PHARMACOKINETICS OF INH AND PZA IN MDR-TB: A REVIEW

S. Ramya, S. Shanmugam
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Abstract

Tuberculosis remains a leading cause of morbidity and mortality in developing countries, including india. Isoniazid and pyrazinamide are powerful drugs administered as the First line and second line Anti-TB drugs in Tuberculosis affected patient. It plays a key role in shortening the TB therapy. Isoniazid (INH), and pyrazinamide (PZA) are the main drugs for the treatment of tuberculosis (TB). Mycobacterium tuberculosis is responsible for causing tuberculosis can acquire multiple drug resistance (MDR) by not responding to the most powerful anti-TB agents. The complications of drug resistance in TB elevates the some of the risk factors like inadequate treatment compliance, noncompliance of the patients to the treatment. Pharmacokinetics provides a basic time course of drugs and their effects in the body. These pharmacokinetic processes referred to as ADME. Key words Isoniazid, Pyrazinamide, MDR, ADME, TB
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inh和pza在耐多药结核病中的药代动力学研究进展
结核病仍然是包括印度在内的发展中国家发病和死亡的主要原因。异烟肼和吡嗪酰胺是结核病患者一线和二线抗结核药物。它在缩短结核病治疗时间方面起着关键作用。异烟肼(INH)和吡嗪酰胺(PZA)是治疗结核病(TB)的主要药物。导致结核病的结核分枝杆菌可因对最有效的抗结核药物无反应而获得多重耐药性(MDR)。结核病耐药并发症增加了一些风险因素,如治疗依从性不足,患者不遵守治疗。药代动力学提供了药物及其在体内作用的基本时间过程。这些药代动力学过程称为ADME。关键词异烟肼,吡嗪酰胺,耐多药,ADME, TB
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