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用于一氧化氮控制释放的分子印迹 S-亚硝酰硫醇纳米粒子作为癌症靶向化疗。

Molecular imprinted S-nitrosothiols nanoparticles for nitric oxide control release as cancer target chemotherapy.

机构信息

College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Shandong Normal University, Jinan, 250014, PR China.

Department of Anesthesiology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, 250014, PR China.

出版信息

Colloids Surf B Biointerfaces. 2019 Jan 1;173:356-365. doi: 10.1016/j.colsurfb.2018.09.078. Epub 2018 Oct 3.

Abstract

It is the goal for the development of cancer target chemotherapy with specific recognition, efficient killing the tumor cells and tissues to avoid the intolerable side effects. Molecular imprinted polymer (MIPs) nanoparticles could introduce kinds of specific bio-markers (template molecules) into the nanoparticles with the subsequent removal, leaving special holes in the structure with predictable recognition specificity with cells. Herein, we design and synthesize a kind of sialic acid (SA) over-expressed tumor target hollow double-layer imprinted polymer nanoparticles with S-nitrosothiols for nitric oxide (NO)-releasing as chemotherapy. Equilibrium/selective bindings properties and probe experimental results implies that the MIPs have an intelligently selective binding to cancer cells featuring high levels of SA glyans, providing precondition for the disulfide polymer assisted cell uptake, intracellular GSH induced decomposition and rapid NO-releasing. Cytotoxicity assay with kinds of cells demonstrates the intelligent in vitro SA over-expressed tumor cells targeting recognition, intracellular delivery and cytotoxicity. In vivo bio-distribution in tumor sites and major organs, significant suppression of tumor growth, tumor-bearing mice survival unit, and the systemic toxicity investigation experiments confirm the effective chemotherapy of the S-nitrosothiols MIPs nanoparticles for the target recognition and the controlled NO release for tumor treatment comparing to the results with S-nitrosothiols CPs as delivery system. The inevitable small amount of NO leakage from S-nitrosothiols MIPs would take part in normal physiological activities and not cause serious side effects. For the first time, this kind of nitric oxide based chemotherapy and molecular-imprinting cell recognition technique both in vitro and in vivo, might provide a solution for accurate therapy to various forms of cancer with specific markers and avoid the intolerable side effects of the traditional chemotherapy treatment.

摘要

这是癌症靶向化疗发展的目标,具有特异性识别、高效杀伤肿瘤细胞和组织,避免不可耐受的副作用。分子印迹聚合物(MIPs)纳米粒子可以将各种特定的生物标志物(模板分子)引入纳米粒子中,随后去除,在结构中留下特殊的孔,具有对细胞的可预测的识别特异性。在此,我们设计并合成了一种唾液酸(SA)过表达肿瘤靶向中空双层印迹聚合物纳米粒子,其具有 S-亚硝基硫醇作为化疗的一氧化氮(NO)释放。平衡/选择性结合特性和探针实验结果表明,MIPs 对 SA 糖含量高的癌细胞具有智能选择性结合,为二硫聚合物辅助细胞摄取、细胞内 GSH 诱导分解和快速 NO 释放提供了条件。用各种细胞进行的细胞毒性试验表明,智能体外 SA 过表达肿瘤细胞靶向识别、细胞内递药和细胞毒性。在肿瘤部位和主要器官中的体内生物分布、肿瘤生长的显著抑制、荷瘤小鼠的生存单位以及全身毒性研究实验证实,与 S-亚硝基硫醇 CP 作为递送系统相比,S-亚硝基硫醇 MIPs 纳米粒子的有效化疗具有针对肿瘤治疗的靶向识别和控制的 NO 释放。从 S-亚硝基硫醇 MIPs 中不可避免的少量 NO 泄漏将参与正常的生理活动,不会引起严重的副作用。这是第一次在体外和体内同时使用基于一氧化氮的化疗和分子印迹细胞识别技术,为具有特定标志物的各种形式的癌症提供了精确治疗的解决方案,并避免了传统化疗治疗的不可耐受的副作用。

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