C. Cross

Publications8
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Citations80
Highly Influential Citations0
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The intraperitoneal penetration of temocillin.
TLDR
It was concluded that 1 g of temocillin twice daily would achieve sufficiently high intraperitoneal levels to inhibit susceptible pathogens.
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The antimicrobial activity of cefpirome, a new cephalosporin.
TLDR
The extended spectrum cephalosporin cef Pirome was bactericidal to all the susceptible strains studied with the exception of Lancefield Group D streptococci and the major target site for cefpirome was PBP 3 and the protein binding was low.
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Comparative in vitro antimicrobial activity of Chinese medicinal herbs.
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In vitro activity of CGP 31523A, a broad-spectrum cephalosporin, in comparison with those of other agents
TLDR
In vitro activity of CGP 31523A was compared with those of cefoxitin, cefuroxime, moxalactam, piperacillin, ciprofloxacin, and other beta-lactams, when appropriate, against 533 recent clinical isolates and known resistant strains of bacteria.
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CHAPTER 28:Antimicrobial Photodynamic Therapy: A Decade of Development and Clinical Study
TLDR
This chapter demonstrates how a Methylene Blue-based sensitizer along with relatively low-power activation can provide the clinician with an alternative to the standard of care, including mechanical debridement, surgery, empirical antibiotic coverage and combinations of steroids and antibiotics in both systemic and topical administration.
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Comparative Inactivation Studies of Listeria Monocytogenes at Room and Refrigeration Temperatures
TLDR
Little to no significant difference was observed for these disinfectants at refrigeration temperature compared to room temperature, and the bactericidal efficacy of liquid disinfectants and the effect that low temperatures have on their efficacy were determined.
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InVitro Activity ofCGP31523A, aBroad-Spectrum Cephalosporin, inComparison withThoseofOtherAgents
Antimicrobial photodynamic disinfection of SARS-COV-2 in a thin-film intranasal model
TLDR
Using standard clinical parameters for intranasal pathogen reduction, APDT proved capable of completely eliminating the RNA signature of wild-type SARS-CoV-2 in vitro, and this work supports further development of APDT as a potent, antiviral modality for inhibition of Sars-Cov-2 transmission.
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