Droplette: A Platform Technology for At-Home, Effective, and Rapid Pulmonary Delivery to Reduce Ventilator Use & Hospitalization
- Funded by National Institutes of Health (NIH)
- Total publications:0 publications
Grant number: 3R43EB026363-01S1
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Key facts
Disease
COVID-19Start & end year
20202021Known Financial Commitments (USD)
$248,206Funder
National Institutes of Health (NIH)Principal Investigator
RATHI SRINIVASResearch Location
United States of AmericaLead Research Institution
NOVOPYXIS INCResearch Priority Alignment
N/A
Research Category
Clinical characterisation and management
Research Subcategory
Supportive care, processes of care and management
Special Interest Tags
N/A
Study Type
Non-Clinical
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Unspecified
Vulnerable Population
Unspecified
Occupations of Interest
Unspecified
Abstract
Significance: COVID-19 causes significant lung damage in a subset of patients leading to a cascade ofinflammatory cytokine activation (cytokine storm) that develops into acute respiratory distress syndrome (ARDS).There are several classes of FDA-approved therapeutics that have significant potential in mitigating thepulmonary inflammation when effectively delivered into the lower airways. However, there is a significanttechnology gap in the ability to safely and rapidly dose and administer these drugs to the lungs.Nebulizers are not used for Covid19 patients due to sterility/transmission risks since their use enables viralparticles to linger in the air for hours; they are also not easy to use or sterilize. Inhalers produce mists that donot reach the lower airways. We have developed a patented platform trans-tissue delivery system (Droplette)comprising the unique combination of a piezoelectric transducer and diaphragm pump to physically deliver largetherapeutics into cells and deep through tissue. We hypothesize that this device will allow deep and more rapiddelivery into the lower airways into the lungs of COVID-19 patients relative to standard nebulizers withoutrequiring active inhalation based on the measured droplet sizes (<3 µm) in the mist generated by the device (i.ethis can function as a rapid, low cost, more effective nebulizer for at-home use). Early intervention and at-home administration will reduce the hospitalization burden and need for ventilation- leading to decreasedhospitalization rates, fewer patients who need to be placed on a ventilator and lower mortality. Additionally, thedevice accepts pre-filled sterile one-time use cartridges containing therapeutic formulations and is Bluetooth-enabled with a paired app, allowing a provider to monitor patients' usage via telemedicine. PreliminaryData: Droplette has been tested extensively across ex vivo, in vivo, and pilot human studies. We have previouslydemonstrated that Droplette can deliver naked large (>1 MDa) mRNA to the basal layer of mucosal tissue andhypothesize that the same mechanism can enable pulmonary delivery. The device generates a fine, low-pressure mist in a unique transitional flow regime and produces consistent spray pattern, plume geometry,droplet size distribution, and particle size. Droplette generates 100% fine mist (<4.7 µm) that dispenses~1mL/min with a flow velocity of 1-5 m/s. Specific Aims: We will demonstrate that Droplette can delivertherapeutics into the lungs & lower airways. In Specific Aim 1 we will Assess efficacy and delivery of Droplettepaired with Hypertonic Saline (7%) (HS-7%) in treating ARDS/Cytokine storm using cascade impaction studiesand cell/animal studies using models that will mimic a COVID-19 like cytokine storm. In Specific Aim 2, we willdo the same set of studies using two classes of therapeutics currently in trials for COVID-19: epinephrine & anti-IL-6 antibodies. Collectively, the results from these studies will demonstrate efficacy of our device for pulmonarydelivery in COVID-19 patients to treat cytokine storms & resulting lung damage.