首页> 外文期刊>International Journal of Nanomedicine >Adenosine diphosphate-decorated chitosan nanoparticles shorten blood clotting times, influencing the structures and varying the mechanical properties of the clots
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Adenosine diphosphate-decorated chitosan nanoparticles shorten blood clotting times, influencing the structures and varying the mechanical properties of the clots

机译:腺苷二磷酸壳聚糖纳米粒子缩短血液凝固时间,影响结构并改变凝块的机械性能

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Abstract: Chitosan nanoparticles (NPs) decorated with adenosine diphosphate (ADP) (ANPs) or fibrinogen (FNPs) were used to fabricate hemostatic NPs that can shorten blood clotting time and prevent severe local hemorrhage. The structure and mechanical properties of the blood clot induced with ANP (clot/ANP) or FNP (clot/FNP) were also investigated. The NPs, ANPs, and FNPs, which had particle sizes of 245.1±14.0, 251.0±9.8, and 326.5±14.5 nm and zeta potentials of 24.1±0.5, 20.6±1.9, and 15.3±1.5 mV (n=4), respectively, were fabricated by ionic gelation and then decorated with ADP and fibrinogen. The zeta potentials and Fourier transform infrared (FTIR) spectroscopy of the NPs confirmed that their surfaces were successfully coated with ADP and fibrinogen. The scanning electron microscope (SEM) micrographs of the structure of the clot induced with "undecorated" chitosan NPs (clot/NP), clot/ANP, and clot/FNP (at 0.05 wt%) were different, after citrated bloods had been recalcified by a calcium chloride solution containing NPs, ANPs, or FNPs. This indicated that many NPs adhered on the membrane surfaces of red blood cells, that ANPs induced many platelet aggregates, and that FNPs were incorporated into the fibrin network in the clots. Measurements of the blood clotting times (Tc) of blood clot/NPs, clot/ANPs, and clot/FNPs, based on 90% of ultimate frequency shifts measured on a quartz crystal microbalance (QCM), were significantly (P<0.05) (n=4) shorter than that of a clot induced by a phosphate-buffered solution (PBS) (clot/PBS) (63.6%±3.1%, 48.3%±6.2%, and 63.2%±4.7%, respectively). The ?F2 values in the spectra of frequency shifts associated with the propagation of fibrin networks in the clot/ANPs and clot/FNPs were significantly lower than those of clot/PBS. Interestingly, texture profile analysis of the compressional properties showed significantly lower hardness and compressibility in clot/NPs and clot/ANPs (P<0.05 or better) (n=4) compared with clot/PBS and clot/FNPs. Accordingly, among the hemostatic NPs, ANP substantially reduced blood clotting times, ?F2 values, and compression flow properties of the clot. Hence, ANPs have potential applications for preventing severe local hemorrhage.
机译:摘要:用腺苷二磷酸二磷酸(ADP)(ANP)或纤维蛋白原(FNPS)装饰的壳聚糖纳米粒子(NPS)用于制造止血NP,可缩短血液凝血时间并防止严重的局部出血。还研究了用ANP(CLOT / ANP)或FNP(CLOT / FNP)诱导的血凝凝块的结构和机械性能。具有245.1±14.0,251.0±9.8和326.5±14.5nm和Zeta电位的NPS,ANP和FNP分别为24.1±0.5,20.6±1.9和15.3±1.5mV(n = 4)的Zeta电位,由离子凝胶化制造,然后用ADP和纤维蛋白原装饰。 NPS的Zeta电位和傅立叶变换红外(FTIR)光谱证实它们的表面成功涂覆了ADP和纤维蛋白原。用“未污染的”壳聚糖NPS(CLOT / NP),CLOT / ANP和CLOT / FNP(0.05wt%)诱导的凝块结构的扫描电子显微镜(SEM)显微照片不同,在重新计算柠檬酸血液后,不同通过含有NPS,ANP或FNPS的氯化钙溶液。这表明许多NPS粘附在红细胞的膜表面上,即ANP诱导许多血小板聚集体,并且FNP被掺入凝块中的纤维蛋白网络中。血凝凝块/ NPS,CLOT / ANP和CLOT / FNPS的血液凝血时间(TC)的测量值显着基于90%的最终频移(QCM),显着(P <0.05)( n = 4)短于磷酸盐缓冲溶液(PBS)(CLOT / PBS)诱导的凝块的短(63.6%±3.1%,分别为63.3%±6.2%,分别为63.2%±4.7%)。与CLOT / ANPS和CLOT / FNPS中纤维蛋白网络传播相关的频移的光谱中的ΔF2值显着低于CLOT / PBS。有趣的是,与CLOT / PBS和CLOT / FNP相比,压缩性能的纹理谱分析显示凝块/ NPS和CLOT / ANPS(p <0.05或更高)(p <0.05或更高)(n = 4)显着降低。因此,在止血NPS中,ANP基本上减少血液凝固时间,αf2值和凝块的压缩流动性。因此,ANP具有防止严重局部出血的潜在应用。

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