Abstract
With severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) showing new characteristics and manifesting new variants, the efficacy of vaccination can be reduced. In the meanwhile, no SARS-CoV-2-specific drug has been introduced in the fight against coronavirus disease 2019 (COVID-19) yet, and currently used drugs have also shown serious side effects in patients under treatment. Thus, it is pivotal to continue researching potential therapeutics to treat COVID-19. Recently, studies have shown that Gallium maltolate disrupts the replication of SARS-CoV-2 and therefore has antiviral activity against this virus. Nevertheless, as Gallium compounds have manifested serious side effects in the human body (e.g., hemoglobin synthesis dysfunction and pulmonary complications), drug delivery methods should be recruited to minimize the possible side effects and to optimize the efficacy of the drug in the fight against COVID-19. Liposomes, as nanocarriers, not only increase the half-life of the conjugated compound but also have shown promising features in the delivery of COVID-19-specific drugs to the target tissue. Herein, we propose that conjugation of Gallium maltolate with liposome nanocarriers can be beneficial to target tissues infected with SARS-CoV-2.
Keywords: SARS-CoV-2, COVID-19, liposomes, galium maltolate, nanoparticles, drug delivery.
Graphical Abstract
[http://dx.doi.org/10.1177/2040206620983780] [PMID: 33353394]
[http://dx.doi.org/10.3390/ijerph7052337] [PMID: 20623028]
[http://dx.doi.org/10.1007/s00259-020-04886-9] [PMID: 32535654]
[http://dx.doi.org/10.1016/S0024-3205(99)00375-6] [PMID: 10503955]
[PMID: 33525252]
[http://dx.doi.org/10.1074/jbc.M400338200] [PMID: 15140896]
[http://dx.doi.org/10.1177/1076029620954911] [PMID: 32936689]
[http://dx.doi.org/10.1111/cts.12923] [PMID: 33135382]
[http://dx.doi.org/10.1023/A:1018955915848] [PMID: 8415397]
[http://dx.doi.org/10.1007/BF01757356] [PMID: 8788232]
[http://dx.doi.org/10.1016/S0022-2275(20)33306-X] [PMID: 9548600]