Cited 0 times in
Magnetic Nanochain-Based Smart Drug Delivery System with Remote Tunable Drug Release by a Magnetic Field
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 손혜영 | - |
dc.contributor.author | 허용민 | - |
dc.date.accessioned | 2022-12-22T03:46:34Z | - |
dc.date.available | 2022-12-22T03:46:34Z | - |
dc.date.issued | 2022-09 | - |
dc.identifier.issn | 1976-0280 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/191982 | - |
dc.description.abstract | 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 μm, MN-2: 2.2 ± 1.1 μm, and MN-3: 5.3 ± 2.0 μm) 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. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Korean Biochip Society | - |
dc.relation.isPartOf | BIOCHIP JOURNAL | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.title | Magnetic Nanochain-Based Smart Drug Delivery System with Remote Tunable Drug Release by a Magnetic Field | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | BioMedical Science Institute (의생명과학부) | - |
dc.contributor.googleauthor | Byunghoon Kang | - |
dc.contributor.googleauthor | Moo-Kwang Shin | - |
dc.contributor.googleauthor | Seungmin Han | - |
dc.contributor.googleauthor | Ilyoung Oh | - |
dc.contributor.googleauthor | Eunjung Kim | - |
dc.contributor.googleauthor | Joseph Park | - |
dc.contributor.googleauthor | Hye Young Son | - |
dc.contributor.googleauthor | Taejoon Kang | - |
dc.contributor.googleauthor | Juyeon Jung | - |
dc.contributor.googleauthor | Yong-Min Huh | - |
dc.contributor.googleauthor | Seungjoo Haam | - |
dc.contributor.googleauthor | Eun-Kyung Lim | - |
dc.identifier.doi | 10.1007/s13206-022-00072-1 | - |
dc.contributor.localId | A04589 | - |
dc.contributor.localId | A04359 | - |
dc.relation.journalcode | J00292 | - |
dc.identifier.eissn | 2092-7843 | - |
dc.identifier.url | https://link.springer.com/article/10.1007/s13206-022-00072-1#article-info | - |
dc.subject.keyword | Magnetic field | - |
dc.subject.keyword | Magnetic nanochain | - |
dc.subject.keyword | Remote tunable | - |
dc.subject.keyword | Drug release | - |
dc.subject.keyword | External triggering | - |
dc.subject.keyword | Smart drug delivery | - |
dc.contributor.alternativeName | Son, Hye Yeong | - |
dc.contributor.affiliatedAuthor | 손혜영 | - |
dc.contributor.affiliatedAuthor | 허용민 | - |
dc.citation.volume | 16 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 280 | - |
dc.citation.endPage | 290 | - |
dc.identifier.bibliographicCitation | BIOCHIP JOURNAL, Vol.16(3) : 280-290, 2022-09 | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.