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Biodegradable polymer based theranostic agents for photoacoustic imaging and cancer therapy

机译:基于生物可降解聚合物的治疗剂,用于光声成像和癌症治疗

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In this study, multifunctional theranostic agents for photoacoustic (PA), ultrasound (US), fluorescent imaging, and for therapeutic drug delivery were developed and tested. These agents consisted of a shell made from a biodegradable Poly(lactide-co-glycolic acid) (PLGA) polymer, loaded with perfluorohexane (PFH) liquid and gold nanoparticles (GNPs) in the core, and lipophilic carbocyanines fluorescent dye DiD and therapeutic drug Paclitaxel (PAC) in the shell. Their multifunctional capacity was investigated in an in vitro study. The PLGA/PFH/DiD-GNPs particles were synthesized by a double emulsion technique. The average PLGA particle diameter was 560 nm, with 50 nm diameter silica-coated gold nano-spheres in the shell. MCF7 human breast cancer cells were incubated with PLGA/PFH/DiD-GNPs for 24 hours. Fluorescent and PA images were recorded using a fluorescent/PA microscope using a 1000 MHz transducer and a 532 nm pulsed laser. For the particle vaporization and drug delivery test, MCF7 cells were incubated with the PLGA/PFH-GNPs-PAC or PLGA/PFH-GNPs particles for 6, 12 and 24 hours. The effects of particle vaporization and drug delivery inside the cells were examined by irradiating the cells with a laser fluence of 100 mJ/cm~2, and cell viability quantified using the MTT assay. The PA images of MCF7 cells containing PLGA/PFH/DiD-GNPs were spatially coincident with the fluorescent images, and confirmed particle uptake. After exposure to the PLGA/PFH-GNP-PAC for 6,12 and 24 hours, the cell survival rate was 43%, 38%, and 36% respectively compared with the control group, confirming drug delivery and release inside the cells. Upon vaporization, cell viability decreased to 20%. The particles show potential as imaging agents and drug delivery vehicles.
机译:在这项研究中,开发并测试了用于光声(PA),超声(US),荧光成像以及用于治疗性药物递送的多功能治疗试剂。这些试剂包括由可生物降解的聚丙交酯-乙醇酸共聚物(PLGA)制成的外壳,核心中装有全氟己烷(PFH)液体和金纳米颗粒(GNP),以及亲脂性花青素荧光染料DiD和治疗药物紫杉醇(PAC)位于外壳中。在一项体外研究中对它们​​的多功能能力进行了研究。 PLGA / PFH / DiD-GNPs颗粒是通过双重乳液技术合成的。 PLGA的平均粒径为560 nm,壳中有直径为50 nm的二氧化硅涂层金纳米球。将MCF7人乳腺癌细胞与PLGA / PFH / DiD-GNPs孵育24小时。使用荧光/ PA显微镜,使用1000 MHz换能器和532 nm脉冲激光,记录荧光和PA图像。为了进行颗粒汽化和药物传递测试,将MCF7细胞与PLGA / PFH-GNPs-PAC或PLGA / PFH-GNPs颗粒孵育6、12和24小时。通过用100mJ / cm〜2的激光通量照射细胞来检查细胞内颗粒汽化和药物递送的效果,并使用MTT测定法定量细胞存活力。含有PLGA / PFH / DiD-GNPs的MCF7细胞的PA图像与荧光图像在空间上重合,并确认了颗粒摄取。暴露于PLGA / PFH-GNP-PAC 6、12和24小时后,细胞存活率与对照组相比分别为43%,38%和36%,证实了药物在细胞内的传递和释放。蒸发后,细胞活力降低至20%。颗粒显示出作为显像剂和药物递送载体的潜力。

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