Stability of Dilute Oral Morphine Solution for Neonatal Abstinence Syndrome

被引:5
作者
Sauberan, Jason [1 ,2 ]
Rossi, Steven
Kim, Jae H. [3 ]
机构
[1] Univ Calif San Diego, Med Ctr, Dept Pharm, San Diego, CA 92103 USA
[2] UCSD Skaggs Sch Pharm & Pharmaceut Sci, San Diego, CA USA
[3] UCSD Sch Med, Dept Pediat, Div Neonatol, San Diego, CA USA
关键词
D O I
10.1097/ADM.0b013e318280f495
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Oral morphine is a recommended option for the treatment of neonatal abstinence syndrome (NAS). Commercially available oral morphine solution products in the United States are not formulated in concentrations appropriate for use in neonates. Objective: To test the stability of a diluted oral morphine solution for treatment of NAS. Methods: Ethanol-free morphine 2 mg/mL oral solution was diluted to 0.4 mg/mL with sterile water and stored in a light protected container at room temperature (20 degrees C-25 degrees C). The change in morphine concentration over time was measured by liquid chromatography mass spectrometry with simultaneous ultraviolet diode array detection. Results: The test morphine solution retained 107% of its original concentration after 60 days. Conclusion: Extemporaneously prepared 0.4 mg/mL oral morphine solution is suitable for use in the treatment of NAS as a potentially safer alternative to opium-containing agents. (J Addict Med 2013;7:113-115)
引用
收藏
页码:113 / 115
页数:3
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