Tumor-Targeted CO Nanodelivery System Design and Therapy for Hepatocellular Carcinoma

In recent years, carbon monoxide (CO) has garnered increased attention as a novel green therapy for hepatocellular carcinoma (HCC) treatment. However, the CO donor is still limited in clinical application due to its lack of targeted ability and unstable release rate. Here, self-assembled amphiphilic nanomicelles glucose-polyethylene glycol (PEG)-lipoic acid (LA)-Fe<sub>2</sub>(CO)<sub>6</sub> (Glu-Fe<sub>2</sub>(CO)<sub>6</sub>) are first designed as a CO donor and synthesized via a chemical method, combining glucose with Fe<sub>2</sub>(CO)<sub>6</sub> through PEG-LA. Some advantages of this tumor-targeted Glu-Fe<sub>2</sub>(CO)<sub>6</sub> delivery system include (I) good water-solubility, (II) the glutathione responsive CO slow release, (III) the active tumor-targeted ability of glucose as targeted ligands, and (IV) outstanding efficacy of antitumor and safety of CO therapy of HCC both in vitro and in vivo. These findings suggest that Glu-Fe<sub>2</sub>(CO)<sub>6</sub> nanomicelles hold promise for enhancing antitumor therapeutic capabilities, presenting a novel tumor-targeted delivery strategy in gas therapy for HCC treatment.

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Publication Details

Journal
Molecular Pharmaceutics
Published
2024-09-20
DOI
https://doi.org/10.1021/acs.molpharmaceut.4c00437
Citations
2
Primary Topic
Heme Oxygenase-1 and Carbon Monoxide
Type
article
Field-Weighted Citation Impact
0.47

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article

Tumor-Targeted CO Nanodelivery System Design and Therapy for Hepatocellular Carcinoma

Congyi Zhang, W.M. Li, Tianwei Li, Haotian Wu et al.
2 citations
Molecular Pharmaceutics
Heme Oxygenase-1 and Carbon Monoxide
0.47
article

Tumor-Targeted CO Nanodelivery System Design and Therapy for Hepatocellular Carcinoma

Congyi Zhang, W.M. Li, Tianwei Li, Haotian Wu, Shizhuan Huang, Minghui Li, Sheng Tai, Kunhao Ding, Zibo Shen
article en
2 citations

Abstract

In recent years, carbon monoxide (CO) has garnered increased attention as a novel green therapy for hepatocellular carcinoma (HCC) treatment. However, the CO donor is still limited in clinical application due to its lack of targeted ability and unstable release rate. Here, self-assembled amphiphilic nanomicelles glucose-polyethylene glycol (PEG)-lipoic acid (LA)-Fe<sub>2</sub>(CO)<sub>6</sub> (Glu-Fe<sub>2</sub>(CO)<sub>6</sub>) are first designed as a CO donor and synthesized via a chemical method, combining glucose with Fe<sub>2</sub>(CO)<sub>6</sub> through PEG-LA. Some advantages of this tumor-targeted Glu-Fe<sub>2</sub>(CO)<sub>6</sub> delivery system include (I) good water-solubility, (II) the glutathione responsive CO slow release, (III) the active tumor-targeted ability of glucose as targeted ligands, and (IV) outstanding efficacy of antitumor and safety of CO therapy of HCC both in vitro and in vivo. These findings suggest that Glu-Fe<sub>2</sub>(CO)<sub>6</sub> nanomicelles hold promise for enhancing antitumor therapeutic capabilities, presenting a novel tumor-targeted delivery strategy in gas therapy for HCC treatment.

Molecular PharmaceuticsVol. 21(10)
Harbin Medical University (CN), King's College London (GB), Second Affiliated Hospital of Harbin Medical University (CN)
Harbin Medical University, National Natural Science Foundation of China, China Postdoctoral Science Foundation, Heilongjiang Provincial Postdoctoral Science Foundation
Good health and well-being
Openalex Percentile: Top 35%
Heme Oxygenase-1 and Carbon Monoxide
0.47
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