2016
DOI: 10.1016/j.msec.2015.09.103
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Characteristics, interactions and coating adherence of heterogeneous polymer/drug coatings for biomedical devices

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Cited by 16 publications
(10 citation statements)
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References 31 publications
(21 reference statements)
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“…Cauda et al developed a heparin-loaded PLGA coating on Double-J polyurethane stent in order to reduce incrustation [ 38 ]. However, PLGA was also successfully used as a coating on other substrates, e.g., on Ti–6Al–4V alloy in the form of a gentamicin-loaded layer intended for prosthetic hips [ 39 ]. PLGA used in our study was synthesized with Zr(acac) 4 initiator (contrary to Sn(oct) 2 in commercially available bioresorbable polyesters) and has been previously presented as a suitable polymer coating for metallic implants [ 39 , 40 , 41 , 42 , 43 ] or as a coating on Parylene C [ 44 ].…”
Section: Introductionmentioning
confidence: 99%
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“…Cauda et al developed a heparin-loaded PLGA coating on Double-J polyurethane stent in order to reduce incrustation [ 38 ]. However, PLGA was also successfully used as a coating on other substrates, e.g., on Ti–6Al–4V alloy in the form of a gentamicin-loaded layer intended for prosthetic hips [ 39 ]. PLGA used in our study was synthesized with Zr(acac) 4 initiator (contrary to Sn(oct) 2 in commercially available bioresorbable polyesters) and has been previously presented as a suitable polymer coating for metallic implants [ 39 , 40 , 41 , 42 , 43 ] or as a coating on Parylene C [ 44 ].…”
Section: Introductionmentioning
confidence: 99%
“…However, PLGA was also successfully used as a coating on other substrates, e.g., on Ti–6Al–4V alloy in the form of a gentamicin-loaded layer intended for prosthetic hips [ 39 ]. PLGA used in our study was synthesized with Zr(acac) 4 initiator (contrary to Sn(oct) 2 in commercially available bioresorbable polyesters) and has been previously presented as a suitable polymer coating for metallic implants [ 39 , 40 , 41 , 42 , 43 ] or as a coating on Parylene C [ 44 ]. The possibility of encapsulating drugs within the layers provides additional advantages like local delivery of the drug, which makes it even more attractive.…”
Section: Introductionmentioning
confidence: 99%
“…To date, various strategies have been reported to modify titanium surfaces with antibacterial properties, which mainly include: (1) loading of antibacterial drugs, such as antibiotics [3], or attaching antimicrobial peptides [4] to the surface; (2) introducing inorganic antibacterial metal elements such as F, Cu, Zn, or Ag by alloy or modification [5];…”
Section: Introductionmentioning
confidence: 99%
“…However, these methods are not only prone to drug resistance, but also usually have a burst phase at the initial stage of drug release, which prevents long-term antibacterial effects. Many methods have also been performed to introduce inorganic antibacterial metal elements to titanium surfaces, such as plasma spraying [11], micro-arc oxidation [12], and ultrasonic spray coating [3]. Compared with organic antibacterial drugs, metal elements exhibit broad-spectrum antibacterial activity, long acting time, and no drug resistance.…”
Section: Introductionmentioning
confidence: 99%
“…After proliferation stimulation, a slight decrease of cell viability was observed for all samples.When cytotoxicity was tested towards PMBC in the presence of Ag/HAP, HAP/Gr and Ag/HAP/Gr, a decrease of healthy immunocompetent PBMC cell survival up to 94.6±4.2 % for Ag/HAP, 39 72.3±4.3 % for HAP/Gr 5 and 79.6±11.2 % for Ag/HAP/Gr 36 compared to the control (S = 100 %) was calculated. According to the classification found in literature,55 all investigated samples could be declared as non-cytotoxic against target PBMC. Having in mind that PBMC cells are the first line of immune defense against any type of implant in the human body, obtained results were encouraging for further investigations.…”
mentioning
confidence: 99%