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Imaging-guided photoacoustic drug release and synergistic chemo-photoacoustic therapy with paclitaxel-containing nanoparticles

机译:含紫杉醇纳米粒子的影像引导光声药物释放和协同化学光声治疗

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摘要

Here, a novel triggered drug release modality was developed for oncotherapy. Paclitaxel (PTX), perfluorohexane (PFH) and gold nanorods (AuNRs) loaded nanoparticles (PTX-PAnP) were synthesized. Folic acid (FA) conjugated PTX-PAnP (PTX-PAnP-FA) could be selectively taken into folate receptor-over expressed tumor cells. Upon pulsed laser irradiation, the PTX-PAnP-FA could be rapidly destructed because of the PFH vaporization, resulting in fast drug release, which induced apoptosis of cancer cells efficiently. Stimulated fragmentation of the PTX-PAnP-FA nanoparticles can facilitate multiple mechanisms such as bubble implosion, shockwave generation, and sonoporation that further enhance the therapeutic efficiency. The in vivo therapy study further confirmed this new approach resulted in efficient tumor suppression. The results demonstrate a unique drug release mechanism based on photoacoustic effect. It provides an all-in-one platform for photoacoustic image-guided drug release and synergistic chemo-photoacoustic therapy. (C) 2016 Elsevier B.V. All rights reserved.
机译:在这里,一种新型的触发药物释放方式被开发用于肿瘤治疗。合成了紫杉醇(PTX),全氟己烷(PFH)和金纳米棒(AuNRs)负载的纳米颗粒(PTX-PAnP)。叶酸(FA)偶联的PTX-PAnP(PTX-PAnP-FA)可以被选择性地吸收到叶酸受体过度表达的肿瘤细胞中。在脉冲激光照射下,由于PFH汽化,PTX-PAnP-FA可以快速破坏,从而导致药物快速释放,从而有效诱导癌细胞凋亡。 PTX-PAnP-FA纳米粒子的受激破碎可以促进多种机制,如气泡破裂,冲击波产生和声穿孔作用,从而进一步提高治疗效率。体内治疗研究进一步证实了这种新方法可有效抑制肿瘤。结果证明了基于光声效应的独特药物释放机制。它为光声图像引导的药物释放和协同化学光声治疗提供了一个多平台的平台。 (C)2016 Elsevier B.V.保留所有权利。

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