Chaoui Mariam, Chevrel Sophie, Perinel-Ragey Sophie, Prévôt Nathalie, Pourchez Jérémie
Mines Saint-Etienne, University Lyon, University Jean Monnet, INSERM, U 1059 Sainbiose, Centre CIS, F -42023, Saint-Etienne, France.
INSERM, U1059, F-42023, Saint Etienne, France.
Pharm Res. 2022 Mar;39(3):587-597. doi: 10.1007/s11095-022-03187-0. Epub 2022 Feb 8.
The performance of new-generation high-power electronic nicotine delivery system (ENDS) for the administration of inhaled terbutaline was assessed.
The formulation of e-liquid was carried out using terbutaline in combination with 1, 3- propanediol. Several terbutaline concentrations (from 0.3125 to 2.500 mg / mL) and power levels (from 15 to 35 W) were assessed using a box type ENDS. The respirable drug dose was determined using a Glass Twin Impinger and quantified by liquid chromatography coupled with a UV-detector. The Next Generation Impactor and the Dekati Low Pressure Impactor were used to measure the aerosol particle size distribution in drug mass. The results were compared with a jet nebulizer (Cirrus TM 2) similar to the usual clinical conditions (2 mL at [terbutaline] of 2.5 mg / mL).
The optimal conditions to maximize terbutaline delivery using ENDS are a drug concentration at 1 mg/mL, and a power level at 30 W, to reach a respirable dose of 8.73 ± 0.90 µg/puff. By contrast, during a 5 min nebulization, the respirable dose of terbutaline was 1040 ± 33 µg whatever the cascade impactors and the aerosol devices used. The mass median aerodynamic diameter (MMAD) remains similar for jet nebulizer and ENDS in the 1.74-2.07 µm range.
Compared to the jet nebulizer, a same respirable dose of terbutaline at the same range of aerosol size distribution was delivered by ENDS if 120 puffs were performed. The ENDS can be considered as an alternative aerosol device for terbutaline delivery.
评估新一代大功率电子尼古丁传送系统(ENDS)吸入特布他林的给药性能。
使用特布他林与 1,3-丙二醇组合进行电子液体配方。使用盒式 ENDS 评估了几种特布他林浓度(0.3125 至 2.500 mg/mL)和功率水平(15 至 35 W)。使用玻璃双冲击器测定可吸入药物剂量,并通过与紫外检测器耦合的液相色谱法进行定量。使用下一代撞击器和 Dekati 低压撞击器测量药物质量中的气溶胶粒度分布。结果与类似于常规临床条件(2.5 mg/mL 时 2 mL)的射流式雾化器(Cirrus TM 2)进行比较。
使用 ENDS 最大化特布他林输送的最佳条件是药物浓度为 1 mg/mL,功率水平为 30 W,以达到 8.73±0.90 µg/吸的可吸入剂量。相比之下,在 5 分钟的雾化过程中,无论使用级联撞击器和气溶胶设备如何,特布他林的可吸入剂量均为 1040±33 µg。射流式雾化器和 ENDS 的质量中值空气动力学直径(MMAD)在 1.74-2.07 µm 范围内保持相似。
与射流式雾化器相比,如果进行 120 次抽吸,可通过 ENDS 输送相同范围的气溶胶尺寸分布的相同可吸入特布他林剂量。ENDS 可以被认为是特布他林输送的另一种气溶胶装置。