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논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2015.6
- 수록면
- 67 - 78 (12page)
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Glycopeptides of the clinically important antibiotic drugs are glycosylated cyclic or polycyclic nonribosomal peptides. Glycopeptides such as vancomycin and teicoplanin are often used for the treatment of gram-positive bacteria in patients. The increased incidence of drug resistance and inadequacy of these therapeutics against gram-positive bacterial infections would be the formation and clinical development of more variable second generation of glycopeptide antibiotics: semisynthetic lipoglycopeptide analogs such as telavancin, dalbavancin, and oritavancin with improved activity and better pharmacokinetic properties. In this review, we describe the development of and bacterial resistance to vancomycin, teicoplanin, and semisynthetic glycopeptides (teicoplanin, dalbavancin, and oritavancin). The clinical influence of resistance to glycopeptides, particularly vancomycin, are also discussed.
목차
INTRODUCTION
CHEMICAL STRUCTURE OF NATURAL GLYCOPEPTIDES
SEMISYNTHETIC GLYCOPEPTIDES
THE MECHANISM OF ACTION
MECHANISMS OF BACTERIAL RESISTANCE
CONCLUSION
REFERENCES
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UCI(KEPA) : I410-ECN-0101-2016-475-001637105