# Innovative Fatty Acid-Guided Biosensor Design for Neutrophil Gelatinase, a Prognostic and Diagnostic Biomarker for Chronic Kidney Disease

**Authors:** Kaustubh Jumle, Priya Paliwal, Mohamed A. M. Ali, Ravi Ranjan Kumar Niraj, Anis Ahmad Chaudhary, Manali Datta

PMC · DOI: 10.3390/bios16020074 · Biosensors · 2026-01-26

## TL;DR

This paper introduces a new fatty acid-based biosensor for detecting NGAL, a biomarker for early-stage chronic kidney disease, offering a cost-effective and sensitive diagnostic approach.

## Contribution

The first fatty acid-based biosensor platform for NGAL detection, demonstrating high sensitivity and cost-effectiveness.

## Key findings

- Linoleic acid showed the strongest binding affinity to NGAL through molecular simulations.
- Differential pulse voltammetry achieved a detection limit of 0.05 ng/mL with high sensitivity.
- The proposed biosensor is the first fatty acid-based method for NGAL detection.

## Abstract

Chronic kidney disease (CKD) afflicts 850 million people worldwide, with an estimate that it is the 5th highest cause of years of life lost (YLLs). Standard confirmatory procedures for disease are blood and urine analysis with ultrasound for confirmation. Neutrophil gelatinase-associated lipocalin (NGAL) has been established as a prognostic biomarker, especially for the pre-clinical stages of CKD, thus presenting itself as a dependable predictor of the progression. With the aim of designing diagnostics, fatty acids were explored as potential biorecognition elements for the selective capture of NGAL. Three fatty acids—linoleic acid, arachidonic acid, and retinoic acid—were shortlisted as plausible candidates based on their known affinity toward lipocalin family proteins. Docking followed by molecular dynamics simulations were employed to evaluate the binding affinity and stability of each complex. Among them, linoleic acid exhibited the most favorable interaction, as evidenced by the lowest binding free energy. Subsequently, fluorescence and electrochemical techniques—square-wave voltammetry, differential pulse voltammetry, cyclic voltammetry, and electrochemical impedance spectroscopy (EIS)—were systematically compared for qualitative and quantitative checking of the accuracy of NGAL detection. Amongst the electrochemical techniques, differential pulse voltammetry DPV demonstrated superior analytical performance with an LOD of 0.05 ng/mL with a sensitivity of 23.2 µA/cm2/pg. To the best of our knowledge, this is the first report of a fatty acid-based biosensor platform for NGAL detection, presenting a novel approach for CKD diagnostics. The sensitivity obtained is comparable with available NGAL detection methods yet cost-effective and robust.

## Linked entities

- **Proteins:** LCN2 (lipocalin 2)
- **Chemicals:** linoleic acid (PubChem CID 5280450), arachidonic acid (PubChem CID 444899), retinoic acid (PubChem CID 444795)
- **Diseases:** Chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313] {aka CLG4, CLG4A, MMP-2, MMP-II, MONA, TBE-1}, A2M (alpha-2-macroglobulin) [NCBI Gene 2] {aka A2MD, CPAMD5, FWP007, S863-7}, LCN2 (lipocalin 2) [NCBI Gene 3934] {aka 24p3, MSFI, NGAL, p25}, GPHB5 (glycoprotein hormone subunit beta 5) [NCBI Gene 122876] {aka B5, GPB5, ZLUT1}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, IGKV4-1 (immunoglobulin kappa variable 4-1) [NCBI Gene 28908] {aka B3, IGKV41}, IGKV7-3 (immunoglobulin kappa variable 7-3 (pseudogene)) [NCBI Gene 28905] {aka B1, IGKV73}
- **Diseases:** renal function (MESH:D058186), CKD (MESH:D051436), injury to (MESH:D014947), tuberculosis (MESH:D014376), kidney injury (MESH:D007674), COVID-19 (MESH:D000086382), ESRD (MESH:D007676), cardiovascular complications (MESH:D002318), anemia (MESH:D000740)
- **Chemicals:** NaOH (MESH:D012972), 11-(dansylamino) undecanoic acid (MESH:C054400), Ethanol (MESH:D000431), arachidonic acid (MESH:D016718), N-hydroxysuccinimide (MESH:C001426), water (MESH:D014867), C (MESH:D002244), 3-Aminopropyl triethoxysilane (MESH:C477625), prostaglandins (MESH:D011453), EDC-NHS (MESH:C000625275), salts (MESH:D012492), LA (MESH:D019787), creatinine (MESH:D003404), hydrogen (MESH:D006859), 1-Ethyl-3-(3-dimethyl-aminopropyl) carbodiimide (MESH:D005022), PBS (MESH:D007854), RA (MESH:D011883), FA (MESH:D005227), urea (MESH:D014508), AA (MESH:D000596), retinoic acid (MESH:D014212), C-NH2 primary amine (-), K3Fe(CN6) (MESH:C028033)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** M20T

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938534/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938534/full.md

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Source: https://tomesphere.com/paper/PMC12938534