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首页> 外文期刊>International Journal of Nanomedicine >The Destruction Of Laser-Induced Phase-Transition Nanoparticles Triggered By Low-Intensity Ultrasound: An Innovative Modality To Enhance The Immunological Treatment Of Ovarian Cancer Cells
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The Destruction Of Laser-Induced Phase-Transition Nanoparticles Triggered By Low-Intensity Ultrasound: An Innovative Modality To Enhance The Immunological Treatment Of Ovarian Cancer Cells

机译:由低强度超声引发的激光诱导的相转移纳米粒子的破坏:一种创新的模态,以增强卵巢癌细胞的免疫处理

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Purpose: Photodynamic therapy (PDT), sonodynamic therapy (SDT), and oxaliplatin (OXP) can induce immunogenic cell death (ICD) following damage-associated molecular patterns (DAMPs) exposure or release and can be united via the use of nanoplatforms to deliver drugs that can impart anti-tumor effects. The aim of this study was to develop phase-transition nanoparticles (OI_NPs) loaded with perfluoropentane (PFP), indocyanine green (ICG), and oxaliplatin (OXP), to augment anti-tumor efficacy and the immunological effects of chemotherapy, photodynamic therapy and sonodynamic therapy (PSDT). Methods: OI_NPs were fabricated by a double emulsion method and a range of physicochemical and dual-modal imaging features were characterized. Confocal microscopy and flow cytometry were used to determine the cellular uptake of OI_NPs by ID8 cells. The viability and apoptotic rate of ID8 cells were investigated using the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) assay and ?ow cytometry. Flow cytometry, Western blotting, and luminometric assays were then used to investigate the exposure or release of crucial DAMPs such as calreticulin (CRT), high mobility group box 1 (HMGB1), and adenosine-5?-triphosphate (ATP). Tumor rechallenge experiments were then used to investigate whether treated ID8 cells underwent ICD. Finally, cytotoxic T lymphocyte (CTL) activity was determined by a lactate dehydrogenase (LDH) assay. Results: Spherical OI_NPs were able to carry OXP, ICG and PFP and were successfully internalized by ID8 cells. The application of OI_NPs significantly enhanced the phase shift ability of PFP and the optical characteristics of ICG, thus leading to a significant improvement in photoacoustic and ultrasonic imaging. When combined with near-infrared light and ultrasound, the application of OI_NPs led to improved anti-tumor effects on cancer cells, and significantly enhanced the expression of DAMPs, thus generating a long-term anti-tumor effect. Conclusion: The application of OI_NPs, loaded with appropriate cargo, may represent a novel strategy with which to increase anti-tumor effects, enhance immunological potency, and improve dual-mode imaging.
机译:目的:光动力疗法(PDT),讽刺性治疗(SDT)和Oxaliplatin(OXP)可以诱导损伤相关的分子模式(潮湿)暴露或释放后的免疫原性细胞死亡(ICD),并且可以通过使用纳米片来提供联合可以赋予抗肿瘤效应的药物。本研究的目的是开发含有全氟化丁烷(PFP),吲哚菁绿(ICG)和Oxaliplatin(OXP)的相过期纳米颗粒(OI_NP),以增加抗肿瘤疗效和化疗,光动力疗法和讽刺动力治疗(PSDT)。方法:通过双乳液法制造OI_NP,其特征在于,其物理化学和双模态成像特征。共聚焦显微镜和流式细胞术用于确定ID8细胞OI_NP的细胞摄取。使用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2- H-四唑溴铵(MTT)测定来研究ID8细胞的活力和凋亡率和ΔOm细胞学。然后使用流式细胞术,蛋白质印迹和发光测定测定来研究关键潮湿的暴露或释放,例如CaltreteLin(CRT),高迁移率组箱1(HMGB1)和腺苷-5α-三磷酸(ATP)。然后使用肿瘤重新检查实验来研究是否接受过ICD的处理过的ID8细胞。最后,细胞毒性T淋巴细胞(CTL)活性由乳酸脱氢酶(LDH)测定法测定。结果:球形OI_NPS能够携带OXP,ICG和PFP,并通过ID8细胞成功内化。 OI_NP的应用显着提高了PFP的相移能力和ICG的光学特性,从而导致光声和超声成像的显着改善。当与近红外光和超声结合时,OI_NPS的应用导致改善对癌细胞的抗肿瘤作用,并显着增强了潮湿的表达,从而产生了长期的抗肿瘤作用。结论:oi_nps的应用,加载适当的货物,可以代表一种新的策略,增加抗肿瘤效应,增强免疫效力,改善双模影像。

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