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化学和结构修饰物对β-壳聚糖补丁止血过程和细胞毒性的影响。

The effect of chemical and structural modifiers on the haemostatic process and cytotoxicity of the beta-chitin patch.

机构信息

Department of Surgery-Otorhinolaryngology, Head and Neck Surgery, University of Adelaide, Adelaide, Australia.

Department of Chemistry, University of Otago, Dunedin, New Zealand.

出版信息

Sci Rep. 2021 Sep 17;11(1):18577. doi: 10.1038/s41598-021-97781-8.

Abstract

Beta-chitin patch has previously been proven to be an effective haemostat, but whether modifying the patch affects its efficacy and safety, remains unanswered. In this study, the patch was modified using polyethylene oxide, Pluronic-F127, calcium, increased thickness or polyphosphate, and their effect on the process of haemostasis and cytotoxicity was tested and compared with standard-of-care, Surgicel and FloSeal. Whole blood collected from volunteers was applied to the patches to test their whole blood clotting and thrombin generation capacities, whilst platelet isolates were used to test their platelet aggregation ability. The fluid absorption capacity of the patches was tested using simulated body fluid. Cytotoxicity of the patches was tested using AlamarBlue assays and PC12 cells and the results were compared with the standard-of-care. In this study, beta-chitin patch modifications failed to improve its whole blood clotting, platelet aggregation and thrombin generation capacity. Compared to non-modified patch, modifications with polyethylene oxide or calcium reduced platelet aggregation and thrombin generation capacity, while increasing the thickness or adding polyphosphate decreased platelet aggregation capacity. The cytotoxicity assays demonstrated that the beta-chitin patches were non-toxic to cells. In vivo research is required to evaluate the safety and efficacy of the beta-chitin patches in a clinical setting.

摘要

β-壳聚糖贴片已被证明是一种有效的止血剂,但改变贴片的性质是否会影响其疗效和安全性,目前仍不得而知。在这项研究中,我们使用聚氧化乙烯、Pluronic-F127、钙、增加厚度或多聚磷酸盐对贴片进行了改性,并对其止血和细胞毒性作用进行了测试,并与标准护理 Surgicel 和 FloSeal 进行了比较。志愿者采集的全血被应用于贴片,以测试其全血凝血和凝血酶生成能力,而血小板分离物则用于测试其血小板聚集能力。使用模拟体液测试了贴片的液体吸收能力。通过 AlamarBlue 测定法和 PC12 细胞测试了贴片的细胞毒性,并将结果与标准护理进行了比较。在这项研究中,β-壳聚糖贴片的改性并未改善其全血凝血、血小板聚集和凝血酶生成能力。与未改性的贴片相比,用聚氧化乙烯或钙进行改性会降低血小板聚集和凝血酶生成能力,而增加厚度或添加多聚磷酸盐会降低血小板聚集能力。细胞毒性测定表明,β-壳聚糖贴片对细胞无毒。需要进行体内研究,以评估β-壳聚糖贴片在临床环境中的安全性和疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e9/8448852/82665ddfc8a6/41598_2021_97781_Fig1_HTML.jpg

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