Tanimoto Sarina, Kaliner Michael, Lockey Richard F, Ebisawa Motohiro, Koplowitz Luana Pesco, Koplowitz Barry, Lowenthal Richard
ARS Pharmaceuticals, Inc, San Diego, California.
Institute for Asthma & Allergy, Wheaton, Maryland.
Ann Allergy Asthma Immunol. 2023 Apr;130(4):508-514.e1. doi: 10.1016/j.anai.2022.10.024. Epub 2022 Nov 2.
Manual intramuscular epinephrine injection is the standard of care for treating severe allergic reactions and anaphylaxis. Epinephrine autoinjectors were approved on the basis of the assumption that their pharmacokinetic and pharmacodynamic profiles are equivalent to manual intramuscular injection; however, although there is emerging evidence for product-related differences in pharmacokinetic profiles, very little is known about the comparative pharmacodynamic profiles.
To compare pharmacokinetic and pharmacodynamic profiles of epinephrine delivered through manual intramuscular injection, autoinjectors, and intranasal spray.
This integrated analysis was based on data from 4 randomized cross-over phase 1 trials that compared the pharmacokinetics and pharmacodynamics of epinephrine using manual intramuscular epinephrine 0.3 mg injection, epinephrine 0.3 mg autoinjectors (Symjepi and EpiPen), and epinephrine 1 mg intranasal spray (neffy).
Data from 175 participants showed that although neffy (1.0 mg intranasal spray) resulted in a maximum concentration (258 pg/mL) that was lower than or comparable with manual epinephrine intramuscular injection (254 pg/mL), Symjepi (438 pg/mL) and EpiPen (503 pg/mL), it led to comparable increases in systolic blood pressure (maximum effect [E], 16.9, 10.9, 14.9, and 18.1 mm Hg, respectively). The effect of neffy on diastolic blood pressure was also markedly more pronounced than that of other products (E, 9.32, 5.51, 5.78, and 5.93 mm Hg, respectively).
Intranasal delivery of epinephrine using neffy increases systolic blood pressure more efficiently than do manual intramuscular injection and epinephrine autoinjectors, despite lower maximum plasma concentrations.
手动肌内注射肾上腺素是治疗严重过敏反应和过敏症的标准治疗方法。肾上腺素自动注射器是在其药代动力学和药效学特征等同于手动肌内注射的假设基础上获得批准的;然而,尽管有新证据表明不同产品的药代动力学特征存在差异,但对于比较药效学特征却知之甚少。
比较通过手动肌内注射、自动注射器和鼻内喷雾给药的肾上腺素的药代动力学和药效学特征。
这项综合分析基于4项随机交叉1期试验的数据,这些试验比较了使用0.3mg手动肌内注射肾上腺素、0.3mg肾上腺素自动注射器(Symjepi和EpiPen)和1mg肾上腺素鼻内喷雾(neffy)时肾上腺素的药代动力学和药效学。
175名参与者的数据显示,尽管neffy(1.0mg鼻内喷雾)产生的最大浓度(258pg/mL)低于或与手动肌内注射肾上腺素(254pg/mL)、Symjepi(438pg/mL)和EpiPen(503pg/mL)相当,但它导致收缩压有类似的升高(最大效应[E]分别为16.9、10.9、14.9和18.1mmHg)。neffy对舒张压的影响也明显比其他产品更显著(E分别为9.32、5.51、5.78和5.93mmHg)。
尽管最大血浆浓度较低,但使用neffy鼻内给药肾上腺素比手动肌内注射和肾上腺素自动注射器更有效地提高收缩压。