JPH0160784B2 - - Google Patents

Description

DETAILED DESCRIPTION OF THE INVENTION The present invention relates to autoradiographic measurements.

After administering a radioactively labeled substance to an organism, the organism or a part of its tissue is used as a sample, and this sample is overlapped with a radiation film such as a high-sensitivity X-ray film for a certain period of time. The film may be exposed to light (or
Autoradiography (also called radioautography), which involves exposing a sample to light and obtaining positional information of a radiolabeled substance in the sample from the photosensitive site, has been known for some time. . This autoradiography is used, for example, to study in detail the metabolism, absorption, and excretion routes and conditions of administered substances in living organisms. Such autoradiography is described, for example, in the following literature.

Biochemistry Experiment Course 6 Tracer Experiment Method (1)
pp. 271-289, "8. Autoradiography" Toru Sueyoshi, Akiyo Shigematsu (1977, published by Tokyo Kagaku Dojin Co., Ltd.) Autoradiography is also used to analyze the tissues of living organisms that have been given a radioactive label. It is also used to obtain positional information of radiolabeled substances in media containing substances derived from living organisms.

For example, a radioactive label is added to a biologically derived polymeric substance such as a protein or a nucleic acid, and the radiolabeled polymeric substance, its derivative, or its decomposition product is subjected to a separation operation such as gel electrophoresis to form a gel-like support. By overlapping the gel-like support and a highly sensitive X-ray film for a certain period of time, the film is exposed to light, and based on the positional information of the radiolabeled substance in the gel obtained from the exposed site. and separation of the polymeric substance,
Methods for identification and evaluation of the molecular weight and characteristics of polymeric substances have also been developed and are in actual use.

Particularly in recent years, autoradiography has been effectively used to determine the base sequence of nucleic acids such as DNA, and has therefore become an extremely useful tool for determining the structure of polymeric substances derived from living organisms. There is.

The method of determining the base sequence of DNA using this autoradiography is as follows.
Maxam-Gilbert method,
and Sanger Coulson
Coulson) law is known. These methods are
DNA has a double helix structure, and the bond between the two chain molecules forming the double helix is
This is due to hydrogen bonds between many bases that are the constituent units of the molecule, and that the many constituent base units are the four atoms of adenine (A), guanine (G), cytosine (C), and thymine (T). Consisting only of types of bases,
Furthermore, by skillfully utilizing the characteristic structure of DNA in which hydrogen bonds between each constituent base unit are realized only in two types of combinations, G-C and A-T, the base sequence can be determined. This is the way to do it.

For example, the Maxam-Gilbert method is carried out by the operations described below.

By bonding a group containing a radioactive isotope of phosphorus (P) to one end of a chain molecule of DNA or a DNA degradation product whose base sequence is to be determined, the target substance can be labeled as a radiolabeled substance. Then, chemical means are used to specifically cleave the bonds between each base of the chain molecule. Next, the DNA obtained by this operation or a mixture of many cleaved and degraded DNA products is separated by gel electrophoresis, and a radiochromatogram ( However, it is possible to obtain (which cannot be seen visually). If this radio chromatogram and a high-sensitivity X-ray film are superimposed for a long time at low temperature,
The portion of the X-ray film facing the position where the cut and decomposed product containing the radioactive isotope in its molecules is exposed to light to form a latent image. By developing the X-ray film on which the latent image has been formed in this manner, a chromatogram including a large number of bands corresponding to the radiochromatogram appears as a visible image on the X-ray film. Then, from this visualized chromatogram and the specific cutting means, it is possible to sequentially determine the bases that are in a certain positional relationship from the end of the chain molecule to which the radioactive isotope is bound, and in this way, the target It is possible to determine the sequence of all the bases of a substance.

The Maxam-Gilbert method summarized above is described in detail in the following document.

METHODS IN ENZYMOLOGY, VOL.65,
PART I (ACADEMIC PRESS, NEW YORK
LONDON TRONTO SYDNEY SAN
FRANCISICO, 1980) The Sanger-Coulson method also focuses on the characteristic structure of DNA, and uses DNA synthase, gel electrophoresis, and autoradiography to analyze DNA.
A brief description of the features and operations of this Sanger-Coulson method and the Maxam-Gilbert method can be found in the following documents.

“Reading genetic information in its original language: Surprising DNA”
``Sequence analysis method'' by Kinichiro Miura, Gendai Kagaku, 1977
September issue, pages 46-54 (Published by Tokyo Kagaku Dojin Co., Ltd.) As mentioned above, autoradiography can be used to collect samples such as tissues of living organisms and media containing biological substances and tissues. It is a very useful means for detecting one-dimensional or two-dimensional positional information of radioactively labeled substances contained in It is possible to efficiently study the metabolism, absorption, and excretion routes and conditions of biomolecules, and to determine the structure of biopolymers.

However, there are several problems when actually utilizing such useful autoradiography.

The first is an autoradiogram, or visualization of the location of radioactive substances in a sample containing the radiolabeled substance, such as an organism or part of the tissue of an organism to which a radiolabeled substance has been administered. In order to do this, the film is exposed to light by overlapping the sample with a radiation film such as a high-sensitivity X-ray film for a certain period of time.
The operation is complicated and requires a long time. That is, in conventional autoradiography, the above exposure operation is performed at low temperatures (for example, 0
℃, and -70 to -90 for exposure of gel chromatograms in nucleic acid base sequencing, etc.
°C) and over a long period of time (eg, several days). This is because samples to be measured by autoradiography generally do not have high radioactivity, so exposure must be long in order to obtain sufficient exposure.
For example, if a sample and a radiation film are kept on top of each other for a long time at a relatively high temperature such as room temperature, the silver salt, which is a photosensitive component of the radiation film, will be chemically fogged by various substances in the sample. This is because it is difficult to obtain highly accurate photosensitive images, and therefore, exposure operations must be performed at low temperatures in order to reduce such chemical fog. In order to alleviate such harsh exposure conditions, it may be possible to further increase the sensitivity of the radiation film, but in conventional autoradiography, the radiation film used is already highly sensitive. Considering the sharpness of the images obtained, it is difficult to dramatically increase the sensitivity of radiation films.

In addition, the silver salt of the photosensitive component of radiation film has the disadvantage that it is easily affected not only by chemical stimuli but also by physical stimuli, which also makes autoradiography difficult to operate and reduces its accuracy. becomes. That is, in autoradiography, it is generally necessary to perform the exposure operation with the radiation film in contact with the sample, so operations such as moving and installing the radiation film are often performed with the radiation film in a bare state. Therefore,
During such work, the chances of the radiation film coming into contact with the operator's hands or equipment increase, and the radiation film tends to cause physical fog due to the physical pressure caused by such contact. This point also causes a decrease in the accuracy of autoradiography. In order to avoid such physical fogging of the radiographic film, a high degree of skill and care is required in handling the film, which results in further complicated autoradiography operations.

Furthermore, since conventional autoradiography involves long exposure operations as described above, the natural radioactivity contained in the sample in addition to the radiolabeled substance is also involved in the exposure of the radiographic film, and the resulting radioactivity is There is a problem in that the accuracy of the positional information of the labeling substance is reduced. In order to eliminate such interference due to natural radioactivity, attempts have been made, for example, to conduct parallel experiments using control samples and to optimize the exposure time. The disadvantage is that the entire operation becomes complicated due to the necessity of preliminary experiments to determine the exposure time.

As a result of intensive research aimed at solving the above-mentioned problems associated with conventional autoradiography, the inventors of the present invention discovered that, instead of a radiation film as a photosensitive material, a stimulable phosphor was used as a binder. The present inventors have discovered that the above-mentioned problems can be solved or the drawbacks reduced by using a stimulable phosphor sheet having a phosphor layer dispersed therein, and have thus arrived at the present invention.

In other words, a stimulable fluorescent material having a phosphor layer made of a stimulable phosphor dispersed in a binder is used as a photosensitive material to obtain positional information of a radiolabeled substance contained in a sample in autoradiography. When using a body sheet, not only can the exposure time be significantly shortened, but also the accuracy of the positional information of the radiolabeled substance in the sample obtained can be improved even at or near ambient temperature. It has been found that exposure can be performed without any deterioration. This point significantly simplifies the exposure operation in autoradiography, which has conventionally been carried out under cooling. Furthermore, by realizing a significant reduction in exposure time, the entire autoradiography operation can be performed efficiently in a short time, which is also very advantageous in practical terms.

Furthermore, by using the above-mentioned stimulable phosphor sheet as a photosensitive material for autoradiography, chemical fog and physical fog, which have been a major problem when using conventional radiation films, are virtually eliminated. It has a very advantageous effect on improving the accuracy and workability of autoradiography.

In addition, when a stimulable phosphor sheet is used as a photosensitive material, there is no need to image it in order to obtain positional information of the radiolabeled substance transferred from the sample to the stimulable phosphor sheet; By scanning the phosphor sheet with electromagnetic waves such as a laser, it is possible to read out the above positional information and convert the positional information into any form such as an image, symbol, numerical value, or a combination thereof. . Furthermore, by further processing the above position information using electrical means, it is also possible to obtain the necessary information in various desired forms.

Furthermore, the effects of natural radioactivity contained in the sample that interfere with accuracy can be easily reduced or eliminated by electrically processing the position information stored in the stimulable phosphor sheet. It is also possible to delete it.

Therefore, the present invention provides one-dimensional or two-dimensional analysis of a radiolabeled substance contained in a sample selected from the group consisting of biological tissue and a medium containing biological tissue and/or biological material. In an autoradiographic measurement method that detects dimensional position information, the sample and a stimulable phosphor sheet having a phosphor layer made of a stimulable phosphor dispersed in a binder are held together for a certain period of time. By overlapping, the phosphor sheet absorbs at least a portion of the radiation energy emitted from the radiolabeled substance in the sample, and then the stimulable phosphor sheet is scanned with electromagnetic waves to absorb the stimulable phosphor sheet. The present invention provides a method comprising emitting radiation energy stored in a body sheet as photostimulated light and detecting the stimulated light to obtain positional information of a radiolabeled substance in a sample.

The present invention also includes a method of obtaining the positional information of the radiolabeled substance in the sample obtained as described above as an image, and a method of obtaining it as information expressed in symbols and/or numerical values. This is what we provide.

The stimulable phosphor sheet used in the present invention is also called a radiation image conversion panel, and an example thereof is described in, for example, Japanese Patent Laid-Open No. 12145/1983, and its general configuration is already known. It is.

In other words, the stimulable phosphor sheet absorbs the radiation energy transmitted through the subject or the radiation energy emitted from the subject into the stimulable phosphor of the panel, and then exposes the stimulable phosphor to visible light and infrared rays. By exciting the stimulable phosphor in a time-series manner using electromagnetic waves (excitation light), the radiation energy stored in the stimulable phosphor is released as fluorescence, and this fluorescence is read photoelectrically to obtain an electrical signal. This electrical signal is reproduced as a visible image on a recording material such as a photosensitive film or a display device such as a CRT, or is expressed as numerical or symbolic position information.

The stimulable phosphor sheet preferably used in the autoradiography of the present invention will be briefly described below.

The basic structure of the above-mentioned stimulable phosphor sheet is a support and a phosphor layer provided on one side of the support. However, a transparent protective film is generally provided on the surface of this phosphor layer opposite to the support (the surface not facing the support).
Protects the phosphor layer from chemical deterioration or physical impact.

The phosphor layer consists of a stimulable phosphor and a binder that contains and supports the stimulable phosphor in a dispersed state. After absorbing radiation, the stimulable phosphor absorbs electromagnetic waves such as visible light and infrared rays. It has the property of emitting light (stimulated luminescence) when irradiated with (excitation light). Therefore, for example, radiation emitted from an object such as a sample containing a radiolabeled substance is absorbed by the phosphor layer of the stimulable phosphor sheet in proportion to the amount of radiation, and the radiation is absorbed by the phosphor layer of the stimulable phosphor sheet. A radiation image of the subject is formed as an image of accumulated radiation energy. This accumulated image can be emitted as stimulated luminescence (fluorescence) by exciting it with electromagnetic waves (excitation light) such as visible light and infrared rays, and this stimulated luminescence can be read photoelectrically and converted into an electrical signal. This allows the accumulation of radiation energy to be converted into a visible image or a radioactive (label) image.
It becomes possible to convert into numerical values, symbols, etc. that indicate the position information of substances.

The support for the stimulable phosphor sheet used in the present invention can be arbitrarily selected from various materials used as supports for intensifying screens in conventional radiography. Examples of such materials include films of plastic materials such as cellulose acetate, polyester, polyethylene terephthalate, polyamide, polyimide, triacetate, polycarbonate, metal sheets such as aluminum foil, aluminum alloy foil, ordinary paper,
Examples include baryta paper, resin-coated paper, pigment paper containing pigments such as titanium dioxide, and paper sized with polyvinyl alcohol. However, when considering the characteristics and handling of the stimulable phosphor sheet as an information recording material, a particularly preferred material for the support in the present invention is plastic film. This plastic film may be kneaded with a light-absorbing substance such as carbon black, or may be kneaded with a light-reflecting substance such as titanium dioxide. The former is a support suitable for a high sharpness type stimulable phosphor sheet, and the latter is a support suitable for a high sensitivity type stimulable phosphor sheet.

In known stimulable phosphor sheets, in order to strengthen the bond between the support and the phosphor layer, or to improve the sensitivity or image quality of the stimulable phosphor sheet, the surface of the support on the side where the phosphor layer is provided is A polymeric substance such as gelatin is coated on the surface to form an adhesion-imparting layer, or a light-reflecting layer made of a light-reflecting substance such as titanium dioxide or a light-absorbing layer made of a light-absorbing substance such as carbon black is provided. is also being carried out. The support used in the present invention can also be provided with these various layers, and their configurations can be arbitrarily selected depending on the desired purpose, use, etc. of the stimulable phosphor sheet.

Furthermore, as disclosed in Japanese Patent Application No. 57-82431 filed by the present applicant, in order to improve the sharpness of the obtained image, the surface of the support on the phosphor layer side (the phosphor layer side of the support) (If the surface of the layer is provided with an adhesion-imparting layer, a light-reflecting layer, a light-absorbing layer, or a metal foil, this means the surface of that layer)
The surface may have unevenness formed thereon.

A phosphor layer is formed on the support as described above. The phosphor layer is basically a layer made of a binder containing and supporting particulate stimulable phosphor in a dispersed state.

As mentioned above, a stimulable phosphor is a phosphor that exhibits stimulated luminescence when irradiated with radiation and then with excitation light, but from a practical point of view, it has a wavelength of 400~
300-500nm with excitation light in the 800nm range
It is desirable that the phosphor exhibits stimulated luminescence in the wavelength range of . Examples of stimulable phosphors used in the stimulable phosphor sheet used in the present invention include those described in U.S. Pat. No. 3,859,527.
Phosphors expressed by composition formulas such as SrS:Ce, Sm, SrS:Eu, Sm, ThO ₂ :Er, and La ₂ O ₂ S:Eu, Sm, as described in JP-A-55-12142.
ZnS: Cu, Pb, BaO・xAl ₂ O ₃ : Eu [However, 0.8
≦x≦10], and M ²⁺ O・xSiO ₂ :A [however,
M ²⁺ is Mg, Ca, Sr, Zn, Cd, or Ba;
A is Ce, Tb, Eu, Tm, Pb, Tl, Bi, or
A phosphor represented by a composition formula such as Mn, and x is 0.5≦x≦2.5] (Ba _1-xy , Mg _x , Ca _y ) is described in JP-A-12143-1983. FX:aEu ²⁺ [However, X
is at least one of Cl and Br,
A phosphor represented by the composition formula: x and y are 0<x+y≦0.6 and xy≠0, and a is 10 ^-6 ≦a≦5×10 ^-2 JP-A-12144-1988 stated in the issue
LnOX: xA [However, Ln is La, Y, Gd, and
At least one of Lu, X is at least one of Cl and Br, A is at least one of Ce and Tb, and x is 0<x<0.1
A phosphor represented by the composition formula of (Ba _1-x , _M〓
At least one of Ca, Sr, Zn, and Cd, X is at least one of Cl, Br, and I, A is Eu, Tb, Ce, Tm, Dy, Pr, Ho,
A phosphor represented by a composition formula of at least one of Nd, Yb, and Er, and x is 0≦x≦0.6, and y is 0≦y≦0.2. M listed in the official bulletin
FX・xA:yLn [However, M〓 is Ba, Ca, Sr,
At least one of Mg, Zn, and Cd, A
are BeO, MgO, CaO, SrO, BaO, ZnO,
Al ₂ O ₃ , Y ₂ O ₃ , La ₂ O ₃ , In ₂ O ₃ , SiO ₂ , TiO ₂ ,
ZrO ₂ , GeO ₂ , SnO ₂ , Nb ₂ O ₅ , Ta ₂ O ₅ , and
At least one of ThO ₂ , Ln is Eu, Tb,
Ce, Tm, Dy, Pr, Ho, Nd, Yb, Er, Sm,
and at least one of Gd, X is Cl,
At least one of Br, and I,
x and y are respectively 5×10 ^-5 ≦x≦0.5 and 0<y≦0.2] A phosphor is described in JP-A-56-116777 (Ba _{1- x} , M〓 _x )F ₂・aBaX ₂ :yEu, zA [However,
M〓 is beryllium, magnesium, calcium,
at least one of strontium, zinc, and cadmium; X is at least one of chlorine, bromine, and iodine; A is at least one of zirconium and scandium;
a, x, y, and z are each 0.5≦a≦1.25,
0≦x≦1, 10 ^-6 ≦y≦2×10 ^-1 , and 0<z
≦10 ^-2 ], described in Japanese Patent Application Laid-Open No. 57-23673 (Ba _1-x , M〓x)F ₂・aBaX ₂ :yEu, zB [However, ,
M〓 is beryllium, magnesium, calcium,
at least one of strontium, zinc, and cadmium;
10 ^-6 ≦y≦2×10 ^-1 and 0<z≦5×10 ^-1 ] A phosphor is described in JP-A-57-23675 (Ba _{1 -x} , M〓 _x )F ₂・aBaX ₂ :yEu, zA [However,
M〓 is beryllium, magnesium, calcium,
at least one of strontium, zinc, and cadmium; X is at least one of chlorine, bromine, and iodine; A is at least one of arsenic and silicon; a, x, y, and z are each 0.5 ≦a≦1.25, 0≦x≦1, 10 ^-6
≦y≦2×10 ^-1 and 0<z≦5×10 ^-1 phosphor, which is M described in Japanese Patent Application No. 167498/1988 filed by the present applicant. 〓OX:xCe〓However, M〓 is Pr,
Nd, Pm, Sm, Eu, Tb, Dy, Ho, Er, Tm,
is at least one trivalent metal selected from the group consisting of Yb and Bi, X is one or both of Cl and Br, and x satisfies 0<x<0.1. The represented phosphor is Ba _1-x M _x/2 L _x/2 FX:yEu ²⁺ [However,
M represents at least one alkali metal selected from the group consisting of Li, Na, K, Rb, and Cs; L represents Sc, Y, La, Ce, Pr, Nd, Pm,
Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu,
represents at least one trivalent metal selected from the group consisting of Al, Ga, In, and Tl; X is Cl,
represents at least one halogen selected from the group consisting of Br, and I; and x is 10 ^-2 ≦
A phosphor ^represented by the compositional formula: ,X is
is at least one halogen selected from the group consisting of Cl, Br, and I; A is a fired product of a tetrafluoroboric acid compound; and x is
10 ^-6 ≦x≦0.1, y is 0<y≦0.1], Patent Application No. 158048/1983 (filed on September 13, 1982) by the present applicant BaFX listed in
xA: yEu ²⁺ [wherein, or a fired product of at least one compound selected from the group of hexafluoro compounds consisting of salts of divalent metals; and x is 10 ^-6 ≦x≦
0.1, y is 0<y≦0.1] A phosphor is described in JP-A-59-56479.
BaFX・xNaX′: aEu ²⁺ [However, X and X′ are
Each is at least one of Cl, Br, and I, and x and a are each 0<x≦2,
and 0<a≦0.2], M〓 described in JP-A No. 59-56480
FX・xNaX′: yEu ²⁺ : zA [However, M〓 is Ba,
at least one alkaline earth metal selected from the group consisting of Sr, and Ca;
X′ is at least one kind of halogen selected from the group consisting of Cl, Br, and I;
is at least one transition metal selected from V, Cr, Mn, Fe, Co, and Ni; and
A phosphor represented by the composition formula where x is 0<x≦2, y is 0<y≦0.2, and z is 0<z≦10 ^-2 , and is described in JP-A-59-75200. There M〓
FX・aM〓X′・bM′〓X″ ₂・cM〓X ₃・xA:
yEu ²⁺ [However, M〓 is at least one kind of alkaline earth metal selected from the group consisting of Ba, Sr, and Ca; M〓 is Li, Na, K, Rb, and Cs
is at least one alkali metal selected from the group consisting of; M′〓 is at least one divalent metal selected from the group consisting of Be and Mg;
M〓 is at least one kind of trivalent metal selected from the group consisting of Al, Ga, In, and Tl; A is a metal oxide; X is at least one kind selected from the group consisting of Cl, Br, and I. X′, X″, and X are at least one kind of halogen selected from the group consisting of F, Cl, Br, and I; and a is 0≦a≦2, and b is 0
≦b≦10 ^-2 , c is 0≦c≦10 ^-2 , and a+b+c
≧10 ^-6 ; x is 0<x≦0.5, y is 0<y≦
0.2], etc. can be mentioned.

However, the stimulable phosphor used in the present invention is not limited to the above-mentioned phosphors, but any phosphor that exhibits stimulated luminescence when irradiated with radiation and then irradiated with excitation light. It may be.

Examples of binders for the phosphor layer include proteins such as gelatin, polysaccharides such as dextran, or natural polymeric substances such as gum arabic; and polyvinyl butyral, polyvinyl acetate, nitrocellulose, ethylcellulose, Examples of binders include synthetic polymeric substances such as vinylidene chloride/vinyl chloride copolymer, polymethyl methacrylate, vinyl chloride/vinyl acetate copolymer, polyurethane, cellulose acetate butyrate, polyvinyl alcohol, linear polyester, etc. . Particularly preferred among such binders are nitrocellulose, linear polyesters, and mixtures of nitrocellulose and linear polyesters.

The phosphor layer can be formed on the support, for example, by the following method.

First, add the above-mentioned stimulable phosphor particles and a binder to a suitable solvent (e.g., lower alcohol, chlorine atom-containing hydrocarbon, ketone, ester, ether), mix thoroughly, and add the binder solution. A coating solution in which phosphor particles are uniformly dispersed is prepared.

The mixing ratio of the binder and stimulable phosphor particles in the coating solution varies depending on the characteristics of the desired stimulable phosphor sheet, the type of phosphor particles, etc., but in general, the mixing ratio of the binder and stimulable phosphor particles is The mixing ratio of is 1:1
It is selected from the range of 1:100 to 1:100 (weight ratio), and particularly preferably selected from the range of 1:8 to 1:40 (weight ratio).

Note that the coating liquid contains a dispersant for improving the dispersibility of the phosphor particles in the coating liquid, and
Various additives such as a plasticizer may be mixed in order to improve the bonding force between the binder and the phosphor particles in the phosphor layer after formation. Examples of dispersants used for such purposes include phthalic acid, stearic acid, caproic acid, lipophilic surfactants, and the like. Examples of plasticizers include phosphoric acid esters such as triphenyl phosphate, tricresyl phosphate, and diphenyl phosphate; phthalic acid esters such as diethyl phthalate and dimethoxyethyl phthalate; and ethyl phthalyl ethyl glycolate and butyl phthalyl butyl glycolate. Glycolic acid esters; and polyesters of polyethylene glycol and aliphatic dibasic acids, such as polyesters of triethylene glycol and adipic acid and polyesters of diethylene glycol and succinic acid.

The coating solution containing the phosphor particles and binder prepared as described above is then uniformly applied to the surface of the support to form a coating film of the coating solution. This coating operation can be carried out using conventional coating means such as a doctor blade, roll coater, knife coater, etc.

The formed coating film is then dried by gradually heating to complete the formation of the phosphor layer on the support. The thickness of the phosphor layer varies depending on the characteristics of the desired stimulable phosphor sheet, the type of phosphor particles, the mixing ratio of the binder and the phosphor particles, etc.
Usually it is 20 μm to 1 mm. However, the thickness of this layer is preferably 50 to 500 μm.

Note that the phosphor layer does not necessarily need to be formed by directly applying a coating liquid onto the support as described above; for example, it is possible to form the phosphor layer by separately applying the coating liquid onto a sheet such as a glass plate, metal plate, plastic sheet, etc. After the phosphor layer is formed by drying, it may be pressed onto the support, or the support and the phosphor layer may be joined by a method using an adhesive.

Preferably, a protective film is provided on the phosphor layer as described above. This protective film is made of, for example, transparent cellulose derivatives such as cellulose acetate and nitrocellulose; polymethyl methacrylate, polyvinyl butyral, polyvinyl formal, polycarbonate, polyvinyl acetate/vinyl acetate copolymer, polyethylene terephthalate, polyethylene, polyvinylidene chloride, polyamide, etc. It is made of a transparent synthetic polymer material. The thickness of the protective film is usually 0.1 to 100 μm, preferably 0.3 to 50 μm.

In autoradiography, the present invention provides:
A stimulable phosphor sheet having the structure described above is used in place of a conventional photosensitive material made of a radiation film, and the exposure operation is performed by exposing a sample containing a radiolabeled substance to a stimulable phosphor sheet. By overlapping these for a certain period of time and performing an exposure operation, at least a portion of the radiation emitted from the radiolabeled substance in the sample is absorbed by the phosphor sheet.

The radiolabeled substance used in the autoradiography of the present invention can be obtained by allowing a sample to be measured to retain a radioactive element using an appropriate method.

The radioactive element used in the present invention is radiation (α
Any nuclide may be used as long as it emits rays, β rays, γ rays, neutron rays, X rays, etc., but typical examples include ³² P, ¹⁴ C, ³⁵ S,
^3H , ^125I , etc.

As described above, the sample to be measured in the autoradiographic measurement method of the present invention is selected from the group consisting of biological tissue and a medium containing biological tissue and/or biological material. The purpose is to obtain positional information of the radiolabeled substances contained in the samples through the phosphor sheet as described above.

The present invention is particularly useful when the sample to be measured is a tissue of an organism and/or a medium containing an organism-derived substance.

Furthermore, the present invention provides a support on which a radiolabeled substance is separated and developed, and the radiolabeled substance is
This is particularly useful in the case of biopolymer substances, derivatives thereof, or decomposition products thereof to which a radioactive label is attached. Here, examples of biopolymer substances include:
Examples include polymeric substances such as proteins, nucleic acids, derivatives thereof, and decomposition products thereof. The present invention can be effectively used, for example, to analyze the entire or partial molecular structures of these biopolymer substances or their basic unit configurations.

In addition, methods for separating and developing radiolabeled substances using supports include, for example, gel-like supports (any shape such as layered or columnar), polymer moldings such as acetate membranes, or various types such as filter paper. Electrophoresis using a support, and thin layer chromatography using a support such as silica gel,
Although these are listed as typical methods, the separation and development method is not limited to these methods.

Furthermore, the support on which the radiolabeled substance has been separated and developed is superimposed on the stimulable phosphor sheet, either as it is or after undergoing an arbitrary process such as drying or fixation of the separated and developed material, thereby exposing the support to the stimulable phosphor sheet. The operation is performed.

In the so-called exposure operation described above, the overlapping state of the sample and stimulable phosphor sheet is usually achieved by bringing the sample and stimulable phosphor sheet into close contact with each other, but it is not necessarily necessary to bring them into close contact with each other. It is sufficient if they are placed close to each other.

In addition, the so-called exposure time depends on the strength of the radioactivity of the radiolabeled substance contained in the sample, the concentration and density of the substance, the sensitivity of the stimulable phosphor sheet, and the positional relationship between the sample and the stimulable phosphor sheet. Although it varies, the exposure operation requires a certain period of time, for example, several seconds or more. However, when a stimulable phosphor sheet is used as a photosensitive material according to the present invention,
The exposure time is significantly reduced compared to that required when using conventional radiation films. In addition, in the operation of reading out the positional information of the radiolabeled substance in the sample that has been transferred and accumulated from the sample to the stimulable phosphor sheet by exposure, the strength, distribution, and desired information of the energy stored in the phosphor sheet can be determined. Since it is possible to change the state of the obtained position information by performing various electrical processes according to the conditions, there is no particular need to strictly control the exposure time during the exposure operation.

Further, although there is no particular restriction on the temperature at which the exposure operation is performed, autoradiography using the stimulable phosphor sheet of the present invention can be performed particularly at an environmental temperature of 10 to 35°C. . however,
The exposure operation may be performed at the low temperatures used in conventional autoradiography (eg, around 5° C. or lower).

Next, regarding the method for reading out the positional information of the radiolabeled substance in the sample transferred and accumulated on the stimulable phosphor sheet in the present invention, an example of the reading device (or reading device) shown in FIG. 1 of the attached drawings will be described. A brief description will be given with reference to the following.

FIG. 1 shows a method for temporarily reading out one-dimensional or two-dimensional positional information of a radiolabeled substance accumulated and recorded on a stimulable phosphor sheet (hereinafter sometimes abbreviated as phosphor sheet) 1. Outline of an example of a readout device comprising a readout section 2 for pre-reading and a readout section 3 for main reading which has a function of reading out the radiation image stored and recorded on the phosphor sheet 1 in order to output position information of a radiolabeled substance The figure shows.

In the prefetch reading unit 2, the following prefetch operation is performed.

The laser light 5 generated from the laser light source 4 passes through the filter 6, whereby a portion of the wavelength range corresponding to the wavelength range of stimulated luminescence generated from the phosphor sheet 1 in response to excitation by the laser light 5 is cut out. Ru. Next, the laser beam is deflected by an optical deflector 7 such as a galvano mirror, reflected by a flat reflecting mirror 8, and then reflected by a phosphor sheet 1.
It is incident on the top with a one-dimensional deflection. The laser light source 4 used here is selected so that the wavelength range of its laser light 5 does not overlap with the main wavelength range of stimulated luminescence emitted from the phosphor sheet 1.

The phosphor sheet 1 is transported in the direction of the arrow 9 under irradiation with the above-mentioned polarized laser light. Therefore, the entire surface of the phosphor sheet 1 is irradiated with the polarized laser light. Note that regarding the output of the laser light source 4, the beam diameter of the laser light 5, the scanning speed of the laser light 5, and the transport speed of the phosphor sheet 1, the energy of the laser light 5 for the pre-reading operation is smaller than the energy used for the main reading operation. It will be adjusted so that

When the phosphor sheet 1 is irradiated with the laser light as described above, it exhibits stimulated luminescence with an amount of light proportional to the accumulated and recorded radiation energy, and this light enters the light guiding sheet 10 for prereading. The light guide sheet 10 has a linear incident surface and is placed close to the scanning line on the phosphor sheet 1 so as to face it, and its exit surface forms an annular ring to allow light such as a photoprint to pass through. It communicates with the light receiving surface of the detector 11. The light guide sheet 10 is made by processing a transparent thermoplastic resin sheet such as acrylic synthetic resin, and allows light incident from the incident surface to be transmitted to the exit surface while being totally reflected inside. It is configured to The stimulated luminescence from the phosphor sheet 1 is guided through the light guide sheet 10 and reaches the exit surface, is emitted from the exit surface, and is received by the photodetector 11.

The preferred shape, material, etc. of the light-guiding sheet are disclosed in Japanese Patent Application Laid-open Nos. 55-87970 and 56-11397.

A filter is attached to the light-receiving surface of the photodetector 11, which transmits only light in the stimulated emission wavelength range and cuts out light in the excitation light (laser light) wavelength range.
It is designed to detect only stimulated luminescence. Stimulated luminescence detected by the photodetector 11 is converted into an electrical signal, which is further amplified by the amplifier 12 and output. The accumulated recording information output from the amplifier 12 is input to the control circuit 13 of the main reading reading section 3. The control circuit 13 operates according to the obtained accumulated recording information so that an image with the most uniform density and contrast and excellent observation and interpretation performance is obtained.
The amplification factor setting value a, the recording scale factor b, and the reproduction image processing condition setting value c are output.

The phosphor sheet 1 whose pre-reading operation has been completed as described above is transferred to the main reading reading section 3.

In the main reading reading section 3, the following main reading operation is performed.

The laser beam 15 emitted from the main reading laser light source 14 passes through a filter 16 having the same function as the filter 6 described above, and then the beam
The beam diameter is precisely adjusted by the expander 17. Next, the laser beam is deflected by a light deflector 18 such as a galvano mirror, reflected by a plane reflecting mirror 19, and then one-dimensionally deflected and incident on the phosphor sheet 1. Note that an fθ lens 2 is provided between the optical deflector 18 and the plane reflecting mirror 19.
0 is arranged so that when the polarized laser beam scans the phosphor sheet 1, a uniform beam speed is always maintained.

The phosphor sheet 1 is transported in the direction of the arrow 21 under irradiation with the above-mentioned polarized laser light. Therefore, as in the pre-reading operation, the entire surface of the phosphor sheet 1 is irradiated with the polarized laser light.

When the phosphor sheet 1 is irradiated with laser light as described above, it emits stimulated luminescence with an amount of light proportional to the accumulated and recorded radiation energy, as in the pre-reading operation, and this light is used as a guide for main reading. The light enters the optical sheet 22. This light-guiding sheet 22 for main reading has the same material and structure as the light-guiding sheet 10 for pre-reading, and the stimulated luminescence guided through the interior of the light-guiding sheet 22 for main reading through repeated total reflections. The light is emitted from the exit surface and is received by the photodetector 23. Note that a filter that selectively transmits only the wavelength region of stimulated luminescence is attached to the light receiving surface of the photodetector 23, so that the photodetector 23 detects only stimulated luminescence.

The stimulated luminescence detected by the photodetector 23 is converted into an electrical signal, which is amplified to an appropriate level electrical signal in the amplifier 24 whose sensitivity is set according to the amplification factor setting value a, and then A/D converted. The signal is input to the device 25. The A/D converter 25 converts the digital signal into a digital signal using a scale factor suitable for the signal variator according to the recording scale factor setting value b, and inputs the digital signal to the signal processing circuit 26 . Signal processing circuit 26
Then, signal processing is performed based on the reproduced image processing condition setting value c so that a visible image with appropriate density and contrast and excellent observation and interpretation performance is obtained. , is transmitted to a recording device (not shown).

Examples of recording devices include those that optically record by scanning a photosensitive material with a laser beam or the like;
There are recording devices based on various principles, such as those that display electronically on CRTs, etc., those that record radiation images displayed on CRTs, etc. on video printers, etc., and those that record on heat-sensitive recording materials using heat rays. Can be used.

However, the recording device is not limited to one that creates a visible image as described above, but also one that converts the one-dimensional or two-dimensional positional information of the radiolabeled substance in the sample into numbers or symbols, as described above. You can also record it by doing something like this.

Regarding the method for reading out the positional information of the radiolabeled substance in the sample transferred and accumulated on the stimulable phosphor sheet in the present invention, the readout operation consisting of the pre-reading operation and the main reading operation was explained above. The read operations that can be utilized in the invention are not limited to the above examples. For example, if the content of the radioactive substance in the sample and the exposure time of the stimulable phosphor sheet for the sample are known in advance, the pre-reading operation can be omitted in the above example.

Furthermore, as a method for reading out the positional information of the radiolabeled substance in the sample that has been transferred and accumulated on the stimulable phosphor sheet in the present invention, it is of course possible to use an appropriate method other than those exemplified above. .

In the present invention, "position information" of a radioactively labeled substance in a sample refers to various information centered on the position of a radioactively labeled substance or an aggregate thereof in a sample, such as an aggregate of radioactive substances present in a sample. Refers to various types of information obtained as one or any combination of information such as the location and shape of the body, the concentration and distribution of radioactive substances at that location, etc.

Next, embodiments of the present invention will be described using as an example the operation of the DNA base sequencing method using the aforementioned Maxam-Gilbert method. The base sequence of the DNA [Escherichia coli plasmid DNA (pBR322)] used in the following Examples and Comparative Examples has already been determined, and the evaluation and analysis of the obtained chromatograms were based on these known data. It was carried out.

Furthermore, the stimulable phosphor sheets used in the following examples were prepared by the following method.

Adding methyl ethyl ketone to a mixture of photostimulable europium-activated barium fluoride bromide phosphor (BaFBr:Eu) particles and linear polyester resin,
Further, nitrocellulose with a degree of nitrification of 11.5% is added to prepare a dispersion containing phosphor particles in a dispersed state. Next, tricresyl phosphate, n
- After adding butanol and methyl ethyl ketone, stir and mix thoroughly using a propeller mixer to prepare a coating solution in which the phosphor particles are uniformly dispersed and the viscosity is 25 to 35 PS (25°C).

Next, the coating solution is uniformly applied using a doctor blade onto a carbon black kneaded polyethylene terephthalate sheet (support, thickness: 250 μm) placed horizontally on a glass plate. After coating, the support on which the coating film was formed was placed in a dryer, and the temperature inside the dryer was gradually raised from 25°C to 100°C to dry the coating film. In this way, a phosphor layer with a layer thickness of 300 μm is formed on the support.

Then, on top of this phosphor layer, a polyester adhesive is applied to one side of a transparent polyethylene terephthalate film (thickness: 12 μm), and the protective film is bonded by placing the adhesive layer side down. A stimulable phosphor sheet composed of a support, a phosphor layer, and a protective film is prepared.

Example 1 (1) Isolation and radioactive labeling of DNA to be sequenced Escherichia coli plasmid DNA was isolated using standard methods.
After cutting (pBR322) with the restriction enzyme Hind-, the 5'-end was labeled with ^32P to create a double-stranded
1 μg of DNA ( ^32P -labeled material) was obtained.

Add 1μg of the above double-stranded DNA to 20μ of 20mM Tris[tris(hydroxymethyl)aminomethane]/hydrochloric acid buffer (PH7.4) containing 5mM magnesium chloride and 1mM dithiothreitol and restriction enzyme Hae - approx. 1 unit was added and a specific decomposition reaction was carried out at 37°C for 1 hour to obtain a decomposition mixture solution containing decomposition products of the above fragments.

Using the above decomposition mixture solution as a sample, a slab gel (1.5 mm x 200 mm x 200 mm) of 8% polyacrylamide (crosslinking agent ratio: 3%), and
Electrophoresis was performed at a voltage of 500V using 50mM Tris-borate buffer (PH8.3) containing 1mM EDTA as an electrode solution. The electrophoresis was stopped when the marker dye previously added to the sample reached the bottom of the gel, and the origin of the coordinate axes was marked with ³² P-containing ink.

The above gel and stimulable phosphor sheet were stacked together and exposed at room temperature (approximately 25°C) for 1 minute. Introduced into the reading device,
Using the position marked with ^32P -containing ink as the origin of the coordinate axis, positional information indicating the migration position of the degradation product of the ^32P -labeled fragment was read out. Next, according to this positional information, the gel portion containing the ³² P-labeled degradation product was cut out using a thin razor and transferred to a test tube.

For confirmation, the remaining gel that had been partially cut out above was superimposed on a stimulable phosphor sheet in the same way, and then it was placed on a reading device using a reading device.
When examining the presence or absence of residual decomposition products with ³² P labels, it was found that the entire amount of decomposition products with ³² P labels had been removed. That is, obtained through the above stimulable phosphor sheet
It was confirmed that the positional information of the decomposition products having the ^32P label was highly accurate.

(2) Specific degradation of separated ³² P-labeled DNA fragments The gel taken out in (1) above was extracted according to a conventional method to separate ³² P-labeled DNA fragments.
The count number of the obtained ^32P -labeled DNA fragment was approximately 1.
×10 ⁶ cpm.

Concentrate the extract under reduced pressure to reduce the total volume to approximately 20μ
This concentrate was divided into four microtubes manufactured by Etzpendorf (West Germany). Using each concentrated solution as a sample, constituent bases were specifically cleaved by a decomposition reaction according to the Maxam-Gilbert method.

The degradation method for specific cleavage is as follows: 1) Guanine (G) 2) Guanine (G) + Adenine (A) 3) Thymine (T) + Cytosine (C) 4) Cytosine (C) We selected conditions that would allow the test to be carried out selectively.

For example, the selective cleavage reaction at the guanine (G) position in 1) above was carried out in the following manner according to a conventional method: 2), 3) and 4)
The same procedure was followed in accordance with the conventional method.

5μ of sample (extract concentrate), 1mM
It was added to 200μ of 50mM sodium cacodylate aqueous solution containing EDTA and cooled to 0°C. 1μ of dimethyl sulfate was added to this, heated to 20°C, and reacted for 15 minutes. This reaction solution was cooled to 0°C.
50μ of aqueous solution containing 1.5M sodium sulfate, 1M mercaptoethanol, and 100μg/m of tRNA
After adding and thoroughly mixing 750μ of ethanol, the mixture was cooled at -70°C for 5 minutes.

The above coolant was centrifuged at 12000G to remove the supernatant, and the precipitate was cooled to 0°C.
Add 250μ of 0.3M sodium acetate solution to DNA
and tRNA were dissolved. Next, add approximately 750μ of ethanol to this solution, perform the same centrifugation operation, and remove the supernatant.
DNA and tRNA were washed. Subsequently, the same washing operation was performed again using 1 m of ethanol.

After drying the obtained precipitate under reduced pressure for several minutes, 100 μ of a freshly distilled 1M aqueous solution of piperidine was added thereto, and the mixture was reacted at 90° C. for 30 minutes.
The reaction solution was freeze-dried to remove piperidine, and then washed twice by freeze-drying using 10μ of water.

10μ of an aqueous solution consisting of 80% formamide, 10mM sodium hydroxide, 1mM EDTA, and BPB (bromophenol blue: marker dye)
Next, the freeze-dried product (decomposition product of DNA fragments) obtained above was dissolved, heated at 90°C for several minutes, and then cooled with ice water to prepare a sample for electrophoresis.

(3) Preparation of gel for electrophoresis 10.69 g of acrylamide, 0.56 g of N,N'-methylenebisacrylamide, 37.8 g of urea, and
Dissolve 9 ml of 1.0 M Tris-borate buffer (PH 8.3) containing 20 mM EDTA in distilled water.
A gel solution with a thickness of 90 m was obtained. After blowing nitrogen gas into this gel solution to remove oxygen, add 10%
of ammonium persulfate aqueous solution 600μ and catalyst
TEMED (Tetramethylethylenediamine) 25μ
added. A mold (0.5 mm x 300 mm x 400 mm) was formed from two thoroughly washed 3 mm thick glass plates using the gel solution treated in this way.
Inject it into the gel solution, and then insert four slots (0.5 mm x 15 mm x 20 mm each) into the top of the gel solution.
After inserting the slot former,
The gel was allowed to gel overnight to prepare a desired gel for electrophoresis having four slots.

(4) Electrophoresis operation After installing the gel with the slot formed in the electrophoresis device and performing a pre-run (preliminary electrophoresis operation) for about 180 minutes at 1000V/40cm, place 1)-(G) into the first slot. Specific decomposition products, in the second slot 2)-
(G+A) Specific decomposition product, 3)- in the third slot
The (T+C) specific decomposition product and the 4)-(C) specific decomposition product were introduced into the fourth slot so that each ³² P count was approximately 2×10 ⁵ cpm.

Next, the sample was similarly subjected to electrophoresis at 1000V/40cm. The electrophoresis continued until the marker dye reached the bottom of the gel and then stopped. One glass plate was then removed and the gel was washed twice in 10% acetic acid. The gel was transferred onto a filter paper, and then heated and dried under reduced pressure.

(5) Exposure operation The dried gel obtained above and the stimulable phosphor sheet were stacked together and stored in a cassette, and exposed for 40 minutes at room temperature (approximately 20°C). It was loaded into a reading device to read out a four-row chromatogram showing the position of the radiolabeled substance on the gel transferred and accumulated on the phosphor sheet, and then the information was stored as digital information.

When a visible image of the chromatogram was obtained based on the above digital information, a clear image was obtained. When this chromatogram was compared with a known chromatogram of E. coli plasmid DNA (pBR322), a sufficient match was found.

Separately, similar readout operations were carried out using the respective chromatograms from the second and third slots as the coordinate axes, and the following comparisons were made using computer processing to determine the base sequence of the DNA of interest.

By comparing the chromatogram of the (G+A) specific decomposition product in the second slot with the chromatogram of the (G) specific decomposition product in the first slot, the positions of G and A are determined, respectively, with respect to the origin of the coordinate axes. do.

Next, by comparing the chromatogram of the (T+C) specific decomposition product in the third slot with the chromatogram of the (C) specific decomposition product in the fourth slot, we can determine the positions of T and C with respect to the origin of the coordinate axes. Determine each. Then, by arranging these in order of distance from the origin of the coordinate axes, the DNA base sequence is obtained.

The nucleotide sequence determined by the computer processing described above matched the known nucleotide sequence of the E. coli plasmid DNA (pBR322), which was the subject of the investigation.

From the above results, it was confirmed that it is fully possible to perform DNA base sequencing based on the Maxam-Gilbert method by using a stimulable phosphor sheet and performing a short exposure operation at room temperature. Ta.

Comparative Example 1 After carrying out the electrophoresis operation described in "(5) Exposure operation" of Example 1, the exposure operation of the stimulable phosphor sheet using dry gel was performed using X instead of the phosphor sheet.
Linear film (RX type: Fuji Photo Film Co., Ltd.)
) and a fluorescent intensifying screen (Lightning Plus, manufactured by DuPont, USA) were used in combination, and the film was stored in a normal X-ray film cassette and exposed under the same conditions as in Example 1 (room temperature, 40 minutes exposure). The exposure operation was performed using The X-ray film was then developed, but no readable chromatogram could be obtained.

Next, the above exposure operation was carried out at -80°C for 1000 minutes according to the usual Maxam-Gilbert method, and then the X-ray film was developed in the same way. It was possible to obtain a chromatogram with a sharpness comparable to that of gram. The chromatogram obtained here matched the chromatogram obtained as a visible image in Example 1.

[Brief explanation of drawings]

FIG. 1 shows an example of a reading device (or reading device) for reading positional information of a radiolabeled substance in a sample that has been transferred and accumulated on a stimulable phosphor sheet in the present invention. 1: stimulable phosphor sheet, 2: readout section for pre-reading, 3: readout section for main reading, 4: laser light source,
5: Laser light, 6: Filter, 7: Optical deflector, 8: Planar reflector, 9: Transfer direction, 10: Light guide sheet for prereading, 11: Photodetector, 12: Amplifier, 13: Control circuit, 14: Laser light source, 1
5: laser beam, 16: filter, 17: beam expander, 18: optical deflector, 19: plane reflecting mirror, 20: fθ lens, 21: transport direction, 2
2: Light guide sheet for main reading, 23: Photodetector, 2
4: Amplifier, 25: A/D converter, 26: Signal processing circuit.

Claims (1)

[Scope of Claims] 1. One-dimensional or two-dimensional radiolabeled substances contained in a sample selected from the group consisting of biological tissues and media containing biological tissues and/or biological substances. In an autoradiographic measurement method that detects dimensional position information, the sample and a stimulable phosphor sheet having a phosphor layer made of a stimulable phosphor dispersed in a binder are held together for a certain period of time. By overlapping, the phosphor sheet absorbs at least a portion of the radiation energy emitted from the radiolabeled substance in the sample, and then the stimulable phosphor sheet is scanned with electromagnetic waves to absorb the stimulable phosphor sheet. A method consisting of emitting radiation energy stored in a body sheet as photostimulated light and detecting the stimulated light to obtain positional information of a radiolabeled substance in a sample. 2. The autoradiographic measurement according to claim 1, wherein the sample containing the radiolabeled substance is a tissue of a living organism to which a radioactive label has been given and/or a medium containing a substance derived from the living organism. Law. 3. A patent characterized in that the medium is a support on which a radiolabeled substance is separated and developed, and the radiolabeled substance is a radiolabeled biopolymer substance, a derivative thereof, or a decomposition product thereof. The autoradiographic measurement method according to claim 2. 4. The autoradiographic measurement method according to claim 3, wherein the support is a support on which a biopolymer substance has been separated and developed by electrophoresis. 5. The autoradiographic measurement method according to claim 4, wherein the biopolymer substance is a nucleic acid, a derivative thereof, or a decomposition product thereof. 6 (1) A support obtained by electrophoresing a mixture of radioactively labeled DNA cleavage products or DNA degradation products on a support, and a stimulable phosphor dispersed in a binder. A step of overlapping a stimulable phosphor sheet having a phosphor layer for a certain period of time so that the phosphor sheet absorbs at least a portion of the radiation energy emitted from the radioactive label in the DNA cut product or DNA degradation product. ; and (2) scanning the stimulable phosphor sheet with electromagnetic waves to emit the radiation energy stored in the stimulable phosphor sheet as photostimulated light, and detecting this photostimulated light to generate support. on the body
6. The autoradiographic measurement method according to claim 5, comprising the step of: detecting positional information of DNA cleavage products or DNA degradation products. 7. Claims 1 to 6, characterized in that the stimulable phosphor sheet comprises a support, a phosphor layer comprising a stimulable phosphor dispersed in a binder, and a protective film. The autoradiographic measurement method described in any of the sections. 8 Information on the one-dimensional or two-dimensional position of radioactively labeled substances contained in a sample selected from the group consisting of biological tissues and media containing biological tissues and/or biological substances. In the autoradiographic measurement method that involves detection, the sample and a stimulable phosphor sheet having a phosphor layer made of a stimulable phosphor dispersed in a binder are overlapped for a certain period of time to detect the stimulable phosphor. After at least a portion of the radiation energy emitted from the radiolabeled substance in the sample is absorbed into the phosphor sheet, the stimulable phosphor sheet is scanned with electromagnetic waves to determine whether the radiation energy is accumulated in the stimulable phosphor sheet. A method consisting of emitting radiation energy as photostimulated light, detecting the stimulated light to obtain positional information of a radiolabeled substance in a sample, and then converting the positional information into an image. 9 One-dimensional or two-dimensional positional information of a radiolabeled substance contained in a sample selected from the group consisting of biological tissue and a medium containing biological tissue and/or biological material. In the autoradiographic measurement method that involves detection, the sample and a stimulable phosphor sheet having a phosphor layer made of a stimulable phosphor dispersed in a binder are overlapped for a certain period of time to detect the stimulable phosphor. After at least a portion of the radiation energy emitted from the radiolabeled substance in the sample is absorbed into the phosphor sheet, the stimulable phosphor sheet is scanned with electromagnetic waves to determine whether the radiation energy is accumulated in the stimulable phosphor sheet. A method consisting of emitting radiation energy as photostimulated light, detecting the stimulated light to obtain positional information of a radiolabeled substance in a sample, and expressing the positional information in symbols and/or numerical values. .