Use of thiamphenicol and derivatives thereof for the preparation of pharmaceutical compositions useful in the treatment of chlamydia pneumoniae infections

Abstract

Use of thiamphenicol and derivatives thereof for the preparation of pharmaceutical compositions useful for the treatment Chlamydia pneumoniae infections is described.

Description

[0001] The present invention relates to the use of thiamphenicol and derivatives thereof for the preparation of pharmaceutical compositions useful in the treatment of Chlamydia pneumoniae infections.

[0002] Chlamydia pneumoniae is an intracellular bacterium recently considered responsible of respiratory infections both of the upper tract and the lower tract.

[0003] This bacterium is one of the most widespread human pathogens and primary infections in children from 5 to 14 years have been supported by documentary evidence. In children the infection is generally mild and asymptomatic, but can be more serious in adult and elderly. Chlamydia pneumoniae is responsible for about 10% of cases of atypical pneumonia and of 5% of cases of bronchitis. It has also been associated with respiratory airways diseases and with new onset asthma and asthmatic bronchitis in the adults. Sinusitis caused by Chlamydia pneumoniae also associated with infections of the lower respiratory tract has been described and, moreover, Chlamydia pneumoniae has been isolated from middle ear fluids of patients with otitis media.

[0004] For a survey of the pathologies associated to Chlamydia pneumoniae infections see F. Blasi, Clinical Microbiology and Infections, vol. 1, Suppl. 1, March 1996, S14-S18.

[0005] Among the antibiotics more commonly used in therapy, azithromycin and, in particular, clarithromycin resulted active in vitro against Chlamydia pneumoniae and others agents involved in these infections and therefore they are potential therapeutical agents in the treatment of Chlamydia pneumoniae infections.

[0006] Some quinolonic antibiotics too, offer a potential therapy for Chlamydia pneumoniae infections.

[0007] In the cases of Chlamydia pneumoniae infection the antibiotic treatment can require a long period and cases of Chlamydia pneumoniae chronic persistent infections in which the antibiotic therapy has failed have already been reported.

[0008] The restricted number of antibiotics useful in the treatment of Chlamydia pneumoniae infections and the increasing importance that these infections are assuming from a clinical point of view, make necessary the identifying of antibiotics active against Chlamydia pneumoniae. Thiamphenicol (The Merck Index, XII ed., No. 9436, page 1587) is a known antibiotic used for the treatment of Gram-positive and Gram-negative bacterial infection. In the treatment of respiratory pathologies thiamphenicol is often used as glycinate hydrochloride or acetylcysteinate, i.e. an ester of thiamphenicol salified with hydrochloric acid or with acetylcysteine respectively.

[0009] To our knowledge no data concerning the activity of thiamphenicol or derivatives thereof versus Chlamydia pneumoniae is reported in the literature. It is known instead that thiamphenicol is active against Chlamydia trachomatis, a pathogen responsible of urogenital apparatus infections, but its activity is markedly lower than that of other antibiotics, such as for example erythromycin [G. Ridgeway et al., J. Antimicrob. Chemother. (1979), 5(4), 483-4]. We have now found that thiamphenicol is particularly effective in the treatment of infections caused by Chlamydia pneumoniae.

[0010] It is therefore an object of the present invention the use of thiamphenicol and derivatives thereof for the preparation of a pharmaceutical compositions useful in the treatment of Chlamydia pneumoniae infections.

[0011] The pharmaceutical compositions useful in the present invention are compositions for enteral or parenteral use containing thiamphenicol or derivatives thereof such as, for example, thiamphenicol glycinate and salts thereof.

[0012] Particularly preferred is the use of thiamphenicol glycinate acetylcysteinate.

[0013] Also preferred is the use of thiamphenicol glycinate hydrochloride.

[0014] The amount of active ingredient, expressed as thiamphenicol, contained in the pharmaceutical composition may change depending on the administration way and on the seriousness of the infection but is generally comprised between 250 mg and 5000 mg per dose, more preferably between 500 mg and 2000 mg.

[0015] The pharmaceutical compositions can be in a solid or liquid form, suitable for administering by injectable, oral or aerosol route.

[0016] Preferred are the pharmaceutical compositions suitable for administering by aerosol or injectable route.

[0017] More preferred are the pharmaceutical compositions suitable for administering by aerosol or injectable route containing thiamphenicol glycinate hydrochloride or acetylcysteinate.

[0018] Particularly suitable are the pharmaceutical compositions already on the market with the trademark FLUIMUCIL ANTIBIOTICO® and GLITISOL®.

[0019] The thiamphenicol efficacy against strains of Chlamydia pneumoniae of recent clinical isolation has been demonstrated in vitro by calculating the MIC (Minimum Inhibitory Concentration) in comparison with other antibiotics. It is important to underline as thiamphenicol showed a MIC completely comparable, or better, with respect to that of reference antibiotics already used in therapy for the treatment of Chlamydia pneumoniae infections.

[0020] With the aim to better illustrate the present invention the following example is now given.

MATERIAL AND METHODS

[0021] Chlamydia pneumoniae Strains

[0022] Chlamydia pneumoniae TW183 and Chlamydia pneumoniae 2023 were obtained from American Type Culture Collection. The other strains (No. 9 isolated) were clinically isolated in the period 1997-1999.

[0023] Antibiotics

[0024] The following antibiotics were used: thiamphenicol glycinate acetylcysteinate (TGA), azithromycin, ciprofloxacin, ceftriaxone, amoxicillin, clarithromycin, doxycycline and tetracycline hydrochloride.

[0025] Cell Cultures

[0026] Monolayers of Hep-2 cells were prepared by seeding 2×105 cell/ml in EMEM with 10% fetal calf serum supplemented with L-glutammine, on 12 mm cover slips and left at 35° C., 5% CO2 for 24 to 48 hours for confluent growth. The growth medium was removed and Hep-2 monolayers were inoculated with the different strains at predetermined concentration calculated to give 3-5×102 inclusions for well.

[0027] The monolayers, inoculated with Chlamydia pneumoniae were centrifuged at 1700 g for 60 minutes at 30° C.

[0028] Supernatant was removed and was replaced with 2.0 ml of EMEM containing 2% fetal calf serum, L-glutammine, cycloheximide 1 μg/ml and different dilutions of the tested antibiotics.

[0029] In positive control no antibiotic was added and negative control were considered wells not inoculated with Chlamydia pneumoniae.

[0030] Cells were incubated at 35° C. in atmosphere additionated with 5% CO2, for 3 days, then the monolayers were fixed with acetone for 10 minutes at −20° C. and stained with a fluorescein-coniugated antibody specific for Chlamydia pneumoniae (Argene Biosoft) and observed under a fluorescence microscope.

[0031] All tests were run in duplicate. The number of inclusions were counted and the MIC (the lowest concentration at which complete inhibition of inclusion formation was observed) was determined.

[0032] Results

[0033] The activities of the tested antibiotics are shown in table 1.

TABLE 1
Antimicrobic activity in vitro against stains
of Chlamydia pneumoniae
ANTIBIOTIC     MIC (μg/ml)
Clarithromycin 0.03-0.25
Azithromycin   0.06-0.5
Amoxicillin    >16
Doxycycline    0.06-0.25
Ciprofloxacin  0.5-2
Ceftriaxone    >16
Tetracycline   0.06-0.5
TGA            0.03-0.25

[0034] Clarithromycin and thiamphenicol glycinate acetylcysteinate (TGA) are the most active antibiotics (MIC range 0.03 and 0.25 μg/ml for both).

[0035] In table 2 the MIC values per strain of each test are shown.

	TABLE 2
	Clarithromycin	azithromycin	Doxycycline	ciprofloxacin	Tetracycline	TGA
	I	II	I	II	I	II	I	II	I	II	I	II
strain	μg/ml	μg/ml	μg/ml	μg/ml	μg/ml	μg/ml
1	0.03	0.03	0.5	0.125	0.06	0.125	1	1	0.06	0.06	0.03	0.06
2	0.25	0.03	0.06	0.25	0.125	0.125	0.5	2	0.06	0.06	0.03	0.03
3	0.03	0.03	0.06	0.06	0.125	0.125	0.5	1	0.125	0.125	0.125	0.125
4	0.125	0.06	0.5	0.5	0.06	0.06	1	1	0.125	0.5	0.25	0.06
5	0.03	0.03	0.25	0.25	0.125	0.06	0.5	0.5	0.125	0.25	0.125	0.125
6	0.03	0.125	0.125	0.25	0.06	0.06	2	2	0.06	0.5	0.03	0.03
7	0.125	0.125	0.25	0.25	0.06	0.06	2	1	0.125	0.125	0.03	0.03
8	0.125	0.125	0.25	0.25	0.25	0.06	0.5	2	0.06	0.06	0.125	0.03
9	0.125	0.03	0.5	0.125	0.25	0.25	0.5	0.5	0.06	0.5	0.125	0.125
ATCC 2023	0.03	0.03	0.06	0.125	0.06	0.06	0.5	0.5	0.06	0.125	0.03	0.03
TW 183	0.03	0.125	0.125	0.25	0.125	0.25	0.5	1	0.06	0.06	0.06	0.03

[0036] All the values are under the break point (thiamphenicol≦16 μg/ml, clarithromycin≦2 μg/ml, amoxicillin≦2 μg/ml, doxycycline≦4 μg/ml, ciprofloxacin≦1 μg/ml, tetracycline≦2 μg/ml) except for azithromycin (≦1 μg/ml) and ceftriaxone (≦2 μg/ml).

[0037] Moreover thiamphenicol has shown the best value of the ratio between MIC (0.03-0.25 μg/ml) and break point (≦16 μg/ml) in comparison with the others antimicrobial compounds the break point values of which are lower than thiamphenicol.

Claims

1) Use of thiamphenicol and derivatives thereof for the preparation of a pharmaceutical composition useful for the treatment of Chlamydia pneumoniae infections.

2) Use according to claim 1 wherein thiamphenicol is used as thiamphenicol glycinate or salts thereof.

3) Use according to claim 2 wherein thiamphenicol is used as thiamphenicol glycinate acetylcysteinate.

4) Use according to claim 2 wherein thiamphenicol is used as thiamphenicol glycinate hydrochloride.

5) Use according to claim 1 wherein the pharmaceutical composition is suitable for aerosol and injectable administration.

6) Use according to claim 1 wherein the amount of thiamphenicol is comprised between 250 mg and 5000 mg.