首页> 美国卫生研究院文献>International Journal of Nanomedicine >1,3-Bis(2-chloroethyl)-1-nitrosourea-loaded bovine serum albumin nanoparticles with dual magnetic resonance–fluorescence imaging for tracking of chemotherapeutic agents
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1,3-Bis(2-chloroethyl)-1-nitrosourea-loaded bovine serum albumin nanoparticles with dual magnetic resonance–fluorescence imaging for tracking of chemotherapeutic agents

机译:1,3-双(2-氯乙基)-1-亚硝基脲装载的牛血清白蛋白纳米颗粒,具有双磁共振-荧光成像技术,可追踪化学治疗剂

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摘要

To date, knowing how to identify the location of chemotherapeutic agents in the human body after injection is still a challenge. Therefore, it is urgent to develop a drug delivery system with molecular imaging tracking ability to accurately understand the distribution, location, and concentration of a drug in living organisms. In this study, we developed bovine serum albumin (BSA)-based nanoparticles (NPs) with dual magnetic resonance (MR) and fluorescence imaging modalities (fluorescein isothiocyanate [FITC]-BSA-Gd/1,3-bis(2-chloroethyl)-1-nitrosourea [BCNU] NPs) to deliver BCNU for inhibition of brain tumor cells (MBR 261-2). These BSA-based NPs are water dispersible, stable, and biocompatible as confirmed by XTT cell viability assay. In vitro phantoms and in vivo MR and fluorescence imaging experiments show that the developed FITC-BSA-Gd/BCNU NPs enable dual MR and fluorescence imaging for monitoring cellular uptake and distribution in tumors. The T1 relaxivity (R1) of FITC-BSA-Gd/BCNU NPs was 3.25 mM−1 s−1, which was similar to that of the commercial T1 contrast agent (R1 =3.36 mM−1 s−1). The results indicate that this multifunctional drug delivery system has potential bioimaging tracking of chemotherapeutic agents ability in vitro and in vivo for cancer therapy.
机译:迄今为止,知道如何在注射后确定化学治疗剂在人体中的位置仍然是一个挑战。因此,迫切需要开发一种具有分子成像跟踪能力的药物输送系统,以准确了解生物体内药物的分布,位置和浓度。在这项研究中,我们开发了具有双重磁共振(MR)和荧光成像方式(异硫氰酸荧光素[FITC] -BSA-Gd / 1,3-bis(2-chloroethyl)的基于牛血清白蛋白(BSA)的纳米颗粒(NPs) -1-亚硝基脲(BCNU)NPs释放BCNU以抑制脑肿瘤细胞(MBR 261-2)。如XTT细胞活力分析所证实,这些基于BSA的NP具有水分散性,稳定性和生物相容性。体外体模以及体内MR和荧光成像实验表明,已开发的FITC-BSA-Gd / BCNU NP能够实现MR和荧光双重成像,以监测肿瘤中细胞的摄取和分布。 FITC-BSA-Gd / BCNU NP的T1弛豫度(R1)为3.25 mM -1 s -1 ,与商用T1造影剂相似( R1 = 3.36 mM -1 s -1 )。结果表明,该多功能药物递送系统具有体外和体内化学疗法对癌症治疗的能力的潜在生物成像追踪。

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