Genipin-crosslinked gelatin microspheres as a strategy to prevent postsurgical peritoneal adhesions: In vitro and in vivo characterization

被引:128
作者
De Clercq, Kaat [1 ]
Schelfhout, Charlotte [1 ]
Bracke, Marc [2 ]
De Wever, Olivier [2 ]
Van Bockstal, Mieke [3 ]
Ceelen, Wim [4 ]
Remon, Jean Paul [1 ]
Vervaet, Chris [1 ]
机构
[1] Univ Ghent, Lab Pharmaceut Technol, Ottergemsesteenweg 460, B-9000 Ghent, Belgium
[2] Univ Ghent, Lab Expt Canc Res, B-9000 Ghent, Belgium
[3] Ghent Univ Hosp, Dept Pathol, Ghent, Belgium
[4] Ghent Univ Hosp, Dept Surg, Ghent, Belgium
关键词
Microspheres; Crosslinking; Genipin; Peritoneal adhesions prevention; Post-operative adhesions; Anti-adhesion barrier; HYPERTHERMIC INTRAPERITONEAL CHEMOTHERAPY; LAPAROSCOPIC MOUSE MODEL; DRUG-DELIVERY SYSTEM; HYALURONIC-ACID; POSTOPERATIVE ADHESIONS; ABDOMINAL ADHESIONS; ENHANCED ADHESIONS; CARCINOMATOSIS; LINKING; HYDROGELS;
D O I
10.1016/j.biomaterials.2016.04.012
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Background: Peritoneal adhesions are a common complication after abdominal surgery. They cause small bowel obstruction, female infertility and chronic abdominal pain. Peritoneal adhesions also hamper uniform drug distribution in the peritoneal cavity, thereby reducing the efficacy of intraperitoneal chemotherapy after cytoreductive surgery. Aim: The goal of this study was to develop a formulation that prevents peritoneal adhesions, evenly distributes in the abdominal cavity, and simultaneously extends residence time and improves local drug concentration. This report describes the formulation and characterization of genipin-crosslinked gelatin microspheres (GP-MS). Methods and results: Spheroid gelatin microspheres were prepared by an emulsification solvent extraction method. A higher degree of crosslinking was obtained by increasing genipin concentration and crosslinking time. The degree of crosslinking allowed to tailor the degradation rate of GP-MS, hence their residence time. GP-MS did not affect cell viability. In vivo experiments showed excellent GP-MS biocompatibility and degradation characteristics. GP-MS were distributed evenly throughout the abdominal cavity. Adhesions were induced in Balb/c mice by application of an abraded peritoneal wall-cecum model. GP-MS-treated mice developed significantly less postsurgical adhesions compared to saline and Hyalobarrier (R) group. Histopathological examination showed a decrease of peritoneal inflammation over time in GP-MS-treated mice with complete recovery of peritoneal wounds postoperative day 14. Conclusion: GP-MS are a promising strategy to prevent postoperative peritoneal adhesions and improve efficacy of postoperative intraperitoneal chemotherapy. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:33 / 46
页数:14
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