Nano-Biointerface studies of mucus-modulating particles containing Remdesivir with respiratory epithelium membrane models in healthy and hyperinflammatory conditions of COVID-19
- Funded by Fundação de Amparo à Pesquisa do Estado de São Paulo [São Paulo Research Foundation] (FAPESP)
- Total publications:0 publications
Grant number: 20/14062-1
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Key facts
Disease
COVID-19Start & end year
20212023Funder
Fundação de Amparo à Pesquisa do Estado de São Paulo [São Paulo Research Foundation] (FAPESP)Principal Investigator
Valtencir ZucolottoResearch Location
BrazilLead Research Institution
Instituto de Física de São Carlos (IFSC). Universidade de São Paulo (USP). São Carlos , SP, BrazilResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Pathogen morphology, shedding & natural history
Special Interest Tags
N/A
Study Type
Non-Clinical
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Not Applicable
Vulnerable Population
Not applicable
Occupations of Interest
Not applicable
Abstract
The most serious cases of COVID-19 are manifested by a state of pulmonary hyperinflammation caused by a cytokine storm, which occurs due to the infection of the lower airways by the SARS-CoV-2 virus. Under these conditions, diffuse alveolar damage leads to severe acute respiratory disease (SARS), with a high mortality rate. Mucus-modulating nanoparticles are potentially useful in the pulmonary administration of drugs and vaccines for the treatment of COVID-19, as they could be designed to overcome the mucus barrier present in the airways and reach the alveolar region, which is covered by the lung surfactant barrier. Thus, the therapeutic and / or preventive success of these carriers depends on interactions occurring at the nano-bio interface of these two barriers present in the pulmonary administration route. The objective of this project is to characterize the nano-biointeractions of mucus-modulating particles containing the model drug remdesivir with real and biomimetic membranes of the respiratory epithelium. The studies will be performed with cells able to producing mucus and lung surfactant. These biointerfaces are relevant to SARS-CoV-2 infection and represent important sites for the release of remdesivir. The characterization of the biophysical properties of biological membranes (extracted from epithelial cells) and biomimetics (produced with synthetic lipids) will be performed using Langmuir films and phospholipid vesicles in the presence of particles in healthy and inflammatory conditions. The project conclusion will allow us to gain mechanistic insights into the main interactions occurring in these nano-biointerfaces that can fundamentally improve the rational design of mucus-modulating particles for pulmonary administration of drugs and vaccines for the treatment of COVID-19 and other serious respiratory syndromes. (AU)