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Folic acid-modified bovine serum albumin nanoparticles with doxorubicin and chlorin e6 for effective combinational chemo-photodynamic therapy

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dc.contributor.authorLee, Hoomin-
dc.contributor.authorKim, Suji-
dc.contributor.authorOh, Cheolwoo-
dc.contributor.authorKhan, Imran-
dc.contributor.authorShukla, Shruti-
dc.contributor.authorBajpai, Vivek K.-
dc.contributor.authorHan, Young-Kyu-
dc.contributor.authorHuh, Yun Suk-
dc.date.accessioned2023-04-27T20:40:46Z-
dc.date.available2023-04-27T20:40:46Z-
dc.date.issued2020-12-
dc.identifier.issn0928-4931-
dc.identifier.issn1873-0191-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/5847-
dc.description.abstractWe herein describe a facile method to synthesize stable bovine serum albumin-based nanoparticles (BNPs) loaded with two anticancer therapeutics, doxorubicin (DOX) and a photosensitizer, chlorin e6 (Ce6), in combination with folic acid (FA) as a target cancer cell receptor for the development of an effective combined chemo and photodynamic (FA-Ce6/DOX/BNPs) therapy against cervical cancer. FA-Ce6/DOX/BNPs exhibited excellent monodispersity with an average diameter of 103.5 +/- 3.8 nm, a negative zeta potential of approximately -30.44 +/- 0.35 mV, and long-term stability. As a result, FA-Ce6/DOX/BNPs exhibited severe toxicity to cervical HeLa cancer cells. Also, a higher drug release rate was observed under acidic pH conditions (pH 5.0). Moreover, FA-Ce6/DOX/BNPs potentiated mitochondrial reactive oxygen species (ROS) production in HeLa cells under 671-nm laser exposure, leading to activation of key regulator proteins of apoptosis such as BH3 interacting-domain death agonist (BID), B-cell lymphoma 2 (Bcl-2), and Bcl-2-associated X (BAX), as well as induction of the caspase cascade and mitochondrial ROS-mediated cell death. Confocal microscopy analysis further validated cellular uptake of FA-Ce6/DOX/BNPs by HeLa cells. Furthermore, results of real-time quantitative PCR (RT-qPCR) and western blot analysis further validated the anticancer effect of FA-Ce6/DOX/BNPs, as evidenced by elevated gene/protein expression levels of apoptotic biomarkers p53, BID, caspase-3, cleaved poly (ADP-ribose) polymerase 1 (PARP-1), and BAX, contrary to levels of the anti-apoptotic marker Bcl-2. Moreover, in vivo toxicity results of FA-Ce6/DOX/BNPs using laser irradiation in zebrafish larvae, as a chemo-photodynamic therapy confirmed that it does not affect the larval development without causing any adverse toxic effect in zebrafish larvae. Altogether these findings strongly support the anticancer effect of FA-Ce6/DOX/BNPs combinational chemo-photodynamic therapy, which could be a promising candidate for cervical cancer therapy.-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER-
dc.titleFolic acid-modified bovine serum albumin nanoparticles with doxorubicin and chlorin e6 for effective combinational chemo-photodynamic therapy-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.msec.2020.111343-
dc.identifier.scopusid2-s2.0-85089560134-
dc.identifier.wosid000571220600006-
dc.identifier.bibliographicCitationMATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, v.117-
dc.citation.titleMATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS-
dc.citation.volume117-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusINHIBITS CELL-PROLIFERATION-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusOVARIAN-CANCER-
dc.subject.keywordPlusSTAT-3 TRANSLOCATION-
dc.subject.keywordPlusVIVO EVALUATION-
dc.subject.keywordPlusDEATH-
dc.subject.keywordPlusHELA-
dc.subject.keywordPlusBSA-
dc.subject.keywordPlusSTATISTICS-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordAuthorPhotodynamic therapy-
dc.subject.keywordAuthorDrug delivery system-
dc.subject.keywordAuthorBiodegradable BNPs-
dc.subject.keywordAuthorROS-
dc.subject.keywordAuthorMitochondrial apoptosis-
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