2002
DOI: 10.1016/s0168-3659(02)00179-7
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In vitro–in vivo characterization of gentamicin bone implants

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Cited by 102 publications
(66 citation statements)
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“…On the protocol in which only half of the medium was replaced, concentration gradient was lower, explaining the slower CHX release kinetics over the 14 days incubation. The observed behavior is in agreement with several studies showing that controlled drug release profiles usually reveal an initial burst release of short duration that is followed by a longer period of continuous but declining release [4,13,18,[42][43][44], and that the release pattern is dependent on the amount of antimicrobial agent adsorbed on biomaterials [13,44].…”
Section: Discussionsupporting
confidence: 91%
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“…On the protocol in which only half of the medium was replaced, concentration gradient was lower, explaining the slower CHX release kinetics over the 14 days incubation. The observed behavior is in agreement with several studies showing that controlled drug release profiles usually reveal an initial burst release of short duration that is followed by a longer period of continuous but declining release [4,13,18,[42][43][44], and that the release pattern is dependent on the amount of antimicrobial agent adsorbed on biomaterials [13,44].…”
Section: Discussionsupporting
confidence: 91%
“…CHX release results from desorption or partial dissolution of the CHX-phosphate binding. As expected, CHX release kinetics was clearly affected by the protocol used, because CHX is prone to leach, especially close to the discs' surface where rapid diffusion of water molecules was facilitated [13,4,42]. This process depends on the concentration gradient between the bulk solution and the disc surface.…”
Section: Discussionmentioning
confidence: 56%
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“…The absorbing properties of HAP have been exploited in the formation of HAP-antibiotic and HAP-drug composites for slow release in situ [14][15][16]. This has proved effective in the treatment of diseases such as osteomyelitis as it allows better recovery from the disease [17].…”
Section: Introductionmentioning
confidence: 99%
“…Besides the polymeric matrix, other controlled release systems based on different materials have been intensively studied in recent years, such as bioceramic and composites. Some examples are antibiotics like gentamicin, released from the matrix composed of calcium phosphates and poly(DL-lactide) (PLA) (Baro et al, 2002) and from the composite of hydroxyapatite/collagen (Martins & Goissis, 2000), and antineoplastic agents like cisplatin, released from calcium phosphate (CaP) nanoparticles (Barroug et al, 2004). The porosity of conventional matrices is highly heterogeneous due to complex chemical composition, which presents as a great disadvantage the difficulty of ensuring homogeneous drug distribution through the matrix, affecting the release rate.…”
Section: Controlled Release Of Drugsmentioning
confidence: 99%