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一种新型两亲性荧光探针BODIPY--CMC-cRGD作为生物标志物和纳米颗粒载体。

A novel amphiphilic fluorescent probe BODIPY--CMC-cRGD as a biomarker and nanoparticle vector.

作者信息

Zhu Tingting, Xiong Ji, Xue Zhongbo, Su Yu, Sun Fengnan, Chai Ran, Xu Jialiang, Feng Yaqing, Meng Shuxian

机构信息

School of Chemical Engineering and Technology, Tianjin University No. 92, Weijin Road, Nankaiwei District Tianjin 300072 P. R. China

Hebei University of Technology P. R. China.

出版信息

RSC Adv. 2018 Jun 4;8(36):20087-20094. doi: 10.1039/c8ra02125b. eCollection 2018 May 30.

Abstract

Fluorescent probes have been demonstrated to be promising candidates as biomarkers and biological carriers. Our study focuses on the development of a novel amphiphilic fluorescent probe with good photostability, high water solubility, excellent specificity and promising loading capability for tumor diagnosis and treatment. At first, BODIPY dye and -carboxymethyl chitosan were prepared a chemical reaction. Then, the prepared BODIPY dye and cRGD were bonded to -carboxymethyl chitosan successively an acylation reaction. Finally, we obtained the desired amphiphilic fluorescent probe: BODIPY--CMC-cRGD, which was based on the fluorescence resonance energy transfer (FRET) principle for selective visualization of tumors . Through a series of experiments, we found that this fluorescent probe possessed better fluorescence characteristics and tumor targeting properties. Simultaneously, by self-assembly, the amphiphilic probe encapsulated the other flexible structure of BODIPY2 and the rigid structure of porphyrin, which formed distinct nanoparticles with different particle sizes. Hence, we could observe different phagocytosis processes of the two nanoparticles in the tumor cells the fluorescence of dyes by confocal laser scanning microscopy. Therefore, the results suggest that the fluorescent probe has advantages in tumor detection, and the constructed tumor-specific nanoparticles show high clinical potential to be utilized not only in visual and precise diagnosis but also in excellent drug delivery for tumor treatment. Henceforth, we will prepare new targeted and visualized pharmaceuticals by replacing BODIPY2 and porphyrin with antineoplastic drugs for future tumor treatment.

摘要

荧光探针已被证明是作为生物标志物和生物载体的有前途的候选者。我们的研究重点是开发一种新型两亲性荧光探针,它具有良好的光稳定性、高水溶性、优异的特异性以及用于肿瘤诊断和治疗的有前景的负载能力。首先,通过化学反应制备了硼二吡咯染料和羧甲基壳聚糖。然后,通过酰化反应将制备的硼二吡咯染料和cRGD依次连接到羧甲基壳聚糖上。最后,我们获得了所需的两亲性荧光探针:基于荧光共振能量转移(FRET)原理用于肿瘤选择性可视化的硼二吡咯-羧甲基壳聚糖-cRGD。通过一系列实验,我们发现这种荧光探针具有更好的荧光特性和肿瘤靶向特性。同时,通过自组装,两亲性探针包裹了硼二吡咯2的另一种柔性结构和卟啉的刚性结构,形成了具有不同粒径的独特纳米颗粒。因此,我们可以通过共聚焦激光扫描显微镜观察肿瘤细胞中两种纳米颗粒通过染料荧光的不同吞噬过程。因此,结果表明该荧光探针在肿瘤检测方面具有优势,并且构建的肿瘤特异性纳米颗粒不仅在视觉和精确诊断中,而且在用于肿瘤治疗的优异药物递送中都显示出很高的临床应用潜力。从今以后,我们将用抗肿瘤药物取代硼二吡咯2和卟啉来制备新的靶向和可视化药物用于未来的肿瘤治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ecf/9080774/a5ecb98ef4fa/c8ra02125b-s1.jpg

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