Comparison of the breaking strength of polyglactin mesh in urine, serum, and cell culture media

Citation
Cd. Best et al., Comparison of the breaking strength of polyglactin mesh in urine, serum, and cell culture media, UROLOGY, 53(6), 1999, pp. 1239-1244
Citations number
26
Categorie Soggetti
Urology & Nephrology
Journal title
UROLOGY
ISSN journal
00904295 → ACNP
Volume
53
Issue
6
Year of publication
1999
Pages
1239 - 1244
Database
ISI
SICI code
0090-4295(199906)53:6<1239:COTBSO>2.0.ZU;2-H
Abstract
Objectives. This study was designed to determine the durability of polyglac tin woven mesh in various in vitro environments, including urine, since pol yglactin 901 mesh has been considered for implementation in urinary tract r econstruction. Methods. Segments of 1 x 1-cm sterile woven and knitted polyglactin 910 mes h with and without collagen coating were exposed to the following condition s: dry (at room temperature and at 37 degrees C, humidified air), in porcin e and human serum and urine, in porcine urine over a range of pH levels, in infected urine, in cell culture media (MCDB 105 with 5% fetal bovine serum ), and in cell culture media with porcine bladder fibroblasts. The mesh bre aking strength was measured at 0, 12, 21, 28, and 36 days. Results. The mean breaking strength for dry, room temperature mesh segments measured 350 g for all time intervals. At day 21, the breaking strength fo r all mesh types in human and porcine serum, cell culture media, and cell c ulture media with bladder fibroblasts was less than 10% of the control, but the human and porcine urine maintained 12% to 24% of the control breaking strength (this difference did not reach statistical significance). There wa s no significant difference in the breaking strength in human and porcine u rine or human and porcine serum. By day 38, the breaking strength for all m esh types in all solutions was less than 5% of the control breaking strengt h. The presence of fibroblasts increased the rate of degradation of the mes h compared with the urine, serum, and cell culture media alone. There was a significant prolongation of degradation with decreasing pH, as well as wit h infected urine. This prolongation was additive; in fact, all mesh types i n low pH (5.0), infected urine showed minimal degradation at 38 days. Conclusions. In acidic infected urine, the durability of polyglactin 910 me sh is significantly prolonged compared with the other conditions tested. Th erefore, when used in urinary tract reconstruction, as in other organ syste ms, the integrity of the polyglactin mesh should diminish rapidly after 3 w eeks as long as the urine is kept sterile and a neutral to alkaline pH is m aintained. UROLOGY 53: 1239-1244, 1999. (C) 1999, Elsevier Science Inc. All rights reserved.