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Levan-based nanocarrier system for peptide and protein drug delivery: Optimization and influence of experimental parameters on the nanoparticle characteristics

机译:基于Levan的用于肽和蛋白质药物递送的纳米载体系统:优化和实验参数对纳米粒子特性的影响

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摘要

Microbial levans are biopolymers produced from sucrose-based substrates by a variety of microorganisms. There is very limited information related to the levan-based drug delivery systems. In this study, bovine serum albumin (BSA) encapsulated-levan nanoparticles were prepared using levan produced by a new Halomonas sp. Effects of polymer and BSA concentrations and rotating speed on in vitro characterization of the nanoparticles were investigated. The size of levan nanoparticles, with the surface charges +4.3 mV to +7.6 mV, changed between 200 nm and 537 nm. The encapsulation capacity of the particles changed between 49.3% and 71.3% depending on the levan concentration used in the formulation. The cumulative in vitro release of protein from the particles was shown to be controlled release of BSA. This study affirmed the suitability of levan by Halomonas sp. to be used as a nanocarrier system for potential delivery of macromolecular drugs such as peptides and proteins.
机译:微生物左旋聚糖是由多种微生物从基于蔗糖的底物中产生的生物聚合物。与基于levan的药物输送系统有关的信息非常有限。在这项研究中,牛血清白蛋白(BSA)封装的levan纳米颗粒是使用新型Halomonas sp。生产的levan制备的。研究了聚合物和BSA浓度以及转速对纳米粒子体外表征的影响。带有表面电荷+4.3 mV至+7.6 mV的levan纳米粒子的大小在200 nm至537 nm之间变化。取决于制剂中所用的levan浓度,颗粒的包封能力在49.3%至71.3%之间变化。蛋白质从颗粒中的累积体外释放被证明是BSA的受控释放。这项研究证实了Halomonas sp。用作纳米载体系统,可潜在地输送大分子药物,例如肽和蛋白质。

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