Page 72 - 《中国药科大学学报》2025年第4期
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468                      学报   Journal of China Pharmaceutical University 2025, 56(4): 460 − 468  第 56 卷

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               常的   30%  以下 ,且与白蛋白结合率降低,游离药                          2025, 16: 1233.
               物浓度升高       [27] 。甲钴胺主要经肾脏排泄,而肝衰竭                [11]   China  Pharmaceutical  University.  Use  of  Mecobalamin  and
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               合并肝肾综合征时肾小球滤过率降低,可能影响其                                Treating Liver Failure: CN, 115998758A[P]. 2023-04-25.
               排泄过程。鉴于健康患者和肝衰竭患者在药物药                            [12]   Alpers DH, Russell-Jones G. Gastric intrinsic factor: the gastric
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               代动力学行为上存在明显差异,这种差异对药物疗
                                                                     journey[J]. Biochimie, 2013, 95(5): 989-94.
               效和毒性反应有着重要影响,值得深入关注。后续                           [13]   Seetharam B, Yammani RR. Cobalamin transport proteins and
               研究将借助肝衰竭模型大鼠,系统研究甲钴胺和头                                their  cell-surface  receptors[J].  Expert  Rev  Mol  Med,  2003,
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               孢曲松钠的药代动力学行为,阐明两药在肝衰竭状
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                    本实验分别建立了          SD  大鼠血浆中甲钴胺和                  quirements  for  Pharmaceuticals  for  Human  Use.  ICH  M10-
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               独给药相比,单次联合给药下两药在健康大鼠体内                                biol B, 2013, 122: 7-14.
               的药代动力学行为无显著性差异,表明甲钴胺与头                           [18]   Ao ZX, Feng SS, Zhao CY, et al. Study on polycyclic macro-
                                                                     molecular drug  solid  stability:  a  case  exploration  of   methyl-
               孢曲松钠进行联合用药时,无基于药代动力学的药
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               物相互作用。                                           [19]   Xu QA, Trissel LA, Williams KY. Compatibility and stability
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