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本文引用的文献

1
Bio-Orthogonal Chemistry and Reloadable Biomaterial Enable Local Activation of Antibiotic Prodrugs and Enhance Treatments against Infections.生物正交化学与可再装填生物材料实现抗生素前药的局部激活并增强感染治疗效果。
ACS Cent Sci. 2018 Dec 26;4(12):1624-1632. doi: 10.1021/acscentsci.8b00344. Epub 2018 Dec 12.
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Enamide Prodrugs of Acetyl Phosphonate Deoxy-d-xylulose-5-phosphate Synthase Inhibitors as Potent Antibacterial Agents.乙酰膦酸脱氧-D-木酮糖-5-磷酸合酶抑制剂的烯酰胺前药作为强效抗菌剂
ACS Infect Dis. 2019 Mar 8;5(3):406-417. doi: 10.1021/acsinfecdis.8b00307. Epub 2019 Jan 18.
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Innate glycosidic activity in metallic implants for localized synthesis of antibacterial drugs.金属植入物中的固有糖苷活性用于局部合成抗菌药物。
Chem Commun (Camb). 2019 Jan 3;55(4):443-446. doi: 10.1039/c8cc08737g.
4
Polyprodrug Antimicrobials: Remarkable Membrane Damage and Concurrent Drug Release to Combat Antibiotic Resistance of Methicillin-Resistant Staphylococcus aureus.聚前药型抗菌剂:通过显著的膜损伤和药物协同释放来克服耐甲氧西林金黄色葡萄球菌的抗生素耐药性。
Small. 2018 Oct;14(41):e1802008. doi: 10.1002/smll.201802008. Epub 2018 Aug 17.
5
Macrophage-targeted drugamers with enzyme-cleavable linkers deliver high intracellular drug dosing and sustained drug pharmacokinetics against alveolar pulmonary infections.具有酶可裂解连接子的巨噬细胞靶向药物偶联物可实现针对肺泡肺部感染的高细胞内药物剂量和持续的药物药代动力学。
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Improved Antibacterial Activity of the Marine Peptide N6 against Intracellular Salmonella Typhimurium by Conjugating with the Cell-Penetrating Peptide Tat via a Cleavable Linker.通过连接一个可裂解的连接子将穿膜肽 Tat 与海洋肽 N6 偶联,提高其对细胞内鼠伤寒沙门氏菌的抗菌活性。
J Med Chem. 2018 Sep 13;61(17):7991-8000. doi: 10.1021/acs.jmedchem.8b01079. Epub 2018 Aug 23.
7
Glutamic acid-valine-citrulline linkers ensure stability and efficacy of antibody-drug conjugates in mice.谷氨酸-缬氨酸-瓜氨酸连接子确保抗体药物偶联物在小鼠体内的稳定性和疗效。
Nat Commun. 2018 Jun 28;9(1):2512. doi: 10.1038/s41467-018-04982-3.
8
Action of antimicrobial peptides and their prodrugs on model and biological membranes.抗菌肽及其前药对模型膜和生物膜的作用。
J Pept Sci. 2018 Jul;24(7):e3086. doi: 10.1002/psc.3086. Epub 2018 May 24.
9
PEGylated prodrugs of antidiabetic peptides amylin and GLP-1.聚乙二醇化的抗糖尿病肽胰淀素和 GLP-1 的前药。
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10
The expanding role of prodrugs in contemporary drug design and development.前药在当代药物设计和开发中的作用不断扩大。
Nat Rev Drug Discov. 2018 Aug;17(8):559-587. doi: 10.1038/nrd.2018.46. Epub 2018 Apr 27.

签收、密封、送达:共轭和前药策略作为抗生素的靶向递送载体

Signed, Sealed, Delivered: Conjugate and Prodrug Strategies as Targeted Delivery Vectors for Antibiotics.

作者信息

Cheng Ana V, Wuest William M

机构信息

Department of Chemistry , Emory University , 1515 Dickey Drive , Atlanta , Georgia 30322 , United States.

Emory Antibiotic Resistance Center , Emory School of Medicine , 201 Dowman Drive , Atlanta , Georgia 30322 , United States.

出版信息

ACS Infect Dis. 2019 Jun 14;5(6):816-828. doi: 10.1021/acsinfecdis.9b00019. Epub 2019 Apr 10.

DOI:10.1021/acsinfecdis.9b00019
PMID:30969100
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6570538/
Abstract

Innate and developed resistance mechanisms of bacteria to antibiotics are obstacles in the design of novel drugs. However, antibacterial prodrugs and conjugates have shown promise in circumventing resistance and tolerance mechanisms via directed delivery of antibiotics to the site of infection or to specific species or strains of bacteria. The selective targeting and increased permeability and accumulation of these prodrugs not only improves efficacy over unmodified drugs but also reduces off-target effects, toxicity, and development of resistance. Herein, we discuss some of these methods, including sideromycins, antibody-directed prodrugs, cell penetrating peptide conjugates, and codrugs.

摘要

细菌对抗生素的固有和后天抗性机制是新型药物设计中的障碍。然而,抗菌前体药物和偶联物在规避抗性和耐受机制方面已显示出前景,它们可通过将抗生素定向递送至感染部位或特定种类或菌株的细菌。这些前体药物的选择性靶向以及更高的渗透性和蓄积性不仅提高了相对于未修饰药物的疗效,还减少了脱靶效应、毒性和抗性的产生。在此,我们讨论其中一些方法,包括铁载体霉素、抗体导向前体药物、细胞穿透肽偶联物和协同药物。