In vivo and in vitro degradatation of monofilament absorbable sutures, PDS® and Maxon®
1990; Elsevier BV; Volume: 11; Issue: 1 Linguagem: Inglês
10.1016/0142-9612(90)90050-z
ISSN1878-5905
AutoresStephen Metz, Nasser Chegini, Byron J. Masterson,
Tópico(s)Orthopedic Surgery and Rehabilitation
ResumoTwo new absorbable monofilament suture materials polydioxanone and Maxon® are being employed increasingly in abdominal surgery because of increased strength retention and decreased tissue reactivity compared with previously available materials. As part of our investigation of the behaviour of suture materials, 3−0 sutures of polydioxanone and Maxon were enclosed in nylon pouches, a technique developed for in vivo experiments to prevent cellular interaction with implanted devices. The pouched sutures were gas sterilized, then implanted in either the extrafascial space or peritoneal cavity for periods of 1–5 wk. Sterilized sutures were also incubated in Ringer's lactate at 37°C. Tensile strength of the exposed sutures was measured. For a given suture material and duration of incubation, there was no significant difference in tensile strength degradation among the three test environments. Although the strength of unexposed Maxon is greater than that of polydioxanone, the residual strength of Maxon decreases more rapidly in use, so that, after 2 wk, the strength of polydioxanone is greater. Scanning electron microscope examination of the suture surfaces reveals that polydioxanone develops surface crazing with time, whereas the surface morphology of Maxon remains relatively unaltered.
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