【24h】

Fortum stability in different disposable infusion devices by pyridine assay.

机译:通过吡啶测定法在不同的一次性输液器中的稳定性。

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摘要

The stability of ceftazidime in 5% dextrose injection and 0.9% sodium chloride injection when stored in a different disposable infusion device was determined. Solutions of ceftazidime 40 mg/ml were used to fill the drug administration devices. Stability was determined for both 5% dextrose injection and 0.9% sodium chloride injection solutions at 37 degrees C in four disposable infusion devices. Ceftazidime and its mean degradation product, pyridine, were simultaneously assayed in triplicate by a stability-indicating high-performance liquid chromatographic (HPLC) method. This method was simple, sensitive (limit of quantitation (LOQ), 2 ng injected for both compounds), rapid (run time was 7 min) and precise (mean recovery was 100.5+/-2.9 and 103.6+/-1.9% for pyridine and ceftazidime, respectively). The ceftazidime stability in the 5% dextrose solution was lower than in the 0.9% sodium chloride solution. When stored at 37 degrees C in a disposable infusion device, the stability of the ceftazidime is included in large hourly range, depending strongly on the manufacturer. The stability of ceftazidime exceed 19 h in none studied cases. The pyridine formed in 24 h was in the range of 100-400 mg depending on devices and infusions.
机译:确定了头孢他啶在5%葡萄糖注射液和0.9%氯化钠注射液中的稳定性(当储存在不同的一次性输液设备中时)。使用头孢他啶40 mg / ml的溶液填充药物给药装置。在四个一次性输液设备中,在37摄氏度下测定了5%葡萄糖注射液和0.9%氯化钠注射液的稳定性。头孢他啶及其平均降解产物吡啶通过指示稳定性的高效液相色谱(HPLC)方法同时进行三次重复测定。该方法简单,灵敏(定量限(LOQ),两种化合物均进样2 ng),快速(运行时间为7分钟)且精确(吡啶的平均回收率为100.5 +/- 2.9和103.6 +/- 1.9%和头孢他啶)。 5%葡萄糖溶液中的头孢他啶稳定性低于0.9%氯化钠溶液中的头孢他啶稳定性。当在37℃下储存在一次性输注装置中时,头孢他啶的稳定性在大的每小时范围内包括在内,这在很大程度上取决于制造商。在没有研究的病例中,头孢他啶的稳定性超过19小时。在24小时内形成的吡啶在100-400 mg范围内,具体取决于器械和输注液。

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