The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Dec. 21, 2021

Filed:

Apr. 28, 2021
Applicants:

Lawrence Jacobowitz, Boynton Beach, FL (US);

Alan M. Victor, Raleigh, NC (US);

Inventors:

Lawrence Jacobowitz, Boynton Beach, FL (US);

Alan M. Victor, Raleigh, NC (US);

Assignee:

Other;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61B 18/18 (2006.01); A61B 18/00 (2006.01); A61B 17/00 (2006.01);
U.S. Cl.
CPC ...
A61B 18/1815 (2013.01); A61B 2017/00159 (2013.01); A61B 2017/00725 (2013.01); A61B 2018/0016 (2013.01); A61B 2018/0072 (2013.01); A61B 2018/00613 (2013.01); A61B 2018/00642 (2013.01); A61B 2018/00678 (2013.01); A61B 2018/00767 (2013.01); A61B 2018/00779 (2013.01); A61B 2018/1823 (2013.01); A61B 2018/1838 (2013.01);
Abstract

A non-invasive electrodynamic radiative electroporation system and method for safe in vivo delivery of specific radiant energy to physiologically inaccessible sites for selective destruction of biomolecular function of virions, particularly Covid-19 and its variants. The system and method applies a computer or like controller to generate, modulate, direct and deliver applied external electric fields from plural antennas to target tissues in the full respiratory tract, including lung microstructures, cardiovascular tissues and neuron networks. Electric fields exceeding a critical threshold-value interact with the virus lipid bilayer membranes, intra-membrane organelles, mRNA, and biomolecular scaffold assemblies, to destroy virion function through irreversible electroporation and electropermeabilization. Polarized electric fields are generated to provide force vectors in optimal dynamic angular distribution to the virion membrane surface and modulated within time-scales short compared to thermal transport characteristic times to effect the electroporation as an adiabatic process that preempts Joule heating of normal tissues.


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