Stability and Compatibility of an Intramuscular Fetal Anesthetic Cocktail for Fetal Intervention.

IF 1.6 3区 医学 Q3 OBSTETRICS & GYNECOLOGY Fetal Diagnosis and Therapy Pub Date : 2024-01-01 Epub Date: 2024-03-30 DOI:10.1159/000538611
Emma L Ross, Cristina L Wood, Michael F Wempe
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Abstract

Introduction: The aim of the study was to evaluate chemical stability and physical compatibility when combining fentanyl, rocuronium, and atropine in a fixed ratio to support intramuscular drug delivery during fetal intervention and surgery.

Methods: A highly concentrated combination of fentanyl, rocuronium, and atropine was created based on common prescribing practices at a maternal-fetal care center. Chemical stability testing was completed using liquid chromatograph mass spectrometry-mass spectrometry (LC/MS-MS) to detect and quantitate atropine, rocuronium, and fentanyl, with fentanyl-d5 being an internal standard at 6, 12, 24, and 36 h following sample preparation. Physical compatibility testing was completed using United States Pharmacopeia (USP) <788> recommended analytical technique of light obscuration in addition to novel backgrounded membrane imaging at 6 and 24 h following sample preparation. Physical compatibility was determined using USP <788> particle count limits for both techniques.

Results: Based on LC/MS-MS results, the samples retained expected medication concentrations at all time points tested. For physical compatibility testing, the particle counts met criteria to be considered compatible per USP <788> large-volume particle count thresholds at 6 h by both methods but exceeded tolerable thresholds at 24 h.

Discussion/conclusion: The combination of rocuronium, fentanyl, and atropine for intramuscular fetal administration is physically compatible and chemically stable for 6 h.

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用于胎儿干预的肌肉注射胎儿麻醉鸡尾酒的稳定性和兼容性。
引言目的:评估芬太尼、罗库洛铵和阿托品按固定比例混合后的化学稳定性和物理相容性,以支持胎儿干预和手术过程中的肌肉给药:方法: 根据孕产妇胎儿护理中心的常见处方做法,制作了芬太尼、罗库洛铵和阿托品的高浓度组合。使用液相色谱-质谱法(LC/MS-MS)完成了化学稳定性测试,以检测和定量阿托品、罗库铵和芬太尼,并以芬太尼-d5 为内标,分别在样品制备后的 6、12、24 和 36 小时进行测试。物理兼容性测试采用美国药典 (USP) 推荐的光掩蔽 (LO) 分析技术以及新型背景膜成像 (BMI),分别在样品制备后 6 小时和 24 小时完成。两种技术的物理兼容性均采用 USP 粒子计数限值来确定:结果:根据 LC/MS-MS 结果,样品在所有测试时间点都保留了预期的药物浓度。在物理兼容性测试中,根据 USP 大容量粒子计数阈值,两种方法在 6 小时内的粒子计数均符合兼容性标准,但在 24 小时内超过了可容忍阈值:讨论/结论:用于胎儿肌肉注射的罗库溴铵、芬太尼和阿托品组合物在 6 小时内具有物理兼容性和化学稳定性。
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来源期刊
Fetal Diagnosis and Therapy
Fetal Diagnosis and Therapy 医学-妇产科学
CiteScore
4.70
自引率
9.10%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The first journal to focus on the fetus as a patient, ''Fetal Diagnosis and Therapy'' provides a wide range of biomedical specialists with a single source of reports encompassing the common discipline of fetal medicine.
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