化工儀器網(wǎng)
資料下載
測量應(yīng)用案例-20210205
閱讀：109 發(fā)布時間：2021-2-23| 提 供 商 | 美國布魯克海文儀器公司 | 資料大小 | 3.5MB |
|---|---|---|---|
| 資料圖片 | 下載次數(shù) | 19次 | |
| 資料類型 | PDF 文件 | 瀏覽次數(shù) | 109次 |
| 免費下載 | 點擊下載 |
作者： Cunfeng Song ;Yugang Li ;Tianliang Li ;Yuming Yang ;Zhicheng Huang ;Jesús Martinez de la Fuente ;Jian Ni ;Daxiang Cui
Institute of Nano Biomedicine and Engineering ,Shanghai Engineering Research Center for Intelligent Instrument for Diagnosis and Therapy ,Department of Instrument Science & Engineering
School of Electronic Information and Electrical Engineering ,Shanghai Jiao Tong University,
800 Dongchuan Road, Shanghai 200240, P. R. China
摘要：Nanocarriers for chemo‐photothermal therapy suffer from insufficient retention at the tumor site and poor penetration into tumor parenchyma. A smart drug‐dye‐based micelle is designed by making the best of the structural features of small‐molecule drugs. P‐DOX is synthesized by conjugating doxorubicin (DOX) with poly(4‐formylphenyl methacrylate‐co‐2‐(diethylamino) ethyl methacrylate)‐b‐polyoligoethyleneglycol methacrylate (P(FPMA‐co‐DEA)‐b‐POEGMA) via imine linkage. Through the π–π stacking interaction, IR780, a near‐infrared fluorescence dye as well as a photothermal agent, is integrated into the micelles (IR780‐PDMs) with the P‐DOX. The IR780‐PDMs show remarkably long blood circulation (t1/2β = 22.6 h). As a result, a progressive tumor accumulation and retention are presented, which is significant to the sequential drug release. Moreover, when entering into a moderate acidic tumor microenvironment, IR780‐PDMs can dissociate into small‐size conjugates and IR780, which obviously increases the penetration depth of drugs, and then improves the lethality to deep‐seated tumor cells. Owing to the high delivery efficiency and superior chemo‐photothermal therapeutic efficacy of IR780‐PDMs, 97.6% tumor growth in the A549 tumor‐bearing mice is suppressed with a low dose of intravenous injection (DOX, 1.5 mg kg−1; IR780, 0.8 mg kg−1). This work presents a brand‐new strategy for long‐acting intensive cancer therapy.