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将氨苄青霉素和庆大霉素功能化用生物合成的铜纳米粒子(CuNPs)改造针对 MDR 临床分离株的抗菌和细胞毒性作用。

Functionalization of ampicillin and gentamicin with biogenic copper nanoparticles (CuNPs) remodel antimicrobial and cytotoxic outcome against MDR clinical isolates.

机构信息

Department of Biotechnology, Fatima Jinnah Women University, Rawalpindi, Pakistan.

Department of Microbiology, Armed Forces Institute of Pathology, Rawalpindi, Pakistan.

出版信息

Arch Microbiol. 2023 Feb 13;205(3):88. doi: 10.1007/s00203-023-03425-y.

Abstract

The present study reports the functionalization of antibiotic-conjugated Alternanthera pungens and Trichodesma indicum copper nanoparticles (CuNPs). Initially, antibiotic profiling of multi-drug resistant (MDR) clinical isolates against five antibiotics was verified and then gentamicin and ampicillin conjugates of CuNPs were prepared. Biosynthesized nanostructures were characterized through UV-visible spectroscopy, Fourier-transformed infrared spectroscopy, X-ray diffraction and scanning electron microscope. Biogenic synthesized CuNPs displayed highest antibacterial activity (24.0-31.3 mm inhibition zones) when capped with gentamicin as compared to the ampicillin-conjugated NPs which showed resistance against most of the bacterial species. A. pungens-derived conjugates of gentamicin (CuAp-GNT) along with the vehicle revealed 4.86 ± 0.20% and 4.25 ± 2.96% hemolytic potential and highest MDA production in S. typhimurium (3.18 ± 1.52 µg/mL and 6.31 ± 3.49 µg/mL) and K. pneumoniae (2.99 ± 0.90 µg/mL and 4.06 ± 1.20 µg/mL). Similarly, CuAp-GNT also showed highest DNA protection ability by displaying 1342.99 ± 11.87 band intensity. All-inclusive, CuAp showed more promising effects when conjugated with gentamicin indicating that capping of gentamicin with the active components of the plant-based copper nanostructures increases the antibacterial capacity of the drug. Hence, conjugation of antibiotics with bio-based sources offers great potential for identifying potent drug leads.

摘要

本研究报告了抗生素偶联的Alternanthera pungens 和 Trichodesma indicum 铜纳米粒子(CuNPs)的功能化。首先,验证了多药耐药(MDR)临床分离株对五种抗生素的抗生素分析,然后制备了庆大霉素和氨苄青霉素偶联的 CuNPs。通过紫外-可见光谱、傅里叶变换红外光谱、X 射线衍射和扫描电子显微镜对生物合成的纳米结构进行了表征。与氨苄青霉素偶联的 NPs 相比,用庆大霉素封端的生物合成 CuNPs 显示出最高的抗菌活性(24.0-31.3 毫米抑制区),而氨苄青霉素偶联的 NPs 对大多数细菌物种表现出耐药性。与载体相比,A. pungens 衍生的庆大霉素偶联物(CuAp-GNT)显示出 4.86 ± 0.20%和 4.25 ± 2.96%的溶血潜能和最高 MDA 产量在 S. typhimurium(3.18 ± 1.52 µg/mL 和 6.31 ± 3.49 µg/mL)和 K. pneumoniae(2.99 ± 0.90 µg/mL 和 4.06 ± 1.20 µg/mL)。同样,CuAp-GNT 还显示出最高的 DNA 保护能力,显示出 1342.99 ± 11.87 条带强度。综上所述,当与庆大霉素偶联时,CuAp 表现出更有前途的效果,表明将庆大霉素与基于植物的铜纳米结构的活性成分偶联可以提高药物的抗菌能力。因此,抗生素与基于生物的来源偶联为识别有效的药物先导物提供了巨大的潜力。

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