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Enhanced MRI-Guided Gadolinium (III) Neutron Capture Therapy by Polymeric Nanocarriers Promoting Tumor Accumulation and Intracellular Delivery

机译:增强的MRI引导钆(III)中子捕获治疗通过聚合物纳米载体促进肿瘤积累和细胞内递送

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摘要

Gadolinium(III) (Gd(III)) chelates are promising compounds for developing MRI-guided neutron capture therapies (NCT). However, despite their success as MRI contrast agents (CAs), current Gd(III) chelates do not present appropriate accumulation in tumors for effective NCT. To overcome this limitation, we developed a series of biocompatible polymeric nanocarriers conjugating Gd(III)-chelates, i. e. Gd-DOTA, as NCT agents with high MRI sensitivity and tumor delivery. These polymers were based on poly(aspartic acid) (P(Asp)) and were modified with poly(ethylene glycol) (PEG) chains having different molecular weight (M-w) for controlling stability and pharmacokinetics. The T-1 relaxivity of the Gd-DOTA conjugated polymers increased 2-fold compared to that of clinically used Gd(III) CAs. In vivo, the PEG-modified polymers promoted the accumulation in tumor tissues, enhancing the MRI contrast of tumors. After neutron irradiation, the nanocarriers effectively suppressed the tumor growth, particularly the PEG-P(Asp-Gd-DOTA) with shorter PEG chain, which promoted higher intracellular delivery, supporting their potential as NCT agents.
机译:钆(III)(GD(III))螯合物是开发MRI引导中子捕获疗法(NCT)的有希望的化合物。然而,尽管其成功作为MRI造影剂(CAS),但目前的GD(III)螯合物在肿瘤中没有适当的积累,以有效NCT。为了克服这种限制,我们开发了一系列的生物相容性聚合物纳米载体缀合Gd(III) - 螯合物,I。 e。 Gd-dota,作为具有高MRI敏感性和肿瘤递送的NCT代理。这些聚合物基于聚(天冬氨酸)(P(ASP)),并用具有不同分子量(M-W)的聚(乙二醇)(PEG)链进行改性,用于控制稳定性和药代动力学。与临床使用的GD(III)CAS相比,GD-DOTA共轭聚合物的T-1的弛豫率增加了2倍。在体内,PEG改性聚合物促进肿瘤组织中的积累,增强了肿瘤的MRI对比度。在中子辐射之后,纳米载体有效地抑制了肿瘤生长,特别是PEG-P(ASP-GD-DOTA)具有较短的PEG链,其促进了更高的细胞内递送,支持它们作为NCT代理的潜力。

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