鼠李糖脂制备氟康唑负载plga纳米颗粒的抗生物膜效果评价

IF 0.5 Q4 MULTIDISCIPLINARY SCIENCES
A. Üstün, Serkan Örtucu
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引用次数: 0

摘要

本研究以聚乙烯醇(PVA)和PVA-鼠李糖脂(R)两种不同的配方制备了负载氟康唑(FLZ)的聚乳酸-羟基乙酸(PLGA)纳米颗粒(NPs),以提高其对白色念珠菌ATCC 90028的抗菌膜活性。比较了这些制剂的包封效率、载药量、体外释放度、表征及抗生物膜活性。利用扫描电子显微镜(SEM)和Zetasizer分析了NPs的表征。用分光光度法测定载药量和包封率。PLGA-NPs呈球形,平均尺寸为~300 nm, FLZ负载的PVA和PVA- r - plga NPs的表面电荷分别为-25、9±1.99、-48、1±2.46。PVA-R PLGA-NPs中FLZ的缓释(6 h后≥60%)。PVA-FLZ-PLGA和PVA-R-FLZ-PLGA的包封率分别为50%和85%。抗菌膜抑制率分别为55%和63%。这些结果表明PVA-R-FLZ-PLGA给药系统是一种新的治疗白色念珠菌感染的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EVALUATION OF THE ANTIBIOFILM EFFECT OF FLUCONAZOLE LOADED PLGA NANOPARTICLES PREPARED USING RHAMNOLIPID
In this study, fluconazole(FLZ) loaded poly(lactic-co-glycolic acid) (PLGA) nanoparticles(NPs) were prepared with two different formulations consisting of polyvinyl alcohol(PVA) and PVA-rhamnolipid(R) in order to improve antibiofilm activity against Candida albicans ATCC 90028. The encapsulation efficiency, drug loading capacity, in-vitro release, characterization and antibiofilm activity of these formulations were compared. Characterization of NPs were analyzed by scanning electron microscopy(SEM) and Zetasizer. Drug loading capacity and encapsulation efficiency percentages were measured by spectrophotometric method. PLGA-NPs were spherical in shape with mean sizes of ~300 nm and surface charge of FLZ loaded PVA and PVA-R-PLGA NPs -25,9±1.99, -48,1±2.46, respectively. Sustained release of FLZ (≥60% after 6 h) were obtained in PVA-R PLGA-NPs. The encapsulation efficiency percentages of PVA-FLZ-PLGA and PVA-R-FLZ-PLGA were 50% and %85 respectively. Antibiofilm inhibition percentages are 55% and 63% respectively. These results show that the PVA-R-FLZ-PLGA drug delivery system is a new therapeutic approach that can be used in infections caused by C.albicans.
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来源期刊
Trakya University Journal of Natural Sciences
Trakya University Journal of Natural Sciences MULTIDISCIPLINARY SCIENCES-
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