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载铁(II)酞菁和 AS1411 适体靶向纳米粒子:用于乳腺癌双重模态成像和光热治疗的纳米复合物。

Iron(II) phthalocyanine Loaded and AS1411 Aptamer Targeting Nanoparticles: A Nanocomplex for Dual Modal Imaging and Photothermal Therapy of Breast Cancer.

机构信息

Department of Nuclear Medicine, The Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, People's Republic of China.

Chongqing Key Laboratory of Ultrasound Molecular Imaging, The Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, People's Republic of China.

出版信息

Int J Nanomedicine. 2020 Aug 11;15:5927-5949. doi: 10.2147/IJN.S254108. eCollection 2020.

Abstract

PURPOSE

A multi-functional nanoplatform with diagnostic imaging and targeted treatment functions has aroused much interest in the nanomedical research field and has been paid more attention in the field of tumor diagnosis and treatment. However, some existing nano-contrast agents have encountered difficulties in different aspects during clinical promotion, such as complicated preparation process and low specificity. Therefore, it is urgent to find a nanocomplex with good targeting effect, high biocompatibility and significant therapeutic effect for the integration of diagnosis and treatment and clinical transformation.

MATERIALS AND METHODS

Nanoparticles (NPs) targeting breast cancer were synthesized by phacoemulsification which had liquid fluorocarbon perfluoropentane(PFP) in the core and were loaded with Iron(II) phthalocyanine (FePc) on the shell. The aptamer (APT) AS1411 was outside the shell used as a molecular probe. Basic characterization and targeting abilities of the NPs were tested, and their cytotoxicity and biological safety in vivo were evaluated through CCK-8 assay and blood bio-chemical analysis. The photoacoustic (PA) and ultrasound (US) imaging system were used to assess the effects of AS1411-PLGA@FePc@PFP (A-FP NPs) as dual modal contrast agent in vitro and in vivo. The effects of photothermal therapy (PTT) in vitro and in vivo were evaluated through MCF-7 cells and tumor-bearing nude mouse models.

RESULTS

A-FP NPs, with good stability, great biocompatibility and low toxicity, were of 201.87 ± 1.60 nm in diameter, and have an active targeting effect on breast cancer cells and tissues. With the help of PA/US imaging, it was proved to be an excellent dual modal contrast agent for diagnosis and guidance of targeted therapy. Meanwhile, it can heat up under near-infrared (NIR) laser irradiation and has achieved obvious antitumor effect both in vitro and in vivo experiments.

CONCLUSION

As a kind of nanomedicine, A-FP NPs can be used in the integration of diagnosis and treatment. The treatment effects and biocompatibility in vivo may provide new thoughts in the clinical transformation of nanomedicine and early diagnosis and treatment of breast cancer.

摘要

目的

具有诊断成像和靶向治疗功能的多功能纳米平台在纳米医学研究领域引起了广泛关注,并在肿瘤诊断和治疗领域受到了更多关注。然而,一些现有的纳米造影剂在临床推广过程中遇到了不同的困难,例如复杂的制备工艺和低特异性。因此,迫切需要找到一种具有良好靶向效果、高生物相容性和显著治疗效果的纳米复合物,用于诊断和治疗的整合以及临床转化。

材料和方法

通过相乳液化法合成靶向乳腺癌的纳米粒子(NPs),其核心为液态氟碳全氟戊烷(PFP),壳层负载铁(II)酞菁(FePc)。外壳外包裹着适配体(APT)AS1411 作为分子探针。测试了 NPs 的基本特性和靶向能力,并通过 CCK-8 测定法和血液生化分析评估了其在体内的细胞毒性和生物安全性。使用光声(PA)和超声(US)成像系统评估 AS1411-PLGA@FePc@PFP(A-FP NPs)作为双模态对比剂在体外和体内的效果。通过 MCF-7 细胞和荷瘤裸鼠模型评估了光热治疗(PTT)的体外和体内效果。

结果

A-FP NPs 具有良好的稳定性、优异的生物相容性和低毒性,粒径为 201.87 ± 1.60nm,对乳腺癌细胞和组织具有主动靶向作用。在 PA/US 成像的帮助下,它被证明是一种出色的双模态对比剂,可用于诊断和指导靶向治疗。同时,它可以在近红外(NIR)激光照射下升温,并在体外和体内实验中均取得了明显的抗肿瘤效果。

结论

作为一种纳米药物,A-FP NPs 可用于诊断和治疗的整合。其体内治疗效果和生物相容性可能为纳米医学的临床转化和乳腺癌的早期诊断和治疗提供新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adc7/7429213/104b240a8bbd/IJN-15-5927-g0009.jpg

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