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首页> 外文期刊>Biochemical Engineering Journal >Chitosan microparticles ionically cross-linked with poly(gamma-glutamic acid) as antimicrobial peptides and nitric oxide delivery systems
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Chitosan microparticles ionically cross-linked with poly(gamma-glutamic acid) as antimicrobial peptides and nitric oxide delivery systems

机译:壳聚糖微粒与聚(γ-谷氨酸)离子交联作为抗菌肽和一氧化氮传递系统

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摘要

The emergence of antibiotic resistance influences the effective development of therapeutics. In this paper, chitosan (CS) and poly-gamma-glutamic acid (gamma-PGA) composite microparticles were prepared and characterized as carriers for antimicrobial peptides (LL-37) and nitric oxide (NO) delivery systems. Using ionic complexation between the positively charged LL-37 and the negatively charged polyelectrolyte gamma-PGA, gamma-PGA/LL-37 microparticles with negative zeta potentials were produced. Transmission and scanning electron microscopy revealed that complexation of gamma-PGA and LL-37 alone leads to nanostructures with irregular shapes; addition of a third component, CS, is required. gamma-PGA/LL-37 composite microparticles were rewrapped by CS to obtain LL-37 loaded spherical CS/gamma-PGA composite microparticles. NO was further loaded on microparticles by the reaction of NO and LL-37 loaded CS/gamma-PGA composite microparticles under high NO pressure. The results indicated that both LL-37 and NO were co-loaded successfully in microparticles, and the composite particles could sustain LL-37 and NO release at pH 7.4, in vitro. (C) 2014 Published by Elsevier B.V.
机译:抗生素抗性的出现影响治疗剂的有效开发。在本文中,制备了壳聚糖(CS)和聚γ-谷氨酸(γ-PGA)复合微粒,并将其表征为抗菌肽(LL-37)和一氧化氮(NO)输送系统的载体。使用带正电的LL-37和带负电的聚电解质γ-PGA之间的离子络合,可制得具有负ζ电位的γ-PGA/ LL-37微粒。透射电子显微镜和扫描电子显微镜显示,仅γ-PGA和LL-37的络合会形成具有不规则形状的纳米结构。需要添加第三个组件CS。通过CS将γ-PGA/ LL-37复合微粒包裹,以获得负载有LL-37的球形CS /γ-PGA复合微粒。通过NO和LL-37负载的CS /γ-PGA复合微粒在高NO压力下的反应,NO进一步负载在微粒上。结果表明,LL-37和NO均成功地负载在微粒中,并且复合颗粒在体外能在pH 7.4下维持LL-37和NO的释放。 (C)2014由Elsevier B.V.发布

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