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Non-invasive neuromodulation assisted by exogenous stimuli-responsive nanoplatforms for Alzheimer’s disease and Parkinson's disease therapy

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  • Corresponding author: yiwang2@hkbu.edu.hk
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    1. Stimuli-responsive nanoplatforms enable non-invasive neuromodulation for Alzheimer’s and Parkinson’s therapy.

      External stimuli enhance drug delivery efficiency in neurodegenerative disease treatment.

      Nanoplatforms respond to brain regions or pathologies like amyloid plaques and dopamine deficits.

      Challenges in precision, safety, and efficacy are addressed through advanced targeting strategies.

  • In recent decades, the incidence of neurodegenerative diseases such as Alzheimer’s disease (AD) and Parkinson’s disease (PD) has risen continuously, significantly impairing patients’ quality of life while imposing growing economic and social burdens. Traditional treatments exhibit limited effectiveness in halting disease progression. Non-invasive neuromodulation techniques, utilizing electromagnetic fields, light, or ultrasound, have emerged as promising strategies to modulate neural activity and alleviate symptoms. However, achieving spatially precise and targeted neuromodulation remains challenging. The integration of stimuli-responsive nanoplatforms addresses this limitation. These nanoplatforms, engineered to respond to specific stimuli, can deliver therapeutic agents to the desired brain regions. By enabling controlled and localized drug release, they facilitate precise neuromodulation. Despite their potential, several hurdles must be overcome, including the optimization of nanoplatform design, elucidating complex nanoplatform-brain interactions, and ensuring long-term safety and efficacy. Nonetheless, combining non-invasive neuromodulation with stimuli-responsive nanoplatforms holds revolutionary potential for neurodegenerative disease therapy, offering targeted, personalized treatments that may halt or slow disease progression. This comprehensive review explores the therapeutic potential and applications of non-invasive neuromodulation assisted by exogenous stimuli-responsive nanoplatforms for AD and PD therapy.
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  • [1] Zhou J., Jangili P., Son S., et al. (2020). Fluorescent diagnostic probes in neurodegenerative diseases. Adv. Mater. 32:e2001945. DOI:10.1002/adma.202001945

    View in Article CrossRef Google Scholar

    [2] Lin M. T. and Beal M. F. (2006). Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases. Nature 443:787−795. DOI:10.1038/nature05292

    View in Article CrossRef Google Scholar Scopus

    [3] Tian M., Ma Z. and Yang G.-Z. (2024). Micro/nanosystems for controllable drug delivery to the brain. The Innovation 5:100548. DOI:10.1016/j.xinn.2023.100548

    View in Article CrossRef Google Scholar Scopus

    [4] Furtado D., Bjornmalm M., Ayton S., et al. (2018). Overcoming the blood-brain barrier: The role of nanomaterials in treating neurological diseases. Adv. Mater. 30:1801362. DOI:10.1002/adma.201801362

    View in Article CrossRef Google Scholar

    [5] Pandit R., Chen L. and Gotz J. (2020). The blood-brain barrier: Physiology and strategies for drug delivery. Adv. Drug Deliv. Rev. 165-166:1−14. DOI:10.1016/j.addr.2019.11.009

    View in Article CrossRef Google Scholar Scopus

    [6] Colombo E., Feyen P., Antognazza M. R., et al. (2016). Nanoparticles: A challenging vehicle for neural stimulation. Front. Neurosci. 10:105. DOI:10.3389/fnins.2016.00105

    View in Article CrossRef Google Scholar Scopus

    [7] Yoo S., Mittelstein D. R., Hurt R., et al. (2022). Focused ultrasound excites cortical neurons via mechanosensitive calcium accumulation and ion channel amplification. Nat. Commun. 13:493. DOI:10.1038/s41467-022-28040-1

    View in Article CrossRef Google Scholar Scopus

    [8] Tortiglione C., Antognazza M. R., Tino A., et al. (2017). Semiconducting polymers are light nanotransducers in eyeless animals. Sci. Adv. 3:e1601699. DOI:10.1126/sciadv.1601699

    View in Article CrossRef Google Scholar Scopus

    [9] Fernandez-Yague M. A., Trotier A., Demir S., et al. (2021). A self-powered piezo-bioelectric device regulates tendon repair-associated signaling pathways through modulation of mechanosensitive ion channels. Adv. Mater. 33:2008788. DOI:10.1002/adma.202008788

    View in Article CrossRef Google Scholar

    [10] Liu H. J. and Xu P. (2022). Strategies to overcome/penetrate the BBB for systemic nanoparticle delivery to the brain/brain tumor. Adv. Drug Deliv. Rev. 191:114619. DOI:10.1016/j.addr.2022.114619

    View in Article CrossRef Google Scholar Scopus

    [11] Majumder J. and Minko T. (2021). Multifunctional and stimuli-responsive nanocarriers for targeted therapeutic delivery. Expert Opin. Drug Deliv. 18:205−227. DOI:10.1080/17425247.2021.1828339

    View in Article CrossRef Google Scholar Scopus

    [12] Zhang Z., You Y., Ge M., et al. (2023). Functional nanoparticle-enabled non-genetic neuromodulation. J. Nanobiotechnol. 21:319. DOI:10.1186/s12951-023-02084-x

    View in Article CrossRef Google Scholar Scopus

    [13] Huang H., Delikanli S., Zeng H., et al. (2010). Remote control of ion channels and neurons through magnetic-field heating of nanoparticles. Nat. Nanotechnol. 5:602−606. DOI:10.1038/nnano.2010.125

    View in Article CrossRef Google Scholar Scopus

    [14] Graff-Radford J., Yong K. X. X., Apostolova L. G., et al. (2021). New insights into atypical Alzheimer's disease in the era of biomarkers. Lancet Neurol. 20:222−234. DOI:10.1016/s1474-4422(20)30440-3

    View in Article CrossRef Google Scholar Scopus

    [15] Kavitha C., Mani V., Srividhya S. R., et al. (2022). Early-stage alzheimer's disease prediction using machine learning models. Front. Public Health 10:853294. DOI:10.3389/fpubh.2022.853294

    View in Article CrossRef Google Scholar

    [16] Busche M. A. and Hyman B. T. (2020). Synergy between amyloid-beta and tau in Alzheimer's disease. Nat. Neurosci. 23:1183−1193. DOI:10.1038/s41593-020-0687-6

    View in Article CrossRef Google Scholar

    [17] Shin W. S., Di J., Cao Q., et al. (2019). Amyloid beta-protein oligomers promote the uptake of tau fibril seeds potentiating intracellular tau aggregation. Alzheimers Res. Ther. 11:86. DOI:10.1186/s13195-019-0541-9

    View in Article CrossRef Google Scholar

    [18] Budimir A. (2011). Metal ions, Alzheimer's disease and chelation therapy. Acta Pharm. 61:1−14. DOI:10.2478/v10007-011-0006-6

    View in Article CrossRef Google Scholar Scopus

    [19] Heneka M. T., Carson M. J., El Khoury J., et al. (2015). Neuroinflammation in Alzheimer's disease. Lancet Neurol. 14:388−405. DOI:10.1016/s1474-4422(15)70016-5

    View in Article CrossRef Google Scholar Scopus

    [20] Irwin M. R. and Vitiello M. V. (2019). Implications of sleep disturbance and inflammation for Alzheimer's disease dementia. Lancet Neurol. 18:296−306. DOI:10.1016/s1474-4422(18)30450-2

    View in Article CrossRef Google Scholar Scopus

    [21] Dubois B., Villain N., Frisoni G. B., et al. (2021). Clinical diagnosis of Alzheimer's disease: Recommendations of the International Working Group. Lancet Neurol. 20:484−496. DOI:10.1016/s1474-4422(21)00066-1

    View in Article CrossRef Google Scholar

    [22] Tao Q.-Q., Cai X., Xue Y.-Y., et al. (2024). Alzheimer's disease early diagnostic and staging biomarkers revealed by large-scale cerebrospinal fluid and serum proteomic profiling. The Innovation 5:100544. DOI:10.1016/j.xinn.2023.100544

    View in Article CrossRef Google Scholar Scopus

    [23] Kalia L. V. and Lang A. E. (2015). Parkinson's disease. Lancet 386:896−912. DOI:10.1016/s0140-6736(14)61393-3

    View in Article CrossRef Google Scholar Scopus

    [24] McGregor M. M. and Nelson A. B. (2019). Circuit mechanisms of Parkinson's disease. Neuron 101:1042−1056. DOI:10.1016/j.neuron.2019.03.004

    View in Article CrossRef Google Scholar Scopus

    [25] Rocha E. M., Keeney M. T., Di Maio R., et al. (2022). LRRK2 and idiopathic Parkinson's disease. Trends Neurosci. 45:224−236. DOI:10.1016/j.tins.2021.12.002

    View in Article CrossRef Google Scholar Scopus

    [26] Malpartida A. B., Williamson M., Narendra D. P., et al. (2021). Mitochondrial dysfunction and mitophagy in Parkinson's disease: From mechanism to therapy. Trends Biochem.Sci. 46:329−343. DOI:10.1016/j.tibs.2020.11.007

    View in Article CrossRef Google Scholar Scopus

    [27] Weintraub D., Aarsland D., Chaudhuri K. R., et al. (2022). The neuropsychiatry of Parkinson's disease: Advances and challenges. Lancet Neurol. 21:89−102. DOI:10.1016/s1474-4422(21)00330-6

    View in Article CrossRef Google Scholar Scopus

    [28] Tolosa E., Garrido A., Scholz S. W., et al. (2021). Challenges in the diagnosis of Parkinson's disease. Lancet Neurol. 20:385−397. DOI:10.1016/s1474-4422(21)00030-2

    View in Article CrossRef Google Scholar Scopus

    [29] Mahoney-Sanchez L., Bouchaoui H., Ayton S., et al. (2021). Ferroptosis and its potential role in the physiopathology of Parkinson's disease. Prog. Neurobiol. 196:101890. DOI:10.1016/j.pneurobio.2020.101890

    View in Article CrossRef Google Scholar Scopus

    [30] Zhang W., Mehta A., Tong Z., et al. (2021). Development of polymeric nanoparticles for blood-brain barrier transfer-strategies and challenges. Adv. Sci. 8:2003937. DOI:10.1002/advs.202003937

    View in Article CrossRef Google Scholar

    [31] Abbott N. J. and Friedman A. (2012). Overview and introduction: The blood-brain barrier in health and disease. Epilepsia 53:1−6. DOI:10.1111/j.1528-1167.2012.03696.x

    View in Article CrossRef Google Scholar

    [32] Bell R. D., Winkler E. A., Sagare A. P., et al. (2010). Pericytes control key neurovascular functions and neuronal phenotype in the adult brain and during brain aging. Neuron 68:409−427. DOI:10.1016/j.neuron.2010.09.043

    View in Article CrossRef Google Scholar

    [33] Ising C. and Heneka M. T. (2018). Functional and structural damage of neurons by innate immune mechanisms during neurodegeneration. Cell Death Dis. 9:120. DOI:10.1038/s41419-017-0153-x

    View in Article CrossRef Google Scholar Scopus

    [34] Stephenson J., Nutma E., van der Valk P., et al. (2018). Inflammation in CNS neurodegenerative diseases. Immunology 154:204−219. DOI:10.1111/imm.12922

    View in Article CrossRef Google Scholar Scopus

    [35] Brighi C., Puttick S., Rose S., et al. (2018). The potential for remodelling the tumour vasculature in glioblastoma. Adv. Drug Deliv. Rev. 136:49−61. DOI:10.1016/j.addr.2018.10.001

    View in Article CrossRef Google Scholar Scopus

    [36] Hernandez C. and Shukla S. (2022). Liposome based drug delivery as a potential treatment option for Alzheimer's disease. Neural Regen. Res. 17:1190−1198. DOI:10.4103/1673-5374.327328

    View in Article CrossRef Google Scholar Scopus

    [37] Has C. and Sunthar P. (2020). A comprehensive review on recent preparation techniques of liposomes. J. Liposome Res. 30:336−365. DOI:10.1080/08982104.2019.1668010

    View in Article CrossRef Google Scholar Scopus

    [38] Elliott R. O. and He M. (2021). Unlocking the power of exosomes for crossing biological barriers in drug delivery. Pharmaceutics 13:122. DOI:10.3390/pharmaceutics13010122

    View in Article CrossRef Google Scholar Scopus

    [39] Mardpour S., Hamidieh A. A., Taleahmad S., et al. (2019). Interaction between mesenchymal stromal cell-derived extracellular vesicles and immune cells by distinct protein content. J. Cell. Physiol. 234:8249−8258. DOI:10.1002/jcp.27669

    View in Article CrossRef Google Scholar Scopus

    [40] Li Z., Liu F., He X., et al. (2019). Exosomes derived from mesenchymal stem cells attenuate inflammation and demyelination of the central nervous system in EAE rats by regulating the polarization of microglia. Int. Immunopharmacol. 67:268−280. DOI:10.1016/j.intimp.2018.12.001

    View in Article CrossRef Google Scholar Scopus

    [41] Armstrong J. P. K., Holme M. N. and Stevens M. M. (2017). Re-engineering extracellular vesicles as smart nanoscale therapeutics. Acs Nano 11:69−83. DOI:10.1021/acsnano.6b07607

    View in Article CrossRef Google Scholar

    [42] Ruan H., Li Y., Zheng D., et al. (2023). Engineered extracellular vesicles for ischemic stroke treatment. The Innovation 4:100394. DOI:10.1016/j.xinn.2023.100394

    View in Article CrossRef Google Scholar Scopus

    [43] Teleanu R. I., Preda M. D., Niculescu A.-G., et al. (2022). Current strategies to enhance delivery of drugs across the blood-brain barrier. Pharmaceutics 14:987. DOI:10.3390/pharmaceutics14050987

    View in Article CrossRef Google Scholar

    [44] Schally A. V. and Nagy A. (2004). Chemotherapy targeted to cancers through tumoral hormone receptors. Trends Endocrinol. Metab. 15:300−310. DOI:10.1016/j.tem.2004.07.002

    View in Article CrossRef Google Scholar Scopus

    [45] Iqbal I., Saqib F., Mubarak Z., et al. (2024). Alzheimer's disease and drug delivery across the blood-brain barrier: Approaches and challenges. Eur. J. Med. Res. 29:313. DOI:10.1186/s40001-024-01915-3

    View in Article CrossRef Google Scholar

    [46] Huang D., Wang J., Song C., et al. (2023). Ultrasound-responsive matters for biomedical applications. The Innovation 4:100421. DOI:10.1016/j.xinn.2023.100421

    View in Article CrossRef Google Scholar Scopus

    [47] Zhang J., Liu H., Du X., et al. (2017). Increasing of blood-brain tumor barrier permeability through transcellular and paracellular pathways by microbubble-enhanced diagnostic ultrasound in a C6 glioma model. Front. Neurosci. 11:86. DOI:10.3389/fnins.2017.00086

    View in Article CrossRef Google Scholar Scopus

    [48] Meng Y., Volpini M., Black S., et al. (2017). Focused ultrasound as a novel strategy for Alzheimer disease therapeutics. Ann. Neurol. 81:611−617. DOI:10.1002/ana.24933

    View in Article CrossRef Google Scholar Scopus

    [49] Park J., Aryal M., Vykhodtseva N., et al. (2017). Evaluation of permeability, doxorubicin delivery, and drug retention in a rat brain tumor model after ultrasound-induced blood-tumor barrier disruption. J. Control. Release 250:77−85. DOI:10.1016/j.jconrel.2016.10.011

    View in Article CrossRef Google Scholar Scopus

    [50] Aryal M., Fischer K., Gentile C., et al. (2017). Effects on p-glycoprotein expression after blood-brain barrier disruption using focused ultrasound and microbubbles. PLoS One 12:e0166061. DOI:10.1371/journal.pone.0166061

    View in Article CrossRef Google Scholar

    [51] Mohapatra A., Uthaman S. and Park I.-K. (2021). External and internal stimuli-responsive metallic nanotherapeutics for enhanced anticancer therapy. Front. Mol. Biosci. 7:597634. DOI:10.3389/fmolb.2020.597634

    View in Article CrossRef Google Scholar

    [52] Rajendrakumar S. K., Cherukula K., Park H. J., et al. (2018). Dual-stimuli-responsive albumin-polyplex nanoassembly for spatially controlled gene release in metastatic breast cancer. J. Control. Release 276:72−83. DOI:10.1016/j.jconrel.2018.02.039

    View in Article CrossRef Google Scholar Scopus

    [53] Wu W., Luo L., Wang Y., et al. (2018). Endogenous pH-responsive nanoparticles with programmable size changes for targeted tumor therapy and imaging applications. Theranostics 8:3038−3058. DOI:10.7150/thno.23459

    View in Article CrossRef Google Scholar Scopus

    [54] Yao J., Feng J. and Chen J. (2016). External-stimuli responsive systems for cancer theranostic. Asian J. Pharm. Sci. 11:585−595. DOI:10.1016/j.ajps.2016.06.001

    View in Article CrossRef Google Scholar Scopus

    [55] Xu Z., Yang D., Long T., et al. (2022). pH-sensitive nanoparticles based on amphiphilic imidazole/cholesterol modified hydroxyethyl starch for tumor chemotherapy. Carbohydr. Polym. 277:118827. DOI:10.1016/j.carbpol.2021.118827

    View in Article CrossRef Google Scholar

    [56] Kanamala M., Wilson W. R., Yang M., et al. (2016). Mechanisms and biomaterials in pH-responsive tumour targeted drug delivery: A review. Biomaterials 85:152−167. DOI:10.1016/j.biomaterials.2016.01.061

    View in Article CrossRef Google Scholar Scopus

    [57] Chu S., Shi X., Tian Y., et al. (2022). pH-responsive polymer nanomaterials for tumor therapy. Front. Oncol. 12:855019. DOI:10.3389/fonc.2022.855019

    View in Article CrossRef Google Scholar

    [58] Zhao Y., Liu X., Peng X., et al. (2022). A poloxamer/hyaluronic acid/chitosan-based thermosensitive hydrogel that releases dihydromyricetin to promote wound healing. Int. J. Biol. Macromol. 216:475−486. DOI:10.1016/j.ijbiomac.2022.06.210

    View in Article CrossRef Google Scholar Scopus

    [59] Chen Q., Jia C., Xu Y., et al. (2022). Dual-pH responsive chitosan nanoparticles for improving in vivo drugs delivery and chemoresistance in breast cancer. Carbohydr. Polym. 290:119518. DOI:10.1016/j.carbpol.2022.119518

    View in Article CrossRef Google Scholar Scopus

    [60] Liu A., Liang C., Liu J., et al. (2022). Reactive oxygen species horizontal line responsive lipid nanoparticles for effective RNAi and corneal neovascularization therapy. ACS Appl. Mater. Interfaces 14:17022−17031. DOI:10.1021/acsami.1c23412

    View in Article CrossRef Google Scholar

    [61] Li Q., Wen Y., You X., et al. (2016). Development of a reactive oxygen species (ROS)-responsive nanoplatform for targeted oral cancer therapy. J. Mat. Chem. B 4:4675−4682. DOI:10.1039/c6tb01016d

    View in Article CrossRef Google Scholar Scopus

    [62] Xu X., Saw P. E., Tao W., et al. (2017). ROS-responsive polyprodrug nanoparticles for triggered drug delivery and effective cancer therapy. Adv. Mater. 29:1700141. DOI:10.1002/adma.201700141

    View in Article CrossRef Google Scholar

    [63] Saravanakumar G., Kim J. and Kim W. J. (2017). Reactive-oxygen-species-responsive drug delivery systems: Promises and challenges. Adv. Sci. 4:1600124. DOI:10.1002/advs.201600124

    View in Article CrossRef Google Scholar

    [64] Xu Q., He C., Xiao C., et al. (2016). Reactive oxygen species (ROS) responsive polymers for biomedical applications. Macromol. Biosci. 16:635−646. DOI:10.1002/mabi.201500440

    View in Article CrossRef Google Scholar

    [65] Jin L., Zhu Z., Hong L., et al. (2023). ROS-responsive 18beta-glycyrrhetic acid-conjugated polymeric nanoparticles mediate neuroprotection in ischemic stroke through HMGB1 inhibition and microglia polarization regulation. Bioact. Mater. 19:38−49. DOI:10.1016/j.bioactmat.2022.03.040

    View in Article CrossRef Google Scholar

    [66] Zhang R., Liu R., Liu C., et al. (2020). A pH/ROS dual-responsive and targeting nanotherapy for vascular inflammatory diseases. Biomaterials 230:119605. DOI:10.1016/j.biomaterials.2019.119605

    View in Article CrossRef Google Scholar Scopus

    [67] Karimi M., Ghasemi A., Zangabad P. S., et al. (2016). Smart micro/nanoparticles in stimulus-responsive drug/gene delivery systems. Chem. Soc. Rev. 45:1457−1501. DOI:10.1039/c5cs00798d

    View in Article CrossRef Google Scholar Scopus

    [68] Mi P. (2020). Stimuli-responsive nanocarriers for drug delivery, tumor imaging, therapy and theranostics. Theranostics 10:4557−4588. DOI:10.7150/thno.38069

    View in Article CrossRef Google Scholar Scopus

    [69] Ovejero J. G., Armenia I., Serantes D., et al. (2021). Selective magnetic nanoheating: Combining iron oxide nanoparticles for multi-hot-spot induction and sequential regulation. Nano Lett. 21:7213−7220. DOI:10.1021/acs.nanolett.1c02178

    View in Article CrossRef Google Scholar

    [70] Wu W., Liu J., Gong P., et al. (2022). Construction of core-shell nanoMOFs@microgel for aqueous lubrication and thermal-responsive drug release. Small 18:e2202510. DOI:10.1002/smll.202202510

    View in Article CrossRef Google Scholar

    [71] Wells C. M., Harris M., Choi L., et al. (2019). Stimuli-responsive drug release from smart polymers. J. Funct. Biomater. 10DOI:10.3390/jfb10030034.

    View in Article Google Scholar

    [72] Puoci F., Hampel S., Parisi O. I., et al. (2013). Imprinted microspheres doped with carbon nanotubes as novel electroresponsive drug-delivery systems. J. Appl. Polym. Sci. 130:829−834. DOI:10.1002/app.39212

    View in Article CrossRef Google Scholar Scopus

    [73] Loh D. M., Nava M. and Nocera D. G. (2022). Polypyrrole-silicon nanowire arrays for controlled intracellular cargo delivery. Nano Lett. 22:366−371. DOI:10.1021/acs.nanolett.1c04033

    View in Article CrossRef Google Scholar

    [74] Wang S., Bai Y., Wang D., et al. (2022). Reversing tumor to “hot”: A NIR light-triggered carrier-free nanoplatform for enhanced tumor penetration and photo-induced immunotherapy. Chem. Eng. J. 442DOI:10.1016/j.cej.2022.136322.

    View in Article Google Scholar

    [75] Roy B., Mengji R., Roy S., et al. (2022). NIR-responsive lysosomotropic phototrigger: An "AIE plus ESIPT" active naphthalene-based single-component photoresponsive nanocarrier with two-photon uncaging and real-time monitoring ability. ACS Appl. Mater. Interfaces 14:4862−4870. DOI:10.1021/acsami.1c19022

    View in Article CrossRef Google Scholar

    [76] Balakrishnan P. B., Silvestri N., Fernandez-Cabada T., et al. (2020). Exploiting unique alignment of cobalt ferrite nanoparticles, mild hyperthermia, and controlled intrinsic cobalt toxicity for cancer therapy. Adv. Mater. 32:e2003712. DOI:10.1002/adma.202003712

    View in Article CrossRef Google Scholar

    [77] You D. G., Deepagan V. G., Um W., et al. (2016). ROS-generating TiO2 nanoparticles for non-invasive sonodynamic therapy of cancer. Sci. Rep. 6:23200. DOI:10.1038/srep23200

    View in Article CrossRef Google Scholar

    [78] Wang J., Xie L., Shi Y., et al. (2021). Early detection and reversal of cell apoptosis induced by focused ultrasound-mediated blood-brain barrier opening. Acs Nano 15:14509−14521. DOI:10.1021/acsnano.1c04029

    View in Article CrossRef Google Scholar

    [79] Son S., Kim J. H., Wang X., et al. (2020). Multifunctional sonosensitizers in sonodynamic cancer therapy. Chem. Soc. Rev. 49:3244−3261. DOI:10.1039/c9cs00648f

    View in Article CrossRef Google Scholar Scopus

    [80] Liu T., Zhang N., Wang Z., et al. (2017). Endogenous catalytic generation of O2 bubbles for in situ ultrasound-guided high intensity focused ultrasound ablation. Acs Nano 11:9093−9102. DOI:10.1021/acsnano.7b03772

    View in Article CrossRef Google Scholar

    [81] Peng X., Han Q., Zhou X., et al. (2022). Effect of pH-sensitive nanoparticles on inhibiting oral biofilms. Drug Deliv. 29:561−573. DOI:10.1080/10717544.2022.2037788

    View in Article CrossRef Google Scholar Scopus

    [82] Sun Y., Gong L., Yin Y., et al. (2022). A gradient pH-sensitive polymer-based antiviral strategy via viroporin-induced membrane acidification. Adv. Mater. 34:2109580. DOI:10.1002/adma.202109580

    View in Article CrossRef Google Scholar

    [83] Wu H., Xia F., Zhang L., et al. (2022). A ROS-sensitive nanozyme-augmented photoacoustic nanoprobe for early diagnosis and therapy of acute liver failure. Adv. Mater. 34:2108348. DOI:10.1002/adma.202108348

    View in Article CrossRef Google Scholar

    [84] Zhou X., Liu X., Yang X., et al. (2021). Tumor progress intercept by intervening in Caveolin-1 related intercellular communication via ROS-sensitive c-Myc targeting therapy. Biomaterials 275:120958. DOI:10.1016/j.biomaterials.2021.120958

    View in Article CrossRef Google Scholar Scopus

    [85] Han L., Zhang X.-Y., Wang Y.-L., et al. (2017). Redox-responsive theranostic nanoplatforms based on inorganic nanomaterials. J. Control. Release 259:40−52. DOI:10.1016/j.jconrel.2017.03.018

    View in Article CrossRef Google Scholar Scopus

    [86] Li Y., Feng S., Dai P., et al. (2022). Tailored Trojan horse nanocarriers for enhanced redox-responsive drug delivery. J. Control. Release 342:201−209. DOI:10.1016/j.jconrel.2022.01.006

    View in Article CrossRef Google Scholar Scopus

    [87] Riber C. F., Smith A. A. A. and Zelikin A. N. (2015). Self-immolative linkers literally bridge disulfide chemistry and the realm of thiol-free drugs. Adv. Healthc. Mater. 4:1887−1890. DOI:10.1002/adhm.201500344

    View in Article CrossRef Google Scholar

    [88] Lv F., Li C., Ma Y., et al. (2019). Fabrication of step-by-step drug release system both sensitive to magnetic field and temperature based on layered double hydroxides and PNIPAM. Nanotechnology 30:055103. DOI:10.1088/1361-6528/aaf095

    View in Article CrossRef Google Scholar Scopus

    [89] Yadav R. and Venkatesu P. (2019). Functionalized carbon nanotubes modulate the phase transition behavior of thermoresponsive polymer via hydrophilic-hydrophobic balance. Polymer 178:121573. DOI:10.1016/j.polymer.2019.121573

    View in Article CrossRef Google Scholar Scopus

    [90] Chen T., Yang Y., Peng H., et al. (2021). Cellulose nanocrystals reinforced highly stretchable thermal-sensitive hydrogel with ultra-high drug loading. Carbohydr. Polym. 266:118122. DOI:10.1016/j.carbpol.2021.118122

    View in Article CrossRef Google Scholar Scopus

    [91] Bauer S. M., Bauer R. J. and Velazquez O. C. (2005). Angiogenesis, vasculogenesis, and induction of healing in chronic wounds. Vasc. Endovasc. Surg. 39:293−306. DOI:10.1177/153857440503900401

    View in Article CrossRef Google Scholar Scopus

    [92] Magaz A., Ashton M. D., Hathout R. M., et al. (2020). Electroresponsive silk-based biohybrid composites for electrochemically controlled growth factor delivery. Pharmaceutics 12:742. DOI:10.3390/pharmaceutics12080742

    View in Article CrossRef Google Scholar Scopus

    [93] Ajdary R., Ezazi N. Z., Correia A., et al. (2020). Multifunctional 3D-printed patches for long-term drug release therapies after myocardial infarction. Adv. Funct. Mater. 30:2003440. DOI:10.1002/adfm.202003440

    View in Article CrossRef Google Scholar

    [94] Donahue M. J., Sanchez-Sanchez A., Inal S., et al. (2020). Tailoring PEDOT properties for applications in bioelectronics. Mater. Sci. Eng. R-Rep. 140:100546. DOI:10.1016/j.mser.2020.100546

    View in Article CrossRef Google Scholar Scopus

    [95] Enshaei H., Puiggali-Jou A., del Valle L. J., et al. (2021). Nanotheranostic interface based on antibiotic-loaded conducting polymer nanoparticles for real-time monitoring of bacterial growth inhibition. Adv. Healthc. Mater. 10:2001636. DOI:10.1002/adhm.202001636

    View in Article CrossRef Google Scholar

    [96] Sun Q., Hou X., Yang J., et al. (2021). Heparin-coated photosensitive metal-organic frameworks as drug delivery nanoplatforms of autophagy inhibitors for sensitized photodynamic therapy against breast cancer. ACS Appl. Mater. Interfaces 13:55577−55590. DOI:10.1021/acsami.1c18055

    View in Article CrossRef Google Scholar

    [97] Tong X., Gan S., Wu J., et al. (2020). A nano-photosensitizer based on covalent organic framework nanosheets with high loading and therapeutic efficacy. Nanoscale 12:7376−7382. DOI:10.1039/c9nr10787h

    View in Article CrossRef Google Scholar Scopus

    [98] Xiao F., Cao B., Wen L., et al. (2020). Photosensitizer conjugate-functionalized poly(hexamethylene guanidine) for potentiated broad-spectrum bacterial inhibition and enhanced biocompatibility. Chin. Chem. Lett. 31:2516−2519. DOI:10.1016/j.cclet.2020.06.038

    View in Article CrossRef Google Scholar Scopus

    [99] Wang Y., Boero G., Zhang X., et al. (2022). Nanopore generation in biodegradable silk/magnetic nanoparticle membranes by an external magnetic field for implantable drug delivery. ACS Appl. Mater. InterfacesDOI:10.1021/acsami.2c10603.

    View in Article Google Scholar

    [100] Deatsch A. E. and Evans B. A. (2014). Heating efficiency in magnetic nanoparticle hyperthermia. J. Magn. Magn. Mater. 354:163−172. DOI:10.1016/j.jmmm.2013.11.006

    View in Article CrossRef Google Scholar Scopus

    [101] Banobre-Lopez M., Teijeiro A. and Rivas J. (2013). Magnetic nanoparticle-based hyperthermia for cancer treatment. Rep. Pract. Oncol. Radiother. 18:397−400. DOI:10.1016/j.rpor.2013.09.011

    View in Article CrossRef Google Scholar Scopus

    [102] Boissenot T., Bordat A., Fattal E., et al. (2016). Ultrasound-triggered drug delivery for cancer treatment using drug delivery systems: From theoretical considerations to practical applications. J. Control. Release 241:144−163. DOI:10.1016/j.jconrel.2016.09.026

    View in Article CrossRef Google Scholar Scopus

    [103] Canavese G., Ancona A., Racca L., et al. (2018). Nanoparticle-assisted ultrasound: A special focus on sonodynamic therapy against cancer. Chem. Eng. J. 340:155−172. DOI:10.1016/j.cej.2018.01.060

    View in Article CrossRef Google Scholar Scopus

    [104] Cesmeli S. and Avci C. B. (2019). Application of titanium dioxide (TiO2) nanoparticles in cancer therapies. J. Drug Target. 27:762−766. DOI:10.1080/1061186x.2018.1527338

    View in Article CrossRef Google Scholar

    [105] Shanei A. and Sazgarnia A. (2019). An overview of therapeutic applications of ultrasound based on synergetic effects with gold nanoparticles and laser excitation. Iran. J. Basic Med. Sci. 22:848−855.

    View in Article Google Scholar Scopus

    [106] Shanei A. and Akbari-Zadeh H. (2019). Investigating the sonodynamic-radiosensitivty effect of gold nanoparticles on HeLa cervical cancer cells. J. Korean Med. Sci. 34:e243. DOI:10.3346/jkms.2019.34.e243

    View in Article CrossRef Google Scholar

    [107] Heinzelman P., Schoborg J. A. and Jewett M. C. (2015). pH responsive granulocyte colony-stimulating factor variants with implications for treating Alzheimer's disease and other central nervous system disorders. Protein Eng. Des. Sel. 28:481−489. DOI:10.1093/protein/gzv022

    View in Article CrossRef Google Scholar Scopus

    [108] Zhang L., Liu X. g., Liu D. q., et al. (2020). A conditionally releasable “do not eat me” CD47 signal facilitates microglia‐targeted drug delivery for the treatment of Alzheimer's disease. Adv. Funct. Mater. 30DOI:10.1002/adfm.201910691.

    View in Article Google Scholar

    [109] Hu B., Dai F., Fan Z., et al. (2015). Nanotheranostics: Congo red/rutin-MNPs with enhanced magnetic resonance imaging and H2O2-responsive therapy of Alzheimer's disease in APPswe/PS1dE9 transgenic mice. Adv. Mater. 27:5499−5505. DOI:10.1002/adma.201502227

    View in Article CrossRef Google Scholar

    [110] Xu S., Yang P., Qian K., et al. (2022). Modulating autophagic flux via ROS-responsive targeted micelles to restore neuronal proteostasis in Alzheimer's disease. Bioact. Mater. 11:300−316. DOI:10.1016/j.bioactmat.2021.06.017

    View in Article CrossRef Google Scholar Scopus

    [111] Ballance W. C., Qin E. C., Chung H. J., et al. (2019). Reactive oxygen species-responsive drug delivery systems for the treatment of neurodegenerative diseases. Biomaterials 217:119292. DOI:10.1016/j.biomaterials.2019.119292

    View in Article CrossRef Google Scholar Scopus

    [112] Pettignano A., Grijalvo S., Haering M., et al. (2017). Boronic acid-modified alginate enables direct formation of injectable, self-healing and multistimuli-responsive hydrogels. Chem. Commun. 53:3350−3353. DOI:10.1039/c7cc00765e

    View in Article CrossRef Google Scholar Scopus

    [113] Yang B., Chen Y. and Shi J. (2019). Reactive oxygen species (ROS)-based nanomedicine. Chem. Rev. 119:4881−4985. DOI:10.1021/acs.chemrev.8b00626

    View in Article CrossRef Google Scholar Scopus

    [114] Liu Z., Zhang B., Xia S., et al. (2021). ROS-responsive and multifunctional anti-Alzheimer prodrugs: Tacrine-ibuprofen hybrids via a phenyl boronate linker. Eur. J. Med. Chem. 212:112997. DOI:10.1016/j.ejmech.2020.112997

    View in Article CrossRef Google Scholar Scopus

    [115] Zhou H., Gong Y., Liu Y., et al. (2020). Intelligently thermoresponsive flower-like hollow nano-ruthenium system for sustained release of nerve growth factor to inhibit hyperphosphorylation of tau and neuronal damage for the treatment of Alzheimer's disease. Biomaterials 237:119822. DOI:10.1016/j.biomaterials.2020.119822

    View in Article CrossRef Google Scholar Scopus

    [116] Georgieva D., Ivanova-Mileva K., Ivanova S., et al. (2020). Thermoresponsive poly(N-isopropylacrylamide) copolymer networks for galantamine hydrobromide delivery. Colloid Polym. Sci. 298:377−384. DOI:10.1007/s00396-020-04621-8

    View in Article CrossRef Google Scholar Scopus

    [117] Geng H., Yuan H., Qiu L., et al. (2020). Inhibition and disaggregation of amyloid beta protein fibrils through conjugated polymer-core thermoresponsive micelles. J. Mat. Chem. B 8:10126−10135. DOI:10.1039/d0tb01863e

    View in Article CrossRef Google Scholar

    [118] Guimard N. K., Gomez N. and Schmidt C. E. (2007). Conducting polymers in biomedical engineering. Prog. Polym. Sci. 32:876−921. DOI:10.1016/j.progpolymsci.2007.05.012

    View in Article CrossRef Google Scholar Scopus

    [119] Xu H., Holzwarth J. M., Yan Y., et al. (2014). Conductive PPY/PDLLA conduit for peripheral nerve regeneration. Biomaterials 35:225−235. DOI:10.1016/j.biomaterials.2013.10.002

    View in Article CrossRef Google Scholar Scopus

    [120] Wu Y., Wang L., Guo B., et al. (2016). Electroactive biodegradable polyurethane significantly enhanced Schwann cells myelin gene expression and neurotrophin secretion for peripheral nerve tissue engineering. Biomaterials 87:18−31. DOI:10.1016/j.biomaterials.2016.02.010

    View in Article CrossRef Google Scholar Scopus

    [121] Xie M., Wang L., Guo B., et al. (2015). Ductile electroactive biodegradable hyperbranched polylactide copolymers enhancing myoblast differentiation. Biomaterials 71:158−167. DOI:10.1016/j.biomaterials.2015.08.042

    View in Article CrossRef Google Scholar Scopus

    [122] Chen J., Dong R., Ge J., et al. (2015). Biocompatible, biodegradable, and electroactive polyurethane-urea elastomers with tunable hydrophilicity for skeletal muscle tissue engineering. ACS Appl. Mater. Interfaces 7:28273−28285. DOI:10.1021/acsami.5b10829

    View in Article CrossRef Google Scholar

    [123] Xie M., Wang L., Ge J., et al. (2015). Strong electroactive biodegradable shape memory polymer networks based on star-shaped polylactide and aniline trimer for bone tissue engineering. ACS Appl. Mater. Interfaces 7:6772−6781. DOI:10.1021/acsami.5b00191

    View in Article CrossRef Google Scholar Scopus

    [124] Li W., Luo R., Lin X., et al. (2015). Remote modulation of neural activities via near-infrared triggered release of biomolecules. Biomaterials 65:76−85. DOI:10.1016/j.biomaterials.2015.06.041

    View in Article CrossRef Google Scholar Scopus

    [125] Kim D., Kwon H. J. and Hyeon T. (2019). Magnetite/ceria nanoparticle assemblies for extracorporeal cleansing of amyloid-beta in Alzheimer's disease. Adv. Mater. 31:1807965. DOI:10.1002/adma.201807965

    View in Article CrossRef Google Scholar

    [126] Dyne E., Prakash P. S., Li J., et al. (2021). Mild magnetic nanoparticle hyperthermia promotes the disaggregation and microglia-mediated clearance of beta-amyloid plaques. Nanomed.-Nanotechnol. Biol. Med. 34:102397. DOI:10.1016/j.nano.2021.102397

    View in Article CrossRef Google Scholar Scopus

    [127] Razzokov J., Yusupov M. and Bogaerts A. (2019). Oxidation destabilizes toxic amyloid beta peptide aggregation. Sci. Rep. 9:5476. DOI:10.1038/s41598-019-41931-6

    View in Article CrossRef Google Scholar Scopus

    [128] Kang S.-g., Tien H., Xia Z., et al. (2013). Hydrophobic interaction drives surface-assisted epitaxial assembly of amyloid-like peptides. J. Am. Chem. Soc. 135:3150−3157. DOI:10.1021/ja310989u

    View in Article CrossRef Google Scholar Scopus

    [129] Karthika V., Sridharan B., Nam J. W., et al. (2024). Neuromodulation by nanozymes and ultrasound during Alzheimer's disease management. J. Nanobiotechnol. 22:139. DOI:10.1186/s12951-024-02406-7

    View in Article CrossRef Google Scholar

    [130] Jiang J., Zhao K., Xiao X., et al. (2012). Synthesis and facet-dependent photoreactivity of BiOCl single-crystalline nanosheets. J. Am. Chem. Soc. 134:4473−4476. DOI:10.1021/ja210484t

    View in Article CrossRef Google Scholar Scopus

    [131] Jang J., Kim K., Yoon J., et al. (2020). Piezoelectric materials for ultrasound-driven dissociation of Alzheimer's β-amyloid aggregate structure. Biomaterials 255:120165. DOI:10.1016/j.biomaterials.2020.120165

    View in Article CrossRef Google Scholar Scopus

    [132] Tzankov B., Tzankova V., Aluani D., et al. (2019). Development of MCM-41 mesoporous silica nanoparticles as a platform for pramipexole delivery. J. Drug Deliv. Sci. Technol. 51:26−35. DOI:10.1016/j.jddst.2019.02.008

    View in Article CrossRef Google Scholar Scopus

    [133] Gombotz W. R. and Wee S. F. (1998). Protein release from alginate matrices. Adv. Drug Deliv. Rev. 31:267−285. DOI:10.1016/s0169-409x(97)00124-5

    View in Article CrossRef Google Scholar Scopus

    [134] Tan J. P. K., Voo Z. X., Lim S., et al. (2019). Effective encapsulation of apomorphine into biodegradable polymeric nanoparticles through a reversible chemical bond for delivery across the blood-brain barrier. Nanomed.-Nanotechnol. Biol. Med. 17:236−245. DOI:10.1016/j.nano.2019.01.014

    View in Article CrossRef Google Scholar

    [135] Pichla M., Bartosz G., Stefaniuk I., et al. (2021). pH-responsive redox nanoparticles protect SH-SY5Y cells at lowered pH in a cellular model of Parkinson's disease. Molecules 26:543. DOI:10.3390/molecules26030543

    View in Article CrossRef Google Scholar Scopus

    [136] Hao C., Qu A., Xu L., et al. (2019). Chiral molecule-mediated porous CuxO nanoparticle clusters with antioxidation activity for ameliorating Parkinson's disease. J. Am. Chem. Soc. 141:1091−1099. DOI:10.1021/jacs.8b11856

    View in Article CrossRef Google Scholar Scopus

    [137] Li S., Liu J., Li G., et al. (2019). Near-infrared light-responsive, pramipexole-loaded biodegradable PLGA microspheres for therapeutic use in Parkinson's disease. Eur. J. Pharm. Biopharm. 141:1−11. DOI:10.1016/j.ejpb.2019.05.013

    View in Article CrossRef Google Scholar Scopus

    [138] Zhou X., Li B., Guo M., et al. (2022). Microneedle patch based on molecular motor as a spatio-temporal controllable dosing strategy of L-DOPA for Parkinson's disease. Chem. Eng. J. 427:131555. DOI:10.1016/j.cej.2021.131555

    View in Article CrossRef Google Scholar Scopus

    [139] Wang M., Li L., Zhang X., et al. (2018). Magnetic resveratrol liposomes as a new theranostic platform for magnetic resonance imaging guided Parkinson's disease targeting therapy. ACS Sustain. Chem. Eng. 6:17124−17133. DOI:10.1021/acssuschemeng.8b04507

    View in Article CrossRef Google Scholar Scopus

    [140] Niu S., Zhang L.-K., Zhang L., et al. (2017). Inhibition by multifunctional magnetic nanoparticles loaded with alpha-synuclein RNAi plasmid in a Parkinson's disease model. Theranostics 7:344−356. DOI:10.7150/thno.16562

    View in Article CrossRef Google Scholar Scopus

    [141] Xu T., Lu X., Peng D., et al. (2020). Ultrasonic stimulation of the brain to enhance the release of dopamine-a potential novel treatment for Parkinsons disease. Ultrason. Sonochem. 63:104955. DOI:10.1016/j.ultsonch.2019.104955

    View in Article CrossRef Google Scholar

    [142] Bond A. E., Shah B. B., Huss D. S., et al. (2017). Safety and efficacy of focused ultrasound thalamotomy for patients with medication-refractory, tremor-dominant Parkinson disease a randomized clinical trial. JAMA Neurol. 74:1412−1418. DOI:10.1001/jamaneurol.2017.3098

    View in Article CrossRef Google Scholar

  • Cite this article:

    Mao M., Komes D., Zhao S., et al. (2025). Non-invasive neuromodulation assisted by exogenous stimuli-responsive nanoplatforms for Alzheimer’s disease and Parkinson's disease therapy. The Innovation Medicine 3:100121. https://doi.org/10.59717/j.xinn-med.2025.100121
    Mao M., Komes D., Zhao S., et al. (2025). Non-invasive neuromodulation assisted by exogenous stimuli-responsive nanoplatforms for Alzheimer’s disease and Parkinson's disease therapy. The Innovation Medicine 3:100121. https://doi.org/10.59717/j.xinn-med.2025.100121

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