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本文引用的文献

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Enzyme-Specific Doxorubicin Drug Beacon as Drug-Resistant Theranostic Molecular Probes.酶特异性阿霉素药物信标作为耐药性诊疗分子探针
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A polymer additive boosts the anti-cancer efficacy of supramolecular nanofibers of taxol.一种聚合物添加剂可提高紫杉醇超分子纳米纤维的抗癌功效。
Biomater Sci. 2014 May 1;2(5):651-654. doi: 10.1039/c3bm60252d. Epub 2013 Dec 12.
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A paclitaxel-loaded recombinant polypeptide nanoparticle outperforms Abraxane in multiple murine cancer models.一种负载紫杉醇的重组多肽纳米颗粒在多种小鼠癌症模型中比白蛋白结合型紫杉醇表现更优。
Nat Commun. 2015 Aug 4;6:7939. doi: 10.1038/ncomms8939.
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New trends in guided nanotherapies for digestive cancers: A systematic review.导向型纳米疗法治疗消化系统癌症的新趋势:系统评价。
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Light-triggered, self-immolative nucleic Acid-drug nanostructures.光触发自毁核酸药物纳米结构。
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Engineering Biomaterial-Drug Conjugates for Local and Sustained Chemotherapeutic Delivery.用于局部和持续化疗给药的工程化生物材料-药物偶联物
Bioconjug Chem. 2015 Jul 15;26(7):1212-23. doi: 10.1021/acs.bioconjchem.5b00046. Epub 2015 Mar 2.
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Synthesis and Self-Assembly of a Mikto-Arm Star Dual Drug Amphiphile Containing both Paclitaxel and Camptothecin.含紫杉醇和喜树碱的米克托臂星型双药两亲分子的合成与自组装
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Site-specific antibody-drug conjugates: the nexus of bioorthogonal chemistry, protein engineering, and drug development.位点特异性抗体-药物偶联物:生物正交化学、蛋白质工程与药物开发的关联点
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Ring-opening polymerization of prodrugs: a versatile approach to prepare well-defined drug-loaded nanoparticles.前药的开环聚合:一种制备结构明确的载药纳米颗粒的通用方法。
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单组分纳米药物

One-component nanomedicine.

作者信息

Su Hao, Koo Jin Mo, Cui Honggang

机构信息

Department of Chemical and Biomolecular Engineering, The Johns Hopkins University, 3400 N Charles Street, Baltimore, MD 21218, USA; Institute for NanoBioTechnology, The Johns Hopkins University, 3400 N Charles Street, Baltimore, MD 21218, USA.

Department of Chemical and Biomolecular Engineering, The Johns Hopkins University, 3400 N Charles Street, Baltimore, MD 21218, USA.

出版信息

J Control Release. 2015 Dec 10;219:383-395. doi: 10.1016/j.jconrel.2015.09.056. Epub 2015 Sep 28.

DOI:10.1016/j.jconrel.2015.09.056
PMID:26423237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4656119/
Abstract

One-component nanomedicine (OCN) represents an emerging class of therapeutic nanostructures that contain only one type of chemical substance. This one-component feature allows for fine-tuning and optimization of the drug loading and physicochemical properties of nanomedicine in a precise manner through molecular engineering of the underlying building blocks. Using a precipitation procedure or effective molecular assembly strategies, molecularly crafted therapeutic agents (e.g. polymer-drug conjugates, small molecule prodrugs, or drug amphiphiles) could involuntarily aggregate, or self-assemble into nanoscale objects of well-defined sizes and shapes. Unlike traditional carrier-based nanomedicines that are inherently multicomponent systems, an OCN does not require the use of additional carriers and could itself possess desired physicochemical features for preferential accumulation at target sites. We review here recent progress in the molecular design, conjugation methods, and fabrication strategies of OCN, and analyze the opportunities that this emerging platform could open for the new and improved treatment of devastating diseases such as cancer.

摘要

单组分纳米药物(OCN)是一类新兴的治疗性纳米结构,仅包含一种化学物质。这种单组分特性使得通过对基础构建单元进行分子工程,能够以精确的方式对纳米药物的载药量和物理化学性质进行微调与优化。利用沉淀法或有效的分子组装策略,经分子设计的治疗剂(如聚合物 - 药物偶联物、小分子前药或药物两亲物)可能会自发聚集,或自组装成尺寸和形状明确的纳米级物体。与本质上是多组分系统的传统基于载体的纳米药物不同,OCN不需要使用额外的载体,并且自身可能具备在靶部位优先积累所需的物理化学特性。我们在此综述OCN在分子设计、偶联方法和制备策略方面的最新进展,并分析这个新兴平台可能为诸如癌症等毁灭性疾病的新型和改进治疗带来的机遇。