Antibacterial activity of a novel glycyrrhizic acid-loaded chitosan composite nanogel in vitro against Staphylococcus aureus small colony variants.

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY Current drug delivery Pub Date : 2023-01-17 DOI:10.2174/1567201820666230117150253
Mujie Ju, Jinhuan Liu, Ding Guan, Nannan Leng, Samah Attia Algharib, Ali Sobhy Dawood, Wanhe Luo
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Abstract

Background This study aimed to improve the sustained and controlled release of glycyrrhizic acid to the infected site of Staphylococcus aureus small colony variants (SCVs). Methods The glycyrrhizic acid-loaded chitosan composite nanogel was prepared by inclusion action, Schiff's base formation, and electrostatic action. Furthermore, the formulation screening, characteristics, in vitro release, and antibacterial activity of the glycyrrhizic acid composite nanogel were explored. Results The final optimal formula comprised 10 mg/mL (chitosan) and 50 μL (glutaraldehyde). The loading capacity, encapsulation efficiency, mean size, polydispersity index, and zeta potential were 8.8%±1.6%, 92.1%±2.8%, 478.3±2.8 nm, 0.37±0.10, and 25.3±3.6 mv, respectively. Scanning electron microscope images showed a spherical shape with a relatively uniform distribution. The in vitro release study showed that glycyrrhizic acid composite nanogel exhibited a biphasic pattern with a sustained release of 52.1%±2.0% at 48 h in the pH 5.5 PBS. The minimum inhibitory and minimum biofilm inhibitory concentrations of glycyrrhizic acid composite nanogel against SCVs were 0.625 μg/mL. The time-killing curves and live/dead bacterial staining showed that glycyrrhizic acid composite nanogel had a stronger curative effect against SCVs strain with concentration-dependent. Conclusion This study provides promising glycyrrhizic acid composite nanogel to improve the treatment of SCV infection.

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新型甘草酸负载壳聚糖复合纳米凝胶在体外对金黄色葡萄球菌小菌落变种的抗菌活性。
背景 本研究旨在改善甘草酸对金黄色葡萄球菌小菌落变种(SCVs)感染部位的持续和可控释放。方法 通过包涵作用、席夫碱形成和静电作用制备了载甘草酸的壳聚糖复合纳米凝胶。此外,还探讨了甘草酸复合纳米凝胶的配方筛选、特性、体外释放和抗菌活性。结果 最终的最佳配方为 10 mg/mL(壳聚糖)和 50 μL(戊二醛)。载量、包封效率、平均尺寸、多分散指数和 zeta 电位分别为 8.8%±1.6%、92.1%±2.8%、478.3±2.8 nm、0.37±0.10 和 25.3±3.6 mv。扫描电子显微镜图像显示其呈球形,分布相对均匀。体外释放研究表明,甘草酸复合纳米凝胶呈现出双相模式,在 pH 值为 5.5 的 PBS 中,48 小时的持续释放率为 52.1%±2.0%。甘草酸复合纳米凝胶对 SCV 的最小抑制浓度和最小生物膜抑制浓度均为 0.625 μg/mL。时间杀灭曲线和活/死细菌染色表明,甘草酸复合纳米凝胶对 SCVs 菌株有更强的抑制作用,且与浓度有关。结论 本研究为甘草酸复合纳米凝胶改善 SCV 感染的治疗提供了前景。
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来源期刊
Current drug delivery
Current drug delivery PHARMACOLOGY & PHARMACY-
CiteScore
5.10
自引率
4.20%
发文量
170
期刊介绍: Current Drug Delivery aims to publish peer-reviewed articles, research articles, short and in-depth reviews, and drug clinical trials studies in the rapidly developing field of drug delivery. Modern drug research aims to build delivery properties of a drug at the design phase, however in many cases this idea cannot be met and the development of delivery systems becomes as important as the development of the drugs themselves. The journal aims to cover the latest outstanding developments in drug and vaccine delivery employing physical, physico-chemical and chemical methods. The drugs include a wide range of bioactive compounds from simple pharmaceuticals to peptides, proteins, nucleotides, nucleosides and sugars. The journal will also report progress in the fields of transport routes and mechanisms including efflux proteins and multi-drug resistance. The journal is essential for all pharmaceutical scientists involved in drug design, development and delivery.
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