# Molecularly Imprinted Polymers as Biomimetic Test Zones in Paper-Based Nucleic Acid Assays—Comparing Vertical and Lateral Flow Formats

**Authors:** Jennifer Marfà, Anaixis del Valle, Maria Del Pilar Taboada Sotomayor, María Isabel Pividori

PMC · DOI: 10.3390/bios16030175 · Biosensors · 2026-03-21

## TL;DR

This paper compares two paper-based nucleic acid test formats using synthetic receptors to detect Escherichia coli, showing their speed and sensitivity differences.

## Contribution

The study introduces biotin-specific molecularly imprinted polymers as stable synthetic receptors in paper-based nucleic acid assays.

## Key findings

- NAVF provided a 3-minute visual readout with a limit of detection of 1.00 × 10−2 ng mL−1.
- NALF achieved a visual limit of detection of 3.17 × 10−2 ng mL−1 with an assay time of less than 15 minutes.
- Biotin-MIPs demonstrated versatility for rapid, low-cost nucleic acid assays with format-specific advantages.

## Abstract

The development of rapid and sensitive point-of-care nucleic acid tests benefits from robust synthetic recognition elements. Here, a biotin-specific molecularly imprinted polymer (MIP) was synthesized using an optimized protocol and integrated as a biomimetic test zone into two paper-based formats: nucleic acid vertical flow (NAVF) and nucleic acid lateral flow (NALF). Both platforms were evaluated for the detection of double-tagged PCR amplicons from Escherichia coli. NAVF enabled a 3 min visual readout with an LOD of 1.00 × 10−2 ng mL−1. NALF provided a total assay time of <15 min and achieved a visual LOD of 3.17 × 10−2 ng mL−1. Overall, the results demonstrate the versatility of biotin-MIPs as stable synthetic receptors for rapid, low-cost paper-based nucleic acid assays, with NAVF prioritizing speed and design flexibility and NALF prioritizing higher analytical sensitivity.

## Linked entities

- **Species:** Escherichia coli (taxon 562)

## Full-text entities

- **Diseases:** tuberculosis (MESH:D014376), HIV (MESH:D015658), injury to (MESH:D014947), COVID-19 (MESH:D000086382), infectious diseases (MESH:D003141)
- **Chemicals:** Ethanol (MESH:D000431), methanol (MESH:D000432), carbon (MESH:D002244), PEG 4000 (MESH:C000595214), polymer (MESH:D011108), Pd (MESH:D010165), AE100 (-), ester (MESH:D004952), hydrogen (MESH:D006859), TRIS (MESH:D014325), Au (MESH:D006046), 3,3',5,5'-tetramethylbenzidine (MESH:C021758), N2 (MESH:D009584), NaCl (MESH:D012965), MIP (MESH:D000082582), alumina (MESH:D000537), water (MESH:D014867), DIG (MESH:D004076), aluminum (MESH:D000535), 2,2'-azobisisobutyronitrile (MESH:C004526), BIO (MESH:D001710), Tween 20 (MESH:D011136), acetic acid (MESH:D019342), CF4 (MESH:C035066), acrylic acid (MESH:C036658), Cellulose (MESH:D002482), polyester (MESH:D011091), platinum (MESH:D010984), EGDMA (MESH:C004919)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

14 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13023435/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023435/full.md

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Source: https://tomesphere.com/paper/PMC13023435