Leveraging immunoliposomes as nanocarriers against SARS-CoV-2 and its emerging variants

被引:3
作者
Faizal, Nur Dini Fatini Mohammad [1 ]
Ramli, Nurul Afina [1 ]
Rani, Nur Najihah Izzati Mat [2 ]
Shaibie, Nur Adania [1 ]
Aarti [4 ]
Poonsawas, Pattaporn [3 ]
Sharma, Sunil K. [4 ]
Amin, Mohd Cairul Iqbal Mohd [1 ]
机构
[1] Univ Kebangsaan Malaysia, Fac Pharm, Ctr Drug Delivery Technol & Vaccine CENTRIC, Kuala Lumpur 50300, Malaysia
[2] Univ Royal Coll Med Perak UniKL RCMP, Fac Pharm, 3 Jalan Greentown, Ipoh 30450, Perak, Malaysia
[3] Thammasat Univ, Fac Econ, Bangkok 10200, Thailand
[4] Univ Delhi, Dept Chem, Delhi 110007, India
关键词
Coronavirus; COVID-19; SARS-CoV-2; Liposomes; Immunoliposomes; DRUG-DELIVERY; LIPOSOMES; STRATEGY; PROTEINS; SPIKE; TRANSPEPTIDATION; NANOPARTICLES; CARBODIIMIDE;
D O I
10.1016/j.ajps.2023.100855
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The global COVID-19 pandemic arising from SARS-CoV-2 has impacted many lives, gaining interest worldwide ever since it was first identified in December 2019. Till 2023, 752 million cumulative cases and 6.8 million deaths were documented globally. COVID-19 has been rapidly evolving, affecting virus transmissibility and properties and contributing to increased disease severity. The Omicron is the most circulating variant of concern. Although success in its treatment has indicated progress in tackling the virus, limitations in delivering the current antiviral agents in battling emerging variants remain remarkable. With the latest advancements in nanotechnology for controlling infectious diseases, liposomes have the potential to counteract SARS-CoV-2 because of their ability to employ different targeting strategies, incorporating monoclonal antibodies for the active and passive targeting of infected patients. This review will present a concise summary of the possible strategies for utilizing immunoliposomes to improve current treatment against the occurrence of SARSCoV-2 and its variants. (c) 2023 Shenyang Pharmaceutical University. Published by Elsevier B.V. ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
引用
收藏
页数:14
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