Poly(Ethylene Glycol)‐Modified Catalase Blocking Reactive Oxygen Species for the Treatment of Hepatic Ischemia

Hepatic ischemia-reperfusion injury (IRI) is a severe clinical condition often leading to liver dysfunction due to oxidative stress and inflammatory responses. This study investigates the therapeutic potential of polyethylene glycol (PEG)-modified catalase (CAT) in alleviating oxidative damage associated with hepatic IRI. Catalase, an enzyme that decomposes hydrogen peroxide into water and oxygen, is modified with PEG to enhance its stability, bioavailability, and to prolong its half-life in vivo. PEGylation significantly improved the pharmacokinetics of CAT by extending its circulation half-life and enhancing its stability against enzymatic degradation. Both in vitro and in vivo experiments demonstrated that PEGylated CAT (CAT-PEG) efficiently reduced reactive oxygen species (ROS) levels, mitigated oxidative stress, and improved liver function post-reperfusion. These findings suggest that CAT-PEG is a promising therapeutic strategy for treating IRI, with potential for broader applications in liver transplantation and other conditions involving oxidative damage.

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Publication Details

Journal
Macromolecular Rapid Communications
Published
2025-05-26
DOI
https://doi.org/10.1002/marc.202500367
Citations
4
Primary Topic
Liver Disease and Transplantation
Type
article
Field-Weighted Citation Impact
5.29

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article

Poly(Ethylene Glycol)‐Modified Catalase Blocking Reactive Oxygen Species for the Treatment of Hepatic Ischemia

Yunfeng Lu, Yijia Zhang, Zeren Han, Qiong Dai et al.
4 citations
Macromolecular Rapid Communications
Liver Disease and Transplantation
5.29
article

Poly(Ethylene Glycol)‐Modified Catalase Blocking Reactive Oxygen Species for the Treatment of Hepatic Ischemia

Yunfeng Lu, Yijia Zhang, Zeren Han, Qiong Dai, Jian Zeng, Yuxi Li, Chaoyong Liu, Jiarui Li, Feifei Li, Dingqi Wu, Liyun Zhang, Rui Ma, Qian He, Sai Gao
article en
4 citations

Abstract

Hepatic ischemia-reperfusion injury (IRI) is a severe clinical condition often leading to liver dysfunction due to oxidative stress and inflammatory responses. This study investigates the therapeutic potential of polyethylene glycol (PEG)-modified catalase (CAT) in alleviating oxidative damage associated with hepatic IRI. Catalase, an enzyme that decomposes hydrogen peroxide into water and oxygen, is modified with PEG to enhance its stability, bioavailability, and to prolong its half-life in vivo. PEGylation significantly improved the pharmacokinetics of CAT by extending its circulation half-life and enhancing its stability against enzymatic degradation. Both in vitro and in vivo experiments demonstrated that PEGylated CAT (CAT-PEG) efficiently reduced reactive oxygen species (ROS) levels, mitigated oxidative stress, and improved liver function post-reperfusion. These findings suggest that CAT-PEG is a promising therapeutic strategy for treating IRI, with potential for broader applications in liver transplantation and other conditions involving oxidative damage.

Macromolecular Rapid CommunicationsVol. 46(17)
University of California, Santa Barbara (US), Shanxi Medical University (CN), Chinese Academy of Sciences (CN), Zhejiang Cancer Hospital (CN), Shanxi Academy of Medical Sciences (CN), Hangzhou Cancer Hospital (CN), Beijing University of Chemical Technology (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 4%
Liver Disease and Transplantation
5.29
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