{"title":"血浆天然荧光特性在口腔潜在恶性疾病早期诊断中的应用。","authors":"Pravda Chidambaranathan, Rajvikram Natarajan, Divyambika Catakapatri Venugopal, Saravanan Ramachandran, Jamal Mohamed Thoufeeq, Anandh Sundaramoorthy, Singaravelu Ganesan, Aruna Prakasarao","doi":"10.1007/s12013-025-01779-2","DOIUrl":null,"url":null,"abstract":"<p><p>Oral potentially malignant disorders (PMD) are heterogenous group of oral conditions characterized by increased risk of malignant transformation that are commonly diagnosed clinically and treated. Tissue biopsy is an invasive tool for diagnosis of oral PMDs. Native fluorescence spectroscopy of biofluids has been considered as an alternative and/or complimentary tool in the characterization of tissues of various pathological conditions. In the present study, it is primarily aimed to characterize different fluorophores present in the blood plasma of normal subjects and PMD patients, using excitation-emission matrix (EEM) and to compare their diagnostic potentials in delineating PMD cases from normal subjects. From EEM measurements of blood plasma, it was observed that there is a maximum emission around 340 ± 5 nm at 307 ± 3 nm excitation for normal subjects and around 337 ± 5 nm emission at 300 ± 3 nm excitation for PMD patients. In addition to the maxima, the contours exhibit other secondary emissions such as 480 ± 5 nm at 335 ± 3 nm excitation for both normal and PMD blood plasma. It was also observed that an emission at 520 ± 5 nm for 440 ± 3 nm excitation is seen for PMD blood plasma and the same is absent in the cases of normal blood plasma. The three contours centred around 340, 480 and 520 nm may be attributed to emissions from tryptophan, NADH and FAD, respectively. Results of stepwise multiple linear discriminant analysis reveal that fluorescence spectral features of NADH classify samples more effectively with 100% sensitivity and 95% specificity.</p>","PeriodicalId":510,"journal":{"name":"Cell Biochemistry and Biophysics","volume":" ","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Native Fluorescence Characterization of Blood Plasma for Early Diagnosis of Oral Potentially Malignant Disorders.\",\"authors\":\"Pravda Chidambaranathan, Rajvikram Natarajan, Divyambika Catakapatri Venugopal, Saravanan Ramachandran, Jamal Mohamed Thoufeeq, Anandh Sundaramoorthy, Singaravelu Ganesan, Aruna Prakasarao\",\"doi\":\"10.1007/s12013-025-01779-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Oral potentially malignant disorders (PMD) are heterogenous group of oral conditions characterized by increased risk of malignant transformation that are commonly diagnosed clinically and treated. Tissue biopsy is an invasive tool for diagnosis of oral PMDs. Native fluorescence spectroscopy of biofluids has been considered as an alternative and/or complimentary tool in the characterization of tissues of various pathological conditions. In the present study, it is primarily aimed to characterize different fluorophores present in the blood plasma of normal subjects and PMD patients, using excitation-emission matrix (EEM) and to compare their diagnostic potentials in delineating PMD cases from normal subjects. From EEM measurements of blood plasma, it was observed that there is a maximum emission around 340 ± 5 nm at 307 ± 3 nm excitation for normal subjects and around 337 ± 5 nm emission at 300 ± 3 nm excitation for PMD patients. In addition to the maxima, the contours exhibit other secondary emissions such as 480 ± 5 nm at 335 ± 3 nm excitation for both normal and PMD blood plasma. It was also observed that an emission at 520 ± 5 nm for 440 ± 3 nm excitation is seen for PMD blood plasma and the same is absent in the cases of normal blood plasma. The three contours centred around 340, 480 and 520 nm may be attributed to emissions from tryptophan, NADH and FAD, respectively. Results of stepwise multiple linear discriminant analysis reveal that fluorescence spectral features of NADH classify samples more effectively with 100% sensitivity and 95% specificity.</p>\",\"PeriodicalId\":510,\"journal\":{\"name\":\"Cell Biochemistry and Biophysics\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2025-05-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell Biochemistry and Biophysics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s12013-025-01779-2\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Biochemistry and Biophysics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s12013-025-01779-2","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Native Fluorescence Characterization of Blood Plasma for Early Diagnosis of Oral Potentially Malignant Disorders.
Oral potentially malignant disorders (PMD) are heterogenous group of oral conditions characterized by increased risk of malignant transformation that are commonly diagnosed clinically and treated. Tissue biopsy is an invasive tool for diagnosis of oral PMDs. Native fluorescence spectroscopy of biofluids has been considered as an alternative and/or complimentary tool in the characterization of tissues of various pathological conditions. In the present study, it is primarily aimed to characterize different fluorophores present in the blood plasma of normal subjects and PMD patients, using excitation-emission matrix (EEM) and to compare their diagnostic potentials in delineating PMD cases from normal subjects. From EEM measurements of blood plasma, it was observed that there is a maximum emission around 340 ± 5 nm at 307 ± 3 nm excitation for normal subjects and around 337 ± 5 nm emission at 300 ± 3 nm excitation for PMD patients. In addition to the maxima, the contours exhibit other secondary emissions such as 480 ± 5 nm at 335 ± 3 nm excitation for both normal and PMD blood plasma. It was also observed that an emission at 520 ± 5 nm for 440 ± 3 nm excitation is seen for PMD blood plasma and the same is absent in the cases of normal blood plasma. The three contours centred around 340, 480 and 520 nm may be attributed to emissions from tryptophan, NADH and FAD, respectively. Results of stepwise multiple linear discriminant analysis reveal that fluorescence spectral features of NADH classify samples more effectively with 100% sensitivity and 95% specificity.
期刊介绍:
Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems
The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized.
Examples of subject areas that CBB publishes are:
· biochemical and biophysical aspects of cell structure and function;
· interactions of cells and their molecular/macromolecular constituents;
· innovative developments in genetic and biomolecular engineering;
· computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies;
· photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design
For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.