Xi Chao-Yun, Zhuang Yuan, Chen Lin Feng, Liu Ya-Qian, Wang Shu-Fang, Wang De-Qing
Department of Blood Transfusion, Chinese PLA General Hospital, Beijing 100853,China.
Department of Blood Transfusion, Chinese PLA General Hospital, Beijing 100853, China. E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2014 Apr;22(2):503-8. doi: 10.7534/j.issn.1009-2137.2014.02.043.
This study was aimed to develop a new generation of ideal hemostatic powder which can be safely, effectively and easily used mainly to first aid anterior to hospital by the synergistic effect of physical and chemical hemostatic mechanisms. The tranexamic acid(TA)-loaded porous starch(PS) (TAPS) was prepared by using PS as carrier and TA as loaded drug component. The absorption property of TAPS was evaluated by water absorption; the hemostatic ability of TAPS was evaluated by test in vitro and in vivo, the blood coagulation time of TAPS was detected by using Lee-white method. The experiment was divided into 3 groups: blank control group, Yunnan Baiyao group and TAPS group, each group with 10 blood samples in vitro test; the 27 SD rats were used to test in vivo, and randomly were divided into 3 groups: PS,Yunnan Baiyao and TAPS, each group consisted of 9 rats for establishing the animal model of liver trauma and detecting the complete hemostasis time. The results showed that the water absorption of PS did not be affected by TA when dose of TA loaded in PS was <0.02 g/g PS. There was no statistic difference in blood coagulation time between TAPS and PS groups(P > 0.05). The complete hemostatic time of TAPS for trauma of left lobe liver was 236.67 ± 55.00 seconds, which was shorter than that of Yunnan Baiyao (340.00 ± 73.48 seconds) and PS (396.67 ± 68.37 seconds) (P < 0.05 and P < 0.01, respectively). It is concluded that PS can load TA and play the hemostatic effect through releasing TA; the TA loading <0.02 g/g PS did not affect the water absorption and pro-coagulation properties. The TA can enhance the hemostatic efficacy of PS, the hemostatic property of TAPS is derived from synergism of physical and chemical hemostatic mechanisms.
本研究旨在开发新一代理想的止血粉,其可通过物理和化学止血机制的协同作用,安全、有效且简便地用于院前急救。以多孔淀粉(PS)为载体、氨甲环酸(TA)为载药成分制备了载氨甲环酸的多孔淀粉(TAPS)。通过吸水性评价TAPS的吸附性能;通过体内外试验评价TAPS的止血能力,采用李氏-怀特法检测TAPS的凝血时间。实验分为3组:空白对照组、云南白药组和TAPS组,每组在体外试验中有10份血样;采用27只SD大鼠进行体内试验,随机分为3组:PS组、云南白药组和TAPS组,每组9只大鼠,用于建立肝创伤动物模型并检测完全止血时间。结果表明,当PS中TA的负载量<0.02 g/g PS时,TA对PS的吸水性无影响。TAPS组和PS组的凝血时间无统计学差异(P>0.05)。TAPS对左叶肝创伤的完全止血时间为236.67±55.00秒,短于云南白药组(340.00±73.48秒)和PS组(396.67±68.37秒)(分别为P<0.05和P<0.01)。结论:PS可负载TA并通过释放TA发挥止血作用;TA负载量<0.02 g/g PS不影响吸水性和促凝血性能。TA可增强PS的止血效果,TAPS的止血性能源于物理和化学止血机制的协同作用。