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1-丁基-3-己基-1-咪唑-2(3)-硒酮的合成、表征及其抗真菌活性的表面增强拉曼光谱评价

Synthesis, Characterization, and Evaluation of Antifungal Activity of 1-Butyl-3-hexyl-1-imidazol-2(3)-selenone by Surface-Enhanced Raman Spectroscopy.

作者信息

Huda Noor Ul, Wasim Muhammad, Nawaz Haq, Majeed Muhammad Irfan, Javed Muhammad Rizwan, Rashid Nosheen, Iqbal Muhammad Adnan, Tariq Anam, Hassan Ahmad, Akram Muhammad Waseem, Jamil Faisal, Imran Muhammad

机构信息

Department of Chemistry, University of Agriculture Faisalabad, Faisalabad 38000, Pakistan.

Department of Bioinformatics and Biotechnology, Government College University Faisalabad (GCUF), Faisalabad 38000, Pakistan.

出版信息

ACS Omega. 2023 Sep 21;8(39):36460-36470. doi: 10.1021/acsomega.3c05436. eCollection 2023 Oct 3.

DOI:10.1021/acsomega.3c05436
PMID:37810682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10552477/
Abstract

In the present research work, a selenium N-heterocyclic carbene (Se-NHC) complex/adduct was synthesized and characterized by using different analytical methods including FT-IR, HNMR, and CNMR. The antifungal activity of the Se-NHC complex against () fungus was investigated with disc diffusion assay. Moreover, the biochemical changes occurring in this fungus due to exposure of different concentrations of the in-house synthesized compound are characterized by surface-enhanced Raman spectroscopy (SERS) and are illustrated in the form of SERS spectral peaks. SERS analysis yields valuable information about the probable mechanisms responsible for the antifungal effects of the Se-NHC complex. As demonstrated by the SERS spectra, this Se-NHC complex caused denaturation and conformational changes in the proteins as well as decomposition of the fungal cell membrane. The SERS spectra were analyzed using two chemometric tools such as principal component analysis (PCA) and partial least-squares discriminant analysis (PLS-DA). The fungal samples' SERS spectra were differentiated using PCA, while various groups of spectra were discriminated with ultrahigh sensitivity (98%), high specificity (99.7%), accuracy (100%), and area under the receiver operating characteristic curve (87%) using PLS-DA.

摘要

在本研究工作中,合成了一种硒氮杂环卡宾(Se-NHC)配合物/加合物,并使用包括傅里叶变换红外光谱(FT-IR)、核磁共振氢谱(HNMR)和核磁共振碳谱(CNMR)在内的不同分析方法对其进行了表征。采用纸片扩散法研究了Se-NHC配合物对()真菌的抗真菌活性。此外,通过表面增强拉曼光谱(SERS)对该真菌因暴露于不同浓度的自制化合物而发生的生化变化进行了表征,并以SERS光谱峰的形式进行了说明。SERS分析提供了有关Se-NHC配合物抗真菌作用可能机制的有价值信息。如SERS光谱所示,这种Se-NHC配合物导致蛋白质变性和构象变化以及真菌细胞膜分解。使用主成分分析(PCA)和偏最小二乘判别分析(PLS-DA)这两种化学计量学工具对SERS光谱进行了分析。使用PCA区分了真菌样品的SERS光谱,而使用PLS-DA以超高灵敏度(98%)、高特异性(99.7%)、准确度(100%)和受试者工作特征曲线下面积(87%)区分了不同组的光谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/bea122a11c24/ao3c05436_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/a30c43306993/ao3c05436_0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/7e17b7270d03/ao3c05436_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/bea122a11c24/ao3c05436_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/a30c43306993/ao3c05436_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/bba2b75dca3a/ao3c05436_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/1fe863e54e31/ao3c05436_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/70da2defb410/ao3c05436_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/788307ef4661/ao3c05436_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/ea9f1f792d97/ao3c05436_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/c4c7ba723389/ao3c05436_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/7e17b7270d03/ao3c05436_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60b/10552477/bea122a11c24/ao3c05436_0009.jpg

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