首页> 外文期刊>Journal of Clinical Pharmacy and Therapeutics >Stability and compatibility of anakinra with intravenous cimetidine hydrochloride or famotidine in 0.9% sodium chloride injection.
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Stability and compatibility of anakinra with intravenous cimetidine hydrochloride or famotidine in 0.9% sodium chloride injection.

机译:Anakinra与0.9%氯化钠注射液中的静脉注射西咪替丁盐酸盐或法莫替丁的稳定性和相容性。

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We designed a study to evaluate the stability and compatibility of anakinra (recombinant human interleukin-1 receptor antagonist) with cimetidine hydrochloride or famotidine in 0.9% sodium chloride injection during a 4-h period at room temperature (22 degrees C) and light. Anakinra was diluted in 0.9% sodium chloride to concentrations of 4 and 36 mg/ml. At each concentration, anakinra was mixed with 3 mg/ml cimetidine or with 1 mg/ml famotidine, in a 50:50 proportion and stored in plastic culture vials with polypropylene caps. The mean concentrations of anakinra, cimetidine hydrochloride, and famotidine exceeded 95% of initial concentrations throughout the study. No changes were noted in the physical appearance, pH, or the chromatograms during the study period. Thus, anakinra appears to be stable and compatible with cimetidine hydrochloride or famotidine when diluted into 0.9% sodium chloride injection for 4 h at ambient room temperature and light.
机译:我们设计了一项研究,以评估anakinra(重组人白介素1受体拮抗剂)与西咪替丁盐酸盐或法莫替丁在0.9%氯化钠注射液中于室温(22摄氏度)和光照下4小时内的稳定性和相容性。将Anakinra在0.9%氯化钠中稀释至4和36 mg / ml的浓度。在每种浓度下,将anakinra与3 mg / ml西咪替丁或1 mg / ml法莫替丁按50:50的比例混合,并保存在带有聚丙烯盖的塑料培养瓶中。在整个研究过程中,anakinra,西咪替丁盐酸盐和法莫替丁的平均浓度超过初始浓度的95%。在研究期间,物理外观,pH或色谱图未见变化。因此,当在室温和光照下稀释到0.9%氯化钠注射液中4h时,anakinra似乎是稳定的并且与西咪替丁盐酸盐或法莫替丁相容。

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