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Development of nanoparticles incorporated with quercetin and ACE2-membrane as a novel therapy for COVID-19.
Fang, Jia-You; Huang, Kuo-Yen; Wang, Tong-Hong; Lin, Zih-Chan; Chen, Chin-Chuan; Chang, Sui-Yuan; Chen, En-Li; Chao, Tai-Ling; Yang, Shuenn-Chen; Yang, Pan-Chyr; Chen, Chi-Yuan.
Afiliación
  • Fang JY; Research Center for Food and Cosmetic Safety and Research Center for Chinese Herbal Medicine, Chang Gung University of Science and Technology, Taoyuan, Taiwan.
  • Huang KY; Graduate Institute of Natural Products, Chang Gung University, Taoyuan, Taiwan.
  • Wang TH; Department of Anesthesiology, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
  • Lin ZC; Department of Clinical Laboratory Sciences and Medical Biotechnology, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Chen CC; National Taiwan University YongLin Institute of Health, Taipei, Taiwan.
  • Chang SY; Graduate School of Advanced Technology (Program for Precision Health and Intelligent Medicine), National Taiwan University, Taipei, Taiwan.
  • Chen EL; Graduate Institute of Natural Products, Chang Gung University, Taoyuan, Taiwan.
  • Chao TL; Graduate Institute of Health Industry Technology, Research Center for Food and Cosmetic Safety and Research Center for Chinese Herbal Medicine, Chang Gung University of Science and Technology, Taoyuan, Taiwan.
  • Yang SC; Biobank, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
  • Yang PC; Liver Research Center, Department of Hepato-Gastroenterology, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
  • Chen CY; Chronic Diseases and Health Promotion Research Center, Chang Gung University of Science and Technology, Chiayi, Taiwan.
J Nanobiotechnology ; 22(1): 169, 2024 Apr 12.
Article en En | MEDLINE | ID: mdl-38609998
ABSTRACT

INTRODUCTION:

Angiotensin-converting enzyme 2 (ACE2) and AXL tyrosine kinase receptor are known to be involved in the SARS-CoV-2 entry of the host cell. Therefore, targeting ACE2 and AXL should be an effective strategy to inhibit virus entry into cells. However, developing agents that can simultaneously target ACE2 and AXL remains a formidable task. The natural compound quercetin has been shown to inhibit AXL expression. MATERIALS AND

METHODS:

In this study, we employed PLGA nanoparticles to prepare nanoparticles encapsulated with quercetin, coated with ACE2-containing cell membranes, or encapsulated with quercetin and then coated with ACE-2-containing cell membranes. These nanoparticles were tested for their abilities to neutralize or inhibit viral infection.

RESULTS:

Our data showed that nanoparticles encapsulated with quercetin and then coated with ACE2-containing cell membrane inhibited the expression of AXL without causing cytotoxic activity. Nanoparticles incorporated with both quercetin and ACE2-containing cell membrane were found to be able to neutralize pseudo virus infection and were more effective than free quercetin and nanoparticles encapsulated with quercetin at inhibition of pseudo virus and SARS-CoV-2 infection.

CONCLUSIONS:

We have shown that the biomimetic nanoparticles incorporated with both ACE-2 membrane and quercetin showed the most antiviral activity and may be further explored for clinical application.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Nanopartículas / COVID-19 Límite: Humans Idioma: En Revista: J Nanobiotechnology Año: 2024 Tipo del documento: Article País de afiliación: Taiwán

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Nanopartículas / COVID-19 Límite: Humans Idioma: En Revista: J Nanobiotechnology Año: 2024 Tipo del documento: Article País de afiliación: Taiwán