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具有阿霉素和二氢卟吩e6的叶酸修饰牛血清白蛋白纳米粒用于有效的联合化学-光动力疗法

Folic acid-modified bovine serum albumin nanoparticles with doxorubicin and chlorin e6 for effective combinational chemo-photodynamic therapy.

作者信息

Lee Hoomin, Kim Suji, Oh Cheolwoo, Khan Imran, Shukla Shruti, Bajpai Vivek K, Han Young-Kyu, Huh Yun Suk

机构信息

Department of Biological Engineering, NanoBio High-Tech Materials Research Center, Inha University, Incheon 22212, Republic of Korea.

Department of Food Science and Technology, National Institute of Food Technology Entrepreneurship and Management (NIFTEM), Sonipat, Haryana 131028, India.

出版信息

Mater Sci Eng C Mater Biol Appl. 2020 Dec;117:111343. doi: 10.1016/j.msec.2020.111343. Epub 2020 Aug 11.

Abstract

We herein describe a facile method to synthesize stable bovine serum albumin-based nanoparticles (BNPs) loaded with two anticancer therapeutics, doxorubicin (DOX) and a photosensitizer, chlorin e6 (Ce6), in combination with folic acid (FA) as a target cancer cell receptor for the development of an effective combined chemo and photodynamic (FA-Ce6/DOX/BNPs) therapy against cervical cancer. FA-Ce6/DOX/BNPs exhibited excellent monodispersity with an average diameter of 103.5 ± 3.8 nm, a negative zeta potential of approximately -30.44 ± 0.35 mV, and long-term stability. As a result, FA-Ce6/DOX/BNPs exhibited severe toxicity to cervical HeLa cancer cells. Also, a higher drug release rate was observed under acidic pH conditions (pH 5.0). Moreover, FA-Ce6/DOX/BNPs potentiated mitochondrial reactive oxygen species (ROS) production in HeLa cells under 671-nm laser exposure, leading to activation of key regulator proteins of apoptosis such as BH3 interacting-domain death agonist (BID), B-cell lymphoma 2 (Bcl-2), and Bcl-2-associated X (BAX), as well as induction of the caspase cascade and mitochondrial ROS-mediated cell death. Confocal microscopy analysis further validated cellular uptake of FA-Ce6/DOX/BNPs by HeLa cells. Furthermore, results of real-time quantitative PCR (RT-qPCR) and western blot analysis further validated the anticancer effect of FA-Ce6/DOX/BNPs, as evidenced by elevated gene/protein expression levels of apoptotic biomarkers p53, BID, caspase-3, cleaved poly(ADP-ribose) polymerase 1 (PARP-1), and BAX, contrary to levels of the anti-apoptotic marker Bcl-2. Moreover, in vivo toxicity results of FA-Ce6/DOX/BNPs using laser irradiation in zebrafish larvae, as a chemo-photodynamic therapy confirmed that it does not affect the larval development without causing any adverse toxic effect in zebrafish larvae. Altogether these findings strongly support the anticancer effect of FA-Ce6/DOX/BNPs combinational chemo-photodynamic therapy, which could be a promising candidate for cervical cancer therapy.

摘要

我们在此描述了一种简便的方法,用于合成负载两种抗癌治疗药物(阿霉素(DOX)和光敏剂二氢卟吩e6(Ce6))的稳定的基于牛血清白蛋白的纳米颗粒(BNPs),并结合叶酸(FA)作为靶向癌细胞受体,以开发针对宫颈癌的有效联合化学和光动力(FA-Ce6/DOX/BNPs)疗法。FA-Ce6/DOX/BNPs表现出优异的单分散性,平均直径为103.5±3.8nm,负ζ电位约为-30.44±0.35mV,并且具有长期稳定性。结果,FA-Ce6/DOX/BNPs对宫颈HeLa癌细胞表现出严重毒性。此外,在酸性pH条件(pH 5.0)下观察到更高的药物释放速率。此外,FA-Ce6/DOX/BNPs在671nm激光照射下增强了HeLa细胞中线粒体活性氧(ROS)的产生,导致凋亡关键调节蛋白如BH3相互作用结构域死亡激动剂(BID)、B细胞淋巴瘤2(Bcl-2)和Bcl-2相关X蛋白(BAX)的激活,以及半胱天冬酶级联反应的诱导和线粒体ROS介导的细胞死亡。共聚焦显微镜分析进一步验证了HeLa细胞对FA-Ce6/DOX/BNPs的细胞摄取。此外,实时定量PCR(RT-qPCR)和蛋白质印迹分析结果进一步验证了FA-Ce6/DOX/BNPs的抗癌作用,凋亡生物标志物p53、BID、半胱天冬酶-3、裂解的聚(ADP-核糖)聚合酶1(PARP-1)和BAX的基因/蛋白质表达水平升高证明了这一点,这与抗凋亡标志物Bcl-2的水平相反。此外,在斑马鱼幼虫中使用激光照射的FA-Ce6/DOX/BNPs的体内毒性结果,作为一种化学光动力疗法,证实其在不影响斑马鱼幼虫发育且不引起任何不良毒性作用的情况下。总之,这些发现有力地支持了FA-Ce6/DOX/BNPs联合化学光动力疗法的抗癌作用,这可能是宫颈癌治疗的一个有前途的候选方法。

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