2020
DOI: 10.1002/jbm.b.34686
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In vitro degradation profiles and in vivo biomaterial–tissue interactions of microwell array delivery devices

Abstract: To effectively apply microwell array cell delivery devices their biodegradation rate must be tailored towards their intended use and implantation location. Two microwell array devices with distinct degradation profiles, either suitable for the fabrication of retrievable systems in the case of slow degradation, or cell delivery systems capable of extensive remodeling using a fast degrading polymer, were compared in this study. Thin films of a poly(ethylene glycol)-poly(butylene terephthal

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Cited by 7 publications
(10 citation statements)
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“…Either in cattle or sheep CE cysts, the presence of a granulomatous reaction is indicative of a foreign body response, which has been widely studied in the biomaterials field [ 25 27 ], where after an acute inflammatory reaction, there is chronic inflammation, followed by either granulomatous tissue or the development of a fibrous capsule [ 27 ]. Here we report that in non-fertile CE cysts, this fibrous capsule changes its location; in cattle it is found surrounding the chronic inflammation tissue, whereas in sheep is found directly surrounding the laminated layer.…”
Section: Discussionmentioning
confidence: 99%
“…Either in cattle or sheep CE cysts, the presence of a granulomatous reaction is indicative of a foreign body response, which has been widely studied in the biomaterials field [ 25 27 ], where after an acute inflammatory reaction, there is chronic inflammation, followed by either granulomatous tissue or the development of a fibrous capsule [ 27 ]. Here we report that in non-fertile CE cysts, this fibrous capsule changes its location; in cattle it is found surrounding the chronic inflammation tissue, whereas in sheep is found directly surrounding the laminated layer.…”
Section: Discussionmentioning
confidence: 99%
“…A similar medium at various pH was applied to assess the degradation profile of the PEOT-PBT and poly(ester urethane) films [11]. Bremrer et al [12] used the guide of [13] for the evaluation of the degradation in vitro potentiality of the poly(ester)urethane-based adhesive.…”
Section: Introductionmentioning
confidence: 99%
“…The primary challenge in developing biodegradable hydrogels for drug delivery lies in accurately measuring their degradation over time, while also simultaneously being able to evaluate the drug-release kinetics. Standard approaches to assess the biodegradation of hydrogels are either by volume or mass loss, the latter of which is more common [13][14][15]. When assessing mass loss, researchers measure the weight of the dried gel at a specified time point [14,15].…”
Section: Introductionmentioning
confidence: 99%
“…Standard approaches to assess the biodegradation of hydrogels are either by volume or mass loss, the latter of which is more common [13][14][15]. When assessing mass loss, researchers measure the weight of the dried gel at a specified time point [14,15]. This procedure is exceptionally cumbersome and time consuming because a dried gel from one time point cannot be reused for subsequent measurements.…”
Section: Introductionmentioning
confidence: 99%