# A Molecularly Imprinted Membrane for High-Density Lipoprotein Extraction in Point-of-Care Testing

**Authors:** Gian Luca de Gregorio, Denis Prim, Alberto Zavattoni, Italo Mottini, Daniele Pezzoli, Federico Roveda, Marc E. Pfeifer, Jean-Manuel Segura

PMC · DOI: 10.3390/bios15100685 · Biosensors · 2025-10-10

## TL;DR

This paper presents a new membrane-based method for extracting HDL from blood to enable point-of-care LDL cholesterol testing.

## Contribution

The study introduces a molecularly imprinted membrane for selective HDL removal in paper-based diagnostic tests.

## Key findings

- Molecularly imprinted polymers showed good HDL selectivity with an uptake capacity of 5.0–7.0 µg of HDL-C/mg of MIP.
- The membrane achieved 68% HDL removal efficiency but faced challenges due to non-specific LDL binding.
- The approach demonstrates a novel way to integrate solid-phase affinity extraction into point-of-care diagnostics.

## Abstract

Cholesterol blood levels in low-density lipoproteins (LDLs) are a key parameter for assessing the risk of cardiovascular diseases. Direct quantification of LDL cholesterol at the point of care would be possible if all other lipoproteins, particularly the high-density lipoproteins (HDLs), could be removed prior to measurement. Here, we investigated whether a molecularly imprinted membrane (MIM) could be used for the solid-phase affinity extraction (SPAE) of HDL in a paper-based lateral flow test. Samples traveled by capillarity through the MIM before reaching a detection zone where LDL cholesterol was quantified enzymatically. MIMs were produced by impregnation of the membrane with a dispersion of molecularly imprinted polymers (MIPs) selective for HDL. MIPs were synthesized using precipitation polymerization and exhibited good selectivity for HDL compared with LDL and an uptake capacity of 5.0–7.0 µg of HDL-C/mg of MIP. The MIM enabled the removal of HDL with an efficiency of typically 68%. However, quantification of LDL cholesterol suffered from strong non-specific binding of LDL, likely due to its inherent colloidal instability. Overall, our results highlight the challenges associated with SPAE of colloidal particles. Furthermore, our study demonstrates a novel, efficient, and potentially generic modality to integrate SPAE into paper-based POC diagnostic tests.

## Full-text entities

- **Genes:** MIP (major intrinsic protein of lens fiber) [NCBI Gene 4284] {aka AQP0, CTRCT15, LIM1, MIP26, MP26}
- **Diseases:** cardiovascular diseases (MESH:D002318)
- **Chemicals:** Cholesterol (MESH:D002784)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12563577/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12563577/full.md

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Source: https://tomesphere.com/paper/PMC12563577