Azithromycin.

Q1 Pharmacology, Toxicology and Pharmaceutics Profiles of drug substances, excipients, and related methodology Pub Date : 2014-01-01 DOI:10.1016/B978-0-12-800173-8.00001-5
Ahmed H H Bakheit, Badraddin M H Al-Hadiya, Ahmed A Abd-Elgalil
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引用次数: 42

Abstract

Azithromycin is an azalide, a subclass of macrolide antibiotics. It is derived from erythromycin, with a methyl-substituted nitrogen atom incorporated into the lactone ring, thus making the lactone ring 15-membered. It prevents bacteria from growing by interfering with their protein synthesis. It binds to the 50S subunit of the bacterial ribosome and thus inhibits translation of mRNA. Azithromycin is used to treat or prevent certain bacterial infections, most often those causing middle ear infections, strep throat, pneumonia, typhoid, bronchitis, and sinusitis. In recent years, it has been used primarily to prevent bacterial infections in infants and those with weaker immune systems. It is also effective against certain sexually transmitted infections, such as nongonococcal urethritis, chlamydia, and cervicitis. Recent studies have indicated it also to be effective against late-onset asthma, but these findings are controversial and not widely accepted. The present study gives a comprehensive profile of azithromycin, including detailed physico-chemical properties, nomenclature, formulae, methods of preparation, and methods of analysis (including compendial, electrochemical, spectroscopic, and chromatographic methods of analysis). Developed validated stability-indicating (HPLC and biodiffusion assay methods under accelerated acidic, alkaline, and oxidative conditions, in addition to effect of different types of light, temperature, and pH. Detailed clinical applications also presented (mechanism of action, ADME profile, clinical uses and doses, side effects, and drug interactions). Each of the above stages includes appropriate figures and tables. More than 80 references were given as a proof of the above-mentioned studies.

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阿奇霉素。
阿奇霉素是一种杜鹃花类抗生素,是大环内酯类抗生素的一个亚类。它来源于红霉素,在内酯环中加入了一个甲基取代的氮原子,使内酯环成为15元。它通过干扰细菌的蛋白质合成来阻止细菌的生长。它与细菌核糖体的50S亚基结合,从而抑制mRNA的翻译。阿奇霉素用于治疗或预防某些细菌感染,最常引起中耳感染、链球菌性咽喉炎、肺炎、伤寒、支气管炎和鼻窦炎。近年来,它主要用于预防婴儿和免疫系统较弱的人的细菌感染。它对某些性传播感染也有效,如非淋球菌性尿道炎、衣原体和宫颈炎。最近的研究表明,它对迟发性哮喘也有效,但这些发现存在争议,没有被广泛接受。本研究全面介绍了阿奇霉素,包括详细的物理化学性质、命名、配方、制备方法和分析方法(包括药典、电化学、光谱和色谱分析方法)。除了不同类型的光、温度和ph值的影响外,还开发了经过验证的稳定性指示(HPLC和生物扩散测定)方法,并详细介绍了临床应用(作用机制、ADME概况、临床使用和剂量、副作用和药物相互作用)。以上每一个阶段都包括适当的图表。本文给出了80多篇文献作为上述研究的佐证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Profiles of drug substances, excipients, and related methodology
Profiles of drug substances, excipients, and related methodology Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
13.10
自引率
0.00%
发文量
4
期刊最新文献
Avanafil: A comprehensive drug profile. Deferasirox: A comprehensive drug profile. Duvelisib: A comprehensive profile. Ponatinib: A comprehensive drug profile. Regorafenib: A comprehensive drug profile.
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