# Oscillatory dynamics in paclitaxel-proteinoid networks

**Authors:** Panagiotis Mougkogiannis, Andrew Adamatzky

PMC · DOI: 10.1007/s44345-026-00047-x · 2026-02-22

## TL;DR

This study explores how paclitaxel interacts with proteinoid microspheres to create electrically active networks with potential applications in bio-inspired signal processing.

## Contribution

The study introduces a novel paclitaxel-proteinoid system that exhibits enhanced conductivity and oscillatory behavior.

## Key findings

- Paclitaxel incorporation into proteinoid microspheres increases electrical conductivity by nearly two orders of magnitude.
- The system shows diffusion-controlled redox behavior and long-term stable electrical oscillations.
- Spectral analysis reveals chaotic behavior in mixed proteinoid systems.

## Abstract

Paclitaxel is a widely used microtubule-targeting chemotherapeutic, yet its intrinsic electrochemical behavior remains poorly understood. Here we investigate the electrochemical and oscillatory properties of paclitaxel incorporated into proteinoid microspheres that mimic cellular environments. Using scanning electron microscopy, cyclic voltammetry, electrochemical impedance spectroscopy, and square-wave voltammetry, we compare pure paclitaxel, proteinoid–paclitaxel mixtures, and related proteinoid systems. Incorporation of paclitaxel induces the formation of interconnected fibrous networks and enhances electrical conductivity by nearly two orders of magnitude relative to pure paclitaxel. The proteinoid–paclitaxel system exhibits diffusion-controlled redox behavior, long-term stable electrical oscillations, and high signal coherence. Spectral and nonlinear analyses reveal distinct dynamical regimes, including chaotic behavior in mixed proteinoid systems. These results establish proteinoid–paclitaxel assemblies as electrically active biomimetic platforms and suggest their potential as model systems for studying microtubule-related bioelectrical phenomena and bio-inspired signal processing.

## Linked entities

- **Chemicals:** paclitaxel (PubChem CID 36314)

## Full-text entities

- **Genes:** AZIN2 (antizyme inhibitor 2) [NCBI Gene 113451] {aka ADC, AZIB1, ODC-p, ODC1L, ODCp}, SUCO (SUN domain containing ossification factor) [NCBI Gene 51430] {aka C1orf9, CH1, OPT, SLP1}
- **Diseases:** peripheral neuropathy (MESH:D010523), depressed (MESH:D003866), epilepsy (MESH:D004827), electrical (MESH:D004556), neurological disorders (MESH:D009461), neurodegeneration (MESH:D019636), cancer (MESH:D009369), Alzheimer's (MESH:D000544)
- **Chemicals:** Calcium (MESH:D002118), diterpenoid (MESH:D004224), H+ (MESH:D006859), dicarboxylic amino acid (MESH:D000600), Cyan (-), cisplatin (MESH:D002945), L-phenylalanine (MESH:D010649), amino acids (MESH:D000596), Omeprazole (MESH:D009853), Ir (MESH:D007495), water (MESH:D014867), amide (MESH:D000577), chloride (MESH:D002712), glycyrrhizic acid (MESH:D019695), Glu (MESH:D018698), oxygen (MESH:D010100), Pt (MESH:D010984), carbon (MESH:D002244), ester (MESH:D004952), lactam (MESH:D007769), nitrogen (MESH:D009584), Paclitaxel (MESH:D017239), AC (MESH:D000186)
- **Species:** Chara corallina (species) [taxon 43696], Paramecium (genus) [taxon 5884], Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562]

## Figures

23 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12961978/full.md

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Source: https://tomesphere.com/paper/PMC12961978