Huynh-Delerme C, Penaud J-F, Lacombe C, Brunhes A, Moriette G
Service de Médecine Néonatale de Port-Royal, UFR Cochin-Port-Royal, Université René-Descartes, Paris, France.
Biol Neonate. 2002;81(3):158-62. doi: 10.1159/000051528.
The aim of this in vitro study was to determine stability and biological activity of epoietin (Epo) beta in a parenteral nutrition solution over 24 h. Epo beta was added to the parenteral nutrition solution which was administered through intravenous tubing and a Posidyne Neo filter. Samples were collected after 0, 4, 12, and 24 h. The Epo concentrations were measured before and after filter passage by an ELISA assay. The Epo biological activity was determined in the UT7/Epo cell line. The Epo concentration in the parenteral nutrition solution remained stable for 24 h. However, 35% of the Epo was adsorbed by the filter. The samples collected induced proliferation of UT7/Epo cells. These results suggest that Epo can be administered in parenteral nutrition solutions, but the dosage would need to be increased when a filter is used.
这项体外研究的目的是确定促红细胞生成素(Epo)β在肠外营养溶液中24小时内的稳定性和生物活性。将Epoβ添加到通过静脉输液管和Posidyne Neo过滤器给药的肠外营养溶液中。在0、4、12和24小时后收集样本。通过ELISA测定法在过滤器通过前后测量Epo浓度。在UT7/Epo细胞系中测定Epo生物活性。肠外营养溶液中的Epo浓度在24小时内保持稳定。然而,35%的Epo被过滤器吸附。收集的样本诱导UT7/Epo细胞增殖。这些结果表明,Epo可以在肠外营养溶液中给药,但使用过滤器时需要增加剂量。