CN1602872A - Antituberculosis pharmaceutical composition - Google Patents

Antituberculosis pharmaceutical composition Download PDF

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Publication number
CN1602872A
CN1602872A CN 03151413 CN03151413A CN1602872A CN 1602872 A CN1602872 A CN 1602872A CN 03151413 CN03151413 CN 03151413 CN 03151413 A CN03151413 A CN 03151413A CN 1602872 A CN1602872 A CN 1602872A
Authority
CN
China
Prior art keywords
drug
pyrazinamide
agent compositions
tablet
antitubercular agent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN 03151413
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Chinese (zh)
Inventor
谢元德
陈春
马越峰
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ZHEJING KELISI'AN PHARMACEUTICAL CO Ltd
Original Assignee
ZHEJING KELISI'AN PHARMACEUTICAL CO Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by ZHEJING KELISI'AN PHARMACEUTICAL CO Ltd filed Critical ZHEJING KELISI'AN PHARMACEUTICAL CO Ltd
Priority to CN 03151413 priority Critical patent/CN1602872A/en
Publication of CN1602872A publication Critical patent/CN1602872A/en
Pending legal-status Critical Current

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  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The invention relates to an antituberculosis drug combination, prepared of rifampicin, isonicotinyl hydrazine, pyrazinamide, ethambutol hydrochloride and other auxiliaries, able to effectively overcome problems of drug resistance, improving compliance of patient, etc. It is applied in a compound form, which can avoid curing by single antituberculosis drug, thus avoiding selective drug resistance caused by single drug; the patients are willing to accept this, avoiding irregular drug application caused by simultaneously taking several drugs and different numbers of drug tablets, or taking more or less drugs.

Description

A kind of antitubercular agent compositions
Technical field
The present invention relates to a kind of pharmaceutical composition, relate in particular to a kind of antitubercular agent compositions.
Background technology
Tuberculosis is a kind of chronic infectious disease, and it has been played vaccine and also can't guarantee to get anything but tuberculosis unlike variola or poliomyelitis.The data introduction is arranged, and in recent years, because people loosen tuberculosis vigilance, poverty and recurrent population roll up, and the appearance of Resistant strain, acquired immune deficiency syndrome (AIDS), and big rise has all appearred in tuberculosis all over the world.World Health Organization's report, tuberculosis remain the first killer of infectious disease, and the whole world has the people of 1/3 (about 2,000,000,000) to infect tulase approximately, and in existing 2,000 ten thousand tuberculosis patients, 95% in developing country.About 9,000,000 patients of the new appearance in the annual whole world, wherein 75% patient age was at 15~50 years old.As not controlling, also will there be 9,000 ten thousand people to fall ill in 10 years from now on.Serious day by day multiple drug resistance case increases, and will threaten tuberculosis to get back to the age of " incurable disease " again.As not taking strong measure immediately, the even more serious popular and threat of tuberculosis will be caused.China remains one of 22 the heaviest countries of the burden of tuberculosis in the world, the whole nation infected number about 400,000,000, the number of hectic reaches more than 600 ten thousand, wherein the infectiousness consumptive more than 200 ten thousand, annual because of the dead number of tuberculosis reaches 250,000 people, be 2 times of all kinds of infectious disease death toll summations.Tuberculosis Epidemiological study result shows, except that teenager tuberculosis morbidity height, the old people in 60-70 year also is onset peak.Its reason one is old people's immunologic function degression, and the old people merges the resume combustion that pulmonary and systemic disease can cause conceal type or old focus in addition.The 2nd, present old people, in adolescence tuberculosis the most rampant popular age on China's history just, the overwhelming majority was subjected to the infection of tuberculosis, but not morbidity.When entering old age, body's immunity descends, and makes the tuberculosis recurrence; Fall ill when also some old tuberculosis is teenager, be subjected at that time that historical conditions limits, do not obtain regular treatment timely, to old recurrence.The 3rd, aged tendency of population, the aging population ratio increases, and old tuberculosis constituent ratio is increased.
Be used for the single medicine that mostly is lungy at present, antiphthisic treatment time is long, and not only the pulmonary tuberculosis bacterium can not kill, and also can produce Resistant strain; And during conventional therapy, patient must take corrected and antitubercular agent capacity, causes that easily the light patient of body weight causes side effect because of high dose, and the high patient of body weight is difficult for obtaining ideal treatment.In addition, because the medication amount of taking simultaneously is more, patient's compliance is bad, easily causes wrong clothes, misses etc. to be unfavorable for the behavior for the treatment of.Medicine can be avoided single antitubercular agent treatment with the form administration of compound recipe, thus the selectivity drug resistance of avoiding single medicine to cause; Patient takes like a shot, and has avoided obeying multiple medications simultaneously and each tablet quantity does not wait the irregular medication that is caused, or the many clothes and the thing of taking medicine less; Simplify the storage management of medicine; Simplify therapeutic scheme, the direct face of being more convenient for is looked down short-course chemotherapy (DOTS) management of administration.
Therefore, develop a kind of novel antituberculosis drug to current treatment pulmonary tuberculosis with to overcome chemical sproof meaning very great.
Summary of the invention
The object of the present invention is to provide a kind ofly can effectively overcome drug resistance, improve patient's compliance, improve the antitubercular agent compositions of therapeutic effect.
A kind of antitubercular agent compositions of the present invention is the medicament of being made by Rimactazid, pyrazinamide, ebutol and other pharmaceutical adjunct; Pharmaceutical adjunct is a microcrystalline Cellulose, pregelatinized Starch, magnesium stearate, dextrin, lactose, micropowder silica gel, one or more mixing in the amylum pregelatinisatum; Said medicament is tablet or capsule; In tablet, contain rifampicin 50g~150g, isoniazid 30g~60g, pyrazinamide 100g~300g, ebutol 65g~150g in per 1000; Optimum content is to contain rifampicin 75g, isoniazid 37.5g, pyrazinamide 200g, ebutol 137.5g, microcrystalline Cellulose 50g, pregelatinized Starch 75g, magnesium stearate 1.5g in the tablet in per 1000; The present invention also provides the preparation method of this antituberculotics tablet, takes by weighing rifampicin, ebutol, isoniazid, pyrazinamide, microcrystalline Cellulose and pregelatinized Starch, magnesium stearate by prescription, and mixing is with 12mm punch die tabletting, promptly.
Antituberculotics of the present invention can be avoided single antitubercular agent treatment with the form administration of compound recipe, thus the selectivity drug resistance of avoiding single medicine to cause; Patient takes like a shot, and has avoided obeying multiple medications simultaneously and each tablet quantity does not wait the irregular medication that is caused, or the many clothes and the thing of taking medicine less.
The specific embodiment
Embodiment: the preparation of the tablet of the present composition
Prescription:
Rifampicin 75.0g
Ebutol 137.5g
Isoniazid 37.5g
Pyrazinamide 200.0g
Microcrystalline Cellulose 50g
Pregelatinized Starch 70g
Magnesium stearate 1.5g
Make 1000
Take by weighing rifampicin, ebutol, isoniazid, pyrazinamide, microcrystalline Cellulose and pregelatinized Starch, magnesium stearate by prescription, mixing with 12mm punch die tabletting, makes tablet, can also wrap film-coat, obtains Film coated tablets.

Claims (6)

1, a kind of antitubercular agent compositions is characterized in that the medicament of being made by Rimactazid, pyrazinamide, ebutol and other pharmaceutical adjunct.
2, a kind of antitubercular agent compositions according to claim 1 is characterized in that other pharmaceutical adjunct is a microcrystalline Cellulose, pregelatinized Starch, magnesium stearate, dextrin, lactose, micropowder silica gel, one or more mixing in the amylum pregelatinisatum.
3, a kind of antitubercular agent compositions according to claim 1 is characterized in that said medicament is tablet or capsule.
4, a kind of antitubercular agent compositions according to claim 3 is characterized in that containing in per 1000 in the tablet rifampicin 50g~150g, isoniazid 30g~60g, pyrazinamide 100g~300g, ebutol 65g~150g.
5,, it is characterized in that containing rifampicin 75g, isoniazid 37.5g, pyrazinamide 200g, ebutol 137.5g, microcrystalline Cellulose 50g, pregelatinized Starch 75g, magnesium stearate 1.5g in per 1000 of the tablet according to claim 3 or 4 described a kind of antitubercular agent compositions.
6, according to the preparation method of the tablet of claim 3,4 or 5 described a kind of antitubercular agent compositions, it is characterized in that taking by weighing rifampicin, ebutol, isoniazid, pyrazinamide, microcrystalline Cellulose and pregelatinized Starch, magnesium stearate by prescription, mixing, with 12mm punch die tabletting, promptly.
CN 03151413 2003-09-29 2003-09-29 Antituberculosis pharmaceutical composition Pending CN1602872A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 03151413 CN1602872A (en) 2003-09-29 2003-09-29 Antituberculosis pharmaceutical composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 03151413 CN1602872A (en) 2003-09-29 2003-09-29 Antituberculosis pharmaceutical composition

Publications (1)

Publication Number Publication Date
CN1602872A true CN1602872A (en) 2005-04-06

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN 03151413 Pending CN1602872A (en) 2003-09-29 2003-09-29 Antituberculosis pharmaceutical composition

Country Status (1)

Country Link
CN (1) CN1602872A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010009572A1 (en) * 2008-07-23 2010-01-28 国防教育研究基金会 New low side effect pharmaceutical composition containing isoniazid
CN102106855A (en) * 2009-12-24 2011-06-29 杭州赛利药物研究所有限公司 Pharmaceutical preparation for resisting tuberculosis and preparation method thereof
WO2012139485A1 (en) * 2011-04-12 2012-10-18 浙江海正药业股份有限公司 Oral solid preparation of compound antituberculosis drug and preparation method thereof
CN104274456A (en) * 2013-07-02 2015-01-14 安徽贝克生物制药有限公司 Quadrigeminal compound preparation of anti-tuberculosis medicines and preparation method thereof
CN104418864A (en) * 2013-08-30 2015-03-18 西南大学 Conjugates of dihydroartemisinin and quinolones compounds as well as preparation method and application thereof
CN108186638A (en) * 2018-03-08 2018-06-22 重庆华邦制药有限公司 The pharmaceutical composition of isoniazid

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010009572A1 (en) * 2008-07-23 2010-01-28 国防教育研究基金会 New low side effect pharmaceutical composition containing isoniazid
CN102137671A (en) * 2008-07-23 2011-07-27 国防教育研究基金会 New low side effect pharmaceutical composition containing isoniazid
CN102137671B (en) * 2008-07-23 2012-10-17 国防教育研究基金会 New low side effect pharmaceutical composition containing isoniazid
CN102106855A (en) * 2009-12-24 2011-06-29 杭州赛利药物研究所有限公司 Pharmaceutical preparation for resisting tuberculosis and preparation method thereof
CN102106855B (en) * 2009-12-24 2014-04-09 杭州赛利药物研究所有限公司 Pharmaceutical preparation for resisting tuberculosis and preparation method thereof
WO2012139485A1 (en) * 2011-04-12 2012-10-18 浙江海正药业股份有限公司 Oral solid preparation of compound antituberculosis drug and preparation method thereof
RU2605388C2 (en) * 2011-04-12 2016-12-20 Чжэцзян Хисун Фармасьютикал Ко., Лтд. Oral solid preparation of compound antituberculosis drug and preparation method thereof
US9555003B2 (en) 2011-04-12 2017-01-31 Zhejiang Hisun Pharmaceutical Co., Ltd. Oral solid formulation of compound anti-tubercular drug and preparation method thereof
CN104274456A (en) * 2013-07-02 2015-01-14 安徽贝克生物制药有限公司 Quadrigeminal compound preparation of anti-tuberculosis medicines and preparation method thereof
CN104418864A (en) * 2013-08-30 2015-03-18 西南大学 Conjugates of dihydroartemisinin and quinolones compounds as well as preparation method and application thereof
CN104418864B (en) * 2013-08-30 2016-06-08 西南大学 Conjugate of dihydroarteannuin and carbostyril compound and its preparation method and application
CN108186638A (en) * 2018-03-08 2018-06-22 重庆华邦制药有限公司 The pharmaceutical composition of isoniazid

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