# Plasma–Nanomedicine Synergistic Therapy for Brain Diseases: Current Status, Applications, and Challenges

**Authors:** Shun-Lian Li, Qiao Li, Jun-Ze Deng, Zhen-Long Zhang, Miao Qi, Xiu-Hua Luo, Yudan Zhang, Qing-Yan Ma, Feng Zhu, Xian-Cang Ma, Dao-Cheng Wu, Shuo Zhang

PMC · DOI: 10.3390/antiox15020166 · Antioxidants · 2026-01-26

## TL;DR

This paper reviews how combining cold plasma with nanomedicine could improve treatments for brain diseases like stroke and Alzheimer's.

## Contribution

The paper systematically reviews plasma-nanomedicine synergy and highlights its potential and challenges in brain disease treatment.

## Key findings

- Plasma-nanomedicine synergy can regulate oxidative stress and improve therapeutic outcomes.
- Four nanomedicine categories are reviewed for brain disease applications.
- Key challenges include limited CAP equipment and incomplete mechanism understanding.

## Abstract

Brain diseases such as ischaemic stroke, Alzheimer’s disease (AD), and glioma were characterized by high mortality and disability rate, and oxidative stress remains a major obstacle in treatment. Plasma–nanomedicine synergistic treatment technology provides a very attractive treatment strategy based on complementarity. This technology integrates cold atmospheric plasma (CAP) with nanomedicine. CAP produces active substances that regulate oxidative stress, while nanomedicine is specially designed for targeted delivery, controlled release, and microenvironmentally responsive activation of therapeutic agents. This integration generates new therapeutic functions and significantly improves the overall therapeutic effect. Despite the broad prospects of this emerging technology, researchers in the fields of medicine, physics, or pharmacy have not yet paid much attention to it. To fill this research gap, this review describes the physicochemical properties and biological effects of CAP and summarizes the latest advances in plasma nanomedicine strategies in the field of brain disease intervention, and reviews the four major nanomedical categories—metal-based, inorganic non-metallic, polymer-based and hydrogel systems—and their clinical applications in the treatment of brain tumors, strokes and neurodegenerative diseases in conjunction with CAP. Finally, we highlight a number of key challenges—limited resources of special CAP equipment, incomplete understanding of the mechanism, obstacles to transformation application—and put forward the future research direction to promote the development of accurate, safe, and clinical transformation value plasma–nanomedicine therapy for brain diseases.

## Linked entities

- **Diseases:** ischaemic stroke (MONDO:1060198), Alzheimer’s disease (MONDO:0004975), glioma (MONDO:0021042)

## Full-text entities

- **Genes:** CAPS (calcyphosine) [NCBI Gene 828] {aka CAPS1}, CLDN5 (claudin 5) [NCBI Gene 7122] {aka AWAL, BEC1, CPETRL1, TMDVCF, TMVCF}, Pik3r1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 18708] {aka PI3K, p50alpha, p55alpha, p85alpha}, Sorbs1 (sorbin and SH3 domain containing 1) [NCBI Gene 686098] {aka CAP, SH3P12}, Bax (BCL2 associated X, apoptosis regulator) [NCBI Gene 24887], MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, App (amyloid beta precursor protein) [NCBI Gene 11820] {aka Abeta, Abpp, Adap, Ag, Cvap, E030013M08Rik}, OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, NQO1 (NAD(P)H quinone dehydrogenase 1) [NCBI Gene 1728] {aka DHQU, DIA4, DTD, NMOR1, NMORI, QR1}, Psen1 (presenilin 1) [NCBI Gene 19164] {aka Ad3h, PS-1, PS1, S182}, MCL1 (MCL1 apoptosis regulator, BCL2 family member) [NCBI Gene 4170] {aka BCL2L3, EAT, MCL1-ES, MCL1L, MCL1S, Mcl-1}, Casp3 (caspase 3) [NCBI Gene 25402] {aka CPP32-beta, Lice, Yama}, Bcl2 (BCL2, apoptosis regulator) [NCBI Gene 24224] {aka Bcl-2}, App (amyloid beta precursor protein) [NCBI Gene 54226] {aka Abeta}, ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 5243] {aka ABC20, CD243, CLCS, ENPAT, GP170, MDR1}, GPX4 (glutathione peroxidase 4) [NCBI Gene 2879] {aka GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}, Map2 (microtubule-associated protein 2) [NCBI Gene 17756] {aka G1-397-34, MAP-2, Mtap-2, Mtap2, repro4}, BCL2L1 (BCL2 like 1) [NCBI Gene 598] {aka BCL-XL/S, BCL2L, BCLX, Bcl-X, PPP1R52}, TAT (tyrosine aminotransferase) [NCBI Gene 6898], EPHA3 (EPH receptor A3) [NCBI Gene 2042] {aka EK4, ETK, ETK1, HEK, HEK4, TYRO4}
- **Diseases:** hypoxia (MESH:D000860), neurofibrillary (MESH:D055956), psoriasis (MESH:D011565), hyperthermia (MESH:D005334), genetic brain diseases (MESH:D030342), neurological deficits (MESH:D009461), ischemia (MESH:D007511), stroke (MESH:D020521), cerebral vascular malformations (MESH:D054079), hypoxic (MESH:D002534), Neurological diseases (MESH:D020271), bleeding (MESH:D006470), autoimmune disease (MESH:D001327), schizophrenia (MESH:D012559), vitiligo (MESH:D014820), traumatic brain injury (MESH:D000070642), cancer (MESH:D009369), cerebral ischaemia (MESH:D002545), neurotoxicity (MESH:D020258), peritoneal cancer (MESH:D010534), mental disorders (MESH:D001523), mitochondrial failure (MESH:D051437), AD (MESH:D000544), mitochondrial dysfunction (MESH:D028361), PD (MESH:D010300), glioma (MESH:D005910), inflammatory (MESH:D007249), neuropsychiatric diseases (MESH:D004194), NDDs (MESH:D019636), injury to (MESH:D014947), infectious brain diseases (MESH:D003141), illnesses (MESH:D002908), Brain Tumor (MESH:D001932), neuronal apoptosis (MESH:D065703), GBM (MESH:D005909), neurological impairments (MESH:D009422), cognitive decline (MESH:D003072), circuit dysfunction (MESH:D006331), peripheral neuropathy (MESH:D010523), breast and colorectal cancer (MESH:D001943), depression (MESH:D003866), infarct (MESH:D007238), bacterial infection (MESH:D001424), degeneration (MESH:D009410), dermatological disorders (MESH:D000168), cytotoxicity (MESH:D064420), cerebral infarction (MESH:D002544), immune dysfunction (MESH:D007154), cardiovascular diseases (MESH:D002318), infections (MESH:D007239), MCAO (MESH:D020244), rare diseases (MESH:D035583), Brain Diseases (MESH:D001927), mental diseases (MESH:D008607), vein thrombosis (MESH:D012170), reperfusion injury (MESH:D015427), Thrombus (MESH:D013927), ALS (MESH:D000690), long-term disability (MESH:D000088562), ischaemic (MESH:D018917)
- **Chemicals:** hyaluronic acid (MESH:D006820), hydroxyl radicals (MESH:D017665), cerium (MESH:D002563), NO (MESH:D009569), NO3 (MESH:C038619), CAC (MESH:C055936), Ag+ (MESH:D012834), IO (MESH:C000499), iron (MESH:D007501), CeO2 (MESH:C030583), 6-OHDA (MESH:D016627), MB (MESH:D008751), Caelyx (MESH:C506643), Fu (MESH:D005472), water (MESH:D014867), NPD@M. (MESH:C065473), MnO2 (MESH:C016552), polymer (MESH:D011108), carbon (MESH:D002244), nitrogen (MESH:D009584), PEG (MESH:D011092), NO2 (MESH:D009585), oxygen (MESH:D010100), phosphorus (MESH:D010758), chitosan (MESH:D048271), nitrate (MESH:D009566), Au (MESH:D006046), singlet oxygen (MESH:D026082), cGMP (MESH:D006152), Pt (MESH:D010984), Metal (MESH:D008670), ROS (MESH:D017382), argon (MESH:D001128), MXene (MESH:C000723374), polyurethane (MESH:D011140), PLGA (MESH:D000077182), OH (MESH:C031356), lipid (MESH:D008055), peroxynitrite (MESH:D030421), glutathione (MESH:D005978), ATP (MESH:D000255), CS (MESH:D002586), PCL (MESH:C016240), TMZ (MESH:D000077204), RNS (MESH:D026361), PVA (MESH:D011142), RON (MESH:C065495), K (MESH:D011188), doxorubicin (MESH:D004317), helium (MESH:D006371), curcumin (MESH:D003474), H2O2 (MESH:D006861), tyramine (MESH:D014439), AgNP (-), superoxide anions (MESH:D013481), O3 (MESH:D010126)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Escherichia coli (E. coli, species) [taxon 562], Homo sapiens (human, species) [taxon 9606], Staphylococcus aureus (species) [taxon 1280], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** PC12 — Rattus norvegicus (Rat), Rat adrenal gland pheochromocytoma, Cancer cell line (CVCL_0481)

## Full text

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## Figures

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## References

102 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938366/full.md

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Source: https://tomesphere.com/paper/PMC12938366