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1)  Biliary copper excretion
胆汁铜排泄
2)  bile excretion
胆汁排泄
1.
Study on bile excretion of scutellarein;
灯盏花乙素苷元的胆汁排泄研究
2.
OBJECTIVE To study pharmacokinetics of luteolin in rats after oral and intraperitoneal administration,and to deter- minate the bile excretion.
目的建立HPLC-UV方法,研究木犀草素灌胃及腹腔给药后原形药物及结合形药物在大鼠体内的药动学,并测定灌胃给药后大鼠胆汁排泄情况。
3.
To compare the characteristics of absorption and pharmacokinetic behavior of ginsenoside Rg_1(Rg_1) with ginsenoside Rb_1(Rb_1) of panax notoginseng saponins(PNS),bile excretion of both Rg_1 and Rb_1 were studied after iv and ig of PNS solution.
分别考察三七总皂苷(PNS)在大鼠灌胃和静脉给药后的人参皂苷Rg1(Rg1)、人参皂苷Rb1(Rb1)的胆汁排泄;采用平衡透析法测定药物的血浆蛋白结合率;并结合药代动力学的实验结果,研究和比较Rg1与Rb1的口服吸收及其体内药代动力学性质。
3)  biliary excretion
胆汁排泄
1.
Aim To study the biliary excretion of genistein and its metabolite at different doses in rats.
kg-1分别给药后,累积以原形从胆汁排泄的药物分别为(42。
2.
OBJECTIVE To evaluate the biliary excretion of hydroxycamptothecin(HCPT) after intravenous injection of its liposomes in rats.
目的研究羟喜树碱不同制剂经大鼠静脉注射给药后的胆汁排泄特征。
4)  excretion of bile
排泄胆汁
5)  biliary excretion
胆汁中排泄
1.
Stereoselectivity in biliary excretion of trans tramadol and trans O-demethyltramadol in rats;
反式曲马朵和反式氧去甲基曲马朵在大鼠胆汁中排泄的立体选择性
6)  bile excretion
胆排泄
1.
Stereoselective bile excretion of ibuprofen glucuronide and the transport mechanism in the biliary efflux;
布洛芬葡萄糖醛酸结合物的立体选择性胆排泄及其机制研究(英文)
2.
AIM:To illustrate the effects of drug transporters on the bile efflux of ibuprofen glucuronide (IBG),the difference of bile excretion and plasma con- centration of ibuprofen(IB)and its glucuronides was stud- ied in EHBR and normal SD rat(SDR).
目的:为阐明药物转运体在布洛芬(IB)葡萄糖醛酸结合物(IBG)胆排泄中的作用,对 IB 和 IBG 在先天性高胆红素血症大鼠(EHBR)和正常 SD 大鼠 (SDR)的胆排泄和血药浓度差异进行了研究。
补充资料:排泄系统的进化涡虫的排泄系统




排泄系统的进化  涡虫的排泄系统  
                                       李瑞端绘
  [图]图

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