{"title":"Nanoengineered phosphorus doped graphitic carbon nitride based ultrasensitive biosensing platform for Swine flu detection","authors":"Vishakha Nirbhaya , Ramesh Chandra , Suveen Kumar","doi":"10.1016/j.colsurfb.2023.113504","DOIUrl":null,"url":null,"abstract":"<div><p><span>In the present study, we developed an amino-polyindole modified phosphorus doped graphitic carbon nitride<span> nanomaterial (APIN/P-g-C</span></span><sub>3</sub>N<sub>4</sub><span>) based immunosensing biochip<span> for Serum amyloid A (SAA) biomarker towards early diagnosis of Swine flu. The P-g-C</span></span><sub>3</sub>N<sub>4</sub><span> was synthesis via polycondensation and functionalized with APIN. Further, the biochip was fabricated by modifying the working area of SPE with APIN/P-g-C</span><sub>3</sub>N<sub>4</sub> using drop cast method, APIN introduced the larger loading of -NH<sub>2</sub> group moieties onto P-g-C<sub>3</sub>N<sub>4</sub> matrix and benefitted to reinforced the biomolecules via covalent linkages. The monoclonal anti-SAA was conjugated onto APIN/P-g-C<sub>3</sub>N<sub>4</sub><span>/SPE using EDC-NHS chemistry<span><span><span><span> and BSA<span> was added for non-specific site blocking. The structural, chemical, composition and </span></span>morphological characteristics<span> of the synthesized, functionalized nanomaterial and fabricated biochips were investigated by XRD, </span></span>XPS<span>, FT-IR spectroscopy, SEM, FE-SEM and TEM techniques. Further, the electrochemical characterization and response studies of fabricated biochip were analyzed using the CV and </span></span>DPV techniques. Based on the analytical performance of the proposed immunosensing biochip i.e. BSA/anti-SAA/APIN/P-g-C</span></span><sub>3</sub>N<sub>4</sub><span>/SPE, it is capable to detect SAA protein with ultra sensitivity of 79.5 μA log (mL ng</span><sup>−1</sup>) cm<sup>−2</sup>, ultralow limit of detection of 5 ng mL<sup>−1</sup> and wider linear detection range of 5 ng mL<sup>−1</sup>-500 μg mL<sup>−1</sup> with quick response time of 10 min. Moreover, the fabricated immunosensing biochips was used to analyse SAA protein in spiked serum samples and the achieved results demonstrated the good agreement with the electrochemical response observed in standard SAA protein samples in analytical solution. The proposed biochip can provide insights for developing a wide range of clinical screening tools for detecting various contagious diseases.</p></div>","PeriodicalId":279,"journal":{"name":"Colloids and Surfaces B: Biointerfaces","volume":"230 ","pages":"Article 113504"},"PeriodicalIF":5.4000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Colloids and Surfaces B: Biointerfaces","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S092777652300382X","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 1
Abstract
In the present study, we developed an amino-polyindole modified phosphorus doped graphitic carbon nitride nanomaterial (APIN/P-g-C3N4) based immunosensing biochip for Serum amyloid A (SAA) biomarker towards early diagnosis of Swine flu. The P-g-C3N4 was synthesis via polycondensation and functionalized with APIN. Further, the biochip was fabricated by modifying the working area of SPE with APIN/P-g-C3N4 using drop cast method, APIN introduced the larger loading of -NH2 group moieties onto P-g-C3N4 matrix and benefitted to reinforced the biomolecules via covalent linkages. The monoclonal anti-SAA was conjugated onto APIN/P-g-C3N4/SPE using EDC-NHS chemistry and BSA was added for non-specific site blocking. The structural, chemical, composition and morphological characteristics of the synthesized, functionalized nanomaterial and fabricated biochips were investigated by XRD, XPS, FT-IR spectroscopy, SEM, FE-SEM and TEM techniques. Further, the electrochemical characterization and response studies of fabricated biochip were analyzed using the CV and DPV techniques. Based on the analytical performance of the proposed immunosensing biochip i.e. BSA/anti-SAA/APIN/P-g-C3N4/SPE, it is capable to detect SAA protein with ultra sensitivity of 79.5 μA log (mL ng−1) cm−2, ultralow limit of detection of 5 ng mL−1 and wider linear detection range of 5 ng mL−1-500 μg mL−1 with quick response time of 10 min. Moreover, the fabricated immunosensing biochips was used to analyse SAA protein in spiked serum samples and the achieved results demonstrated the good agreement with the electrochemical response observed in standard SAA protein samples in analytical solution. The proposed biochip can provide insights for developing a wide range of clinical screening tools for detecting various contagious diseases.
在本研究中,我们开发了一种基于氨基多吲哚修饰的磷掺杂石墨氮化碳纳米材料(APIN/P-g-C3N4)的免疫传感生物芯片,用于血清淀粉样蛋白A(SAA)生物标志物,以早期诊断猪流感。通过缩聚反应合成了P-g-C3N4,并用APIN对其进行了功能化。此外,通过滴注法用APIN/P-g-C3N4修饰SPE的工作面积来制备生物芯片,APIN在P-g-C3N3基体上引入了更大的-NH2基团部分负载量,并有利于通过共价键增强生物分子。使用EDC-NHS化学将单克隆抗SAA偶联到APIN/P-g-C3N4/SPE上,并加入BSA进行非特异性位点阻断。利用XRD、XPS、FT-IR、SEM、FE-SEM和TEM等技术对合成的功能化纳米材料和制备的生物芯片的结构、化学、组成和形态特征进行了研究。此外,使用CV和DPV技术分析了所制备的生物芯片的电化学特性和响应研究。基于所提出的免疫传感生物芯片BSA/抗SAA/APIN/P-g-C3N4/SPE的分析性能,它能够检测SAA蛋白,具有79.5μA log(mL ng-1)cm-2的超灵敏、5 ng mL-1的超低检测极限和5 ng mL-1-500μg mL-1的较宽线性检测范围,快速响应时间为10分钟。此外,将所制备的免疫传感生物芯片用于分析加标血清样品中的SAA蛋白,所获得的结果与分析溶液中标准SAA蛋白样品中观察到的电化学反应非常一致。所提出的生物芯片可以为开发用于检测各种传染病的广泛临床筛查工具提供见解。
期刊介绍:
Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields.
Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication.
The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.