Unveiling Synergistic Antimicrobial Action with Nisin-Silver Nanoconjugate-Loaded Dissolving Microneedles

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Dnyaneshwari Domb, Pravin Shende
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Abstract

Purpose

The research aimed to develop nisin-silver nanoconjugates within a dissolving microneedle formulation using green synthesis chemistry and solvent casting methods. The objective was to assess potential of these nanoconjugates to enhance antimicrobial efficacy against gram-positive and gram-negative bacteria, such as Bacillus subtilis and Escherichia coli, offering an alternative to conventional antibiotics that often cause resistance and side effects.

Methods

Nisin-silver nanoconjugates were developed using green synthesis chemistry and incorporated into dissolving microneedles through solvent casting methods. Optimization was conducted using 32 factorial design. Characterization included measuring particle size (288 ± 5.49 nm), polydispersity index (0.381 ± 0.57), and zeta potential (-21.4 ± 1.54 mV). ATR-FTIR studies confirmed conjugation by identifying a characteristic C-O-C stretch peak at 1019 cm^-1, and DSC studies revealed an endothermic peak at 242 °C. The microneedle formulation was tested for in-vitro release of Nisin Z over 48 h. Antimicrobial efficacy was assessed using agar disc diffusion method, demonstrating significant zones of inhibition against Bacillus subtilis, Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa.

Results

The microneedle formulation (DMN 3) showed in-vitro release of 85.03 ± 0.53% over 48 h. The antimicrobial efficacy tests showed significant inhibition zones for Bacillus subtilis (20 ± 0.5 mm), Escherichia coli (12 ± 4 mm), Staphylococcus aureus (19 ± 4 mm), and Pseudomonas aeruginosa (11 ± 3 mm).

Conclusion

The study successfully developed nisin-silver nanoconjugates incorporated into dissolving microneedles. These nanoconjugates demonstrated synergistic antimicrobial action, showing promise for treating bacterial infections effectively. This suggests they could be viable alternative to traditional antibiotics, potentially reducing the risks of resistance and side effects associated with conventional treatments.

Abstract Image

目的 该研究旨在利用绿色合成化学和溶剂浇铸方法,在可溶微针配方中开发尼生素-银纳米共轭物。目的是评估这些纳米共轭物在增强对革兰氏阳性和革兰氏阴性细菌(如枯草杆菌和大肠杆菌)的抗菌效力方面的潜力,从而为经常导致耐药性和副作用的传统抗生素提供一种替代品。采用 32 个因子设计进行了优化。表征包括测量粒度(288 ± 5.49 nm)、多分散指数(0.381 ± 0.57)和 zeta 电位(-21.4 ± 1.54 mV)。ATR-FTIR 研究通过确定 1019 cm^-1 处的特征性 C-O-C 伸展峰确认了共轭作用,DSC 研究显示了 242 °C 处的内热峰。使用琼脂盘扩散法评估了抗菌效果,结果显示对枯草杆菌、大肠杆菌、金黄色葡萄球菌和铜绿假单胞菌有显著的抑制作用。抗菌效力测试显示,对枯草杆菌(20 ± 0.5 mm)、大肠杆菌(12 ± 4 mm)、金黄色葡萄球菌(19 ± 4 mm)和铜绿假单胞菌(11 ± 3 mm)有明显的抑制区。这些纳米共轭物具有协同抗菌作用,有望有效治疗细菌感染。这表明它们可以成为传统抗生素的可行替代品,有可能降低耐药性风险和与传统疗法相关的副作用。
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来源期刊
Journal of Pharmaceutical Innovation
Journal of Pharmaceutical Innovation PHARMACOLOGY & PHARMACY-
CiteScore
3.70
自引率
3.80%
发文量
90
审稿时长
>12 weeks
期刊介绍: The Journal of Pharmaceutical Innovation (JPI), is an international, multidisciplinary peer-reviewed scientific journal dedicated to publishing high quality papers emphasizing innovative research and applied technologies within the pharmaceutical and biotechnology industries. JPI''s goal is to be the premier communication vehicle for the critical body of knowledge that is needed for scientific evolution and technical innovation, from R&D to market. Topics will fall under the following categories: Materials science, Product design, Process design, optimization, automation and control, Facilities; Information management, Regulatory policy and strategy, Supply chain developments , Education and professional development, Journal of Pharmaceutical Innovation publishes four issues a year.
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