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纳洛酮产品在标签有效期过后的化学稳定性。

Chemical stability of naloxone products beyond their labeled expiration dates.

机构信息

Department of Pharmaceutical Sciences, Appalachian College of Pharmacy, Oakwood, Virginia.

Commonwealth of Virginia, Richmond, Virginia.

出版信息

J Opioid Manag. 2022 Jan-Feb;18(1):39-46. doi: 10.5055/jom.2022.0693.

Abstract

OBJECTIVE

The purpose of this study was to evaluate the chemical stability of previously dispensed, expired naloxone products.

SETTING

When properly stored, certain products maintain stable, defined as within compendia acceptability, beyond their manufacturer's expiration date. Stockpiling life-saving medications such as the opioid overdose reversing agent naloxone nasal spray (NNS) or injection (NIJ) is of utmost importance to ensure public health emergency preparedness and response. Design/interventions/methods: After each naloxone product was stored at room temperature for several months (6-19) past their labeled expiration date, the level of active therapeutic content and the presence of degradation impurity, 2,29'-bisnaloxone, were evaluated via chromatographic separation with waters higher performance liquid chromatography integrated using the Waters X-Select CSHC-18. The effluent was detected at 229 nm.

MAIN OUTCOME MEASURE

Active naloxone presence and the presence of degradation impurity, 2,29'-bisnaloxone, were evaluated.

RESULTS

The mean potency of naloxone in both NNS and NIJ, up to 10 and 19 months post-expiration, respectively, is within the 90-110 percent United States Pharmacopeia acceptance limit (NNS: 102.8 ± 2.6 percent and NIJ: 106.0 ± 1.3 percent). No impurity was detected in any chromatogram of the expired products.

CONCLUSION

In summary, since both NNS and NIJ were found to be chemically stable beyond 10 months of the expiration date, shelf-life extension of climate controlled, commercially available naloxone products should be further investigated as a potential cost savings measure for national strategic stockpiles, emergency medical services, hospitals, and public responders.

摘要

目的

本研究旨在评估已配药过期的纳洛酮产品的化学稳定性。

背景

在适当储存的情况下,某些产品在制造商规定的有效期之后仍能保持稳定,符合药典的可接受范围。储备救命药物,如阿片类药物过量逆转剂纳洛酮鼻喷雾剂(NNS)或纳洛酮注射液(NIJ),对于确保公共卫生应急准备和应对至关重要。

设计/干预措施/方法:在每个纳洛酮产品在室温下储存超过标签有效期数月(6-19 个月)后,通过 Waters 更高性能液相色谱与 Waters X-Select CSHC-18 的集成,评估活性治疗成分的水平和降解杂质 2,29'-双纳洛酮的存在。在 229nm 处检测流出物。

主要观察指标

评估活性纳洛酮的存在和降解杂质 2,29'-双纳洛酮的存在。

结果

在有效期后 10 个月和 19 个月时,NNS 和 NIJ 的纳洛酮平均效价均在 90-110%美国药典接受限度内(NNS:102.8±2.6%和 NIJ:106.0±1.3%)。在过期产品的任何色谱图中均未检测到杂质。

结论

总之,由于 NNS 和 NIJ 在有效期后 10 个月以上均被发现化学稳定,因此应进一步研究控制气候、市售纳洛酮产品的保质期延长问题,作为国家战略储备、急救医疗服务、医院和公共应急响应者的潜在成本节约措施。

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