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用于肿瘤靶向近红外二区光诊疗的乳腺癌细胞膜伪装脂质纳米颗粒

Breast Cancer Cell Membrane Camouflaged Lipid Nanoparticles for Tumor-Targeted NIR-II Phototheranostics.

作者信息

Xu Mengze, Yang Yu, Yuan Zhen

机构信息

Cancer Center, Faculty of Health Sciences, University of Macau, Macau 999078, China.

Centre for Cognitive and Brain Sciences, University of Macau, Macau 999078, China.

出版信息

Pharmaceutics. 2022 Jun 28;14(7):1367. doi: 10.3390/pharmaceutics14071367.

Abstract

Photoacoustic imaging and photothermal therapy that employ organic dye in the second near-infrared window (NIR-II) became an attractive theranostical strategy for eliminating solid tumors, in which IR1048 was previously reported to be a good candidate. However, the further biomedical application of IR1048 was blocked by its poor water-solubility and lack of tumor-targeting. To solve this problem, liposome camouflaged with 4T1 cell membrane fragments was employed to encapsulate IR1048 (thereafter called MLI), and its application for photoacoustic and thermo-imaging and photothermal therapy were explored in vitro and in vivo. The results showed that MLI exhibited spherical morphology around 92.55 ± 5.41 nm coated by monolayer adventitial fragments, and uniformly dispersed in PBS with high loading efficiency and encapsulation efficiency to IR1048. In addition, both free IR1048 and MLI presented strong absorption in NIR-II, and upon 1064 nm laser irradiation the MLI showed awesome photothermal performance that could rapidly elevate the temperature to 50.9 °C in 6 min. Simultaneously, phantom assay proved that MLI could dramatically enhance the photoacoustic amplitudes by a linear concentration-dependent way. Moreover, either flow cytometry or confocal analysis evidenced that MLI was the most uptaked by 4T1 cells among other melanoma B16 cells and Hek293 cells and coexist of IR1048 and 1064 nm laser irradiation were indispensable for the photothermal cytotoxicity of MLI that specifically killed 96.16% of 4T1 cells far outweigh the B16 cells while hardly toxic to the Hek293 normal cells. Furthermore, PA imaging figured out that 4 h post tail-vein injection of MLI was the best time to give 1064 nm irradiation to conduct the photothermal therapy when the average tumor-accumulation of MLI achieved the highest. In the NIR-II photothermal therapy, MLI could significantly inhibit the tumor growth and almost ablated the tumors with slight body weight variation and the highest average life span over the therapy episode and caused no damage to the normal organs. Hence, MLI could pave the way for further biomedical applications of IR-1048 by homologous tumor-targeting and dual-modal imaging directed NIR-II accurate photothermal therapy with high efficacy and fine biosafety.

摘要

在近红外二区(NIR-II)使用有机染料的光声成像和光热疗法成为一种有吸引力的用于消除实体瘤的诊疗策略,此前有报道称IR1048是一个很好的候选物。然而,IR1048进一步的生物医学应用受到其水溶性差和缺乏肿瘤靶向性的阻碍。为了解决这个问题,用4T1细胞膜片段伪装的脂质体用于包裹IR1048(此后称为MLI),并在体外和体内探索其在光声和热成像以及光热疗法中的应用。结果表明,MLI呈现出球形形态,直径约为92.55±5.41nm,被单层外膜片段包裹,并且以高负载效率和包封效率均匀分散在PBS中。此外,游离的IR1048和MLI在NIR-II中均表现出强烈的吸收,在1064nm激光照射下,MLI表现出出色的光热性能,能够在6分钟内迅速将温度升高到50.9℃。同时,模型分析证明MLI能够以线性浓度依赖的方式显著增强光声信号幅度。此外,流式细胞术或共聚焦分析均证明,在其他黑色素瘤B16细胞和Hek293细胞中,4T1细胞对MLI的摄取最多,并且IR1048和1064nm激光照射的共同存在对于MLI的光热细胞毒性是必不可少的,MLI特异性杀死了96.16%的4T1细胞,远远超过B16细胞,而对Hek293正常细胞几乎没有毒性。此外,光声成像表明,尾静脉注射MLI后4小时是进行1064nm照射以实施光热疗法的最佳时间,此时MLI的平均肿瘤蓄积量达到最高。在NIR-II光热疗法中,MLI能够显著抑制肿瘤生长,几乎消除肿瘤,体重变化轻微,在治疗期间平均寿命最长,并且对正常器官没有损害。因此,MLI可以通过同源肿瘤靶向和双模态成像引导的NIR-II精确光热疗法,以高疗效和良好的生物安全性为IR-1048的进一步生物医学应用铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4267/9319009/92d440e73adc/pharmaceutics-14-01367-g001.jpg

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