2013
DOI: 10.1016/j.medengphy.2012.08.021
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Effects of through-hole drug reservoirs on key clinical attributes for drug-eluting depot stent

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Cited by 20 publications
(13 citation statements)
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“…The modification of these stents brought both its own advantages and disadvantages the same as all previous stent technologies. They have improved the duration of drug release from the stent although they have failed in mechanical integrity required for stent backbone in most cases (Hsiao et al 2013 ). Polymer-free stents also indicated a capability for long-term safety in comparison to traditional coated DES (Farah 2018 ).…”
Section: More New Stent Systemsmentioning
confidence: 99%
“…The modification of these stents brought both its own advantages and disadvantages the same as all previous stent technologies. They have improved the duration of drug release from the stent although they have failed in mechanical integrity required for stent backbone in most cases (Hsiao et al 2013 ). Polymer-free stents also indicated a capability for long-term safety in comparison to traditional coated DES (Farah 2018 ).…”
Section: More New Stent Systemsmentioning
confidence: 99%
“…The literature review shows that this type of modification of stents has brought many advantageous features. The duration of drug release from the stent has been improved, although the mechanical integrity required for the stent backbone has been problematic in most cases [ 159 ]. However, it is worth noting that their long-term safety distinguishes polymer-free stents compared to traditional DES-coated stents [ 15 ].…”
Section: New Stent Systemsmentioning
confidence: 99%
“…For instance: 1) in the shell, soluble porogenic additives (such poly(ethylene glycol) or poly(vinylpyrrolidone)) could be used to regulate the drug release behavior, as is currently the case in some particle-based drug depots [59]; 2) the approach could be extended to achieve the sustained release of soluble drugs (a major challenge in pharmaceutics); 3) drug delivery systems with more complicated drug release profiles could be achieved, e.g. multiple-phase release of a drug using a pure drug exterior compartment; 4) combined therapies with temporally sequential drug release characteristics could be explored; 5) an extremely wide range of un-spinnable fluids including dilute polymer solutions [60], surfactant or electrolyte solutions could be explored as the outer fluid in modified tri-axial processes, in order to create numerous nanoscale biomaterials with complicated nanostructures.…”
Section: Figmentioning
confidence: 99%