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            美國(guó)布魯克海文儀器公司>公司動(dòng)態(tài)>Paclitaxel-loaded polymeric nanoparticles combined with chronomodulated chemotherapy on lung cancer: In vitro and in vivo evaluation

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            Paclitaxel-loaded polymeric nanoparticles combined with chronomodulated chemotherapy on lung cancer: In vitro and in vivo evaluation

            閱讀:440          發(fā)布時(shí)間:2017-9-26
             作者 Jie Hua. Shaozhi Fua. Qiuxia Penga. YunWei Hana. Jie Xieb. Ning Zana. Yue Chenc. Juan Fana.

            a

            Department of Oncology, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, China

            b

            Department of Orthopedics, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, China

            c

            Department of Nuclear Medicine, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, China

             

            摘要:The objective of our study was to examine the anti-tumor effect of paclitaxel (PTX)-loaded polymeric nanoparticles (PTX-NPs) combined with circadian chronomodulated chemotherapy. Our intention was to screen out the best time of the day for the drug to be administered. PTX-NPs with a diameter of approximay 168 nm were prepared through a thin film dispersion technique. The PTX in PTX-NPs showed an initial fast release subsequently a slower and sustained release. The cytotoxicity of chronomodulated administration of PTX-NPs in vitro confirmed that its cytotoxic effect was lower than that of PTX injection, and showed a time-dependent effect. In addition, anti-tumor effect was examined by analysing tumor growth inhibition rate, micro-vessel density (MVD), cell proliferation and cell apoptosis, following either injection with PTX or administration of PTX-NPs. Micro fluorine-18-deoxyglucose PET/computed tomography (18F-FDG PET/CT) was used to evaluate tumor reactivity to PTX-NPs combined with chronomodulated chemotherapy. Taken these results into consideraion, our experiment indicates that PTX-NPs exhibit greater anti-tumor activity against A549 cells, in comparison with PTX injection, and the anti-tumor effect at 15 h after light onset (HALO) administration is the best in all groups. Therefore, prepared PTX-NPs combined with chronomodulated chemotherapy could be a potential treatment for lung cancer.

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