School of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI, 53705, USA.
Assistance Publique, Hôpitaux de Marseille, Centre Hospitalier Universitaire La Timone, Service de Cardiologie, Marseille, France.
Drugs R D. 2022 Mar;22(1):61-70. doi: 10.1007/s40268-021-00378-9. Epub 2022 Feb 12.
Vasovagal syncope is a common cause of syncope which, if recurrent, can have multiple negative consequences such as injury and occupational disability. Various medications can be used to decrease the recurrence of vasovagal syncope but there are no drugs that can be used by patients to interrupt a perceived vasovagal episode.
A phase I study was performed to evaluate the tolerability and safety of a gel formulation containing capsaicin (1 mg), phenylephrine HCL (PE) and caffeine citrate (200 mg) (CPC) in normal adult volunteers. Secondary objectives were to characterize the pharmacokinetics (PK) of the CPC formulation and the highest dose of PE needed to achieve a target increase in systolic BP of at least 40 mmHg. After receiving the first dose, a second dose of the CPC mixture was administered at 2 h. Suboptimal changes in systolic blood pressure (SBP) were noted at PE doses of 0.6, 1.2, and 1.8 mg, therefore a second cohort was studied at PE doses of 10, 20, and 30 mg. Blood samples were collected in rapid sequence and were assayed for all three drugs.
A total of 17 subjects received the drug with no serious adverse effects reported. All doses were well tolerated, although the capsaicin content usually caused expected temporary oral and gastric discomfort. One subject did not complete the study because of a vasovagal reaction that was associated with the frequent blood sampling. There was a 5-25 min lag in the appearance of measurable blood concentrations of capsaicin and phenylephrine. Most subjects had baseline caffeine concentrations from dietary use, with a gradual increase noted after 15 min consistent with GI absorption. Although the intended criterion of a 40 mmHg increase in SBP was not reached, a clinically significant increase in BP for at least 15 min was noted in the six subjects who received the highest dose of PE (30 mg), with a gradual decline over the next 2 h.
The ternary mixture of capsaicin, phenylephrine, and caffeine was well tolerated when administered as two sublingual/oral doses over a 2-h period.
血管迷走性晕厥是晕厥的常见原因,如果反复发作,可能会导致多种负面后果,如受伤和职业残疾。各种药物可用于减少血管迷走性晕厥的复发,但尚无药物可供患者用于中断感知到的血管迷走性发作。
进行了一项 I 期研究,以评估含有辣椒素(1 毫克)、盐酸苯福林(PE)和柠檬酸咖啡因(200 毫克)(CPC)的凝胶制剂在正常成年志愿者中的耐受性和安全性。次要目标是描述 CPC 制剂的药代动力学(PK)和达到至少 40mmHg 收缩压目标增加所需的最高 PE 剂量。在接受第一剂后,在 2 小时时给予 CPC 混合物的第二剂。在 0.6、1.2 和 1.8mg 的 PE 剂量下,注意到收缩压(SBP)的变化不理想,因此在 10、20 和 30mg 的 PE 剂量下研究了第二队列。快速顺序采集血样,并检测所有三种药物。
共有 17 名受试者接受了药物治疗,没有报告严重不良事件。所有剂量均耐受良好,尽管辣椒素含量通常会导致预期的暂时口腔和胃部不适。一名受试者因与频繁采血相关的血管迷走反应而未完成研究。在可测量的辣椒素和苯福林血药浓度出现之前,有 5-25 分钟的延迟。大多数受试者由于饮食原因基线咖啡因浓度升高,15 分钟后逐渐增加,与 GI 吸收一致。尽管未达到收缩压增加 40mmHg 的预期标准,但在接受最高剂量 PE(30mg)的六名受试者中,至少 15 分钟内血压有临床显著增加,在接下来的 2 小时内逐渐下降。
在 2 小时内给予两次舌下/口服剂量时,辣椒素、苯福林和咖啡因的三元混合物耐受性良好。