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dc.contributor.authorChang, Ju-Yaoen_US
dc.contributor.authorJu, Tsai-Kaien_US
dc.contributor.authorChen, Nelson G.en_US
dc.contributor.authorHsiao, Chun-Jenen_US
dc.contributor.authorWang, Chin-Yuen_US
dc.date.accessioned2019-09-02T07:46:19Z-
dc.date.available2019-09-02T07:46:19Z-
dc.date.issued2019-01-01en_US
dc.identifier.issn2169-3536en_US
dc.identifier.urihttp://dx.doi.org/10.1109/ACCESS.2019.2928900en_US
dc.identifier.urihttp://hdl.handle.net/11536/152694-
dc.description.abstractWhen treating cancer with chemotherapy, serious side effects are caused by the inability of the drug to be solely delivered to the tumor. As a result, a portion of the drug agents is inevitably delivered elsewhere and destroy normal cells. We report the first results on combining ultrasound with an aptamer-doxorubicin conjugate to treat cancer cells. Enhancement of therapeutic effects combined with a reduction in side effects indicates the potential of this approach. Although many studies have noted that ultrasound can enhance drug delivery, ultrasound has not addressed the goal of reducing side effects. To both reduce side effects and enhance the efficiency of killing cancer cells, this study mainly uses a specially targeted aptamer conjugated to the anticancer drug doxorubicin (DOX), which was applied in combination with ultrasound for cancer treatment. We also compared the results between cancer and normal cell lines to explore the targeting effect of the aptamer. Both breast cancer cells (MCF-7) and breast cells (MCF-10A) were used for the experiments. The results show that the aptamer conjugated to an anticancer drug can be used to target cancer cells and ultrasound can enhance drug delivery. This method can significantly reduce the side effects of the anticancer drug and achieve favorable therapeutic effects.en_US
dc.language.isoen_USen_US
dc.subjectAptameren_US
dc.subjectcanceren_US
dc.subjectdrug deliveryen_US
dc.subjectultrasounden_US
dc.titleUltrasound-Enhanced Delivery of an Aptamer-Doxorubicin Conjugate to Breast Cancer Cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1109/ACCESS.2019.2928900en_US
dc.identifier.journalIEEE ACCESSen_US
dc.citation.volume7en_US
dc.citation.spage94189en_US
dc.citation.epage94194en_US
dc.contributor.department分子醫學與生物工程研究所zh_TW
dc.contributor.department電機工程學系zh_TW
dc.contributor.departmentInstitute of Molecular Medicine and Bioengineeringen_US
dc.contributor.departmentDepartment of Electrical and Computer Engineeringen_US
dc.identifier.wosnumberWOS:000477867900040en_US
dc.citation.woscount0en_US
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