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载甲氨蝶呤 PLGA 纳米气泡用于超声成像及 HIFU 消融后残留肿瘤的协同靶向治疗。

Methotrexate-loaded PLGA nanobubbles for ultrasound imaging and Synergistic Targeted therapy of residual tumor during HIFU ablation.

机构信息

Department of Obstetrics and Gynecology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, PR China.

Institution of Ultrasound Imaging, Second Affiliated Hospital, Chongqing Medical University, Chongqing 400010, PR China.

出版信息

Biomaterials. 2014 Jun;35(19):5148-61. doi: 10.1016/j.biomaterials.2014.02.036. Epub 2014 Mar 28.

Abstract

High intensity focused ultrasound (HIFU) has attracted the great attention in tumor ablation due to its non-invasive, efficient and economic features. However, HIFU ablation has its intrinsic limitations for removing the residual tumor cells, thus the tumor recurrence and metastasis cannot be avoided in this case. Herein, we developed a multifunctional targeted poly(lactic-co-glycolic acid) (PLGA) nanobubbles (NBs), which not only function as an efficient ultrasound contrast agent for tumor imaging, but also a targeted anticancer drug carrier and excellent synergistic agent for enhancing the therapeutic efficiency of HIFU ablation. Methotrexate (MTX)-loaded NBs were synthesized and filled with perfluorocarbon gas subsequently using a facile but general double emulsion evaporation method. The active tumor-targeting monoclonal anti-HLA-G antibodies (mAbHLA-G) were further conjugated onto the surface of nanobubbles. The mAbHLA-G/MTX/PLGA NBs could enhance the ultrasound imaging both in vitro and in vivo, and the targeting efficiency to HLA-G overexpressing JEG-3 cells has been demonstrated. The elaborately designed mAbHLA-G/MTX/PLGA NBs can specifically target to the tumor cells both in vitro and in vivo, and their blood circulation time in vivo was much longer than non-targeted MTX/PLGA NBs. Further therapeutic evaluations showed that the targeted NBs as a synergistic agent can significantly improve the efficiency of HIFU ablation by changing the acoustic environment, and the focused ultrasound can promote the on-demand MTX release both in vitro and in vivo. The in vivo histopathology test and immunohistochemical analysis showed that the mAbHLA-G/MTX/PLGA NBs plus HIFU group presented most serious coagulative necrosis, the lowest proliferation index and the highest apoptotic index. Therefore, the successful introduction of targeted mAbHLA-G/MTX/PLGA NBs provides an excellent platform for the highly efficient, imaging-guided and non-invasive HIFU synergistic therapy of cancer with the supplementary functions of killing residual tumor cells and preventing tumor recurrence/metastasis.

摘要

高强度聚焦超声(HIFU)由于其非侵入性、高效和经济的特点,在肿瘤消融中引起了极大的关注。然而,HIFU 消融对于清除残留的肿瘤细胞存在固有局限性,因此在这种情况下无法避免肿瘤的复发和转移。在此,我们开发了一种多功能靶向聚(乳酸-共-乙醇酸)(PLGA)纳米泡(NBs),它不仅可以作为肿瘤成像的高效超声造影剂,还可以作为靶向抗癌药物载体,并作为增强 HIFU 消融治疗效果的优异协同剂。采用简便但通用的双乳液蒸发法合成了载甲氨蝶呤(MTX)的 NB,并随后填充全氟碳气体。活性肿瘤靶向单克隆抗 HLA-G 抗体(mAbHLA-G)进一步偶联到纳米泡的表面。mAbHLA-G/MTX/PLGA NBs 可以增强体外和体内的超声成像,并且已经证明了对 HLA-G 过表达 JEG-3 细胞的靶向效率。精心设计的 mAbHLA-G/MTX/PLGA NBs 可以在体外和体内特异性靶向肿瘤细胞,并且它们在体内的血液循环时间比非靶向 MTX/PLGA NBs 长得多。进一步的治疗评估表明,作为协同剂的靶向 NBs 可以通过改变声环境显著提高 HIFU 消融的效率,并且聚焦超声可以在体外和体内按需释放 MTX。体内组织病理学检查和免疫组织化学分析表明,mAbHLA-G/MTX/PLGA NBs 加 HIFU 组呈现出最严重的凝固性坏死,最低的增殖指数和最高的凋亡指数。因此,靶向 mAbHLA-G/MTX/PLGA NBs 的成功引入为高效、成像引导和非侵入性 HIFU 协同治疗癌症提供了一个极好的平台,具有杀伤残留肿瘤细胞和防止肿瘤复发/转移的附加功能。

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