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dc.contributor.author Khan, Tunazzina Zaman -
dc.contributor.author Newaj, Shekh Md -
dc.contributor.author Rahman, Ashikur -
dc.contributor.author Tabassum, Rahnuma -
dc.contributor.author Tasnim, Khandaker Nujhat -
dc.contributor.author Reza, Hasan Mahmud -
dc.contributor.author Reza, Md. Selim -
dc.contributor.author Hong, Seonki -
dc.contributor.author Sharker, Shazid Md. -
dc.date.accessioned 2023-12-18T14:40:20Z -
dc.date.available 2023-12-18T14:40:20Z -
dc.date.created 2023-10-27 -
dc.date.issued 2023-10 -
dc.identifier.issn 2633-5409 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/46677 -
dc.description.abstract In this study, we developed NIR-light responsive poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) by incorporating the ICG dye for the local delivery of small-molecule drugs and therapeutics. Since NIR light can penetrate the skin up to a depth of 2 mm, it allows externally controlled photothermal-induced drug release. The synthesized NPs had a size of approximately 100 nm upon conjugation with a model anticancer drug, doxorubicin (Dox), which demonstrated in vivo NIR-derived heat generation exceeding 45 °C within 5 minutes. The in vivo efficacy of these NPs was evaluated by administering them via the tail vein route in DMBA/TPA-treated mice, resulting in a significant decrease in tumor size (from 15 to 1 mm3). Histological results obtained from sacrificed tumor tissue also clearly supported the therapeutic activity of the developed NPs. This study indicates that NIR-guided PLGA-based NPs allow the localized delivery of therapeutics in a spatially controlled manner, potentially improving overall patient care. © 2023 The Author(s). -
dc.language English -
dc.publisher Royal Society of Chemistry -
dc.title NIR-light-triggered delivery of doxorubicin-loaded PLGA nanoparticles for synergistic cancer therapy on DMBA/TPA induced tumor-bearing mice -
dc.type Article -
dc.identifier.doi 10.1039/d3ma00375b -
dc.identifier.scopusid 2-s2.0-85174283371 -
dc.identifier.bibliographicCitation Materials Advances, v.4, no.21, pp.5175 - 5183 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordPlus IN-VITRO -
dc.subject.keywordPlus CARBON NANOPARTICLES -
dc.subject.keywordPlus PHOTOTHERMAL THERAPY -
dc.subject.keywordPlus GRAPHENE -
dc.subject.keywordPlus RELEASE -
dc.subject.keywordPlus MICROENVIRONMENT -
dc.subject.keywordPlus NANOPLATFORM -
dc.subject.keywordPlus PACLITAXEL -
dc.subject.keywordPlus EFFICACY -
dc.subject.keywordPlus MOUSE -
dc.citation.endPage 5183 -
dc.citation.number 21 -
dc.citation.startPage 5175 -
dc.citation.title Materials Advances -
dc.citation.volume 4 -
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Department of Physics and Chemistry Bioinspired Organic Materials Laboratory 1. Journal Articles

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