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Biodegradable Amphiphilic Tri-block Copolymeric Nanoparticles for Controlled MTB Drug Delivery

机译:用于受控MTB药物递送的可生物降解的两亲三嵌段共聚物纳米颗粒

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A series of biodegradable amphiphilic tri-block copolymers (PLGA-PEG-PLGA) have been derived from the di-block copolymer poly (lactic-co-glycolic acid (PLGA)) and polyethylene glycol (PEG). The mycobacterium tuberculosis (MTB) drag pyrazinamide (PZA) loaded polymer nanoparticles (NPs) have been prepared by probe-sonication followed by w/o/w double emulsification technique. The copolymers have been characterized by FTIR and 'HNMR spectroscopic techniques, TG-DTA analysis, GPC analysis and powder XRD pattern. The MTB drag loaded polymeric NPs have been characterized by FESEM, powder XRD, HRTEM and XPS analysis. The drag loading efficiency, drag content and in vitro drag release studies have been carried out by spectrophotometry. The drug loading efficiency and drug content of triblock copolymeric NPs were higher than these of diblock copolymeric microparticles (MPs). The in vitro drag release studies indicate that the NPs exhibit initial burst release followed by controlled release of PZA for longer durations. The drag release kinetics mechanism has been evaluated by zero order, first order, Korsemeyer-Peppas (KP) and Higuchi models.
机译:一系列生物可降解的两性三嵌段共聚物的(PLGA-PEG-PLGA)已经从二嵌段共聚物的聚(乳酸 - 共 - 乙醇酸(PLGA))和聚乙二醇(PEG)衍生的。结核分枝杆菌(MTB)拖动吡嗪酰胺(PZA)加载聚合物纳米颗粒(NP)已被制备探针超声处理,随后的w / o / w的双重乳化技术。该共聚物已经用FTIR和“技术HNMR光谱,TG-DTA分析,GPC分析和粉末X射线衍射图案。的MTB拖动加载聚合物纳米粒的特点是FESEM,粉末XRD,HRTEM和XPS分析。拖动装载效率,阻力含量和体外药物释放的研究已经通过分光光度法完成。载药量和三嵌段共聚物纳米颗粒的药物含量均低于这些嵌段共聚物微粒(MPS)的高。体外药物释放研究表明,纳米颗粒显示出初始突释,随后更长的持续时间PZA的受控释放。牵引解除动力学机制已经由零级,一级,Korsemeyer-Peppas(KP)和樋口模型中评估。

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