Gd(3+)- dtpa - meglumi -阴离子线性球状树突状物G1:新型纳米低毒肿瘤分子MR显像剂。

ISRN Pharmaceutics Pub Date : 2013-01-01 Epub Date: 2013-02-26 DOI:10.1155/2013/378452
Tahmineh Darvish Mohamadi, Massoud Amanlou, Negar Ghalandarlaki, Bita Mehravi, Mehdi Shafiee Ardestani, Parichehr Yaghmaei
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引用次数: 10

摘要

尽管在癌症的早期诊断和治疗方面做出了巨大努力,但这种疾病继续增长,仍然是全球杀手。在疾病的早期,癌症的治疗效率相对较高。因此,早期诊断是癌症治疗的关键因素。在各种诊断方法中,分子显像是最快、最安全的方法之一。由于其独特的特性,磁共振成像在大多数研究中占有特殊的地位。为了提高磁共振图像的对比度,目前已知和使用了许多药物。Gadopentetate(商业名称为Magnevist)是美国食品和药物管理局批准的第一种磁共振成像造影剂。在这项研究中,首先合成了加佐戊二酸酯,然后将其附着在一种由聚乙二醇核和周围的柠檬酸基团形成的树状聚合物上。对该药物进行了稳定性研究,以确保正确合成。然后,观察药物对肝细胞的摄取情况及药物的细胞毒性。最后对新合成药物进行体外和体内磁共振成像。基于本研究的发现,将枝状聚合物表面连接可以产生一种更强、更安全、更有效的造影剂。Gd(III)-五乙酸二乙三胺-三聚氰胺-树突状药物具有进入细胞的能力,不产生明显的细胞毒性。它还增加了组织的松弛性,增强了MR图像的对比度。所得结果证实了加佐戊酸与柠檬酸树状大分子的结合产生了一种新的、可生物降解的、稳定的、强的旧造影剂的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Gd(3+)-DTPA-Meglumine-Anionic Linear Globular Dendrimer G1: Novel Nanosized Low Toxic Tumor Molecular MR Imaging Agent.

Gd(3+)-DTPA-Meglumine-Anionic Linear Globular Dendrimer G1: Novel Nanosized Low Toxic Tumor Molecular MR Imaging Agent.

Gd(3+)-DTPA-Meglumine-Anionic Linear Globular Dendrimer G1: Novel Nanosized Low Toxic Tumor Molecular MR Imaging Agent.

Gd(3+)-DTPA-Meglumine-Anionic Linear Globular Dendrimer G1: Novel Nanosized Low Toxic Tumor Molecular MR Imaging Agent.

Despite the great efforts in the areas of early diagnosis and treatment of cancer, this disease continues to grow and is still a global killer. Cancer treatment efficiency is relatively high in the early stages of the disease. Therefore, early diagnosis is a key factor in cancer treatment. Among the various diagnostic methods, molecular imaging is one of the fastest and safest ones. Because of its unique characteristics, magnetic resonance imaging has a special position in most researches. To increase the contrast of MR images, many pharmaceuticals have been known and used so far. Gadopentetate (with commercial name Magnevist) is the first magnetic resonance imaging contrast media that has been approved by the US Food and Drug Administration. In this study, gadopentetate was first synthesized and then attached to a tree-like polymer called dendrimer which is formed by polyethylene glycol core and surrounding citric acid groups. Stability studies of the drug were carried out to ensure proper synthesis. Then, the uptake of the drug into liver hepatocellular cell line and the drug cytotoxicity were evaluated. Finally, in vitro and in vivo MR imaging were performed with the new synthetic drug. Based on the findings of this research, connecting gadopentetate to dendrimer surface produces a stronger, safer, and more efficient contrast media. Gd(III)-diethylenetriamine pentaacetate-meglumine-dendrimer drug has the ability to enter cells and does not produce significant cytotoxicity. It also increases the relaxivity of tissue and enhances the MR images contrast. The obtained results confirm the hypothesis that the binding of gadopentetate to citric acid dendrimer produces a new, biodegradable, stable, and strong version of the old contrast media.

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