩尔比的胆固醇中开发出了脂质体。结果表明,通过薄膜水化法,使用100mg药物,以60:50的摩尔比和60的胆固醇制造的脂质体的最高包封率为92.11%。发现胆固醇和药物的制备方法和含量会影响包封。通过水口控制机制,优化的蛋白质组制剂在28小时内显示出98.04%的体外释放显着延迟。使用金黄色葡萄球菌进行的体外抗菌研究表明,与常规剂型(17mm)相比,磺胺嘧啶银的尼古丁制剂显示出更好的抑制区(18mm)。综上所述,该研究表明,该氟尿嘧啶制剂可作为有希望的缓释方法用于局部递送磺胺嘧啶银治疗烧伤。关键字:磺胺嘧啶银;抗菌研究;烧伤;包封效率;跨度60

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