Pinnas J L, Bhatt B D, Campbell S C, Kemp J P, Tinkelman D G
Chest. 1987 Apr;91(4):533-9. doi: 10.1378/chest.91.4.533.
Bitolterol mesylate, a new beta 2 adrenergic bronchodilator, is a "pro-drug" which is activated by esterases in the lung. In order to determine the optimal bronchodilator dose of bitolterol, six doses, (0.5 mg, 1.0 mg, 1.5 mg, 2.0 mg, 2.5 mg and 3.0 mg), were administered by closed-port, intermittent-flow nebulization (CPIF) to asthmatic patients on different days. For most patients, the onset of bronchodilator activity (FEV1 increase of at least 15 percent above baseline) occurred within 5 minutes and lasted at least 8 hours. Maximum mean increases in FEV1 were 46-50 percent at the 1.0 mg to 3.0 mg doses. Beyond the 1.0 mg dose, there was no significant improvement in bronchodilator effect, but adverse effects, particularly tremor, increased at higher doses. The optimal dose of bitolterol administered by CPIF was determined to be 1.0 mg which is similar to the dose of bitolterol recommended for use by metered-dose inhaler (MDI) which is 0.7 mg to 1.1 mg. If continuous-flow nebulization is used, two-three times more drug may be needed for a comparable effect. Bitolterol appears to be a safe, effective and long-lasting bronchodilator when administered by jet nebulization.
甲磺酸比托特罗是一种新型的β2肾上腺素能支气管扩张剂,它是一种“前体药物”,在肺中被酯酶激活。为了确定比托特罗的最佳支气管扩张剂量,在不同日期对哮喘患者采用密闭端口间歇流雾化(CPIF)方式给予六个剂量(0.5毫克、1.0毫克、1.5毫克、2.0毫克、2.5毫克和3.0毫克)。对于大多数患者,支气管扩张活性的起效(第一秒用力呼气量[FEV1]比基线增加至少15%)在5分钟内出现,并持续至少8小时。在1.0毫克至3.0毫克剂量时,FEV1的最大平均增加量为46%-50%。超过1.0毫克剂量后,支气管扩张效果没有显著改善,但在更高剂量下不良反应,尤其是震颤,会增加。经CPIF给药的比托特罗最佳剂量确定为1.0毫克,这与定量吸入器(MDI)推荐使用的比托特罗剂量(0.7毫克至1.1毫克)相似。如果使用连续流雾化,为获得相当的效果可能需要两到三倍的药物。通过喷射雾化给药时,比托特罗似乎是一种安全、有效且作用持久的支气管扩张剂。