Your browser doesn't support javascript.
loading
Generation of purified nitric oxide from liquid N2O4 for the treatment of pulmonary hypertension in hypoxemic swine.
Lovich, Mark A; Fine, David H; Denton, Ryan J; Wakim, Matt G; Wei, Abraham E; Maslov, Mikhail Y; Gamero, Lucas G; Vasquez, Gregory B; Johnson, Bryan J; Roscigno, Robert F; Gilbert, Richard J.
Affiliation
  • Lovich MA; Department of Anesthesiology, Pain Medicine, and Critical Care, Steward St. Elizabeth's Medical Center, Boston, MA, United States. Electronic address: Mark.Lovich@steward.org.
  • Fine DH; GeNO LLC, Cocoa, FL, United States.
  • Denton RJ; GeNO LLC, Cocoa, FL, United States.
  • Wakim MG; Department of Anesthesiology, Pain Medicine, and Critical Care, Steward St. Elizabeth's Medical Center, Boston, MA, United States.
  • Wei AE; Department of Anesthesiology, Pain Medicine, and Critical Care, Steward St. Elizabeth's Medical Center, Boston, MA, United States.
  • Maslov MY; Department of Anesthesiology, Pain Medicine, and Critical Care, Steward St. Elizabeth's Medical Center, Boston, MA, United States.
  • Gamero LG; GeNO LLC, Cocoa, FL, United States.
  • Vasquez GB; GeNO LLC, Cocoa, FL, United States.
  • Johnson BJ; GeNO LLC, Cocoa, FL, United States.
  • Roscigno RF; GeNO LLC, Cocoa, FL, United States.
  • Gilbert RJ; Department of Chemistry and Chemical Biology, Northeastern University, Boston, MA, United States.
Nitric Oxide ; 37: 66-72, 2014 Feb 15.
Article in En | MEDLINE | ID: mdl-24513304
ABSTRACT
Inhaled nitric oxide (NO) selectively dilates pulmonary blood vessels, reduces pulmonary vascular resistance (PVR), and enhances ventilation-perfusion matching. However, existing modes of delivery for the treatment of chronic pulmonary hypertension are limited due to the bulk and heft of large tanks of compressed gas. We present a novel system for the generation of inhaled NO that is based on the initial heat-induced evaporation of liquid N2O4 into gas phase NO2 followed by the room temperature reduction to NO by an antioxidant, ascorbic acid cartridge just prior to inhalation. The biologic effects of NO generated from liquid N2O4 were compared with the effects of NO gas, on increased mean pulmonary artery pressure (mPAP) and PVR in a hypoxemic (FiO2 15%) swine model of pulmonary hypertension. We showed that NO concentration varied directly with the fixed cross sectional flow of the outflow aperture when studied at temperatures of 45, 47.5 and 50°C and was independent of the rate of heating. Liquid N2O4-sourced NO at 1, 5, and 20 ppm significantly reduced the elevated mPAP and PVR induced by experimental hypoxemia and was biologically indistinguishable from gas source NO in this model. These experiments show that it is feasible to generate highly purified NO gas from small volumes of liquid N2O4 at concentrations sufficient to lower mPAP and PVR in hypoxemic swine, and suggest that a miniaturized ambulatory system designed to generate biologically active NO from liquid N2O4 is achievable.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hypertension, Pulmonary / Hypoxia / Nitric Oxide / Nitrogen Oxides Limits: Animals Language: En Journal: Nitric Oxide Journal subject: BIOQUIMICA / QUIMICA Year: 2014 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hypertension, Pulmonary / Hypoxia / Nitric Oxide / Nitrogen Oxides Limits: Animals Language: En Journal: Nitric Oxide Journal subject: BIOQUIMICA / QUIMICA Year: 2014 Document type: Article