2011
DOI: 10.7547/1010146
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In Vitro Antimicrobial Activity of Calcium Sulfate and Hydroxyapatite (Cerament Bone Void Filler) Discs Using Heat-Sensitive and Non–Heat-sensitive Antibiotics Against Methicillin-Resistant Staphylococcus aureus and Pseudomonas aeruginosa

Abstract: The calcium sulfate and hydroxyapatite Cerament Bone Void Filler was an excellent carrier vehicle for multiple antibiotics creating in vitro significant zones of inhibition, thus demonstrating susceptibility against Staphylococcus aureus and Pseudomonas aeruginosa, which holds tremendous promise in treating osteomyeilits.

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Cited by 20 publications
(11 citation statements)
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“…Traditional local antimicrobial application involves the off‐label use of polymethylmethacrylate (PMMA) as a delivery device, which elutes antibiotics such as vancomycin, tobramycin, and/or gentamicin . Other safe carriers for antibiotic delivery include ceramic‐based resorbable bone void fillers, such as calcium phosphate and calcium sulfate cements …”
mentioning
confidence: 99%
“…Traditional local antimicrobial application involves the off‐label use of polymethylmethacrylate (PMMA) as a delivery device, which elutes antibiotics such as vancomycin, tobramycin, and/or gentamicin . Other safe carriers for antibiotic delivery include ceramic‐based resorbable bone void fillers, such as calcium phosphate and calcium sulfate cements …”
mentioning
confidence: 99%
“…CSS resorbable properties could limit its employment in collapses secondary to malignancies because, if a malignancy is able to erode a normal bone, it may be able to do the same with CSS too, considering its composition, leading to recollapse. However, there are some circumstances in which CSS is employed with the double purpose of being both bone void filler and antibiotic carrier [52,53]. It should be, therefore, plausible to venture that CSS could also be an antineoplastic drug carrier, hence widening its employment to nonosteoporotic VCFs.…”
Section: Discussionmentioning
confidence: 97%
“…Therefore, there is the compelling need to develop novel drug delivery to overcome this resistance [3]. Ticarcillin is an antibiotic belonging to the carboxypenicillin subgroup of third-generation penicillins and covers gram-negative bacteria such as P. aeruginosa , but nowadays, this drug is susceptible to degradation by P. aeruginosa beta-lactamases [4,5]. Like other antibiotics, increasing time and usage have led to resistance to ticarcillin and so, a delivery system that reducing the ticarcillin-resistant while increasing its therapeutic index is of great interest, and nanoliposomes can provide these benefits [6,7].…”
Section: Introductionmentioning
confidence: 99%