Biodegradable Polymer-Coated Multifunctional Graphene Quantum Dots for Light-Triggered Synergetic Therapy of Pancreatic Cancer
In this work, we reported the synthesis of an engineered novel nanocarrier composed of biodegradable charged polyester vectors (BCPVs) and graphene quantum dots (GQDs) for pancreatic cancer (MiaPaCa-2 cells) therapy applications. Such a nanocarrier was utilized to co-load doxorubicin (DOX) and small...
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Published in | ACS applied materials & interfaces Vol. 11; no. 3; pp. 2768 - 2781 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
American Chemical Society
23.01.2019
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Abstract | In this work, we reported the synthesis of an engineered novel nanocarrier composed of biodegradable charged polyester vectors (BCPVs) and graphene quantum dots (GQDs) for pancreatic cancer (MiaPaCa-2 cells) therapy applications. Such a nanocarrier was utilized to co-load doxorubicin (DOX) and small interfering ribonucleic acid (siRNA), resulting in the formation of GQD/DOX/BCPV/siRNA nanocomplexes. The resulting nanocomplexes have demonstrated high stability in physiologically mimicking media, excellent K-ras downregulation activity, and effective bioactivity inhibition for MiaPaCa-2 cells. More importantly, laser light was used to generate heat for the nanocomplexes via the photothermal effect to damage the cells, which was further employed to trigger the release of payloads from the nanocomplexes. Such triggered release function greatly enhanced the anticancer activity of the nanocomplexes. Preliminary colony formation study also suggested that GQD/DOX/BCPV/siRNA nanocomplexes are qualified carrier candidates in subsequent in vivo tests. |
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AbstractList | In this work, we reported the synthesis of an engineered novel nanocarrier composed of biodegradable charged polyester vectors (BCPVs) and graphene quantum dots (GQDs) for pancreatic cancer (MiaPaCa-2 cells) therapy applications. Such a nanocarrier was utilized to co-load doxorubicin (DOX) and small interfering ribonucleic acid (siRNA), resulting in the formation of GQD/DOX/BCPV/siRNA nanocomplexes. The resulting nanocomplexes have demonstrated high stability in physiologically mimicking media, excellent K-ras downregulation activity, and effective bioactivity inhibition for MiaPaCa-2 cells. More importantly, laser light was used to generate heat for the nanocomplexes via the photothermal effect to damage the cells, which was further employed to trigger the release of payloads from the nanocomplexes. Such triggered release function greatly enhanced the anticancer activity of the nanocomplexes. Preliminary colony formation study also suggested that GQD/DOX/BCPV/siRNA nanocomplexes are qualified carrier candidates in subsequent in vivo tests. In this work, we reported the synthesis of an engineered novel nanocarrier composed of biodegradable charged polyester vectors (BCPVs) and graphene quantum dots (GQDs) for pancreatic cancer (MiaPaCa-2 cells) therapy applications. Such a nanocarrier was utilized to co-load doxorubicin (DOX) and small interfering ribonucleic acid (siRNA), resulting in the formation of GQD/DOX/BCPV/siRNA nanocomplexes. The resulting nanocomplexes have demonstrated high stability in physiologically mimicking media, excellent K-ras downregulation activity, and effective bioactivity inhibition for MiaPaCa-2 cells. More importantly, laser light was used to generate heat for the nanocomplexes via the photothermal effect to damage the cells, which was further employed to trigger the release of payloads from the nanocomplexes. Such triggered release function greatly enhanced the anticancer activity of the nanocomplexes. Preliminary colony formation study also suggested that GQD/DOX/BCPV/siRNA nanocomplexes are qualified carrier candidates in subsequent in vivo tests.In this work, we reported the synthesis of an engineered novel nanocarrier composed of biodegradable charged polyester vectors (BCPVs) and graphene quantum dots (GQDs) for pancreatic cancer (MiaPaCa-2 cells) therapy applications. Such a nanocarrier was utilized to co-load doxorubicin (DOX) and small interfering ribonucleic acid (siRNA), resulting in the formation of GQD/DOX/BCPV/siRNA nanocomplexes. The resulting nanocomplexes have demonstrated high stability in physiologically mimicking media, excellent K-ras downregulation activity, and effective bioactivity inhibition for MiaPaCa-2 cells. More importantly, laser light was used to generate heat for the nanocomplexes via the photothermal effect to damage the cells, which was further employed to trigger the release of payloads from the nanocomplexes. Such triggered release function greatly enhanced the anticancer activity of the nanocomplexes. Preliminary colony formation study also suggested that GQD/DOX/BCPV/siRNA nanocomplexes are qualified carrier candidates in subsequent in vivo tests. |
Author | Xu, Gaixia Birowosuto, Muhammad Danang Permatasari, Fitri Aulia Lin, Wei-Jen Zeng, Shuwen Yin, Mingjie Ogi, Takashi Chen, Chih-Kuang Chan, Kok Ken Yang, Chengbin Wang, Xiaomei Okuyama, Kikuo Iskandar, Ferry Yong, Ken-Tye Lin, Guimiao |
AuthorAffiliation | Department of Fiber and Composite Materials Guangdong Key Laboratory for Biomedical Measurements and Ultrasound Imaging, School of Biomedical Engineering, Health Sciences Center School of Electrical and Electronic Engineering Department of Physics, Faculty of Mathematics and Natural Sciences Hiroshima University Department of Chemical and Materials Engineering CINTRA CNRS/NTU/THALES UMI 3288 Department of Physiology, School of Basic Medical Sciences, Health Sciences Center Department of Chemical Engineering, Graduate School of Engineering |
AuthorAffiliation_xml | – name: Department of Chemical and Materials Engineering – name: Department of Chemical Engineering, Graduate School of Engineering – name: Department of Physiology, School of Basic Medical Sciences, Health Sciences Center – name: Department of Fiber and Composite Materials – name: CINTRA CNRS/NTU/THALES UMI 3288 – name: School of Electrical and Electronic Engineering – name: Department of Physics, Faculty of Mathematics and Natural Sciences – name: Guangdong Key Laboratory for Biomedical Measurements and Ultrasound Imaging, School of Biomedical Engineering, Health Sciences Center – name: Hiroshima University |
Author_xml | – sequence: 1 givenname: Chengbin orcidid: 0000-0001-9672-7412 surname: Yang fullname: Yang, Chengbin – sequence: 2 givenname: Kok Ken orcidid: 0000-0002-0592-4427 surname: Chan fullname: Chan, Kok Ken organization: School of Electrical and Electronic Engineering – sequence: 3 givenname: Gaixia surname: Xu fullname: Xu, Gaixia email: xugaixia@szu.edu.cn – sequence: 4 givenname: Mingjie surname: Yin fullname: Yin, Mingjie organization: School of Electrical and Electronic Engineering – sequence: 5 givenname: Guimiao surname: Lin fullname: Lin, Guimiao – sequence: 6 givenname: Xiaomei surname: Wang fullname: Wang, Xiaomei – sequence: 7 givenname: Wei-Jen surname: Lin fullname: Lin, Wei-Jen organization: Department of Fiber and Composite Materials – sequence: 8 givenname: Muhammad Danang orcidid: 0000-0002-9997-6841 surname: Birowosuto fullname: Birowosuto, Muhammad Danang organization: CINTRA CNRS/NTU/THALES UMI 3288 – sequence: 9 givenname: Shuwen orcidid: 0000-0003-2188-7213 surname: Zeng fullname: Zeng, Shuwen organization: CINTRA CNRS/NTU/THALES UMI 3288 – sequence: 10 givenname: Takashi orcidid: 0000-0003-3982-857X surname: Ogi fullname: Ogi, Takashi organization: Hiroshima University – sequence: 11 givenname: Kikuo surname: Okuyama fullname: Okuyama, Kikuo organization: Hiroshima University – sequence: 12 givenname: Fitri Aulia surname: Permatasari fullname: Permatasari, Fitri Aulia organization: Department of Physics, Faculty of Mathematics and Natural Sciences – sequence: 13 givenname: Ferry surname: Iskandar fullname: Iskandar, Ferry organization: Department of Physics, Faculty of Mathematics and Natural Sciences – sequence: 14 givenname: Chih-Kuang orcidid: 0000-0002-7896-2424 surname: Chen fullname: Chen, Chih-Kuang email: chihkuan@yuntech.edu.tw organization: Department of Chemical and Materials Engineering – sequence: 15 givenname: Ken-Tye orcidid: 0000-0001-7936-2941 surname: Yong fullname: Yong, Ken-Tye email: ktyong@ntu.edu.sg organization: School of Electrical and Electronic Engineering |
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Title | Biodegradable Polymer-Coated Multifunctional Graphene Quantum Dots for Light-Triggered Synergetic Therapy of Pancreatic Cancer |
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