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ArticleCell biochemistry and biophysics2025

Native Fluorescence Characterization of Blood Plasma for Early Diagnosis of Oral Potentially Malignant Disorders.

Pravda Chidambaranathan, Rajvikram Natarajan, Divyambika Catakapatri Venugopal, Saravanan Ramachandran, Jamal Mohamed Thoufeeq, Anandh Sundaramoorthy, Singaravelu Ganesan, Aruna Prakasarao

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Article in Cell biochemistry and biophysics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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8 authors.

Pravda ChidambaranathanDepartment of Oral Medicine & Radiology, Dr.M.G.R. Educational and Research Institute, Chennai, Tamil Nadu, India. drcpravda.dental@sathyabama.ac.in.
Rajvikram NatarajanDepartment of Orthodontics, Dr.M.G.R. Educational and Research Institute, Chennai, Tamil Nadu, India.
Divyambika Catakapatri VenugopalDepartment of Oral Medicine & Radiology, Sri Ramachandra Dental College & Hospital, Chennai, Tamil Nadu, India.
Saravanan RamachandranDepartment of Orthodontics, Dr.M.G.R. Educational and Research Institute, Chennai, Tamil Nadu, India.
Jamal Mohamed ThoufeeqDepartment of Medical Physics, Anna University, Chennai, Tamil Nadu, India.
Anandh SundaramoorthyDepartment of Medical Physics, Anna University, Chennai, Tamil Nadu, India.
Singaravelu GanesanSchool of Basic and Applied Sciences, Hindustan Institute of Technology and Science, Chennai, Tamil Nadu, India.
Aruna PrakasaraoDepartment of Medical Physics, Anna University, Chennai, Tamil Nadu, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Early Detection of CancerMouth NeoplasmsAdultAgedCase-Control StudiesFemaleFlavin-Adenine DinucleotideFluorescenceHumansMaleMiddle AgedNADSpectrometry, FluorescenceTryptophanFlavin-Adenine DinucleotideNADTryptophan

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