DIAGNOSTIC DRUG, DIAGNOSTIC METHOD AND DIAGNOSTIC DEVICE FOR PERMEABILITY OF INTESTINAL MUCOSA

Abstract

Provided is a diagnostic drug for evaluating permeability of intestinal mucosa, including chitin and/or chitosan as a main component. The chitin and/or chitosan to be used preferably has a weight average molecular weight prepared to a range of from 1,000 to 11,600.

Claims

1-4. (canceled)

5. A diagnostic method, comprising: orally administering or enema administering chitin and/or chitosan to an animal, the animal being other than a human; and measuring a concentration of the administered substance in blood after a lapse of a predetermined period of time, to thereby evaluate permeability of intestinal mucosa of the animal.

6. A diagnostic method, comprising: orally administering or enema administering chitin and/or chitosan to a test subject; and measuring a concentration of the administered substance in blood after a lapse of a predetermined period of time, to thereby evaluate permeability of intestinal mucosa of the test subject.

7. A diagnostic method according to claim 5 or 6, wherein the chitin and/or chitosan has a weight average molecular weight prepared to a range of from 1,000 to 11,600.

8. A diagnostic method according to claim 6, wherein a dose of the chitin and/or chitosan is set to a range of from 8.33 mg to 20.83 mg per kg of body weight.

9. (canceled)

10. A food and drink evaluation method, comprising: allowing a test subject to eat and drink a single or a plurality of specific foods and drinks; allowing the test subject to orally ingest chitin and/or chitosan during the eating and drinking, or before or after the eating and drinking; and measuring a concentration of the ingested substance in blood after a lapse of a predetermined period of time from the oral ingestion, to thereby determine whether the foods and drinks have a potential to serve as a factor affecting permeability of intestinal mucosa of the test subject.

11. (canceled)

12. An evaluation method, comprising: administering a given substance; separately orally administering or enema administering chitin and/or chitosan; and measuring blood concentrations of the orally administered substance or the enema administered substance before and after the administration of the given substance, to thereby evaluate whether the given substance has a normalizing action on permeability of intestinal mucosa, and how strong the normalizing action, when present, is.

13-14. (canceled)

Description

BRIEF DESCRIPTION OF DRAWINGS

[0058] FIG. 1 are test outlines of an AO model and an IR model.

[0059] FIG. 2 are photographs for showing a normal state of an intestinal tract and an LGS-induced state thereof.

[0060] FIG. 3 is a graph for showing the results of a lactulose-mannitol test for the AO model.

[0061] FIG. 4 are graphs for showing the results of an FITC-dextran test for the AO model.

[0062] FIG. 5 is a graph for showing the results of an FITC-dextran test for the IR model.

[0063] FIG. 6 are graphs for showing the measurement results of chitin-chitosan concentrations for the AO model and the IR model.

[0064] FIG. 7 is a graph for showing the manner of distribution of samples containing chitin-chitosan having weight average molecular weights of 1,000, 3,000, and 11,600 as main components.

[0065] FIG. 8 is a graph for showing the blood concentrations of chitin-chitosan at various molecular weights for the IR(20) model.

[0066] FIG. 9 is a graph for showing the blood concentrations of chitin-chitosan at various molecular weights for the IR(10) model.

[0067] FIG. 10 is a graph for showing results for the IR(20) model obtained by orally administering a diagnostic agent having a weight average molecular weight of 1,000 at each of 1.25 mg/mouse and 0.625 mg/mouse, and measuring its blood concentration.

[0068] FIG. 11 are schematic diagrams of distribution modes of the molecular weight of a diagnostic drug and concentration measurement results.

[0069] FIG. 12 is a graph for showing the manner of molecular weight distribution of a purified sample.

[0070] FIG. 13 are a graph for showing the measurement results of a chitin-chitosan concentration using the purified sample, and the external appearance of an intestinal tract and an HE-stained image, for the IR(20) model.

[0071] FIG. 14 is a graph of the measurement of a temporal change in chitin-chitosan amount in circulating blood in the IR(10) model in which the purified sample was orally administered to mice.

[0072] FIG. 15 are graphs of the measurement of a temporal change in blood concentration of chitin-chitosan in the case where the purified sample was intravenously administered to mice not subjected to ischemia-reperfusion treatment.

[0073] FIG. 16 is an explanatory diagram for illustrating a protocol for inducing OVA allergy.

[0074] FIG. 17 is a graph for showing the blood concentration of chitin-chitosan using OVA-IgE mice.

[0075] FIG. 18 are graphs for showing the blood concentrations of chitin-chitosan for a high-fat diet model and a NASH-inducing diet model.

[0076] FIG. 19 are photographs for showing a whole intestine image and HE-stained image before onset in a DSS-induced ulcerative colitis model. Comparative images without the administration of DSS are also shown.

[0077] FIG. 20 is a graph for showing the blood concentrations of chitin-chitosan before onset in the DSS-induced ulcerative colitis model.

[0078] FIG. 21 is a conceptual diagram for illustrating a time lag between an increase in permeability of intestinal mucosa and the occurrence of inflammation or disorder.

DESCRIPTION OF EMBODIMENTS

Construction of LGS-induced Models

[0079] In this embodiment, LGS was assumed as an example in which the leakiness of an intestinal tract was evaluated, and first, induction tests therefor were performed.

[0080] One model uses aspirin and omeprazole (hereinafter referred to as “AO model” as appropriate). Conditions were modified on the basis of the literature (Innate Immun. 2015 July;21(5):537-45).

[0081] An outline of the test is as follows: per kg of body weight of mice, 100 mg of aspirin (100 mg/kg) is orally administered twice a day for 6 days and 10 mg of omeprazole (10 mg/kg) is intraperitoneally administered twice a day for 6 days, and the degree of LGS is measured on the 7th day.

[0082] Another model is an intestinal tract ischemia-reperfusion model (hereinafter referred to as “IR model” as appropriate). Conditions were modified on the basis of the literature (Gastroenterology. 2001 February;120(2):460-9.) and the like.

[0083] An outline of the test is as follows: an intestinal tract is clipped continuously for 30 minutes to be brought into an ischemia state, and then unclipped to achieve reperfusion, and 30 minutes later, the degree of LGS is measured. As an expression specifying an ischemia time of 30 minutes, this model is referred to as “IR 30) model” as appropriate.

[0084] Outlines of both models are illustrated in FIG. 1. In FIG. 1b, an IR(20) model and an IR(10) model, which are described later, are also illustrated.

[0085] In FIG. 2, external appearance photographs, HE-stained images, and electron micrographs of the intestinal tract are shown. As compared to a normal tissue, in the AO model, cracks are found in intestinal villi, and hence the occurrence of mild LGS is recognized. In addition, in the IR(30) model, intestinal villi are significantly damaged, and hence the occurrence of severe LGS is recognized.

Evaluation of Degree of LGS

[0086] The above-mentioned models were used to determine leakiness based on a difference in molecular weight.

[0087] First, a lactulose-mannitol test was performed for the AO model. Lactulose and mannitol were both orally administered at 500 mg/kg, urine was collected for 4 hours, and an L/M ratio was measured. The results are shown in FIG. 3. As compared to mice administered with none of aspirin and omeprazole and not having LGS induced, i.e., a control, the AO model had an about 2-fold increase in L/M ratio. It was able to be confirmed from the foregoing that a state in which the leakiness of a substance having a molecular weight of more than 300, such as mannitol, was raised was found.

[0088] Next, an FITC-dextran test was performed for the AO model. FITC-dextran was orally administered at 600 mg/kg, blood was collected 60 minutes later, and the concentration in plasma thereof was measured. The results are shown in FIGS. 4. It was able to be confirmed that the concentration of dextran in the plasma was increased to some degree as compared to the control (FIG. 4b).

[0089] In addition, an FITC-dextran test was performed for the IR(30) model. FITC-dextran was orally administered at 600 mg/kg, ischemia was started 30 minutes later, blood was collected 30 minutes after reperfusion, and the concentration in plasma thereof was measured. The results are shown in FIG. 5. The dextran concentration in plasma had an increase as high as about 15-fold as compared to the control.

[0090] As apparent from a comparison between FIG. 4a and FIG. 5, the IR(30) model may be said to be a model capable of inspecting a state in which a substance having a large molecular weight is allowed to migrate to blood more easily, as compared to the AO model. In other words, the IR (30) model may be said to be a model capable of evaluating severe LGS.

[0091] On the other hand, on the basis of a comparison between FIG. 3 and FIG. 4b, the AO model may be said to be a model capable of inspecting a state that is not so severe as to allow a substance having a large molecular weight to easily migrate to blood. In other words, the AO model may be said to be a model capable of evaluating mild LGS.

Evaluation of LGS using Chitin-Chitosan

[0092] Next, evaluation of LGS using chitin-chitosan was performed.

[0093] First, the shell of a crab was deproteinized, decalcified, and deacetylated to provide a mixture of chitin and chitosan. Subsequently, the mixture of chitin and chitosan was decomposed into small molecules to provide a chitin-chitosan sample having a weight average molecular weight of 7,900. As a method for the decomposition into small molecules, which is not particularly limited, there are given a method involving hydrolyzing the mixture of chitin and chitosan with concentrated hydrochloric acid (JP 5714963 B2), and a method involving dissolving the mixture with hydrochloric acid or an organic acid, such as acetic acid, citric acid, or lactic acid, and then decomposing the mixture into small molecules using a chitosanase enzyme (JP 2013-79217 A).

[0094] Next, for the AO model, 2.50 mg of the above-mentioned sample was orally administered on the 7th day, blood was collected 60 minutes later, and the concentration of chitin-chitosan in plasma was measured (see FIG. 1a).

[0095] In addition, for the IR(30) model, 2.50 mg of the above-mentioned sample was orally administered 30 minutes before the start of ischemia, blood was collected 30 minutes after reperfusion, and the concentration of chitin-chitosan in plasma was measured (see FIG. 1B).

[0096] For the measurement, first, the plasma was extracted from the blood by a conventional method, and chitin-chitosan in the plasma was decomposed into chitose (2,5-anhydro-D-mannose) serving as a constituent monosaccharide by a nitrous acid decomposition method. Next, its aldehyde group was allowed to react with 3-methyl-2-benzothiazolinone hydrazone hydrochloride (MBTH) and iron (III) chloride to develop a blue color. Finally, the degree of the blue color was measured with an absorbance meter, and the concentration was calculated on the basis of the dye amount.

[0097] The results are shown in FIGS. 6. As shown in FIG. 6, it can be confirmed that chitin-chitosan is allowed to migrate into the blood more remarkably in the IR(30) model than in the AO model. This means a larger molecular weight of the sample used, and agrees with the relationship between FIG. 4b and FIG. 5.

[0098] In view of the foregoing, the inventors of the present invention have decided to investigate the applicability of the chitin-chitosan as a diagnostic drug for the degree of LGS, and by extension, a diagnostic drug for diagnosing permeability of intestinal mucosa (evaluation drug for evaluating permeability of intestinal mucosa). The concentration evaluation has been performed with the absorbance in the foregoing, but is not limited thereto, and chitin and chitosan do not particularly need to be distinguished from each other as long as the blood concentration can be detected. Therefore, in the present invention, the expression “chitin-chitosan” is used, and means chitin and/or chitosan.

[0099] First, a solution of hydrochloric acid or an organic acid was prepared, and the chitin-chitosan sample having a weight average molecular weight of 7,900 was fractionated using UF membranes (having molecular weight cut-offs of 3,000, 6,000, 10,000, and the like) into chitin-chitosan having weight average molecular weights of 1,000, 3,000, 7,900, and 11,600. In FIG. 7, the manner of distribution of the prepared samples is shown. In addition, a measurement method for the weight average molecular weight is also described.

[0100] Next, for the IR model, 2.5 mg each of the above-mentioned samples was orally administered, and the blood concentration of the chitin-chitosan was measured. It was considered that an ischemia time of 30 minutes caused excessively large damage to an intestinal tract, and hence, in this case, a test was performed with the ischemia time shortened to 20 minutes. This model is referred to as “IR(20) model”.

[0101] For the IR(20) model, the measurement results of the blood concentrations of the chitin-chitosan at various molecular weights are shown in FIG. 8. In FIG. 8, the results of a control, i.e., without ischemia-reperfusion are also shown. As apparent from FIG. 8, although the concentration at a weight average molecular weight of 11,600 is slightly small, in general, the sample having any molecular weight has migrated into blood.

[0102] In view of the foregoing, the ischemia time was changed to 10 minutes to further reduce the degree of LGS, inducing medium-degree LGS, and sample-screening performance was investigated. This test is referred to as “IR(10) model”.

[0103] For the IR(10) model, the measurement results of the blood concentrations of the chitin-chitosan at various molecular weights are shown in FIG. 9. As can be seen in FIG. 9, it can be confirmed that a sample having a smaller weight average molecular weight is more liable to leak, and a sample having a larger weight average molecular weight is less liable to leak.

[0104] As apparent from the above-mentioned experiments, through the use of the chitin-chitosan, evaluation can be performed regarding the following: how large the molecular weight of a substance that leaks through the intestinal tract is; and a state in which a substance having how large a molecular weight leaks through the intestinal tract to what degree is found.

[0105] That is, the chitin and/or chitosan can be used for evaluation of permeability of intestinal mucosa through oral administration and blood concentration measurement after a lapse of a predetermined period of time.

[0106] In other words, it may be said that a diagnostic drug for evaluating permeability of intestinal mucosa, containing chitin and/or chitosan as a main component, was able to be obtained.

[0107] In addition, it may also be said that a diagnostic drug for evaluating permeability of intestinal mucosa, containing chitin and/or chitosan as a main component, the diagnostic drug being used by allowing a test subject to orally ingest the diagnostic drug and measuring a blood concentration thereof after a lapse of a predetermined period of time, was able to be obtained.

[0108] It may also be said that an evaluation technology for an increase in intestinal mucosal permeability was able to be obtained.

[0109] As shown in FIG. 8 and FIG. 9, the IR model can induce LGS of any degree from mild to severe through the adjustment of the ischemia time, and may be said to be a model capable of constructing a versatile and objective evaluation system.

[0110] For the IR(20) model, a diagnostic drug having a weight average molecular weight of 1,000 was orally administered at each of 1.25 mg/mouse and 0.625 mg/mouse, and a blood concentration in the case where the dose was reduced was measured. The results are shown in FIG. 10. As apparent from FIG. 10, it was found that significant concentration measurement was possible even at 0.625 mg/mouse. When this value is converted for a human having a body weight of 60 kg, the dose of the diagnostic drug is 1.25 g. In addition, in terms of measurement limit taking also a control into consideration, significant concentration measurement is in theory possible even at 0.500 g of oral ingestion for a 60 kg human. That is, it is appropriate that the dose or the intake be set to a range of from 8.33 mg to 20.83 mg per kg of body weight. In consideration of individuals ranging from a child having a body weight of 5 kg to an adult having a body weight of 200 kg, it may be said that the oral intake may be set to a range of from 0.04 g to 4.20 g. In any case, an oral intake of as much as 15 g required in the lactulose-mannitol test is not required, and hence the diagnostic drug may be said to relieve a burden on the test subject.

[0111] It is considered that the same applies to the case of enema administration.

[0112] In addition, although depending on a detection system, it is preferred that the diagnostic drug have a weight average molecular weight prepared to a range of from 200 to 20,000, more preferably from 1,000 to 11,600. FIG. 11 are schematic diagrams of distribution modes of the molecular weight of the diagnostic drug and concentration measurement results. In FIG. 11a, a single-peak diagnostic drug is shown. Whether a state in which a substance having at least up to this molecular weight leaks is found can be determined. In FIG. 11b, a multi-peak diagnostic drug is shown. How large the maximum molecular weight of a substance that is liable to leak is can be determined. In FIG. 11c, a diagnostic drug having a uniform spread of molecular weights is shown. Also in this case, how large the maximum molecular weight of a substance that is liable to leak is can be determined.

[0113] The diagnostic drug or diagnostic method described above has the following advantages.

Having no toxicity (Usable for a human. Allowing an animal experiment as well.).
Orally administrable.
Not produced in a living body including an intestine (Allowing direct concentration measurement.).
Not easily decomposed in a living body (Allowing direct concentration measurement.).
Hardly absorbed from an intestinal tract in a normal state.
Allowing the adjustment of a molecular weight.

Test Using Highly Purified Chitin-Chitosan

[0114] Next, a test was performed using chitin-chitosan having a sharper molecular weight distribution. FIG. 12 is a graph for showing the manner of molecular weight distribution of a chitin-chitosan sample used in the following test. The sample is a highly purified sample which has a sharp distribution as compared to FIG. 7, and in which, according to the results of separate analysis, molecules having molecular weights of from 823 to 1,984 (having molecular weights of from about 1, 000 to about 1,200 as hydrochlorides) account for 98 wt % of the entirety. This sample is referred to as “purified sample” as appropriate.

[0115] For the IR(20) model, a chitin-chitosan concentration in serum was measured using the purified sample. The measurement results, and the external appearance of an intestinal tract and an HE-stained image thereof are shown in FIG. 13. It is found from the HE-stained image that a mucosal disorder has only slightly advanced, but as with FIG. 8, it can be confirmed that a state in which chitin-chitosan having a molecular weight of about 1,000 leaks into blood is found.

Safety Confirmation

[0116] In the IR(10) model in which the purified sample was orally administered to mice, a temporal change in chitin-chitosan amount in circulating blood was measured. A temporal change from 30 minutes after reperfusion is shown in FIG. 14. An oral dose was set to 2.5 mg/mouse.

[0117] The circulating blood amount of a mouse is estimated to be an amount corresponding to 1/13 of its body weight, and hence the amount is 1.93 ml when the body weight is 25 g. Meanwhile, the Area Under the Curve (AUC) shown in FIG. 14 was 162.16 μg/ml between 0 h and 8 h. Therefore, the amount of the chitin-chitosan that leaked into circulating blood in 8 hours is 162.16*1.93=312.97 μg. It may be said from the foregoing that 12.5% of the oral dose of the purified sample leaked into circulating blood (312.97 μg/2.5 mg=0.125) . The mice remained alive even after 8 hours.

[0118] In addition, 2.5 mg of the purified sample was intravenously administered to nontreated mice, i.e., mice not subjected to ischemia-reperfusion treatment, and a temporal change in blood concentration of the chitin-chitosan was measured. The measurement results are shown in FIG. 15. It was confirmed that the blood concentration was about 70 μg/ml even when the intravenous administration was performed (the blood concentration estimated by extrapolation was about 150 μg/ml even immediately after the administration), and the chitin-chitosan rapidly disappeared from the blood in about 2 hours (the concentration decrease was linear when replotted on a logarithmic scale) . This is considered to be due to renal excretion. No shock symptom due to the intravenous administration was found, and the mice remained alive even after 2 hours.

[0119] The following may be said in consideration of the two tests.

1) The mice continued to live even after the tests, and hence it was able to be confirmed again that the chitin-chitosan was safe for a living body (at least the possibility of immediately seriously affecting the living body is extremely low).
2) The chitin-chitosan can be said to be safe to a living body also because of rapid disappearance thereof from the blood.
3) Under the above-mentioned conditions, the chitin-chitosan in the blood was detected from the blood even after 8 hours . Accordingly, the chitin-chitosan allows concentration measurement even after a lapse of some time from administration, and hence is useful as a diagnostic drug/evaluation drug. In addition, a temporal change can also be grasped.
4) The chitin-chitosan rapidly disappears after leaking into blood, and hence, through oral administration or enema administration thereof, a real-time state of the leakiness or permeability of an intestine can be grasped. More simply, it may be said that the state of the intestine can be grasped.

Permeability Evaluation with Model other than IR Model

[0120] Next, evaluation of permeability or leakiness was performed for models other than the above-mentioned evaluation test involving directly applying a load to the intestine like ischemia-reperfusion.

Permeability Evaluation with Food Allergy Model

[0121] First, mucosal permeability evaluation of the small intestine was performed for mice having egg allergy, i.e., OVA-IgE mice. A protocol for inducing OVA allergy is as illustrated in FIG. 16. First, mice were sensitized by being intraperitoneally administered with ovalbumin (OVA), followed continuously by oral administration therewith. 28 Days after the sensitization, the mice were orally administered with OVA and the purified sample and evaluated. In the OVA-IgE mice, severe diarrhea, a typical symptom of food allergy, was found.

[0122] The blood concentration measurement results of the chitin-chitosan are shown in FIG. 17. For comparison, the results of a lactulose-mannitol test are also shown. As shown in FIG. 17, it was able to be found that, when diarrhea resulting from food allergy occurred, a state in which the permeability of the intestine was raised was found. It was also found that the raising of permeability was able to be more clearly judged by the evaluation than by the lactulose-mannitol test.

Permeability Evaluation with High-fat Diet Model and NASH-inducing Diet Model

[0123] Next, permeability evaluation was performed for mice kept fed with a high-fat diet and a nonalcoholic steatohepatitis (NASH)-inducing diet, respectively.

[0124] The components of the high-fat diet and the NASH-inducing diet are as shown below.

TABLE-US-00001 TABLE 1 High-fat diet NASH-inducing diet (g/100 g of feed) Carbohydrate 26 45 Protein 26 22 Lipid 35 20 Cholesterol amounts in the lipid and fructose amounts in the carbohydrate are as shown below. High-fat diet NASH-inducing diet (g) Cholesterol in lipid 0.028 2 Fructose in carbohydrate 0 22

[0125] High-fat diet model: 6-Week-old male C57BL/6 mice were allowed to ingest the high-fat diet ad libitum for 5 weeks, and then given neither water nor feed for 21 hours. After that, 2.5 mg of the purified sample was orally administered to the mice, and 1 hour after that, blood was collected from the inferior vena cava, and a chitin-chitosan amount was measured.

[0126] NASH-inducing diet model: 6-Week-old male C57BL/6 mice were allowed to ingest the NASH-inducing diet ad libitum for 4 weeks, and then given neither water nor feed for 21 hours. After that, 2.5 mg of the purified sample was orally administered to the mice, and 1 hour after that, blood was collected from the inferior vena cava, and a chitin-chitosan amount was measured.

[0127] The results are shown in FIG. 18. Although the permeability is not raised for the high-fat diet, the permeability is clearly raised in the case of the NASH-inducing diet . Thus, first, it has been able to be confirmed that it may be said that nonalcoholic steatohepatitis induces a state in which the permeability of the intestine is raised. Next, the leakiness of the intestine was not raised with the ingestion of the high-fat diet of the composition for the period of time. Thus, it has been found, conversely, that the use of the chitin-chitosan enables screening on how the intestine is affected by what diet.

Permeability Evaluation with DSS-induced Ulcerative Colitis Model

[0128] Next, permeability evaluation was performed for mice having ulcerative colitis induced with dextran sodium sulfate (DSS).

[0129] Ulcerative colitis model: First, mice were allowed to drink water having dissolved therein 2.5 wt % of DSS ad libitum. After 72 hours from the start of the ad libitum water drinking, the mice were enema administered or orally administered with the purified sample, and the blood concentrations of the chitin-chitosan were measured 1 hour after the administration for the mice subjected to the enema administration, and 4 hours after the administration for the mice subjected to the oral administration.

[0130] FIG. 19 are whole intestine images and HE-stained images of the case of allowing the drinking of water with DSS for 72 hours (3 days) and the case of not allowing water drinking. As shown in FIG. 19, at 72 hours from the start of the ad libitum water drinking, inflammation was not found in intestinal mucosa, and no clear change was observed anywhere across even the whole intestine.

[0131] However, as shown in FIG. 20, in both the oral administration and the enema administration, leakage of the chitin-chitosan into blood was observed. In addition, as a result of continued observation, it was separately confirmed that the mice that had drunk water with DSS ad libitum developed inflammation 96 hours (4 days) after the start of the water drinking.

[0132] That is, surprisingly, it was able to be confirmed that the use of the chitin-chitosan enabled the detection of an abnormal increase in permeability of intestinal mucosa before the onset of ulcerative colitis.

Chitin-Chitosan as Evaluation Agent for Pharmacological Action

[0133] As illustrated in FIG. 21, an increase in permeability of intestinal mucosa in general, not limited to that before the onset of ulcerative colitis, is considered to occur long before the occurrence of inflammation or disorder. Therefore, grasping of permeability or leakiness through the use of the chitin-chitosan enables pre-onset diagnosis, onset prevention, onset prediction, and evaluation of the pharmacological action of a therapeutic drug or the like.

[0134] First, in the case where inflammation is caused by food ingestion or the like, whereas it has hitherto been impossible to judge what is a causative food or a causative food group without continuing the ingestion until onset, the ingestion can be stopped before onset to relieve a burden and effective screening can be performed.

[0135] Next, the chitin-chitosan can also be used for screening for drug discovery of an LGS therapeutic drug, an LGS alleviating drug, an intestinal mucosal permeability modulatory drug, and the like. That is, by: administering a given substance (candidate substance); separately orally administering or enema administering chitin and/or chitosan; and measuring blood concentrations of chitin and/or chitosan before and after the administration of the candidate substance, it is possible to evaluate whether the candidate substance has a normalizing action on permeability of intestinal mucosa, and how strong the normalizing action, when present, is. The chitin-chitosan may also be provided as an evaluation agent containing chitin and/or chitosan as a main component, the evaluation agent being used as described above.

[0136] In addition, it also becomes possible to accumulate findings on inflammatory bowel diseases (IBDs), such as ulcerative colitis and Crohn's disease, and eosinophilic gastroenteritis. Findings on irritable bowel syndrome can also be accumulated. That is, it becomes possible to determine the active period or remission of pathology, determine a therapeutic effect and a drug efficacy evaluation, and predict pathology.

Application of Diagnostic Drug

[0137] In addition, when the results shown in FIG. 18 are also taken into consideration, the chitin-chitosan can also be used as an evaluation drug for a food and drink.

[0138] That is, by: allowing a test subject to eat and drink a single or a plurality of specific foods and drinks; allowing the test subject to orally ingest an evaluation drug containing the chitin-chitosan as a main component during the eating and drinking, or before or after the eating and drinking; and measuring a concentration of the chitin-chitosan in blood after a lapse of a predetermined period of time from the oral ingestion, it is possible to determine whether the foods and drinks affect permeability of intestinal mucosa of the test subject.

[0139] In the case of LGS, it can be determined whether LGS is induced or LGS is inhibited. The evaluation drug may be orally ingested before the eating and drinking, during the eating and drinking, or after the eating and drinking as appropriate in accordance with, for example, the kind of the food and drink.

[0140] Through the use of the evaluation drug, not only screening of a general inducer or inhibitor can be performed, but also screening of an inducer or inhibitor for an individual can be performed. That is, a risk factor for an individual can be identified.

[0141] For example, a test subject is allowed to first take the evaluation drug, and then eat meat while drinking beer . Concurrently, blood is collected every 10 minutes, and thereby, a temporal transition of LGS can be monitored. As a result, when that combination of food and drink causes the onset of medium-degree LGS in about 20 minutes for that person, the person can be advised to avoid such combination.

[0142] Further, through the use of the food and drink evaluation drug, there can be provided, for example, an objective performance index for a food touted as a conditioner for gut flora or an intestinal environment, i.e., a probiotic food. Moreover, a prebiotic food can also be evaluated.

[0143] A diagnostic device having applied thereto the technology described above can also be constructed.

[0144] That is, a diagnostic device can be obtained by including: concentration-measuring means for measuring a concentration of chitin and/or chitosan in blood collected from a test subject; and evaluation means for evaluating permeability of intestinal mucosa of the test subject on the basis of the concentration measured by the concentration-measuring means.

[0145] As a component technology of the concentration-measuring means, for example, chromatography may be used. A process from sample introduction to concentration calculation may be automated as appropriate through the use of a general technology.

[0146] The evaluation means maybe configured to, for example, determine the degree of leakiness through analysis of the position and height of a peak in an obtained chromatogram, the calculation of a peak area, and the like. Not only a mere determination as severe LGS or mild LGS, but also such a diagnosis as the following can be made on the basis of the distribution and unevenness of peaks in consideration of past data as well: being predisposed to constantly having mild LGS though not predisposed to having medium-degree LGS or severe LGS; predisposed to having medium-degree LGS by taking exercise; or having an intestinal disease other than LGS.

[0147] Besides, a specific detection antibody maybe generated, and an ELISA kit using the antibody may be adopted. With this, a large number of samples can be evaluated at once.

[0148] The blood used for measurement and diagnosis is disposed of without being returned to a human body.

INDUSTRIAL APPLICABILITY

[0149] According to the present invention, an objective index and diagnosis system for LGS can be constructed. In addition, involvement of LGS in various diseases can be explored. For example, its relationship with chronic renal disorder, bronchitic asthma, type I diabetes, food allergy, alcoholic hepatitis, nonalcoholic steatohepatitis, or the like can be investigated. A contribution can also be made to the development of a therapeutic drug for an intestinal disease.