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用于体内分子成像和高特异性癌症治疗的一氧化氮激活“双钥匙一锁”纳米探针。

Nitric Oxide-Activated "Dual-Key-One-Lock" Nanoprobe for in Vivo Molecular Imaging and High-Specificity Cancer Therapy.

机构信息

Molecular Science and Biomedicine Laboratory (MBL), State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering , Hunan University , Changsha 410082 , P. R. China.

出版信息

J Am Chem Soc. 2019 Aug 28;141(34):13572-13581. doi: 10.1021/jacs.9b05901. Epub 2019 Aug 13.

Abstract

Cancer treatments are confounded by severe toxic effects toward patients. To address these issues, activatable nanoprobes have been designed for specific imaging and destruction of cancer cells under the stimulation of specific cancer-associated biomarkers. Most activatable nanoprobes were usually activated by some single-factor stimulation, but this restricts therapeutic specificity between diseased and normal tissue; therefore, multifactor activation is highly desired. To this end, we herein develop a novel dual-stimuli responsive theranostic nanoprobe for simultaneously activatable cancer imaging and photothermal therapy under the coactivation of "dual-key" stimulation of "nitric oxide (NO)/acidity", so as to further improve the therapeutic specificity. Specifically, we have integrated a weak electron acceptor (benzo[][1,2,5]thiadiazole-5,6-diamine) into a donor-π-acceptor-π-donor type chromophore. When the weak acceptor was oxidized by NO in acidic conditions to form a stronger acceptor (5-[1,2,3]triazolo[4,5-]-2,1,3-benzothiadiazole), the molecule absorption was significantly increased in the near-infrared region, based on the intramolecular charge transfer (ICT) mechanism. Under the dual-key stimulation of NO/acidity within the tumor associated with inflammation, the nanoprobe can correspondingly output dual signals for ratiometric photoacoustic and photothermal imaging of cancer in vivo and do so with enhanced accuracy and specificity. Our novel nanoprobe exhibited higher photoacoustic signal enhancement under dual-factor activation at 9.8 times that of NO and 132 times that of acidity alone, respectively. Moreover, through such dual activation of NO/acidity, the nanoprobe produces more differentiation of hyperthermia between tumor and normal tissues, to afford satisfactory photothermal therapy with minimal toxic side effects. Thus, our work presents a promising strategy for significantly improving the precision and specificity of cancer imaging and therapy.

摘要

癌症治疗受到严重的毒性作用对患者的影响。为了解决这些问题,已经设计了可激活的纳米探针,以便在特定癌症相关生物标志物的刺激下对癌细胞进行特定的成像和破坏。大多数可激活的纳米探针通常是通过单一因素的刺激来激活的,但是这限制了病变组织和正常组织之间的治疗特异性;因此,强烈需要多因素激活。为此,我们开发了一种新型的双重刺激响应治疗性纳米探针,用于在“一氧化氮(NO)/酸度”的“双钥匙”刺激下同时激活癌症成像和光热治疗,以进一步提高治疗特异性。具体来说,我们已经将弱电子受体(苯并[][1,2,5]噻二唑-5,6-二胺)整合到供体-π-受体-π-供体型发色团中。当弱受体在酸性条件下被 NO 氧化形成更强的受体(5-[1,2,3]三唑[4,5-]-2,1,3-苯并噻二唑)时,基于分子内电荷转移(ICT)机制,分子吸收在近红外区域显著增加。在与炎症相关的肿瘤中,NO/酸度的双重键刺激下,纳米探针可以相应地输出用于体内癌症的比率光声和光热成像的双重信号,并且具有更高的准确性和特异性。在双重因素激活下,纳米探针的光声信号增强了 9.8 倍,分别是 NO 的 132 倍。此外,通过这种对 NO/酸度的双重激活,纳米探针在肿瘤和正常组织之间产生了更明显的热区分,从而可以进行令人满意的光热治疗,而副作用最小。因此,我们的工作为显著提高癌症成像和治疗的精度和特异性提供了一种有前途的策略。

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