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Determination of Non-Transferrin Bound Iron Transferrin Bound Iron Drug Bound Iron and Total Iron in Serum in a Rats after IV Administration of Sodium Ferric Gluconate Complex by Simple Ultrafiltration Inductively Coupled Plasma Mass Spectrometric Detection

机译:简易超滤电感耦合等离子体质谱法测定葡萄糖酸钠铁复合物静脉给药后大鼠血清中非转铁蛋白结合铁转铁蛋白结合铁药物结合铁和总铁

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摘要

A rapid, sensitive and specific ultrafiltration inductively-coupled plasma mass spectrometry method was developed and validated for the quantification of non-transferrin bound iron (NTBI), transferrin bound iron (TBI), drug bound iron (DI) and total iron (TI) in the same rat serum sample after intravenous (IV) administration of iron gluconate nanoparticles in sucrose solution (Ferrlecit®). Ultrafiltration with a 30 kDa molecular cut-off filter was used for sample cleanup. Different elution solvents were used to separate each form of iron from sample serum. Isolated fractions were subjected to inductively-coupled mass spectrometric analysis after microwave digestion in 4% nitric acid. The reproducibility of the method was evaluated by precision and accuracy. The calibration curve demonstrated linearity from 5–500 ng/mL with a regression (r2) of more than 0.998. This method was effectively implemented to quantify rat pharmacokinetic study samples after intravenous administration of Ferrlecit®. The method was successfully applied to a pharmacokinetic (PK) study of Ferrlecit in rats. The colloidal iron followed first order kinetics with half-life of 2.2 h and reached background or pre-dose levels after 12 h post-dosing. The drug shown a clearance of 0.31 mL/min/kg and volume of distribution of 0.05 L/kg. 19.4 ± 2.4 mL/h/kg.
机译:建立了快速,灵敏,特异的超滤电感耦合等离子体质谱方法,并验证了非转铁蛋白结合铁(NTBI),转铁蛋白结合铁(TBI),药物结合铁(DI)和总铁(TI)的定量在蔗糖溶液中静脉内(IV)给予葡萄糖酸铁纳米颗粒(Ferrlecit ®)后,在相同的大鼠血清样品中提取了相同的样品。带有30 kDa分子截止过滤器的超滤用于样品净化。使用不同的洗脱溶剂从样品血清中分离出每种形式的铁。在4%硝酸中微波消解后,分离出的馏分进行电感耦合质谱分析。该方法的重现性通过精密度和准确性进行评估。校正曲线显示线性范围为5–500 ng / mL,回归(r 2 )大于0.998。该方法有效地定量了静脉注射Ferrlecit ®后的大鼠药代动力学研究样品。该方法已成功地应用于Ferrlecit在大鼠中的药代动力学(PK)研究。胶态铁遵循一级动力学,半衰期为2.2小时,给药后12小时达到背景或给药前水平。该药物的清除率为0.31 mL / min / kg,分布体积为0.05 L / kg。 19.4±2.4毫升/小时/千克。

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