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出 处:《药学学报》1996年第6期406-410,共5页Acta Pharmaceutica Sinica
摘 要:用灵敏的夹心酶联免疫法(ELISA)建立了检测重组人hGM-CSF药代动力学的方法。此方法hGM~CSF在12.5~0.39ng·ml ̄(-1)范围内,检测呈线性相关。最低检测灵敏度为0.4ng·ml ̄(-1)。本方法不受血清中潜在干扰因素的影响,检测具高度特异性。大鼠schGM-CSF50,100,200μg·kg ̄(-1)后15min,血中即有较高浓度的hGM-CSF,1h左右达峰浓度,以后快速下降。皮下给药,尿中可检测到原型hGM-CSF,但累积排泄率较低。本研究为临床合理用药提供依据。A sensitive and reliable sandwich enzyme linked immunosobent assay(ELISA)has been developed for determination of concentration of recombinant human granulocyte-macrophagecolony-stimulating factor(hGM-CSF).The assay is quantitative between 0.39~12.5 ng·ml ̄(-1)forbacterially synthesized hGM-CSF in rat serum and urine. The methed was shown to be highly specificand did not significantly alter the determination when adding some potential interfering substances.After single sc injection of hGM-CSF 501 100 or 200μg·kg(-1), a high GM-CSF level was detectedabout 1 5 min in rat serum, the highest level of hGM-CSF was two apparent phases with half-livesT_(1/2α) of 0.72,0.70,0. 80 h and T_(1/2β) of 8. 77,8. 87 and 5. 58h.A detectable urinary excretionoccured after sc injection of hGM-CSF 200μg· kg(-1),but the total urinary excretion of unchangedhGM-CSF was verv low.
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