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酶武装纳米清洁剂通过双重作用机制提供卓越的解毒效果,对抗有机磷化合物。

Enzyme-armed nanocleaner provides superior detoxification against organophosphorus compounds via a dual-action mechanism.

机构信息

Tianjin Key Laboratory of Risk Assessment and Control Technology for Environment and Food Safety, Military Medical Sciences Academy, Tianjin, 300050, China.

Hebei Key Laboratory of Public Health Safety, College of Public Health, Hebei University, Baoding, 071002, China.

出版信息

J Nanobiotechnology. 2024 Sep 30;22(1):593. doi: 10.1186/s12951-024-02869-8.


DOI:10.1186/s12951-024-02869-8
PMID:39343894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11440912/
Abstract

By inhibiting acetylcholinesterase (AChE) activity, organophosphate compounds (OPs) can quickly cause severe injury to the nervous system and death, making it extremely difficult to rescue victims after OP exposure. However, it is quite challenging to construct scavengers that neutralize and eliminate these harmful chemical agents promptly in the blood circulation system. Herein, we report an enzyme-armed biomimetic nanoparticle that enables a 'targeted binding and catalytic degradation' action mechanism designed for highly efficient in vivo detoxification (denoted as 'Nanocleaner'). Specifically, the resulting Nanocleaner is fabricated with polymeric cores camouflaged with a modified red blood cell membrane (RBC membrane) that is inserted with the organophosphorus hydrolase (OPH) enzyme. In such a subtle construct, Nanocleaner inherits abundant acetylcholinesterase (AChE) on the surface of the RBC membrane, which can specifically lure and neutralize OPs through biological binding. The OPH enzyme on the membrane surface breaks down toxicants catalytically. The in vitro protective effects of Nanocleaner against methyl paraoxon (MPO)-induced inhibition of AChE activity were validated using both preincubation and competitive regimens. Furthermore, we selected the PC12 neuroendocrine cell line as an experimental model and confirmed the cytoprotective effects of Nanocleaner against MPO. In mice challenged with a lethal dose of MPO, Nanocleaner significantly reduces clinical signs of intoxication, rescues AChE activity and promotes the survival rate of mice challenged with lethal MPO. Overall, these results suggest considerable promise of enzyme-armed Nanocleaner for the highly efficient removal of OPs for clinical treatment.

摘要

通过抑制乙酰胆碱酯酶(AChE)的活性,有机磷化合物(OPs)能迅速对神经系统造成严重损伤,导致暴露于 OPs 后的患者救治极为困难。然而,构建能在血液循环系统中迅速中和并消除这些有害化学物质的清除剂极具挑战性。在此,我们报告了一种酶武装仿生纳米颗粒,其能实现“靶向结合和催化降解”的作用机制,从而设计出高效的体内解毒(表示为“Nanocleaner”)。具体来说,所得的 Nanocleaner 是由聚合物核心构建的,聚合物核心伪装成经过修饰的红细胞膜(RBC 膜),其中插入有机磷水解酶(OPH)酶。在这种微妙的结构中,Nanocleaner 继承了 RBC 膜表面丰富的乙酰胆碱酯酶(AChE),其可以通过生物结合特异性地吸引和中和 OPs。膜表面的 OPH 酶可以催化分解有毒物质。我们通过预孵育和竞争方案验证了 Nanocleaner 对甲基对氧磷(MPO)诱导的 AChE 活性抑制的体外保护作用。此外,我们选择 PC12 神经内分泌细胞系作为实验模型,证实了 Nanocleaner 对 MPO 的细胞保护作用。在接受致死剂量 MPO 挑战的小鼠中,Nanocleaner 显著减轻了中毒的临床症状,挽救了 AChE 活性,并提高了接受致死剂量 MPO 挑战的小鼠的存活率。总的来说,这些结果表明酶武装的 Nanocleaner 具有很高的去除 OPs 的潜力,有望用于临床治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/99977c57c8b6/12951_2024_2869_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/f59d9a9a2a64/12951_2024_2869_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/bd010bcc9d65/12951_2024_2869_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/61e315aba6ed/12951_2024_2869_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/eb4c5934ad1d/12951_2024_2869_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/2d7473c916b6/12951_2024_2869_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/5e8b8b270b17/12951_2024_2869_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/cba2303c717d/12951_2024_2869_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/f5c1b834d4d0/12951_2024_2869_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/99977c57c8b6/12951_2024_2869_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/f59d9a9a2a64/12951_2024_2869_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/bd010bcc9d65/12951_2024_2869_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/61e315aba6ed/12951_2024_2869_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/eb4c5934ad1d/12951_2024_2869_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/2d7473c916b6/12951_2024_2869_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/5e8b8b270b17/12951_2024_2869_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/cba2303c717d/12951_2024_2869_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/f5c1b834d4d0/12951_2024_2869_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc54/11440912/99977c57c8b6/12951_2024_2869_Fig9_HTML.jpg

相似文献

[1]
Enzyme-armed nanocleaner provides superior detoxification against organophosphorus compounds via a dual-action mechanism.

J Nanobiotechnology. 2024-9-30

[2]
Dual-Modal Nanoscavenger for Detoxification of Organophosphorus Compounds.

ACS Appl Mater Interfaces. 2022-9-21

[3]
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[4]
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J Hazard Mater. 2018-11-2

[5]
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J Control Release. 2016-12-31

[6]
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ACS Nano. 2015-6-23

[7]
Combined effect of organophosphorus hydrolase and oxime on the reactivation rate of diethylphosphoryl-acetylcholinesterase conjugates.

Biochem Pharmacol. 1998-1-15

[8]
Effect of organophosphorus hydrolysing enzymes on obidoxime-induced reactivation of organophosphate-inhibited human acetylcholinesterase.

Arch Toxicol. 2004-6

[9]
Testing of antidotes for organophosphorus compounds: experimental procedures and clinical reality.

Toxicology. 2007-4-20

[10]
In silico and in vitro evaluation of two novel oximes (K378 and K727) in comparison to K-27 and pralidoxime against paraoxon-ethyl intoxication.

Toxicol Mech Methods. 2017-8-4

本文引用的文献

[1]
Biomimetic single Al-OH site with high acetylcholinesterase-like activity and self-defense ability for neuroprotection.

Nat Commun. 2023-9-28

[2]
Cellular and molecular responses to ethyl-parathion in undifferentiated SH-SY5Y cells provide neurotoxicity pathway indicators for organophosphorus impacts.

Toxicol Sci. 2023-2-17

[3]
Exosomes decorated with a recombinant SARS-CoV-2 receptor-binding domain as an inhalable COVID-19 vaccine.

Nat Biomed Eng. 2022-7

[4]
Dissection of the antibacterial mechanism of zinc oxide nanoparticles with manipulable nanoscale morphologies.

J Hazard Mater. 2022-5-15

[5]
A Bioinspired Five-Coordinated Single-Atom Iron Nanozyme for Tumor Catalytic Therapy.

Adv Mater. 2022-4

[6]
Self-Protecting Biomimetic Nanozyme for Selective and Synergistic Clearance of Peripheral Amyloid-β in an Alzheimer's Disease Model.

J Am Chem Soc. 2020-12-30

[7]
Cellular Nanosponges Inhibit SARS-CoV-2 Infectivity.

Nano Lett. 2020-6-17

[8]
Designing multifunctionalized selenium nanoparticles to reverse oxidative stress-induced spinal cord injury by attenuating ROS overproduction and mitochondria dysfunction.

J Mater Chem B. 2019-3-21

[9]
The Experimental Oxime K027-A Promising Protector From Organophosphate Pesticide Poisoning. A Review Comparing K027, K048, Pralidoxime, and Obidoxime.

Front Neurosci. 2019-5-22

[10]
Cell-Membrane-Cloaked Oil Nanosponges Enable Dual-Modal Detoxification.

ACS Nano. 2019-5-22

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