Method and apparatus of measuring the specific activity of dehydrogenases in tissue

Claim 1

A method of measuring the specific activity of dehydrogenases by using a specimen prepared through a first procedure of causing dehydrogenases in tissue flake to be measured to be reacted with a substrate for a predetermined time and dyeing the same with tetrazolium salt and a second procedure of dyeing the protein in said flake with naphthol yellows, the improvement comprising: providing a third procedure of washing the enzyme-dyed flake with alcohol for a predetermined time after said first procedure, microphotometering a specimen prepared through said first, second and third procedures, by the use of three predetermined wavelengths in the vicinity of 450 nm, 570 nm and 700 nm to obtain the degree of light absorption, I, at each of said predetermined wavelengths, and applying said values to the formula I.sub.570 /I.sub.450 -I.sub.700 to thereby obtain said specific activity, and measuring the specific activity of the dehydrogenases from data obtained corresponding to the respective wavelengths.

Claim 2

A method of measuring the specific activity of dehydrogenases by using a specimen prepared through a first procedure of causing dehydrogenases in tissue flake to be measured to be reacted with a substrate for a predetermined time and dyeing the same with tetrazolium salt and a second procedure of dyeing the protein in said flake with naphthol yellows, the improvement comprising: providing a third procedure of washing the enzyme-dyed flake with alcohol for a predetermined time after said first procedure, microphotometering a specimen prepared through said first, second and third procedures, by the use of three predetermined wavelengths in the vicinity of 450 nm, 570 nm and 700 nm to obtain the degree of light absorption, I, at each of said predetermined wavelengths, and applying said values to the formula I.sub.570 /I.sub.450 -I.sub.700 to thereby obtain said specific activity, and measuring the specific activity of the dehydrogenases from data obtained corresponding to the respective wavelengths.

Claim 6

An apparatus for measuring the specific activity of dehydrogenases by using a specimen prepared through a first procedure of causing dehydrogenases in tissue flake to be measured to be reacted with a substrate for a predetermined time and dyeing the same with tetrazolium salt, a second procedure of dyeing the protein of said flake with naphthol yellows and a third procedure of washing the enzyme-dyed flake with alcohol for a predetermined time after said first procedure, said apparatus including: (a) a microphotometer capable of microphotometry by three predetermined wavelengths in the vicinity of 450 nm, 570 nm and 700 nm; said microphotometer having: a white light source; an optical system for condensing the light beam from said light source on a predetermined region of said specimen; a light path splitting device for splitting the light beam passed through said specimen into a first, a second and a third light path; first, second and third filter means disposed in said three light paths, respectively; said filter means being capable of passing therethrough only wavelengths in the vicinity of 450 nm, 570 nm and 700 nm; first, second and third photoelectric converter means corresponding to said three filter means, respectively, and for receiving the light beams passed through said three filter means; and an optical system for condensing the light beams passed through said filter means on said photoelectric converter means; (b) processing means having at least a first, a second and a third processing circuit provided corresponding to said three wavelengths, respectively; (c) control means for distributing the metering outputs corresponding to said three wavelengths to said three processing circuits, said control means being a line for connecting said first, second and third photoelectric converter means to the corresponding first, second and third processing circuits; and (d) an operational device for effecting a predetermined operation between the output signals of said three processing circuits.

Claim 7

An apparatus for measuring the specific activity of dehydrogenases by using a specimen prepared through a first procedure of causing dehydrogenases in tissue flake to be measured to be reacted with a substrate for a predetermined time and dyeing the same with tetrazolium salt, a second procedure of dyeing the protein of said flake with naphthol yellows and a third procedure of washing the enzyme-dyed flake with alcohol for a predetermined time after said first procedure, said apparatus including: (a) a microphotometer capable of microphotometry by three predetermined wavelengths in the vicinity of 450 nm, 570 nm and 700 nm; said microphotometer having: a white light source; an optical system for condensing the light beam from said light source on a predetermined region of said specimen; a light path splitting device for splitting the light beam passed through said specimen into a first, a second and a third light path; first, second and third filter means disposed in said three light paths, respectively; said filter means being capable of passing therethrough only wavelengths in the vicinity of 450 nm, 570 nm and 700 nm; first, second and third photoelectric converter means corresponding to said three filter means, respectively, and for receiving the light beams passed through said three filter means; and an optical system for condensing the light beams passed through said filter means on said photoelectric converter means; (b) processing means having at least a first, a second and a third processing circuit provided corresponding to said three wavelengths, respectively; (c) control means for distributing the metering outputs corresponding to said three wavelengths to said three processing circuits, said control means being a line for connecting said first, second and third photoelectric converter means to the corresponding first, second and third processing circuits; and (d) an operational device for effecting a predetermined operation between the output signals of said three processing circuits.

Claim 10

An apparatus for measuring the specific activity of dehydrogenases by using a specimen prepared through a first procedure of causing dehydrogenases in tissue flake to be measured to be reacted with a substrate for a predetermined time and dyeing the same with tetrazolium salt, a second procedure of dyeing the protein of said flake with naphtol yellows and a third procedure of washing the enzyme dyed flake with alcohol for a predetermined time after said first procedure, said apparatus including: (a) a microphotometer capable of microphotometry by three predetermined wavelengths in the vicinity of 450 nm, 570 nm and 700 nm, said microphotometer having: a white light source; an optical system for condensing the light beam from said light source on a predetermined region of said specimen; photoelectric converter means for receiving the light beam passed through said speciman; an optical system for condensing the light beam from said specimen on said converter means; and a dispersing element provided in the light path between said light source and said photoelectric converter means, said dispersing element being capable of selectively emitting light beams in the vicinity of wavelengths 450 nm, 570 nm and 700 nm; (b) processing means having at least a first, a second and a third processing circuit provided corresponding to said three wavelengths, respectively; (c) control means for distributing the metering outputs corresponding to said three wavelengths to said three processing circuits; and (d) an operational device for effecting a predetermined operation between the output signals of said three processing circuits; wherein said control means is operable to apply the output of said photoelectric converter means to the processing circuit corresponding to the wavelength selected by said dispersing element.

Claim 11

An apparatus for measuring the specific activity of dehydrogenases by using a specimen prepared through a first procedure of causing dehydrogenases in tissue flake to be measured to be reacted with a substrate for a predetermined time and dyeing the same with tetrazolium salt, a second procedure of dyeing the protein of said flake with naphtol yellows and a third procedure of washing the enzyme dyed flake with alcohol for a predetermined time after said first procedure, said apparatus including: (a) a microphotometer capable of microphotometry by three predetermined wavelengths in the vicinity of 450 nm, 570 nm and 700 nm, said microphotometer having: a white light source; an optical system for condensing the light beam from said light source on a predetermined region of said specimen; photoelectric converter means for receiving the light beam passed through said speciman; an optical system for condensing the light beam from said specimen on said converter means; and a dispersing element provided in the light path between said light source and said photoelectric converter means, said dispersing element being capable of selectively emitting light beams in the vicinity of wavelengths 450 nm, 570 nm and 700 nm; (b) processing means having at least a first, a second and a third processing circuit provided corresponding to said three wavelengths, respectively; (c) control means for distributing the metering outputs corresponding to said three wavelengths to said three processing circuits; and (d) an operational device for effecting a predetermined operation between the output signals of said three processing circuits; wherein said control means is operable to apply the output of said photoelectric converter means to the processing circuit corresponding to the wavelength selected by said dispersing element.

Claim 12

A method of measuring the specific activity of dehydrogenases by using a specimen prepared through a first procedure of causing dehydrogenases in tissue flake to be measured to be reacted with a substrate for a predetermined time and dyeing the same with tetrazolium salt and a second procedure of dyeing the protein in said flake with naphthol yellows, the improvement comprising: providing a third procedure of washing the enzyme-dyed flake with alcohol for a predetermined time after said first procedure, microphotometering a specimen prepared through said first, second, third procedures, by the use of three predetermined wavelengths in the vicinity of 450 nm, 570 nm, and 700 nm to obtain the degree of light transmittivity T, at each of said predetermined wavelengths, and applying said value of T to the formula ##EQU2## to thereby obtain said specific activity, and measuring the specific activity of the dehydrogenases from data obtained corresponding to the respective wavelengths.

Claim 13

A method of measuring the specific activity of dehydrogenases by using a specimen prepared through a first procedure of causing dehydrogenases in tissue flake to be measured to be reacted with a substrate for a predetermined time and dyeing the same with tetrazolium salt and a second procedure of dyeing the protein in said flake with naphthol yellows, the improvement comprising: providing a third procedure of washing the enzyme-dyed flake with alcohol for a predetermined time after said first procedure, microphotometering a specimen prepared through said first, second, third procedures, by the use of three predetermined wavelengths in the vicinity of 450 nm, 570 nm, and 700 nm to obtain the degree of light transmittivity T, at each of said predetermined wavelengths, and applying said value of T to the formula ##EQU2## to thereby obtain said specific activity, and measuring the specific activity of the dehydrogenases from data obtained corresponding to the respective wavelengths.