Medical therapeutic apparatus, method of using medical therapeutic apparatus, and method of applying reactive gas
First Claim
1. A medical therapeutic apparatus which generates plasma and blows out a reactive gas generated by the generated plasma toward a target object from an outlet,wherein a temperature of the reactive gas at a target surface positioned at a distance of 1 mm or more and 10 mm or less from the outlet is 40°
- C. or less, and at least one of the following requirements is satisfied;
(1) a hydroxyl radical concentration is 0.1 to 300 μ
mol/L, and (2) a singlet oxygen concentration is 0.1 to 300 μ
mol/L,wherein the hydroxy radical concentration is measured by a method comprising applying the reactive gas to 0.4 mL of a 0.2 mol/L solution of DMPO (5,5-dimethyl-1-pyrroline-N-oxide) for 30 seconds with a distance from the outlet to a liquid surface of the solution being 5.0 mm, and measuring a hydroxyl radical concentration of the resulting solution by electron spin resonance (ESR) method, andthe singlet oxygen concentration is measured by a method comprising applying the reactive gas to 0.4 mL of a 0.1 mol/L solution of TPC (2,2,5,5-tetramethyl-3-pyrroline-3-carboxamide) for 30 seconds with a distance from the outlet to a liquid surface of the solution being 5.0 mm, and measuring a singlet oxygen concentration of the resulting solution by electron spin resonance (ESR) method.
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Abstract
The present invention discloses a medical therapeutic apparatus (100) which generates plasma and blows out an reactive gas generated by the generated plasma toward a target object from an outlet, wherein a temperature of the reactive gas at a target surface positioned at a distance of 1 mm or more and 10 mm or less from the outlet is 40° C. or less, and a radical concentration is 0.1 to 300 μmol/L as determined by a hydroxy radical concentration measuring method comprising applying the reactive gas to 0.4 mL of a 0.2 mol/L solution of DMPO (5,5-dimethyl-1-pyrroline-N-oxide) for 30 seconds with a distance from the outlet to a liquid surface of the solution being 5.0 mm, and measuring a hydroxyl radical concentration of the resulting solution by electron spin resonance (ESR) method.
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Citations
8 Claims
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1. A medical therapeutic apparatus which generates plasma and blows out a reactive gas generated by the generated plasma toward a target object from an outlet,
wherein a temperature of the reactive gas at a target surface positioned at a distance of 1 mm or more and 10 mm or less from the outlet is 40° - C. or less, and at least one of the following requirements is satisfied;
(1) a hydroxyl radical concentration is 0.1 to 300 μ
mol/L, and (2) a singlet oxygen concentration is 0.1 to 300 μ
mol/L,wherein the hydroxy radical concentration is measured by a method comprising applying the reactive gas to 0.4 mL of a 0.2 mol/L solution of DMPO (5,5-dimethyl-1-pyrroline-N-oxide) for 30 seconds with a distance from the outlet to a liquid surface of the solution being 5.0 mm, and measuring a hydroxyl radical concentration of the resulting solution by electron spin resonance (ESR) method, and the singlet oxygen concentration is measured by a method comprising applying the reactive gas to 0.4 mL of a 0.1 mol/L solution of TPC (2,2,5,5-tetramethyl-3-pyrroline-3-carboxamide) for 30 seconds with a distance from the outlet to a liquid surface of the solution being 5.0 mm, and measuring a singlet oxygen concentration of the resulting solution by electron spin resonance (ESR) method. - View Dependent Claims (2, 3, 4)
- C. or less, and at least one of the following requirements is satisfied;
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5. A method of applying an reactive gas to a target object, excluding medical practice on human body, comprising applying a voltage to a plasma generating gas to generate plasma, and applying a reactive gas generated by the plasma to a target object selected from a cell, a living tissue and a whole body of an organism, to thereby promote cleaning, activation or healing of abnormalities of the target object,
wherein a temperature of the reactive gas at a target surface positioned at a distance of 1 mm or more and 10 mm or less from the outlet is 40° - C. or less, and at least one of the following requirements is satisfied;
(1) a hydroxyl radical concentration is 0.1 to 300 μ
mol/L, and
12) a singlet oxygen concentration is 0.1 to 300 μ
mol/L,wherein the hydroxy radical concentration is measured by a method comprising applying the reactive gas to 0.4 mL of a 0.2 mol/L solution of DMPO (5,5-dimethyl-1-pyrroline-N-oxide) for 30 seconds with a distance from the outlet to a liquid surface of the solution being 5.0 mm, and measuring a hydroxyl radical concentration of the resulting solution by electron spin resonance (ESR) method, and the singlet oxygen concentration is measured by a method comprising applying the reactive gas to 0.4 mL of a 0.1 mol/L solution of TPC (2,2,5,5-tetramethyl-3-pyrroline-3-carboxamide) for 30 seconds with a distance from the outlet to a liquid surface of the solution being 5.0 mm, and measuring a singlet oxygen concentration of the resulting solution by electron spin resonance (ESR) method. - View Dependent Claims (6, 7, 8)
- C. or less, and at least one of the following requirements is satisfied;
Specification