Applied Microbiology · 1963 · 22 citations · 13 references
Life SciencesMicrobiologyAntimicrobial PharmacologyAntimicrobial ResistanceMedical MicrobiologyAntibacterial ResistanceAntibiotic ResistanceAntibiotic Resistance MechanismsAntimicrobial Susceptibility TestingMultidrug ResistanceResistance In Gram-positive BacteriaAntibiotic Susceptibility TestingCephalosporin ResistanceClinical Laboratory EvaluationLaboratory Test EvaluationPenicillin ResistanceResistance Mechanisms In StaphylococciSpectrum Of CephalosporinsSpectrum Of Penicillins
Cephalothin is 7-(thiophene-2-acetamido) cephalosporanic acid; it was prepared by N-acylation of the nucleus of cephalosporin C, 7-aminocephalosporanic acid. Cephalothin had a broad spectrum of antibiotic activity that was essentially unaffected by human serum or inoculum level, the activity of penicillinase, or pH variation of the growth medium. In vitro development of resistance by staphylococci could not be demonstrated, but the gram-negative organisms did develop a stepwise type of resistance to the antibiotic. Staphylococci made resistant in vitro to 5-methyl-3-phenyl-4-isoxazole penicillin were also resistant to cephalothin and to 6-(2,6-dimethoxybenzamido) penicillin; however, the mechanism of resistance to each antibiotic may have differed. Some complications involved in the laboratory evaluation methods currently in use in the field of antibiotics are examined.
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Synthesis of Penicillin: 6-Aminopenicillanic Acid in Penicillin Fermentations
F. R. Batchelor, F. P. Doyle, J. H. C. Nayler et al. · Nature · 1959 · 389 citations
The structure of cephalosporin C
E. P. Abraham, G. G. F. Newton · Biochemical Journal · 1961 · 295 citations · Full text
BACTERIOLOGICAL STUDIES ON A NEW PENICILLIN—BRL.1241
G. N. Rolinson, F. R. Batchelor, Shirley Stevens et al. · The Lancet · 1960 · 146 citations