2014
DOI: 10.1016/j.trsl.2014.01.014
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Regenerative implants for cardiovascular tissue engineering

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Cited by 44 publications
(32 citation statements)
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“…Because of biocompatible degradation properties, PCL is approved for use in human beings by the US Food and Drug Administration 22. Gelatin is a mixture of peptides and proteins produced by partial hydrolysis of collagen extracted from animals.…”
Section: Discussionmentioning
confidence: 99%
“…Because of biocompatible degradation properties, PCL is approved for use in human beings by the US Food and Drug Administration 22. Gelatin is a mixture of peptides and proteins produced by partial hydrolysis of collagen extracted from animals.…”
Section: Discussionmentioning
confidence: 99%
“…Transplantation of vascular cells has tremendous potential for vascular regeneration either by restoring blood flow to ischemic tissues or implanting a tissue engineered blood vessel [70, 71]. So far no clinical trials have been performed using these cells due to a concern for potential tumorigenicity abilities of these cells [7274].…”
Section: Regenerative Therapymentioning
confidence: 99%
“…Scaffolds can be generated from either synthetic matrices, such as polylactic acid and polyglycolic acid, which are often used for simpler constructs, or from biologically derived matrices, such as fibrin, collagen and tissue ECM. For synthetic matrices, properties such as composition, porosity, biodegradation rate and architecture can be precisely controlled, but these materials often fail to recapitulate the properties of native tissue and can be poor substrates for cell attachment and growth (2). In contrast, biologically derived ECM matrices, if left in a native state, can provide natural cues for cell migration, proliferation and differentiation, but scaffolds made from single ECM components often lack the sophistication to develop into a functional tissue.…”
Section: Scaffoldsmentioning
confidence: 99%