4.4 Article

Magnetic Nanochain-Based Smart Drug Delivery System with Remote Tunable Drug Release by a Magnetic Field

Journal

BIOCHIP JOURNAL
Volume 16, Issue 3, Pages 280-290

Publisher

KOREAN BIOCHIP SOCIETY-KBCS
DOI: 10.1007/s13206-022-00072-1

Keywords

Magnetic field; Magnetic nanochain; Remote tunable; Drug release; External triggering; Smart drug delivery

Funding

  1. National Research Foundation (NRF) of Korea - Ministry of Science and ICT (MSIT) of Korea [NRF-2021M3E5E3080379, NRF-2018M3A9E2022821, NRF-2018M3A9E2022819, NRF-2022R1C1C1008815]
  2. Korea Evaluation Institute of Industrial Technology (KEIT) - Korea government (MOTIE) [RS-2022-00154853]
  3. Korea Environment Industry & Technology Institute (KEITI) - Ministry of Environment (ME) of Korea [2021003370003, RE202101004]
  4. Korea Health Industry Development Institute (KHIDI) - Ministry of Health & Welfare, Republic of Korea [HI21C2461]
  5. KRIBB Research Initiative Program [1711134081]

Ask authors/readers for more resources

Considerable attention is given to drug delivery technology, and nanotechnology has been used to develop various strategies for targeted drug delivery. In this study, a delivery system was designed to control drug release through external magnetic fields, and it demonstrated superior therapeutic efficacy in treating cancer cells.
Considerable attention is given to drug delivery technology that efficiently delivers appropriate levels of drug molecules to diseased sites with significant therapeutic efficacy. Nanotechnology has been used to develop various strategies for targeted drug delivery, while controlling the release of drugs because of its many benefits. Here, a delivery system was designed to control drug release by external magnetic fields using porous silica and magnetic nanoparticles. Magnetic nanochains (MNs) of various lengths (MN-1: 1.4 +/- 0.8 mu m, MN-2: 2.2 +/- 1.1 mu m, and MN-3: 5.3 +/- 2.0 mu m) were synthesized by controlling the exposure time of the external magnetic force in magnetic nanoaggregates (MNCs). Mesoporous silica-coated magnetic nanochains (MSMNs) (MSMN-1, MSMN-2, and MSMN-3) were prepared by forming a porous silica layer through sol-gel polymerization. These MSMNs could load the drug doxorubicin (DOX) into the silica layer (DOX-MSMNs) and control the release behavior of the DOX through an external rotating magnetic field. Simulations and experiments were used to verify the motion and drug release behavior of the MSMNs. Furthermore, a bio-receptor (aptamer, Ap) was introduced onto the surface of the DOX-MSMNs (Ap-DOX-MSMNs) that could recognize specific cancer cells. The Ap-DOX-MSMNs demonstrated a strong therapeutic effect on cancer cells that was superior to that of the free DOX. The potent ability of these MSMNs as an external stimulus-responsive drug delivery system was proven.

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