Patent Application
20060142243
The present invention relates to the use of N-acetyl-D-glucosamine in the manufacture of a medicament for treating urogenital tract infection.
2. Background Art
Urogenital tract infection is a common disease, which is chronic and refractory and greatly interferes a patient's normal life. At present, the main medicaments for treating urogenital tract infection mainly are broad spectrum antibiotics and Chinese lotion. However, the abuse of broad spectrum antibiotics results in drug resistance in microorganisms causing urogenital tract infection, so that the therapeutical effect became worse and worse although the dose of antibiotics increases gradually. On the other hand, the conventional treatment with antibiotics can hardly bring about better effect. For example, condyloma acuminatum virus can hardly be treated. In addition, the treatment of urogenital tract infection with Chinese lotion also has disadvantages, for main examples, unremarkable effect, inconvenient use, and contamination of clothing. Hence, a medicament for effectively treating urogenital tract infection is in need all the time.
In the research of “bio-waves” theory, the present inventor has set up a bacterial wave growth model. Through researching, it is known that this wave is of its intrinsic regulation mechanism: some chemical substances are able to participate the regulation in the bio-wave process, so as to transform an abnormal periodic slow wave into a normal physiological chaotic quick wave, and this kind of substances are known as promoting wave factors. Through separating, purifying and identifying, it is determined that one of the factors is N-acetyl-D-glucosamine, the promoting wave function of which is shown in regulating the coupling oscillation of cellular membrane protein and sugar coating. Many biochemical and physiological process of human body need the participation of the promoting wave factors, and it would lead to an abnormal state, if this kind of promoting wave factors is lacked in the living body.
N-acetyl-D-glucosamine is a chemical reagent. From the 1990's, it is continually used to treat diseases such as pericementitis (WO9102530A1), intestinal inflammation (WO9953929A1), cornea disease (JP10287570A2), hypertrophy of the prostate (US05116615), organic pathologic changes of lower digestive tract mucous membrane (WO93/14765), etc., as tissue growth regulation agent (WO/8702244), and in cosmetology (JP59013708A2), shampoo preparation (JP2011505A2), etc., but is has not been used in the manufacture of a medicament for treating urogenital tract infection.
The present invention surprisingly discovers that N-acetyl-D-glucosamine can be used to effective treat urogenital tract infection. This discovery is surprising because the heal of urogenital tract infection needs to control microorganism infection, to treat topical exudation, to eliminate tissue inflammatory edema and pains, to promote tissue repair, and so on, and a doctor usually provides a combination of several medicaments, while N-acetyl-D-glucosamine could be used as the only active Ingredient in a medicament for healing urogenital tract infection.
Based on the above discovery, the present application relates to the use of N-acetyl-D-glucosamine and pharmaceutical acceptable salt thereof in the manufacture of a medicament for treating urogenital tract infection.
On the other hand, the present invention relates to a method for treating urogenital tract infection, comprising administrating to a patient in need of this treatment an effective amount of N-acetyl-D-glucosamine or a pharmaceutical acceptable salt thereof.
N-acetyl-D-glucosamine is a compound of the following formula.
N-acetyl-D-glucosamine is commercially available from market or prepared according to a known method. For instance, WO97/31121 discloses a method for preparing N-acetyl-D-glucosamine from chitin by enzyme method. JP63273493 has discloses a method comprising partially hydrolyzing chitin to obtain N-acetyl-chitose, and then treating it with an enzyme to obtain N-acetyl-D-glucosamine.
The pharmaceutical acceptable salts of N-acetyl-D-glucosamine that can be mentioned are the salts formed with pharmaceutical acceptable acids, for instance, the salts formed with inorganic acids such as hydrochloride, hydrobromide, borate, phosphate, sulfate, hydrosulfate and hydrophosphate, and the salts formed with organic acids, such as citrate, benzoate, ascorbate, methyl sulfate, naphthalene-2-sulfonate, picrate, fumarate, maleate, malonate, oxalate, succinate, acetate, tartrate, mesylate, tosylate, isethionate, α-ketoglutarate, α-glyceryl phosphate and glucose-1-phosphate.
The compound of the formula (I) or its pharmaceutically acceptable salt is used as main active component in combination with several pharmaceutically acceptable excipients and/or carriers to prepare a topical formulation form such as aqua, emulsion, cream, lotion, ointment, suppository, etc. for treatment of urogenital tract infection. The amount of the active component is 0.1 to 10%, preferably 0.2 to 6% relative to the whole formulation. The daily dose of said medicament is 10 to 10000 mg, preferably 50 to 5000 mg, more preferably 100 to 2000 mg of N-acetyl-D-glucosamine per person.
The composition of the present invention in form of topical formulation, such as solution, emulsion, suspension, viscoloid, cream, ointment, etc. for topically daubing or washing, can be prepared by mixing the active component with one or more pharmaceutically acceptable carriers and additives, such as water, polyethylene glycol, glycerin, Vaseline, xanthan gum, alcohols, etc. as dissolving agent, lubricant, binder, preservative, stabilizer, and in combination with an ecological regulator such as lactic acid according to general techniques as well known by the person skilled in the art. In addition, a propellant can be added to said formulation to prepare an aerosol for topically spraying. For example, an aerosol has a formulation comprising 1% N-acetyl-D-glucosamine, 3% lactic acid and 0.3% sodium benzoate.
Unrestricted to any theory, the inventor deems the effect of the compound of formula (I) of the present invention for treatment of urogenital tract infection is achieved by adjusting the redistribution of body cells. “Cell redistribution” means the continue position alternation of body tissue cells or microorganism cells and the rhythmic alternation of coagulation-dissolution state of biological macromolecules in cells. N-acetyl-D-glucosamine brings about a special function by regulating cell redistribution in different levels. The alternation of macroscopic cell position represents the feature of the cell growth in wave manner. N-acetyl-D-glucosamine regulates the growth of body cells and microorganism cells in normal wave manner, so that microorganisms cannot be topically transplanted. As for microecological function, the normal bacteria growth is supported, and the supplement of ecological bacteria is not employed, so that the disadvantage of adaptability of the supplementary bacteria is avoided. In terms of promoting repair of skin and mucous membrane tissues, the product of the present invention exhibits unique effects for controlling inflammation, damage infection, and exudation. Thus, the product of the present invention can be widely used for controlling conditions and for essential treatment.
The following experimental examples are used to illustrate the promoting wave function, low toxicity, activity for suppressing microorganism transplantation, and clinical effect for treatment of urogenital tract infection.
1. Promoting Wave Test of the Compound of Formula (I)
1. Experimental Materials and Method:
1.1 Samples: Pure Compound of Formula (I)
1.2 Experimental Materials:
Culture medium: modified LB culture medium (the components of said medium are: 1% trytones, 0.5% yeast extract, 1% sodium chloride, 0.1% glucose, 0.002% TTC, and pH=7.2 to 7.4).
1.3 Experimental Method:
The Proteus Mirabilis were inoculated at the center of LB plate incubating at 37° C. for 9 hours, then there were concentric rings emerged, which were extended outward continually with an interval of 3 hours, and this was taken as a control; adding the compound of formula (I) with final concentration of 0.5% onto the LB plate, the Proteus Mirabilis were inoculated by the same method, cultured at 37° C., and the result showed that not only the concentric rings formed with an interval of 3 hours were emerged, comparing with the control, it can be seen that there were also many fine waves on each ring emeraged.
The liquid culture results showed that the compound of formula (I) could promote the growth of lactobacillus.
2. Experimental Results and Evaluation:
The experiment adopts a bio-wave model which is used to research the promoting wave function of the compound of formula (1). It can be seen from the result that the compound of formula (I) was not only able to cause bacterial cell to reveal a normal bio-wave characteristic, but also cause the wave reveal finer wave mode, and these indicated that the compound of formula (I) have promoting function to bio-waves, and the promoting wave function is able to participate the repair and redistribution of skin cells.
II. Toxicological Test of the Compound of Formula (I), Including:
1. Acute toxicity test: including tests of oral administration, intravenous injection administration, and maximum limit amount for administration.
2. Ames test:
3. Micronucleus test of mouse bone marrow cell;
4. Abnormality test of mouse sperm;
5. Aberration test of mouse testis chromosome;
6. Chronic lethal test;
7. Subchronic toxicity (feed for 90 days) test;
8. Traditional deformity-inducing test.
The results from these tests showed that in the acute toxicity test of the compound of formula (I), the dosage more that 2 g/kg was taken, which was 300 times than the injection dosage for human being, but the acute toxicosis reaction had not appeared yet; in the long-period toxicity test, the maximum dosage had reached up to 1 g/kg, and after the treatment and observation for four weeks, there was no intoxication reaction yet; and in the reproduction test, the mouse was feed from routine dosage of 7 mg/kg for 3 generations, it had been proved that the compound of formula (I) had no influence on the pregnancy, birth, nurse and the growth of baby mouse, so that the compound of formula (I) is a substance without toxicity.
III. Tests of Effect for Suppressing Bacterial Transplantation
1. Test of effect for suppressing bacillus pyocyaneus transplantation on skin
2. Test of suppressing bacteria
The results of these two tests indicated that the compound of formula (I) essentially exhibited no bactericidal or bacteriostasis effect, but it suppressed the transplantation and growth of bacillus pyocyaneus so as to achieve the object of anti-infection.
IV. Clinic Tests
1. 170 patients suffering various venereal diseases were picked out, including 50 patients suffering gonorrhea, 50 patients suffering syphilis, 20 patients suffering condyloma acuminatum virus infection, 40 patients suffering trichomonas vaginalis infection, and 10 patients suffering candida albicans. 2% N-acetyl-D-glucosamine aerosol was topically sprayed to infected areas, and the effects of the compound of formula (I) for treatment of urogenital tract infections were determined by smearing and microscopic examination, and by isolation and culture. The results showed that the effective rate of N-acetyl-D-glucosamine for treatment of various urogenital tract infections is 79% as depicted in the following table.
Observation of therapeutical effect of N-acetyl-D-glucosamine for treatment of urogenital tract infections
The present invention pioneers a novel medial use of N-acetyl-D-glucosamine, extends the application range of N-acetyl-D-glucosamine, and increases the use value of N-acetyl-D-glucosamine. The external formulations in various forms prepared with N-acetyl-D-glucosamine as active component are used as medicament for prevention and treatment of urogenital tract infections, and exhibit advantages of easy preparation and no toxic and side effect. Since it is a colorless, insipid and nonirritant substance, and has a novel action route, its use exhibits unique therapeutical effect and avoids disadvantages of other products.
| Number | Date | Country | Kind |
|---|---|---|---|
| 01215486.9 | Aug 2002 | CN | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/CN03/00664 | 8/13/2003 | WO | 10/11/2005 |
