2008
DOI: 10.1016/j.actbio.2007.12.009
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Characterization of chlorhexidine-releasing, fast-setting, brushite bone cements

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Cited by 53 publications
(57 citation statements)
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References 30 publications
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“…Additional advantages are provided if the material is injectable, biodegradable, sets at ambient temperature, has both near neutral pHs and a large surface area [36,37]. These properties make self-setting calcium orthophosphate formulations to be very attractive candidates as drug carriers for therapeutic peptides [537], antibiotics [538][539][540][541][542][543][544][545][546][547], anticancer drugs [578], anti-inflammatory drugs [549,550], cytokines [551], hormones [552] and bone morphogenetic proteins [432,[553][554][555][556][557]. For example, a "growth factor cement" has been reported [558].…”
Section: Drug Delivery Applicationsmentioning
confidence: 99%
See 1 more Smart Citation
“…Additional advantages are provided if the material is injectable, biodegradable, sets at ambient temperature, has both near neutral pHs and a large surface area [36,37]. These properties make self-setting calcium orthophosphate formulations to be very attractive candidates as drug carriers for therapeutic peptides [537], antibiotics [538][539][540][541][542][543][544][545][546][547], anticancer drugs [578], anti-inflammatory drugs [549,550], cytokines [551], hormones [552] and bone morphogenetic proteins [432,[553][554][555][556][557]. For example, a "growth factor cement" has been reported [558].…”
Section: Drug Delivery Applicationsmentioning
confidence: 99%
“…After setting, the drugs are slowly released through the cement pores [210,[543][544][545][546]562,563]. For example, a group of investigators added flomoxef sodium to a cement formulation and found that the release of antibiotic could be easily controlled in vivo by adjusting the content of sodium alginate in the formula [210].…”
Section: Drug Delivery Applicationsmentioning
confidence: 99%
“…The drug release from CPCs has commonly been monitored using pre-set specimens, which were allowed to set for different periods, varying from 10-20 min [8], overnight [9], or 24 h [10][11][12][13][14][15][16][17] up to 7 days [10]. Moreover, in several studies [18][19][20][21][22] the conditions used were not indicated.…”
Section: Introductionmentioning
confidence: 99%
“…Additional advantages are provided if the biomaterial is injectable, biodegradable, sets at ambient temperature, has both near neutral pHs and a large surface area [52,53]. These properties make self-setting calcium orthophosphate formulations to be very attractive candidates as drug carriers for therapeutic peptides [617], antibiotics [26,[618][619][620][621][622][623][624][625][626][627][628][629], anticancer [630][631][632][633][634] and anti-inflammatory agents [635,636], cytokines [637], hormones [638], bone morphogenetic proteins [488,[639][640][641][642][643] and other biologically active compounds [644][645][646][647][648][649][650][651]. For example, a -growth factor cement‖ has been reported [652].…”
Section: Drug Deliverymentioning
confidence: 99%
“…According to a topical review on the subject [219], there are 3 options of drug existence inside the matrix: (a) dissolved in the remaining liquid phase within the existing pores among the newly formed inorganic crystals; (b) adsorbed or chemically bound on the surface of the crystals; or (c) in a solid form inside pores ( Figure 15). Studies on drug release are the second most important topic on drugs incorporation into the self-setting formulations [238,[623][624][625][626]656,657]. This process is regulated by the microstructure of the set formulations (i.e., their porosity), as well as by presence or absence of additives able to influence the movement of drug molecules within the solid matrix.…”
Section: Drug Deliverymentioning
confidence: 99%