# Effective Coupling of Light Emitting Diode to a Commercial Capillary Electrophoresis Laser-Induced Fluorescence Instrument for High-Sensitivity Analysis of Fluorescently Labeled Glycans

**Authors:** Filip Duša, Pavlína Dadajová, Jozef Šesták, Jana Lavická

PMC · DOI: 10.1021/acs.analchem.5c05248 · 2025-10-17

## TL;DR

This paper describes a cost-effective way to improve fluorescence detection in capillary electrophoresis using LEDs, enabling highly sensitive glycan analysis with small sample amounts.

## Contribution

A novel LED coupling method for commercial CE-LIF instruments that significantly enhances sensitivity and enables analysis of minute glycan samples.

## Key findings

- A direct coupling design with a single ball lens increased fluorescence signal by 10.7-fold.
- A two-lens design increased signal by 31.2-fold and achieved detection limits between 99 and 105 nmol/L.
- The optimized method enabled N-linked glycan analysis from as little as 7.49 ng of ribonuclease B.

## Abstract

Light-emitting diodes offer a low-cost, power-efficient,
and compact
solution for fluorescence excitation in analytical instrumentation.
This study discusses the coupling of a near-ultraviolet light-emitting
diode (340 nm) to a commercial capillary electrophoresis instrument
and presents two feasible strategies: a simple, robust, and low-cost
option with moderate efficiency and a more complex but significantly
more efficient design for applications demanding maximum sensitivity.
The coupling efficiency was assessed using capillary zone electrophoresis
of maltooligosaccharides labeled with the UV-excitable fluorophore,
6-[4-(4-methylpiperazin-1-yl)­phenyl]­pyridine-3-carbohydrazide. Compared
to a commonly used indirect light guide coupling approach, the new
direct coupling design, incorporating a single ball lens, provided
a 10.7-fold increase in the fluorescence signal. The design incorporating
two plano-convex lenses increased the fluorescence signal by a factor
of 31.2 and achieved limits of detection between 99 and 105 nmol/L
for the analyzed labeled maltooligosaccharides. This optimized configuration
enabled the successful N-linked glycan analysis from
minute sample quantities, specifically, 28.8 ng of ovalbumin and 7.49
ng of ribonuclease B.

## Linked entities

- **Proteins:** Serpinb2 (serine (or cysteine) peptidase inhibitor, clade B, member 2)

## Full-text entities

- **Chemicals:** maltooligosaccharides (MESH:C021705), 6-[4-(4-methylpiperazin-1-yl)phenyl]pyridine-3-carbohydrazide (-), Glycans (MESH:D011134)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12573225/full.md

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Source: https://tomesphere.com/paper/PMC12573225