Handheld Device for Saliva Pretreatment to Improve Cortisol Detection

Summary

This protocol describes a rapid saliva pretreatment method for improving cortisol detection. A handheld filtration device is used to remove mucins and other interfering substances while preserving the target analyte. The pretreated saliva exhibits improved capillary flow, thereby enabling more consistent and reproducible assay performance.

Abstract

Salivary cortisol detection offers a noninvasive alternative to blood-based analysis. However, its practical implementation remains limited by the intrinsic viscosity of saliva and the presence of interfering components. In particular, mucins and salivary proteins impede capillary-driven flow and compromise the reliability of subsequent lateral flow assays (LFAs), thereby necessitating effective and accessible pretreatment strategies. Here, we present a handheld saliva pretreatment device, termed SaliFilter, for point-of-care cortisol detection. The device employs a filtration mechanism that selectively removes high-molecular-weight interfering components while allowing the passage of small molecules, including cortisol. Operated by simple manual pressure, it enables rapid sample processing (~2 min) without the need for external equipment, making it suitable for decentralized settings. The performance of the device was evaluated using turbidity measurements, protein quantification, and SDS-PAGE, which confirmed efficient removal of mucin and salivary proteins. Treated samples exhibited enhanced capillary flow, resulting in stable and reliable LFA operation. Quantitative analysis demonstrated improved signal reproducibility, and cortisol detection achieved a limit of detection of 1.47 ng mL⁻¹ over clinically relevant concentration ranges. This protocol establishes an effective saliva pretreatment strategy that improves analytical sensitivity and reliability without compromising analyte integrity. The proposed approach provides a practical, portable solution for saliva-based diagnostics, with potential applicability for point-of-care testing and self-monitoring.

Introduction

Cortisol, a glucocorticoid hormone secreted by the adrenal cortex, is a key biomarker for assessing physiological stress^1,2. It can be measured in multiple biological fluids, including serum, plasma, urine, interstitial fluid, and saliva, with blood and saliva being the most commonly used in clinical practice³. Although blood-based measurements provide reliable quantitative information, they require invasive venipuncture and trained personnel, which limits their suitability for frequent or longitudinal monitoring^4,5,6. In contrast, salivary cortisol measurement offers a noninvasive and convenient alternative, enabling point-of-care and self-monitoring applications^7,8. Notably, salivary cortisol levels correlate strongly with blood concentrations, supporting saliva as a reliable surrogate sample⁹. However, the intrinsic viscosity of saliva and the presence of interfering components significantly hinder analytical performance, necessitating effective pretreatment prior to analysis^10,11,12.

Various pretreatment strategies have been explored to address these challenges. Centrifugation is widely used to remove large components such as mucins, proteins, and cellular debris. However, it requires bulky laboratory equipment and multiple processing steps, which limits its applicability in decentralized settings^13,14. Dilution with buffer solutions can reduce viscosity and improve sample flow¹⁵. Nevertheless, it simultaneously lowers analyte concentration, thereby compromising analytical sensitivity. As a result, existing approaches remain insufficient for point-of-care applications, where rapid, equipment-free processing and preservation of target analytes are essential.

To overcome these limitations, we developed SaliFilter, a handheld device for saliva pretreatment tailored to point-of-care cortisol detection. The device employs a filtration mechanism that selectively removes high-molecular-weight interfering substances while permitting the passage of small molecules, including cortisol¹⁶. Operated manually, the device enables rapid, user-friendly processing without the need for external instrumentation. By eliminating interfering components, this approach improves capillary flow in lateral flow assays, thereby enhancing analytical reliability. This protocol describes the fabrication of the device and its application for rapid saliva pretreatment prior to cortisol detection using lateral flow assays.

Protocol

Commercially obtained de-identified pooled human saliva was used in this study. No human participants were recruited, and institutional ethics approval was not required.

1. Saliva sample preparation

1. Instruct participants to refrain from eating or drinking for at least 30 min prior to sample collection.
2. Prepare the saliva sample according to the supplier’s instructions.
   NOTE: This study used commercially available pooled human saliva for protocol-level validation.
3. Gently mix the saliva sample before use to ensure homogeneity.
4. Store the saliva samples at 4 °C and use them within the supplier's recommended storage period.

2. Preparation of the RBCM-coated membrane (Figure 1A)

1. Isolate RBCM from whole blood according to a previously reported protocol¹⁶.
   1. Use commercially obtained human whole blood anticoagulated with K2EDTA as the RBCM source.
   2. Centrifuge the whole blood at 800 × g for 5 min and collect the red blood cell fraction after removing the plasma and buffy coat.
   3. Wash the isolated red blood cell pellet three times with ice-cold 1× phosphate-buffered saline (PBS) using gentle manual mixing.
   4. Resuspend the washed red blood cell pellet in ice-cold 0.25× PBS for 30 min to induce hemolysis.
   5. Separate free hemoglobin by centrifuging the lysed suspension at 20,000 × g for 30 min and collecting the RBCM pellet.
   6. Wash the collected RBCM pellet three additional times with 0.25× PBS and store the pale pink RBCM pellet at −80 °C until further use.
2. Prepare a polyethersulfone (PES) membrane with a pore size of 30 nm and a diameter of 13 mm.
3. Deposit 100 µL of 2% (w/v) RBCM solution onto one side of the PES membrane. Gently spread or dispense the solution dropwise until the entire membrane surface is fully wetted.
4. Incubate the membrane at 50 °C for 30 min to ensure uniform coating and drying.
5. Store the coated membrane at room temperature and use it within 15 days after preparation¹⁷.
   NOTE: Detailed characterization of the RBCM-coated PES membrane has been described in our previous study¹⁶.

3. Fabrication of the SaliFilter device (Figure 1B)

1. Place the RBCM-coated membrane into the designated filter holder.
2. Assemble the device by securely connecting the inlet and outlet components.
3. Attach a 1 mL syringe to the inlet of the device.
   CAUTION: Ensure that all components are tightly sealed to prevent leakage during operation.

4. Saliva pretreatment

1. Load 500 µL of saliva into the syringe connected to the SaliFilter device.
2. Apply gentle manual pressure to pass the saliva sample through the membrane (~ 2 min).
3. Collect the pretreated saliva from the outlet.
4. Use the pretreated sample immediately or store it at 4 °C until further analysis.

5. SDS-PAGE analysis of salivary proteins

1. Mix 15 µL of the sample with 5 µL of Laemmli sample buffer.
2. Load the mixture into separate wells of an 8% SDS-PAGE gel.
3. Perform electrophoresis at 150 V for 40 min.
4. Stain the gel with Coomassie blue for 2 h.
5. Destain the gel in distilled water overnight.
6. Capture images of the gel using a smartphone or imaging system.

6. Cortisol detection using Lateral Flow Assay (LFA)

1. Apply 150 µL of pretreated saliva to the sample pad of the LFA strip.
2. Allow the sample to migrate along the strip for 10 min.
3. Capture images of the test results using a smartphone or imaging system.
4. Open the LFA image in ImageJ and use Image > Color > Split Channels to separate the RGB channels.
5. Use the green channel image for test-line intensity analysis.
6. Select a rectangular Region of Interest (ROI) of 100 × 10 pixels covering the test-line and apply the same ROI size to all strip images.
7. Measure the mean intensity value of the test-line ROI. Select an adjacent blank membrane region with the same ROI size and measure the background intensity.
8. Calculate the normalized test-line intensity as follows: normalized intensity = test-line intensity − background intensity.

7. Statistical analysis

1. Present quantitative data as mean ± standard deviation (SD), unless otherwise stated. Define error bars as SD.
   NOTE: In this study, all reported N values represent technical replicates performed using aliquots of commercially obtained pooled human saliva.
2. Perform linear regression analysis using the normalized test-line intensity values obtained from cortisol concentrations of 0–8 ng mL⁻¹ and calculate the coefficient of determination (R²) from the fitted curve.
3. Calculate the limit of detection (LOD) using the following equation: LOD = 3.3 × SE / |slope|, where SE is the standard error of the y-intercept and |slope| is the absolute value of the slope obtained from the linear regression equation. Use the absolute value of the slope because the competitive LFA produces a negative slope.
   NOTE: In this study, no inferential statistical tests were performed, and no significance criteria were applied.

Results

Effective saliva pretreatment requires removing interfering components, including mucins and proteins, that compromise downstream analytical performance. The filtration capability of SaliFilter was first evaluated by comparing turbidity changes with those obtained using commercial saliva collection kits (Figure 2A). Untreated saliva exhibited high turbidity, whereas SaliFilter-treated samples appeared visibly clear, indicating efficient removal of mucins and suspended components. In contrast...

Discussion

Saliva-based diagnostics offer a noninvasive alternative to blood analysis. However, their broader adoption has been constrained by the intrinsic viscosity of saliva and the presence of interfering components such as mucins and proteins. These factors disrupt capillary-driven flow and compromise the performance of simple analytical platforms, including LFAs, thereby necessitating effective sample pretreatment.

In this study, we demonstrate that the proposed handheld filtration device, SaliFilt...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Artificial saliva	Solarbio, China	A7990
Bio-Rad Protein Assay Dye Reagent	Bio-Rad, USA	5000006	For bradford assay
Coomassie blue	Abcam, UK	ab119211	For protein band visualization
Cortisol ELISA Kit	Abcam, UK	ab154996
Cortisol LFA	In-house
Hot plate	Daihan Scientific, Republic of Korea)
Hydrocortisone (Cortisol)	Sigma-Aldrich, USA	PHR1014
Laemmli sample buffer	GenDEPOT, USA	L1200-001	For protein denaturation prior to SDS-PAGE
Membrane holder	GVS Filter Technology	1220950	13mm diameter holder
Mini-PROTEAN® Tetra Cell for 0.75 mm Gels	Bio-Rad, USA	1658000	For gel electrophoresis
Mucin	Sigma-Aldrich, USA	M2378
NanoDrop 2000 spectrophotometer	Thermo Fisher Scientific, USA		For protein assay
PES membranes	STERLITECH, USA	PES00313100	0.03 Micron, 13 mm PES membrane
Phosphate-buffered saline (PBS)	DUKSAN, Republic of Korea	LB004
Pooled Human Saliva	Innovative Research Inc., USA	IRHUSL5ML
RBCM	In-house
Resolving Gel Buffer for PAGE	Bio-Rad, USA	1610798	For resolving gel preparation
Salivette Cortisol	SARSTEDT, Germany	51.1534.500	Saliva collection kit
Stacking Gel Buffer for PAGE	Bio-Rad, USA	1610799	For stacking gel preparation
Super•SAL™	Oasis Diagnostics, USA	SSAL-601	Saliva collection kit
Syringe	koreavaccine, Republic of Korea)		1 mL volume
TEMED	Bio-Rad, USA	1610800	For acrylamide polymerization