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用于增强 OSCC 骨侵犯的光热和缺氧激活化疗的靶向骨红细胞-癌细胞杂化膜伪装纳米颗粒。

Bone-targeted erythrocyte-cancer hybrid membrane-camouflaged nanoparticles for enhancing photothermal and hypoxia-activated chemotherapy of bone invasion by OSCC.

机构信息

College of Stomatology, Chongqing Medical University, Chongqing, 401147, China.

Chongqing Key Laboratory of Oral Diseases and Biomedical Sciences, Chongqing, 401147, China.

出版信息

J Nanobiotechnology. 2021 Oct 26;19(1):342. doi: 10.1186/s12951-021-01088-9.

Abstract

BACKGROUND

Jaw bones are the most common organs to be invaded by oral malignancies, such as oral squamous cell carcinoma (OSCC), because of their special anatomical relationship. Various serious complications, such as pathological fractures and bone pain can significantly decrease the quality of life or even survival outcomes for a patient. Although chemotherapy is a promising strategy for bone invasion treatment, its clinical applications are limited by the lack of tumor-specific targeting and poor permeability in bone tissue. Therefore, it is necessary to develop a smart bone and cancer dual targeting drug delivery platform.

RESULTS

We designed a dual targeting nano-biomimetic drug delivery vehicle Asp8[H40-TPZ/IR780@(RBC-H)] that has excellent bone and cancer targeting as well as immune escape abilities to treat malignancies in jaw bones. These nanoparticles were camouflaged with a head and neck squamous cell carcinoma WSU-HN6 cell (H) and red blood cell (RBC) hybrid membrane, which were modified by an oligopeptide of eight aspartate acid (Asp8). The spherical morphology and typical core-shell structure of biomimetic nanoparticles were observed by transmission electron microscopy. These nanoparticles exhibited the same surface proteins as those of WSU-HN6 and RBC. Flow cytometry and confocal microscopy showed a greater uptake of the biomimetic nanoparticles when compared to bare H40-PEG nanoparticles. Biodistribution of the nanoparticles in vivo revealed that they were mainly localized in the area of bone invasion by WSU-HN6 cells. Moreover, the Asp8[H40-TPZ/IR780@(RBC-H)] nanoparticles exhibited effective cancer growth inhibition properties when compared to other TPZ or IR780 formulations.

CONCLUSIONS

Asp8[H40-TPZ/IR780@(RBC-H)] has bone targeting, tumor-homing and immune escape abilities, therefore, it is an efficient multi-targeting drug delivery platform for achieving precise anti-cancer therapy during bone invasion.

摘要

背景

颌骨是口腔恶性肿瘤(如口腔鳞状细胞癌,OSCC)最常侵犯的器官,这是由于其特殊的解剖关系。各种严重的并发症,如病理性骨折和骨痛,会显著降低患者的生活质量,甚至影响生存结果。尽管化疗是治疗骨侵犯的一种有前途的策略,但由于缺乏肿瘤特异性靶向性和在骨组织中的渗透性差,其临床应用受到限制。因此,有必要开发一种智能的骨和癌症双重靶向药物递送平台。

结果

我们设计了一种双重靶向的纳米仿生药物递送载体 Asp8[H40-TPZ/IR780@(RBC-H)],该载体具有优异的骨和癌症靶向以及免疫逃逸能力,可用于治疗颌骨中的恶性肿瘤。这些纳米颗粒被一种由 8 个天冬氨酸组成的寡肽(Asp8)修饰的头颈鳞状细胞癌 WSU-HN6 细胞(H)和红细胞(RBC)混合膜伪装。透射电子显微镜观察到仿生纳米颗粒具有球形形态和典型的核壳结构。这些纳米颗粒表现出与 WSU-HN6 和 RBC 相同的表面蛋白。流式细胞术和共聚焦显微镜显示,与 bare H40-PEG 纳米颗粒相比,仿生纳米颗粒的摄取量更大。体内纳米颗粒的分布表明,它们主要定位于 WSU-HN6 细胞侵犯的骨区域。此外,与其他 TPZ 或 IR780 制剂相比,Asp8[H40-TPZ/IR780@(RBC-H)]纳米颗粒表现出更有效的抑制肿瘤生长的特性。

结论

Asp8[H40-TPZ/IR780@(RBC-H)]具有骨靶向、肿瘤归巢和免疫逃逸能力,因此,它是一种有效的多靶向药物递送平台,可实现骨侵犯期间的精确抗癌治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a5b/8549398/ef33c249b617/12951_2021_1088_Sch1_HTML.jpg

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