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壳聚糖-富血小板血浆植入物改善大型动物模型中的肩袖修复:关键研究。

Chitosan-Platelet-Rich Plasma Implants Improve Rotator Cuff Repair in a Large Animal Model: Pivotal Study.

作者信息

Chevrier Anik, Hurtig Mark B, Lavertu Marc

机构信息

Chemical Engineering Department, Polytechnique Montreal, 2900 Boul. Édouard-Montpetit, Montreal, QC H3T 1J4, Canada.

Department of Clinical Studies, University of Guelph, Guelph, ON N1G 2W1, Canada.

出版信息

Pharmaceutics. 2021 Nov 18;13(11):1955. doi: 10.3390/pharmaceutics13111955.

Abstract

The purpose of this study was to assess the safety and efficacy of chitosan-platelet-rich plasma (PRP) hybrid implants used as an adjunct to surgical rotator cuff repair in a pivotal Good Laboratory Practice (GLP)-compliant study. The infraspinatus tendon was transected in 48 skeletally mature ewes and repaired with a transosseous-equivalent (TOE) technique. In the two treatment groups, a chitosan-PRP solution was injected at the footprint between the tendon and the bone and on top of the repaired site (2 mL or 3 mL doses, = 12 per group). To further assess chitosan safety, a chitosan-water solution was injected at the same sites (3 mL, = 12). Outcome measures included Magnetic Resonance Imaging (MRI) assessment and clinical pathology at 3 months and 6 months and histopathology at 6 months. The tendon gap was decreased at 3 months on MRI images and certain histopathological features were improved at 6 months by chitosan-PRP treatment compared to controls. The group treated with chitosan-water was not different from controls. Chitosan-PRP treatment induced no negative effects in the sheep, which suggests high safety. This study provides further evidence on the safety and efficacy of chitosan-PRP for rotator cuff repair augmentation, which could eventually be used in a clinical setting.

摘要

本研究的目的是在一项符合药品非临床研究质量管理规范(GLP)的关键研究中,评估壳聚糖-富血小板血浆(PRP)混合植入物作为手术修复肩袖的辅助手段的安全性和有效性。在48只骨骼成熟的母羊中切断冈下肌腱,并用骨替代物(TOE)技术进行修复。在两个治疗组中,将壳聚糖-PRP溶液注射到肌腱与骨骼之间的足迹处以及修复部位的上方(2 mL或3 mL剂量,每组n = 12)。为了进一步评估壳聚糖的安全性,在相同部位注射壳聚糖水溶液(3 mL,n = 12)。结果指标包括3个月和6个月时的磁共振成像(MRI)评估和临床病理学检查,以及6个月时的组织病理学检查。与对照组相比,壳聚糖-PRP治疗在MRI图像上3个月时肌腱间隙减小,6个月时某些组织病理学特征得到改善。壳聚糖水溶液治疗组与对照组无差异。壳聚糖-PRP治疗对绵羊未产生负面影响,这表明其安全性高。本研究为壳聚糖-PRP用于增强肩袖修复的安全性和有效性提供了进一步的证据,最终可应用于临床。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06a8/8622568/2fa823f7ab64/pharmaceutics-13-01955-g001.jpg

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