Dear editor,The role of the oral cavity in the genesis, progression, and dissemination of COVID-19 has been revealed by breakthroughs in SARS-CoV-2 research [1]. As a result, in 2020, our research group presented a recommendation for PHTALOX® mouthwash for reducing COVID-19 infection and progression [2]. On this occasion, we revealed the first clinical findings in patients with COVID-19 who utilized PHTALOX®, an antiviral phthalocyanine derivative (APD), in a gargle/rinse mouthwash protocol [3]. We updated the information with new insights on the usage of the APD method since PHTALOX® was indicated against SARS-CoV-2 (Table 1 (Tab. 1)).
Table 1
Summarized results for the use of PHTALOX® against COVID-19
Hence, combined with immunizations, the activity of products containing PHTALOX® may help prevent patients from transmitting SARS-CoV-2 and thus help prevent others from contracting COVID-19. Following this logic, additional findings from our study group underscore the positive impact of APD. In epidemiological research, the usage of products containing APD reduced virus dissemination and COVID-19 symptoms [4]. In a population-based study with a sample that used APD, a reduction (p<0.05) in the incidence of COVID-19 was observed compared to a control population without APD exposure [5]. Thus, while vaccines are the most important tool in combating the COVID-19 pandemic, they are not 100% effective in those vaccinated, and even after the initial dose, antibody production takes several days to mature, followed by reinforcement with additional doses [6], at which point gargle-and-rinse solutions may be an effective option.As previously indicated, we emphasize how important it is for scientists and governments to evaluate the impact of APD policies in hospitals and the general community on SARS-COV-2 VL, hence reducing the virus's transmission and severity of COVID-19.
Notes
Competing interests
All authors submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr. Vilhena reports personal fees from TRIALS Inc. while conducting the study. In addition, Dr. Vilhena has a patent pending. Dr. da Silva Santos reports grants from CNPq process nº. 309525/2018-7. The other authors claim no conflicts of interest.
Acknowledgments
This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Brazil (Finance Code 001).
ORCID-ID of the Authors
Bernardo da Fonseca Orcina:https://orcid.org/0000-0003-3367-483XVerônica Caroline Brito Reia:https://orcid.org/0000-0003-1352-5474Andrea Name Colado Simão:https://orcid.org/0000-0002-2073-6782Audrey Alesandra Stinghen Garcia Lonni:https://orcid.org/0000-0001-6498-2806Thais Maria Freire Fernandes:https://orcid.org/ 0000-0002-4368-8568Marcelo Lupion Poleti:https://orcid.org/0000-0003-1904-5762Fabiano Vieira Vilhena:https://orcid.org/0000-0003-3840-3633Paulo Sérgio da Silva Santos:https://orcid.org/0000-0002-0674-3759
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