Cited 26 time in
In Vitro and In Vivo Evaluation of PEGylated Starch-Coated Iron Oxide Nanoparticles for Enhanced Photothermal Cancer Therapy
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Amatya, Reeju | - |
| dc.contributor.author | Hwang, Seungmi | - |
| dc.contributor.author | Park, Taehoon | - |
| dc.contributor.author | Min, Kyoung Ah | - |
| dc.contributor.author | Shin, Meong Cheol | - |
| dc.date.accessioned | 2022-12-26T10:16:06Z | - |
| dc.date.available | 2022-12-26T10:16:06Z | - |
| dc.date.issued | 2021-06 | - |
| dc.identifier.issn | 1999-4923 | - |
| dc.identifier.issn | 1999-4923 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/3636 | - |
| dc.description.abstract | Iron oxide nanoparticles (IONPs) possess versatile utility in cancer theranostics, thus, they have drawn enormous interest in the cancer research field. Herein, we prepared polyethylene glycol (PEG)-conjugated and starch-coated IONPs ("PEG-starch-IONPs"), and assessed their applicability for photothermal treatment (PTT) of cancer. The prepared PEG-starch-IONPs were investigated for their physical properties by transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, and dynamic light scattering (DLS). The pharmacokinetic study results showed a significant extension in the plasma half-life by PEGylation, which led to a markedly increased (5.7-fold) tumor accumulation. When PEG-starch-IONPs were evaluated for their photothermal activity, notably, they displayed marked and reproducible heating effects selectively on the tumor site with laser irradiation. Lastly, efficacy studies demonstrated that PEG-starch-IONPs-based PTT may be a promising mode of cancer therapy. | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | MDPI | - |
| dc.title | In Vitro and In Vivo Evaluation of PEGylated Starch-Coated Iron Oxide Nanoparticles for Enhanced Photothermal Cancer Therapy | - |
| dc.type | Article | - |
| dc.publisher.location | 스위스 | - |
| dc.identifier.doi | 10.3390/pharmaceutics13060871 | - |
| dc.identifier.scopusid | 2-s2.0-85108592674 | - |
| dc.identifier.wosid | 000666060600001 | - |
| dc.identifier.bibliographicCitation | PHARMACEUTICS, v.13, no.6 | - |
| dc.citation.title | PHARMACEUTICS | - |
| dc.citation.volume | 13 | - |
| dc.citation.number | 6 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
| dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
| dc.subject.keywordPlus | DRUG-DELIVERY | - |
| dc.subject.keywordPlus | MAGNETIC HYPERTHERMIA | - |
| dc.subject.keywordPlus | POTENTIAL TOXICITY | - |
| dc.subject.keywordPlus | CONTRAST | - |
| dc.subject.keywordPlus | SIZE | - |
| dc.subject.keywordPlus | PEG | - |
| dc.subject.keywordPlus | STABILITY | - |
| dc.subject.keywordAuthor | iron oxide nanoparticle | - |
| dc.subject.keywordAuthor | polyethylene glycol | - |
| dc.subject.keywordAuthor | plasma half-life | - |
| dc.subject.keywordAuthor | photothermal therapy | - |
| dc.subject.keywordAuthor | cancer | - |
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