Cited 2 time in
Externally Controlled Cellular Transport of Magnetic Iron Oxide Particles with Polysaccharide Surface Coatings
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Cho, Kwan Hyung | - |
| dc.contributor.author | Shin, Meong Cheol | - |
| dc.contributor.author | Min, Kyoung Ah | - |
| dc.date.accessioned | 2022-12-26T14:33:49Z | - |
| dc.date.available | 2022-12-26T14:33:49Z | - |
| dc.date.issued | 2019-09 | - |
| dc.identifier.issn | 1085-9195 | - |
| dc.identifier.issn | 1559-0283 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/8788 | - |
| dc.description.abstract | Recently, due to their promising applications in biomedicine, magnetic iron oxide nanoparticles (MPs) have become one of the research hotspots in the nanomedicine field. Since various synthetic modifications have been widely applied to these nanoparticles for better targeting behaviors, it is meaningful to apply the optimal magnetic field condition for each case. This will enable creating a safe and efficient drug targeting using different types of MPs. In the present study, we aimed to find out any changes of transepithelial transport of polysaccharide-coated MPs by applying the continuous or the pulsatile magnetic field condition. Our results with heparin-functionalized MPs indicate that the particle concentrations and the external magnetic field could influence the transepithelial permeability of the particles. In the presence of a continuously applied magnetic density, heparin-MPs at high concentrations, by forming magnetically-induced aggregation of particles over the cell surface layer, showed a lower cellular transport than those at low concentrations. Furthermore, the results from the quantitative chemical assays and imaging analyses showed that transepithelial transport of heparin-MPs (negatively charged) under the pulsatile magnetic field was higher than that under the continuous magnetic field (CP), whereas the starch-MPs (neutrally charged) showed a small difference in transepithelial transport or cell retention between pulsatile vs. continuous magnetic field conditions. Taken together, our results suggest that the external magnetic field should be differentially applied to control the cellular drug transport depending on the physicochemical properties of the surface chemistry of magnetic particles. | - |
| dc.format.extent | 13 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | HUMANA PRESS INC | - |
| dc.title | Externally Controlled Cellular Transport of Magnetic Iron Oxide Particles with Polysaccharide Surface Coatings | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1007/s12013-019-00874-5 | - |
| dc.identifier.scopusid | 2-s2.0-85066146865 | - |
| dc.identifier.wosid | 000485937300004 | - |
| dc.identifier.bibliographicCitation | CELL BIOCHEMISTRY AND BIOPHYSICS, v.77, no.3, pp 213 - 225 | - |
| dc.citation.title | CELL BIOCHEMISTRY AND BIOPHYSICS | - |
| dc.citation.volume | 77 | - |
| dc.citation.number | 3 | - |
| dc.citation.startPage | 213 | - |
| dc.citation.endPage | 225 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
| dc.relation.journalResearchArea | Biophysics | - |
| dc.relation.journalResearchArea | Cell Biology | - |
| dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
| dc.relation.journalWebOfScienceCategory | Biophysics | - |
| dc.relation.journalWebOfScienceCategory | Cell Biology | - |
| dc.subject.keywordPlus | DRUG-PERMEABILITY | - |
| dc.subject.keywordPlus | NANOPARTICLES | - |
| dc.subject.keywordPlus | DELIVERY | - |
| dc.subject.keywordPlus | CACO-2 | - |
| dc.subject.keywordPlus | GENE | - |
| dc.subject.keywordAuthor | Magnetic nanoparticles | - |
| dc.subject.keywordAuthor | Polysaccharide | - |
| dc.subject.keywordAuthor | Controlled magnetic field | - |
| dc.subject.keywordAuthor | Transepithelial transport | - |
| dc.subject.keywordAuthor | Cell surface | - |
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