2015
DOI: 10.1097/dcr.0000000000000346
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Functional and Histological Evidence for the Targeted Therapy Using Biocompatible Polycaprolactone Beads and Autologous Myoblasts in a Dog Model of Fecal Incontinence

Abstract: This study shows that an injection of polycaprolactone beads containing autologous myoblasts may improve anal sphincter function in an animal model of fecal incontinence.

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Cited by 27 publications
(44 citation statements)
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“…In our study, the anal pressures were comparable with the other animal studies although there are slight variations—possibly due to different techniques (balloon vs. double‐triple‐lumen‐catheter, electrical stimulation vs. spontaneous contraction) and different size of the anal canal in different species 13, 16, 19. Salcedo et al stated that rat anal pressures tend to return to baseline after sphincterotomy at 4 weeks even without intervention, but this does not occur after pudendal nerve transection 42.…”
Section: Discussionsupporting
confidence: 83%
“…In our study, the anal pressures were comparable with the other animal studies although there are slight variations—possibly due to different techniques (balloon vs. double‐triple‐lumen‐catheter, electrical stimulation vs. spontaneous contraction) and different size of the anal canal in different species 13, 16, 19. Salcedo et al stated that rat anal pressures tend to return to baseline after sphincterotomy at 4 weeks even without intervention, but this does not occur after pudendal nerve transection 42.…”
Section: Discussionsupporting
confidence: 83%
“…In another study, myogenic stem cells improved external sphincter function after transection of both the internal and external sphincter only when injected along with a biogel scaffold 2 weeks after sphincter damage . Other studies conducted in dog models of FI with internal and external sphincter injury have also injected myoblasts incorporated in polycaprolactone beads . The resting and contractile pressures were improved.…”
Section: Discussionmentioning
confidence: 98%
“…The durability of the typical PCL polymer varies between two and four years, which sometimes is not suitable for certain applications like tissue engineering where a shorter degradation time is required. To shorten the degradation of PCL, other biodegradable polymers are often incorporated or copolymerized with it [11,12].…”
Section: Introductionmentioning
confidence: 99%