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      Remotely Controlled Surface Charge Modulation of Magnetoelectric Nanogenerators for Swift and Efficient Drug Delivery

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          Abstract

          We have developed a highly efficient technique of magnetically controlled swift loading and release of doxorubicin (DOX) drug using a magnetoelectric nanogenerator (MENG). Core–shell nanostructured MENG with a magnetostrictive core and piezoelectric shell act as field-responsive nanocarriers and possess the capability of field-triggered drug release in a cancerous environment. MENGs generate a surface electric dipole when subjected to a magnetic field due to the strain-mediated magnetoelectric effect. The capability of directional magnetic field-assisted modulation of the surface electrical dipole of MENG provides a mechanism to create/break ionic bonds with DOX molecules, which facilitates efficient drug attachment and on-demand swift detachment of the drug at a targeted site. The magnetic field-assisted drug-loading mechanism was minutely analyzed using spectrophotometry and Raman spectroscopy. The detailed time-dependent analysis of controlled drug release by the MENG under unidirectional and rotating magnetic field excitation was conducted using field-emission scanning electron microscopy, energy-dispersive X-ray, and atomic force microscopic measurements. In vitro, experiments validate the cytocompatibility and magnetically assisted on-demand and swift DOX drug delivery by the MENG near MCF-7 breast cancer cells, which results in a significant enhancement of cancer cell killing efficiency. A state-of-the-art experiment was performed to visualize the nanoscale magnetoelectric effect of MENG using off-axis electron holography under Lorentz conditions.

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          Mitochondria-specific drug release and reactive oxygen species burst induced by polyprodrug nanoreactors can enhance chemotherapy

          Cancer cells exhibit slightly elevated levels of reactive oxygen species (ROS) compared with normal cells, and approximately 90% of intracellular ROS is produced in mitochondria. In situ mitochondrial ROS amplification is a promising strategy to enhance cancer therapy. Here we report cancer cell and mitochondria dual-targeting polyprodrug nanoreactors (DT-PNs) covalently tethered with a high content of repeating camptothecin (CPT) units, which release initial free CPT in the presence of endogenous mitochondrial ROS (mtROS). The in situ released CPT acts as a cellular respiration inhibitor, inducing mtROS upregulation, thus achieving subsequent self-circulation of CPT release and mtROS burst. This mtROS amplification endows long-term high oxidative stress to induce cancer cell apoptosis. This current strategy of endogenously activated mtROS amplification for enhanced chemodynamic therapy overcomes the short lifespan and action range of ROS, avoids the penetration limitation of exogenous light in photodynamic therapy, and is promising for theranostics.
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            Polymeric micelles in drug delivery: An insight of the techniques for their characterization and assessment in biorelevant conditions

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              Magnetic Nanoparticles in Cancer Therapy and Diagnosis

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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                15 June 2024
                02 July 2024
                : 9
                : 26
                : 28937-28950
                Affiliations
                []Department of Electrical Engineering, Indian Institute of Technology Delhi , Hauz Khas, New Delhi 110016, India
                []Center for Biomedical Engineering, Indian Institute of Technology Delhi , Hauz Khas, New Delhi110016, India
                [§ ]Department of Chemistry, Indian Institute of Technology Delhi , Hauz Khas, New Delhi110016, India
                Author notes
                Author information
                https://orcid.org/0000-0002-1383-6224
                https://orcid.org/0000-0002-7880-4880
                https://orcid.org/0000-0002-8580-2015
                Article
                10.1021/acsomega.4c03825
                11223158
                cb9127f4-1e99-4293-9fc2-037ea7246a20
                © 2024 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 22 April 2024
                : 17 May 2024
                : 14 May 2024
                Funding
                Funded by: Department of Science and Technology, Ministry of Science and Technology, doi 10.13039/501100001843;
                Award ID: CRG/2021/003525
                Funded by: I-Hub Foundation for Cobotics, doi 10.13039/501100022758;
                Award ID: GP/2023/NR/038
                Funded by: Ministry of Human Resource Development, doi 10.13039/501100004541;
                Award ID: NA
                Funded by: Department of Science and Technology, Ministry of Science and Technology, doi 10.13039/501100001843;
                Award ID: SCP/2022/000878
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                Custom metadata
                ao4c03825
                ao4c03825

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