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使用带有发光体和嵌入剂的DNA缠绕金纳米颗粒辅助递送抗肿瘤铂类药物:迈向新一代具有增强作用的多模态纳米载体。

Assisted delivery of anti-tumour platinum drugs using DNA-coiling gold nanoparticles bearing lumophores and intercalators: towards a new generation of multimodal nanocarriers with enhanced action.

作者信息

Caballero Ana B, Cardo Lucia, Claire Sunil, Craig James S, Hodges Nikolas J, Vladyka Anton, Albrecht Tim, Rochford Luke A, Pikramenou Zoe, Hannon Michael J

机构信息

School of Chemistry , University of Birmingham , Edgbaston , Birmingham B15 2TT , UK . Email:

Physical Sciences for Health Centre , University of Birmingham , Edgbaston , Birmingham B15 2TT , UK.

出版信息

Chem Sci. 2019 Aug 13;10(40):9244-9256. doi: 10.1039/c9sc02640a. eCollection 2019 Oct 28.

Abstract

New gold and lipoic based nanocarriers for the delivery of platinum(ii) and platinum(iv) drugs are developed, which allow enhanced loading of the drug on the surface of the nanocarriers and release in a pH-dependent fashion, with superior release at lower pHs which are associated with many tumours. The conjugate nanoparticles and their conjugates enter cells rapidly (within 3 hours). They tend to cluster in vesicles and are also observed by light and electron microscopies in the cytoplasm, endoplasmic reticulum and nucleus. We further incorporate aminoanthraquinone units that are both fluorophores and DNA intercalators. This results in nanocarriers that after drug release will remain surface decorated with DNA-binders challenging the conventional design of the nanocarrier as an inert component. The outcome is nanocarriers that themselves have distinctive, remarkable and unusual DNA binding properties being able to bind and wrap DNA (despite their anionic charge) and provide enhanced cytotoxic activity beyond that conferred by the platinum agents they release. DNA coiling is usually associated with polycations which can disrupt cell membranes; anionic nanoparticles that can cause novel and dramatic effects on DNA may have fascinating potential for new approaches to in-cell nucleic acid recognition. Our findings have implications for the understanding and interpretation of the biological activities of nanoparticles used to deliver other DNA-binding drugs including clinical drug doxorubicin and its formulations.

摘要

新型基于金和硫辛酸的纳米载体被开发用于递送铂(II)和铂(IV)药物,其能使药物在纳米载体表面实现增强负载,并以pH依赖的方式释放,在与许多肿瘤相关的较低pH值下有更优的释放效果。共轭纳米颗粒及其共轭物能迅速进入细胞(3小时内)。它们倾向于聚集在囊泡中,并且通过光学显微镜和电子显微镜也能在细胞质、内质网和细胞核中观察到。我们进一步引入了兼具荧光团和DNA嵌入剂功能的氨基蒽醌单元。这导致纳米载体在药物释放后表面仍装饰有DNA结合剂,这对将纳米载体设计为惰性成分的传统理念提出了挑战。结果是纳米载体本身具有独特、显著且异常的DNA结合特性,能够结合并包裹DNA(尽管其带负电荷),并提供超出其释放的铂类药物所赋予的增强细胞毒性活性。DNA卷曲通常与可破坏细胞膜的聚阳离子相关;能够对DNA产生新颖且显著影响的阴离子纳米颗粒可能在细胞内核酸识别新方法方面具有迷人的潜力。我们的研究结果对于理解和解释用于递送其他DNA结合药物(包括临床药物阿霉素及其制剂)的纳米颗粒的生物活性具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c11e/7003971/7a2f600f26cb/c9sc02640a-f1.jpg

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