Comprehensive Dermatologic Drug Therapy 2021
DOI: 10.1016/b978-0-323-61211-1.00009-7
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Systemic Antibacterial Agents

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Cited by 7 publications
(9 citation statements)
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“…Vancomycin is a broad-spectrum glycopeptide antibiotic that specifically binds Gram-positive bacteria, including staphylococci, streptococci, and most enterococci, through hydrogen bonds between its carbonyl and amine groups and the peptidoglycans found onto the cell wall [ 91 , 92 , 93 ]. The mechanisms of action mainly involve the inhibition of the cell wall synthesis by forming non-covalent complexes with the C-terminal L-Lys-D-Ala-D-Ala motif within the bacterial peptidoglycan precursors and the inhibition of RNA synthesis [ 92 , 93 , 94 ].…”
Section: Microbial Targeting Strategiesmentioning
confidence: 99%
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“…Vancomycin is a broad-spectrum glycopeptide antibiotic that specifically binds Gram-positive bacteria, including staphylococci, streptococci, and most enterococci, through hydrogen bonds between its carbonyl and amine groups and the peptidoglycans found onto the cell wall [ 91 , 92 , 93 ]. The mechanisms of action mainly involve the inhibition of the cell wall synthesis by forming non-covalent complexes with the C-terminal L-Lys-D-Ala-D-Ala motif within the bacterial peptidoglycan precursors and the inhibition of RNA synthesis [ 92 , 93 , 94 ].…”
Section: Microbial Targeting Strategiesmentioning
confidence: 99%
“…Vancomycin is a broad-spectrum glycopeptide antibiotic that specifically binds Gram-positive bacteria, including staphylococci, streptococci, and most enterococci, through hydrogen bonds between its carbonyl and amine groups and the peptidoglycans found onto the cell wall [ 91 , 92 , 93 ]. The mechanisms of action mainly involve the inhibition of the cell wall synthesis by forming non-covalent complexes with the C-terminal L-Lys-D-Ala-D-Ala motif within the bacterial peptidoglycan precursors and the inhibition of RNA synthesis [ 92 , 93 , 94 ]. While the administration of vancomycin has resulted in the development of vancomycin-resistant Staphylococcus aureus , vancomycin-intermediate Staphylococcus aureus , and vancomycin-resistant enterococci [ 92 ], its attachment onto the surface of nanoparticles has allowed for the capture of both Gram-positive and Gram-negative bacteria within complex samples, such as urine or blood [ 91 ].…”
Section: Microbial Targeting Strategiesmentioning
confidence: 99%
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“…It is highly lipophilic, allowing it to reach high drug concentrations in the skin and nail unit. 2 Patients taking minocycline long term and at high doses are at greatest risk for pigment deposition. 3,4 Minocycline-induced hyperpigmentation is classified into 3 types.…”
Section: The Diagnosismentioning
confidence: 99%
“…Its mechanism of action involves reversibly binding to the 30S ribosomal subunit to prevent bacterial protein synthesis. It is commonly used for short-term therapy in the treatment of acute infections, such as ones caused by methicillin-resistant Staphylococcus aureus, and in the long-term management of acne vulgaris [ 1 , 2 ].…”
Section: Introductionmentioning
confidence: 99%