We use cookies to improve your experience. By continuing to browse this site, you accept our cookie policy.×
Skip main navigation
Aging Health
Bioelectronics in Medicine
Biomarkers in Medicine
Breast Cancer Management
CNS Oncology
Colorectal Cancer
Concussion
Epigenomics
Future Cardiology
Future Medicine AI
Future Microbiology
Future Neurology
Future Oncology
Future Rare Diseases
Future Virology
Hepatic Oncology
HIV Therapy
Immunotherapy
International Journal of Endocrine Oncology
International Journal of Hematologic Oncology
Journal of 3D Printing in Medicine
Lung Cancer Management
Melanoma Management
Nanomedicine
Neurodegenerative Disease Management
Pain Management
Pediatric Health
Personalized Medicine
Pharmacogenomics
Regenerative Medicine
Research Article

Magnetoelectric ‘spin’ on stimulating the brain

    Rakesh Guduru

    Department of Cellular Biology & Pharmacology, Herbert Wertheim College of Medicine, Florida International University, Miami, FL 33199, USA

    Department of Electrical & Computer Engineering, Florida International University, Miami, FL 33174, USA

    ,
    Ping Liang

    Department of Electrical & Computer Engineering, University of California, Riverside, CA 92521, USA

    ,
    J Hong

    Department of Electrical Engineering & Computer Science, University of California, Berkeley, CA 94720, USA

    ,
    Alexandra Rodzinski

    Department of Cellular Biology & Pharmacology, Herbert Wertheim College of Medicine, Florida International University, Miami, FL 33199, USA

    ,
    Ali Hadjikhani

    Department of Electrical & Computer Engineering, Florida International University, Miami, FL 33174, USA

    ,
    Jeffrey Horstmyer

    Neuroscience Centers of Florida Foundation, Miami, FL 33124, USA

    ,
    Ernest Levister

    School of Medicine, University of California, Irvine, CA 92697, USA

    &
    Sakhrat Khizroev

    *Author for correspondence:

    E-mail Address: khizroev@fiu.edu

    Department of Cellular Biology & Pharmacology, Herbert Wertheim College of Medicine, Florida International University, Miami, FL 33199, USA

    Department of Electrical & Computer Engineering, Florida International University, Miami, FL 33174, USA

    Neuroscience Centers of Florida Foundation, Miami, FL 33124, USA

    Published Online:https://doi.org/10.2217/nnm.15.52

    Aim: The in vivo study on imprinting control region mice aims to show that magnetoelectric nanoparticles may directly couple the intrinsic neural activity-induced electric fields with external magnetic fields. Methods: Approximately 10 µg of CoFe2O4–BaTiO3 30-nm nanoparticles have been intravenously administrated through a tail vein and forced to cross the blood–brain barrier via a d.c. field gradient of 3000 Oe/cm. A surgically attached two-channel electroencephalography headmount has directly measured the modulation of intrinsic electric waveforms by an external a.c. 100-Oe magnetic field in a frequency range of 0–20 Hz. Results: The modulated signal has reached the strength comparable to that due the regular neural activity. Conclusion: The study opens a pathway to use multifunctional nanoparticles to control intrinsic fields deep in the brain.

    Papers of special note have been highlighted as: • of interest

    References

    • 1 Marblestone AH et al. Physical principles for scalable neural recording. Front. Comput. Neurosci. 7, 137 (2013).• Gives a unique technology angle on the current state of neuroengineering.Crossref, MedlineGoogle Scholar
    • 2 Hopfield JJ. Neurons with graded response have collective computational properties like those of two-state neurons. Proc. Natl Acad. Sci. USA 81, 3088–3092 (1984).Crossref, Medline, CASGoogle Scholar
    • 3 De Kramer J. The electrical circuitry of an olfactory sensillum in Antheraea polyphemus. J. Neurosci. 5, 2484–2493 (1985).• Presents the concept of the brain's electric circuitry.Crossref, Medline, CASGoogle Scholar
    • 4 Srikanth M, Kessler JA. Nanotechnology – novel therapeutics for central nervous system disorders. Nat. Rev. Neurol. 8, 307–318 (2012).• Gives an overview of using nanotechnology for treating CNS disorders.Crossref, Medline, CASGoogle Scholar
    • 5 Yue K et al. Magneto-electric nano-particles for non-invasive brain stimulation. PLoS ONE 7, e44040 (2012).• Gives a theoretical insight into using magnetoelectric nanoparticles for noninvasive brain stimulation.Crossref, Medline, CASGoogle Scholar
    • 6 Brambilla D, Le Droumaguet B, Nicolas J et al. Nanotechnologies for Alzheimer's disease: diagnosis, therapy, and safety issues. Nanomedicine 7, 521–540 (2011).Crossref, Medline, CASGoogle Scholar
    • 7 Kringelbach ML, Jenkinson N, Owen SL, Aziz TZ. Translational principles of deep brain stimulation. Nat. Rev. Neurol. 8, 623–635 (2007).Crossref, CASGoogle Scholar
    • 8 Stefani A et al. Bilateral deep brain stimulation of the pedunculopontine and subthalamic nuclei in severe Parkinson's disease. Brain 130, 1596–1607 (2007).Crossref, MedlineGoogle Scholar
    • 9 Schlaepfer TE et al. Deep brain stimulation to reward circuitry alleviates anhedonia in refractory major depression. Neuropsychopharmacology 33, 368–377 (2008).Crossref, MedlineGoogle Scholar
    • 10 Barker AT, Jalinous R, Freeston IL. Non-invasive magnetic stimulation of human motor cortex. Lancet 325, 1106–1107 (1985).CrossrefGoogle Scholar
    • 11 Pascual-Leone A. Transcranial magnetic stimulation: studying the brain–behaviour relationship by induction of ‘virtual lesions’. Philos. Trans. R. Soc. Lond. B Biol. Sci. 354, 1229–1238 (1999).Crossref, Medline, CASGoogle Scholar
    • 12 Nitsche MA, Paulus W. Sustained excitability elevations induced by transcranial DC motor cortex stimulation in humans. Neurology 57, 1899–1901 (2001).Crossref, Medline, CASGoogle Scholar
    • 13 Boggio PS, Ferrucci R, Rigonatti SP et al. Effects of transcranial direct current stimulation on working memory in patients with Parkinson's disease. J. Neurol. Sci. 249, 31–38 (2006).Crossref, MedlineGoogle Scholar
    • 14 Fregni F, Pascual-Leone A. Technology insight: noninvasive brain stimulation in neurology – perspectives on the therapeutic potential of rTMS and tDCS. Nat. Clin. Pract. Neuro. 3, 383–393 (2007).Crossref, MedlineGoogle Scholar
    • 15 Yoo SS, Bystritsky A, Lee JH et al. Focused ultrasound modulates region-specific brain activity. Neuroimage 56, 1267–1275 (2011).Crossref, MedlineGoogle Scholar
    • 16 Huang YZ, Sommer M, Thickbroom G et al. Consensus: new methodologies for brain stimulation. Brain Stimul. 2, 2–13 (2009).Crossref, MedlineGoogle Scholar
    • 17 Coenen AM. Neuronal activities underlying the electroencephalogram and evoked potentials of sleeping and waking: implications for information processing. Neurosci. Biobehav. Rev. 19, 447–463 (1995).Crossref, Medline, CASGoogle Scholar
    • 18 Zhao Z, Zhou Z, Bao J. Octapod iron oxide nanoparticles as high-performance T2 contrast agents for magnetic resonance imaging. Nat. Commun. 4, 2266 (2013).Crossref, MedlineGoogle Scholar
    • 19 Corral-Flores V, Bueno-Baques D, Ziolo R. Synthesis and characterization of novel CoFe2O4–BaTiO3 multiferroic core–shell-type nanostructures. Acta Mater. 58, 764–769 (2010).Crossref, CASGoogle Scholar
    • 20 Kitagawa Y, Hiraoka Y, Honda T, Ishikura T, Nakamura H, Kimura T. Low-field magnetoelectric effect at room temperature. Nat. Mater. 9, 797–802 (2010).Crossref, Medline, CASGoogle Scholar
    • 21 Luo W et al. Room-temperature simultaneously enhanced magnetization and electric polarization in BiFeO3 ceramic synthesized by magnetic annealing. Appl. Phys. Lett. 94, 202507 (2009).CrossrefGoogle Scholar
    • 22 Nair M, Guduru R, Liang P, Hong J, Sagar V, Khizroev S. Externally controlled on-demand release of anti-HIV drug using magneto-electric nanoparticles as carriers. Nat. Commun. 4, 1707 (2013).Crossref, MedlineGoogle Scholar
    • 23 Guduru R, Khizroev S. Magnetic field‐controlled release of paclitaxel drug from functionalized magnetoelectric nanoparticles. Part. Part. Syst. Char. 31(5), 605–611 (2013).CrossrefGoogle Scholar
    • 24 Calvo P, Gouritin B, Chacun H et al. Long-circulating PEGylated polycyanoacrylate nanoparticles as new drug carrier for brain delivery. Pharm. Res. 18(8), 1157–1166 (2001).Crossref, Medline, CASGoogle Scholar
    • 25 Guduru R, Liang P, Runowicz C, Nair M, Alturi V, Khizroev S. Magnetetolectric nanoparticles to enable field-controlled high-specificity drug delivery to eradicate ovarian cancer cells. Sci. Rep. 3, 2953 (2013).Crossref, MedlineGoogle Scholar
    • 26 Eskandar E, Rabinov J, Barker FG. Tracking neural stem cells in patients with brain trauma. N. Engl. J. Med. 355(22), 2376–2378 (2006).Crossref, MedlineGoogle Scholar
    • 27 Kim DK, Zhang Y, Kehr J, Klason T, Bjelke B, Muhammed M. Characterization and MRI study of surfactant-coated superparamagnetic nanoparticles administrated into the rat brain. J. Mag. Mag. Mat. 225, 256–261 (2001).Crossref, CASGoogle Scholar
    • 28 Goodwill PW, Scott GC, Stang PP, Conolly SM. Narrowband magnetic particle imaging. IEEE Trans. Med. Imaging 28, 1231–1237 (2009).Crossref, MedlineGoogle Scholar
    • 29 Weizenecker J, Gleich B, Rahmer J, Dahnke H, Borgert J. Three-dimensional real-time in vivo magnetic particle imaging. Phys. Med. Biol. 54, L1 (2009).Crossref, Medline, CASGoogle Scholar
    • 30 Yassa MA, Muftuler LT, Stark CE. Ultrahigh-resolution microstructural diffusion tensor imaging reveals perforant path degradation in aged humans in vivo. Proc. Natl Acad. Sci. USA 107, 12687–12691 (2010).Crossref, Medline, CASGoogle Scholar
    • 31 Khizroev SK, Bain JA, Kryder MH. Considerations in the design of probe heads for 100 Gbit/in 2 recording density. IEEE. Trans. Magn. 33, 2893–2895 (1997).CrossrefGoogle Scholar
    • 32 Koch C, Tononi G. Can machines be conscious? IEEE Spectrum 45(6), 55 (2008).• Presents a concept of reverse-brain engineering.CrossrefGoogle Scholar