Fluoroquinolones

被引:66
作者
O'Donnell, JA
Gelone, SP
机构
[1] Med Coll Penn & Hahnemann Univ, Sch Med, Dept Med, Div Infect Dis, Philadelphia, PA USA
[2] Temple Univ, Sch Pharm, Dept Pharm Practice, Philadelphia, PA 19122 USA
[3] Temple Univ, Sch Pharm, Infect Dis Sect, Philadelphia, PA 19122 USA
[4] Temple Univ, Sch Med, Infect Dis Sect, Philadelphia, PA 19122 USA
[5] Temple Univ, Sch Med, Dept Pharm Practice, Philadelphia, PA 19122 USA
关键词
D O I
10.1016/S0891-5520(05)70260-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The era of quinolone antibiotics began with the serendipitous discovery of the prototype quinolone antibiotic, nalidixic acid, during the synthesis of the antimalarial agent, chloroquine, in the early 1960s.(50) Nalidixic acid never became a useful agent to treat systemic infections because of its narrow antibacterial spectrum, poor tissue penetrability, rapid emergence of bacterial resistance, and frequent adverse central nervous system (CNS) effects(72); however, nalidixic acid did provide the chemical foundation upon which to build the modifications that subsequently would improve therapeutic properties and limit adverse effects of the quinolones. To date more than 10,000 analogues of nalidixic acid have undergone an initial screening process. More than 20 years passed, however, before such an analogue, the first fluoroquinolone (FQ) antibiotic, was approved for clinical use. Over the last decade, the FQs have become a dominant class of antimicrobial agents. No other class of antimicrobial agents has grown so rapidly or been developed with such interest by pharmaceutical research companies. Through the 1990s and into the new millennium, this drug class will likely double in size, with several approvals currently before the Food and Drug Administration (FDA) in the United States. In the past 3 years, four new agents have been released into the US market, including levofloxacin, sparfloxacin, grepafloxacin, and trovafloxacin. Moxifloxacin and gatifloxacin are two additional FQs that have been recently approved for use. Clinafloxacin, gemafloxacin, and tosufloxacin are on the horizon. With the rapid expansion of the FQs comes the potential for confusion regarding appropriate use, tolerability, safety profiles, drug interactions, and dosing issues. This review provides an overview of the FQ class including mechanisms of action and emerging resistance, spectrum of activity, and pharmacology, paying particular attention to the newer agents. In addition, we provide a clinically relevant overview of use of these agents.
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页码:489 / +
页数:26
相关论文
共 98 条
[1]   Community-acquired pneumonia in adults: Guidelines for management [J].
Bartlett, JG ;
Breiman, RF ;
Mandell, LA ;
File, TM .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (04) :811-838
[2]  
*BAY PHARM, 1997, CIPR PROD INFOR
[3]   Alterations in topoisomerase IV and DNA gyrase in quinolone-resistant mutants of Mycoplasma hominis obtained in vitro [J].
Bébéar, CM ;
Renaudin, H ;
Charron, A ;
Bové, JM ;
Bébéar, C ;
Renaudin, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (09) :2304-2311
[4]   Effects on growth of single short courses of fluoroquinolones [J].
Bethell, DB ;
Hien, TT ;
Phi, LT ;
Day, NPJ ;
Vinh, H ;
Duong, NM ;
VanLen, N ;
VanChuong, L ;
White, NJ .
ARCHIVES OF DISEASE IN CHILDHOOD, 1996, 74 (01) :44-46
[5]   COMPARATIVE-STUDY WITH ENOXACIN AND NETILMICIN IN A PHARMACODYNAMIC MODEL TO DETERMINE IMPORTANCE OF RATIO OF ANTIBIOTIC PEAK CONCENTRATION TO MIC FOR BACTERICIDAL ACTIVITY AND EMERGENCE OF RESISTANCE [J].
BLASER, J ;
STONE, BB ;
GRONER, MC ;
ZINNER, SH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (07) :1054-1060
[6]  
Blondeau JM, 1999, CLIN THER, V21, P3
[7]  
BOEREMA JBJ, 1989, DRUG INVEST, V1, P18
[8]  
BRAND HS, 1990, CLIN EXP RHEUMATOL, V8, P393
[9]   Quinolone resistance locus nfxD of Escherichia coli is a mutant allele of the parE gene encoding a subunit of topoisomerase IV [J].
Breines, DM ;
Ouabdesselam, S ;
Ng, EY ;
Tankovic, J ;
Shah, S ;
Soussy, CJ ;
Hooper, DC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (01) :175-179
[10]   Prevalence of a putative efflux mechanism among fluoroquinolone-resistant clinical isolates of Streptococcus pneumoniae [J].
Brenwald, NP ;
Gill, MJ ;
Wise, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (08) :2032-2035