# Emerging biomimetic biopolymer-based composites: advancing accessible and sustainable neural disease models and therapeutics

**Authors:** Daniela Duc, Jacob Pattem, Benjamin Gambrill, Polina Prokopovich, Aybike Kocatürkmen, Matthew Church, Amber Mays, Akash Bedi, Emmanuel Brousseau, Oommen P. Oommen

PMC · DOI: 10.3389/fbioe.2025.1720254 · Frontiers in Bioengineering and Biotechnology · 2026-02-19

## TL;DR

This review explores how biomimetic biopolymer composites can create sustainable and accessible models for studying and treating neurological diseases.

## Contribution

The paper introduces a roadmap for developing and scaling biomimetic biopolymer composites for neurological disease research and therapy.

## Key findings

- Biomimetic biopolymers offer accessible and sustainable solutions for neuronal disease models.
- Nanocellulose-based and glycosaminoglycan composites are promising for advanced neuronal modeling.
- Translation barriers include manufacturing and commercialization challenges.

## Abstract

Neurological diseases are leading causes of death globally and disability-adjusted life years (DALYs) globally. Because of this, urgency in providing technologies and essential medicines to tackle this issue is currently recognized as key in reversing this trend. Global health strategies have recognized tissue engineering as a pillar element in progressing both neurological disease research and therapy discovery. Over time, various biomaterials have been developed with a few barriers appearing along the way when considering translation for routine neurological disorders research and therapy. These barriers include accessibility, sustainability, cost-effectiveness and affordability. In this review, we discuss how biopolymers, namely biomimetic advanced biopolymers composites have emerged to answer this issue. We will explore various types of biomimetic nanocellulose-based, self-assembling peptides, glycosaminoglycan composite, advanced functionalized nanoparticles amongst others are used to create a range of innovative state-of -the-art neuronal models that can be employed for neuronal disease investigation and therapy. Finally, we will review the current factors enabling and hindering their translation and scalability (e.g. manufacturing, characterization and commercialization) and provide a Research and Development Roadmap that can be explored to facilitate their development and provision to answer the pressing global need for these technologies in positively impacting neurological disorders.

## Full-text entities

- **Genes:** PTPRZ1 (protein tyrosine phosphatase receptor type Z1) [NCBI Gene 5803] {aka HPTPZ, HPTPzeta, PTP-ZETA, PTP18, PTPRZ, PTPZ}, SKAP2 (src kinase associated phosphoprotein 2) [NCBI Gene 8935] {aka PRAP, RA70, SAPS, SCAP2, SKAP-HOM, SKAP55R}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}, PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295] {aka AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha}, CCR5 (C-C motif chemokine receptor 5) [NCBI Gene 1234] {aka CC-CKR-5, CCCKR5, CCR-5, CD195, CKR-5, CKR5}, APCS (amyloid P component, serum) [NCBI Gene 325] {aka HEL-S-92n, PTX2, SAP}, SPOCK1 (SPARC (osteonectin), cwcv and kazal like domains proteoglycan 1) [NCBI Gene 6695] {aka SPOCK, TESTICAN, TIC1}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, ACAN (aggrecan) [NCBI Gene 176] {aka AGC1, AGCAN, CSPG1, CSPGCP, MSK16, SEDK}, FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, Cdh2 (cadherin 2) [NCBI Gene 12558] {aka CDHN, N-CAD, Ncad}, MBP (myelin basic protein) [NCBI Gene 4155], Ngf (nerve growth factor) [NCBI Gene 18049] {aka Ngfb, beta-NGF}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], CCL5 (C-C motif chemokine ligand 5) [NCBI Gene 6352] {aka D17S136E, RANTES, SCYA5, SIS-delta, SISd, TCP228}, Fgf2 (fibroblast growth factor 2) [NCBI Gene 14173] {aka Fgf-2, Fgf2a, Fgfb, bFGF}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, PLG (plasminogen) [NCBI Gene 5340] {aka HAE4}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, BCAN (brevican) [NCBI Gene 63827] {aka BEHAB, CSPG7}, VCAN (versican) [NCBI Gene 1462] {aka CSPG2, ERVR, GHAP, PG-M, WGN, WGN1}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, CALML3 (calmodulin like 3) [NCBI Gene 810] {aka CLP}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, NCAN (neurocan) [NCBI Gene 1463] {aka CSPG3}, Egf (epidermal growth factor) [NCBI Gene 13645]
- **Diseases:** amyloid (MESH:C000718787), neuronal damage (MESH:D009410), C6 glioma (MESH:C567307), infarct (MESH:D007238), NPC (MESH:D002292), GBM (MESH:D005909), Brain tumors (MESH:D001932), death (MESH:D003643), brain injury (MESH:D001930), brain diseases (MESH:D001927), middle cerebral artery occlusion (MESH:D020244), long-term disability (MESH:D000088562), tumor metastasis (MESH:D009362), epilepsy (MESH:D004827), ischemic stroke (MESH:D002544), Stroke (MESH:D020521), neuronal disease (MESH:D016472), brain oedema (MESH:D001929), Neurological diseases (MESH:D020271), bleeding (MESH:D006470), hemolysis (MESH:D006461), Neurological disorders (MESH:D009461), neuroblastoma (MESH:D009447), SCI (MESH:D013119), peripheral nerve injury (MESH:D059348), Parkinson's disease (MESH:D010300), inflammation (MESH:D007249), muscle atrophy (MESH:D009133), injury (MESH:D014947), disease (MESH:D004194), neurodegenerative diseases (MESH:D019636), glioma (MESH:D005910), TBI (MESH:D000070642), neuroinflammation (MESH:D000090862), neural disorders (MESH:D015441), AD (MESH:D000544), tumor (MESH:D009369), brain ischemia (MESH:D002545)
- **Chemicals:** lipids (MESH:D008055), PLA (MESH:C033616), biopolymer (MESH:D001704), pyrrole (MESH:D011758), agarose (MESH:D012685), polythiophene (MESH:C066730), maleimide (MESH:C043592), steroid (MESH:D013256), carboxymethylcellulose (MESH:D002266), polyphenylene (MESH:C041325), D-glucosamine (MESH:D005944), berberine (MESH:D001599), ROS (MESH:D017382), dopamine (MESH:D004298), myr (MESH:D019814), lysine (MESH:D008239), PLGA (MESH:D000077182), heparin (MESH:D006493), H2 (MESH:D006859), Cellulose (MESH:D002482), PVDF (MESH:C024865), tripolyphosphate (MESH:C005692), Pluronic F127 (MESH:D020442), GAG (MESH:D006025), RGD (MESH:C047981), hydroxyproline (MESH:D006909), glycerol (MESH:D005990), Na + (MESH:D012964), Heparan sulphate (MESH:D006497), sebacic acid (MESH:C011107), HAMA (-), Si (MESH:D012825), genipin (MESH:C007834), curcumin (MESH:D003474), riboflavin (MESH:D012256), HA (MESH:D017886), PCL (MESH:C016240), PVC (MESH:D011143), fatty acid (MESH:D005227), N-acetyl-D-glucosamine (MESH:D000117), PVA (MESH:D011142), thiol (MESH:D013438), dexamethasone (MESH:D003907), TMZ (MESH:D000077204), MTT (MESH:C070243), amino acid (MESH:D000596), carbon nanotube (MESH:D037742), diphenylalanine (MESH:C000712934), Ti (MESH:D014025), peptides (MESH:D010455), catechol (MESH:C034221), carbodiimide (MESH:D002234), molybdenum dioxide (MESH:C539565), RADA-16I (MESH:C546681), palladium (MESH:D010165), water (MESH:D014867), phospholipids (MESH:D010743), polyaniline (MESH:C416807), PEO-PPO-PEO (MESH:C116176), salinomycin (MESH:C010327)
- **Species:** PX clade (clade) [taxon 569578], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** SH-SY5Y — Homo sapiens (Human), Neuroblastoma, Cancer cell line (CVCL_0019), GPE86 — Mus musculus (Mouse), Transformed cell line (CVCL_8956), PC12 — Rattus norvegicus (Rat), Rat adrenal gland pheochromocytoma, Cancer cell line (CVCL_0481), GBM12 — Homo sapiens (Human), Glioblastoma, Cancer cell line (CVCL_DG57), L929 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_AR58)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12960564/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12960564/full.md

## References

278 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960564/full.md

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Source: https://tomesphere.com/paper/PMC12960564