Macrolides are the effective antibiotics in the treatment of MP infection.
大环内酯类抗生素是治疗MP感染的有效抗生素。
Therapeutic effects of macrolides antibiotic and adrenal cortex hormone are effective.
大环内酯类抗菌素和肾上腺皮质激素疗效效果。
Objective to investigate the macrolides resistant phenotype and genotype in Streptococcus pyogenes.
目的研究酿脓链球菌对大环内酯类抗菌药物的耐药表型与基因型。
Tetracyclines macrolides and quinolones are the effective antibiotics in the treatment of these diseases.
四环素类、大环内酯类、喹诺酮类抗生素是治疗解脲支原体感染的主要有效药物。
ABSTRACT Objective to investigate the macrolides resistant phenotype and genotype in Streptococcus pyogenes.
目的研究酿脓链球菌对大环内酯类抗菌药物的耐药表型与基因型。
Therefore, it has attracted extensive attention to develop new potent macrolides against resistant bacteria.
因此，开发新的抗耐药菌大环内酯抗生素已成为当前药物研究的热点。
OBJECTIVE: To investigate the in vitro activity of domestic roxithromycin and compare it with other macrolides.
目的：研究国产罗红霉素体外杭菌作用，并同大环内醋类其它杭生素进行比较。
It has been reported that many macrolides antibiotics may affect functions of neutrophil and induce its apoptosis.
研究证实，多种大环内酯类抗菌素能影响中性粒细胞的功能，并诱导其凋亡。
Anti-infectious agents like quinolones, macrolides, TCM with anti-infectious effect and biologicals & biochemicals, vitamins had grown.
喹诺酮类、 大环内酯类、抗感染中成药类抗感染药物以及生物制品与生化药物、维生素类药物均有增长；
METHODS: By collecting the literatures and making aggregate analysis of 8 representative drugs depending on the classifications of macrolides, quinolones and tetracyclines.
方法：查阅相关文献，按大环内酯类、喹诺酮类、四环素类分类对8种代表药物进行综合分析。
Conclusion: New generation of macrolides, azithromycin is a safe and effective antibacterial agent for the treatment of acute bacterial infections of lower respiratory tract.
结论：新一代大环内酯类抗生素阿奇霉素注射剂，治疗急性细菌性下呼吸道感染安全有效。
Results of all these 4 macrolides, the higher susceptibilities to gonococci were azithromycin and roxithromycin, in turn, the percentages of susceptibility were 100 %, 96. 04 %, respectively.
结果在测定的4种大环内酯类药物中，淋球菌对阿奇霉素敏感性最高，达100 %；其次为罗红霉素，为96。04 %。
The mechanism of macrolide's action indicates that the binding sites of macrolides are located inside the nascent peptide exit tunnel of the ribosomal 50S subunit near the peptidyl transferase center.
抗菌机制研究表明：大环内酯抗生素的作用靶点位于50S亚基肽通道的出口处，紧邻肽酰转移酶中心。
The mechanism of macrolide's action indicates that the binding sites of macrolides are located inside the nascent peptide exit tunnel of the ribosomal 50S subunit near the peptidyl transferase center.
抗菌机制研究表明：大环内酯抗生素的作用靶点位于50S亚基肽通道的出口处，紧邻肽酰转移酶中心。
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