Targeted, Site-Specific, Delivery Vehicles of Therapeutics for COVID-19 Patients. Brief Review

Author:

Kipshidze Nicholas1,Iversen Patrick2,Porter Thomas R.3,Kipshidze Nodar4,Siddiqui Fakiha5ORCID,Dangas George6,Fareed Jawed57ORCID

Affiliation:

1. NY Cardiovascular Research, New York, NY, USA

2. USAMRID, Fort Detrick, MD, USA

3. University of Nebraska Medical Center, Omaha, NE, USA

4. NYU Langone Health, New York, NY, USA

5. Department of Pathology and Laboratory Medicine, Cardiovascular Research Institute, Loyola University Chicago, Health Sciences Division, Maywood, IL, USA

6. Icahn School of Medicine at Mount Sinai, New York, NY, USA

7. Department of Pharmacology and Neuroscience, Cardiovascular Research Institute, Loyola University Chicago, Health Sciences Division, Maywood, IL, USA

Abstract

Definitive pharmacological therapies for COVID-19 have yet to be identified. Several hundred trials are ongoing globally in the hope of a solution. However, nearly all treatments rely on systemic delivery but COVID-19 damages the lungs preferentially. The use of a targeted delivery approach is reviewed where engineered products are able to reach damaged lung tissue directly, which includes catheter-based and aerosol-based approaches. In this review we have outlined various target directed approaches which include microbubbles, extracellular vesicles including exosomes, adenosine nanoparticles, novel bio-objects, direct aerosol targeted pulmonary delivery and catheter-based drug delivery with reference to their relative effectiveness for the specific lesions. Currently several trials are ongoing to determine the effectiveness of such delivery systems alone and in conjunction with systemic therapies. Such approaches may prove to be very effective in the controlled and localized COVID-19 viral lesions in the lungs and potential sites. Moreover, localized delivery offered a safer delivery mode for such drugs which may have systemic adverse effects.

Publisher

SAGE Publications

Subject

Hematology,General Medicine

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