# Systematic evaluation of surgical insertion of flexible neural probe arrays into deeper brain targets using length modulation methods

**Authors:** Yingyi Gao, Zhouxiao Lu, Xuechun Wang, Zihan Jin, Alberto Esteban-Linares, Jeffery Guo, Huijing Xu, Kee Scholten, Dong Song, Ellis Meng

PMC · DOI: 10.1088/1741-2552/ae385c · Journal of Neural Engineering · 2026-02-02

## TL;DR

This study compares two methods for inserting flexible neural probes into deep brain regions, finding that a simpler dip coating technique works as well as a more complex bracing method.

## Contribution

A systematic comparison of two length modulation methods for inserting flexible neural probes into deep brain targets, with a focus on simplicity and surgical feasibility.

## Key findings

- Dip coating at high withdrawal speeds produced uniform coatings on pMEA shanks.
- Both dip coating and molded brace methods showed similar critical buckling and insertion forces.
- Dip coated pMEAs were successfully implanted in rat hippocampus without significant tissue damage.

## Abstract

Objective. Penetrating polymer-based microelectrode arrays (pMEAs) offer the potential for long term high-quality electrophysiological recordings of dynamic neural activity. Compared to rigid metal wire and silicon MEAs, improved device-tissue interface stability has been reported. However, accurate surgical placement of long, thin shanks in deeper brain regions is challenging as flexibility is achieved at the expense of axial stiffness. This study systematically evaluates then compares two pMEA placement strategies—dissolvable dip coating and molded brace, both with bare, exposed pMEA tips—to address the need for consistent, reliable, and accurate surgical targeting. These methods were selected based on the criteria of ease of fabrication, surgical feasibility, and mechanical performance. Approach. Sham (mechanical model with no electrodes) and fully functional pMEAs with shanks up to 5.5 mm long were fabricated and then modified using biodegradable polyethylene glycol (PEG) to support implantation. PEG was applied to shanks by motorized dip coating or a mechanical mold. Dissolution time and insertion in agarose gel brain models and rat cortex were evaluated followed by targeting of dip coated pMEAs to the rat hippocampus. Main results. Dip coating at high withdrawal speeds achieved uniform coating on shanks. Both strategies yielded similar critical buckling forces and insertion forces for single shank and arrayed pMEAs. Dip coated pMEAs were successfully placed in hippocampal regions without severe tissue damage as confirmed by histology and recordings obtained. Significance. Dip coating is a simpler method to prepare pMEAs for surgical targeting of deep brain regions compared to the bracing technique, as it does not require both a specialized mold and application process. This work provides a guide for researchers using single or multi-shank pMEAs to an accessible insertion strategy for implanting into deep brain regions in rodents and other small animal models.

## Linked entities

- **Chemicals:** polyethylene glycol (PubChem CID 9033), PEG (PubChem CID 174)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Rbfox3 (RNA binding fox-1 homolog 3) [NCBI Gene 287847] {aka Hrnbp3, Neun, RGD1560070}, Gfap (glial fibrillary acidic protein) [NCBI Gene 24387]
- **Diseases:** inflammation (MESH:D007249), weight loss (MESH:D015431), neuronal death (MESH:D009410)
- **Chemicals:** PBS (MESH:D007854), DAB (MESH:C000469), paraffin (MESH:D010232), PMEA (MESH:C053001), hematoxylin (MESH:D006416), dextran (MESH:D003911), Maltose (MESH:D008320), water (MESH:D014867), Ti (MESH:D014025), Saline (MESH:D012965), isoflurane (MESH:D007530), paraformaldehyde (MESH:C003043), polydimethylsiloxane (MESH:C013830), Si (MESH:D012825), ethanol (MESH:D000431), acetone (MESH:D000096), Polymer (MESH:D011108), oxide (MESH:D010087), eosin (MESH:D004801), saccharose (MESH:D013395), AZ 4620 (-), isopropyl alcohol (MESH:D019840), PEG (MESH:D011092), 3,3'-diaminobenzidine (MESH:D015100), xylene (MESH:D014992), metal (MESH:D008670), tungsten (MESH:D014414), Au (MESH:D006046), FA (MESH:D005557), N2 (MESH:D009584), Pt (MESH:D010984), Parylene (MESH:C011055), Agarose (MESH:D012685)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rodentia (rodent, order) [taxon 9989], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Mutations:** C-80  C, C for 3-5

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## Figures

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## References

82 references — full list in the complete paper: https://tomesphere.com/paper/PMC12862595/full.md

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Source: https://tomesphere.com/paper/PMC12862595