Nace G S, Wood A J
Clin Pharmacokinet. 1987 Jul;13(1):51-64. doi: 10.2165/00003088-198713010-00003.
Beta-adrenoceptor antagonists are among the most commonly prescribed classes of drugs. They are indicated for the treatment of diseases such as hypertension and angina pectoris, in which long term therapy is often required. Since many beta-adrenoceptor antagonists have short plasma elimination half-lives, divided daily dosing has often been necessary in order to provide continuous beta-blockade throughout the day. However, such multiple-dose schedules may promote patient non-compliance and failure of the prescribed regimen. Long acting propranolol is a sustained release formulation of propranolol which has been developed to maintain therapeutic plasma propranolol concentrations throughout a 24-hour period while allowing once-daily dosing. Compared with conventionally formulated propranolol, long acting propranolol has a prolonged terminal half-life (8 to 11 hours), due to slower absorption from the gut. Systemic bioavailability of long acting propranolol is 30 to 50% less than that of the conventional formulation. This difference may result from increased hepatic metabolism. Peak drug concentrations are significantly lower than following identical doses of conventional propranolol, and the time to peak drug concentrations following administration is delayed. Relatively constant plasma concentrations and clinically significant inhibition of exercise-induced tachycardia are maintained throughout a 24-hour dosing interval following once-daily long acting propranolol. Once-daily long acting propranolol is as effective as divided doses of conventional propranolol for the treatment of hypertension and angina pectoris. Efficacy also appears comparable with once-daily administration of long acting conventional beta-adrenoceptor antagonists such as atenolol and nadolol. Once-daily long acting propranolol provides clinically significant sustained beta-adrenoceptor blockade and offers the potential for improved patient compliance due to once-daily dosing. Since provision of sustained beta-adrenoceptor blockade appears to be particularly important in the treatment of angina, this may be the principal indication for which long acting propranolol has a therapeutic advantage independent of its potential to improve compliance.
β-肾上腺素受体拮抗剂是最常用的处方药类别之一。它们适用于治疗高血压和心绞痛等疾病,这些疾病通常需要长期治疗。由于许多β-肾上腺素受体拮抗剂的血浆消除半衰期较短,因此通常需要每日分次给药,以便在一天中持续进行β受体阻滞。然而,这种多剂量给药方案可能会导致患者不依从以及规定治疗方案失败。长效普萘洛尔是普萘洛尔的缓释制剂,其开发目的是在24小时内维持治疗性血浆普萘洛尔浓度,同时允许每日一次给药。与传统剂型的普萘洛尔相比,长效普萘洛尔的终末半衰期延长(8至11小时),这是由于其从肠道吸收较慢。长效普萘洛尔的全身生物利用度比传统剂型低30%至50%。这种差异可能是由于肝脏代谢增加所致。药物峰值浓度明显低于相同剂量的传统普萘洛尔,给药后达到药物峰值浓度的时间延迟。在每日一次服用长效普萘洛尔后的24小时给药间隔内,血浆浓度相对恒定,并且对运动诱发的心动过速具有临床显著的抑制作用。每日一次的长效普萘洛尔在治疗高血压和心绞痛方面与传统普萘洛尔分次给药一样有效。其疗效似乎也与每日一次服用长效传统β-肾上腺素受体拮抗剂(如阿替洛尔和纳多洛尔)相当。每日一次的长效普萘洛尔可提供具有临床意义的持续β-肾上腺素受体阻滞,并且由于每日一次给药,有可能提高患者的依从性。由于在心绞痛治疗中提供持续的β-肾上腺素受体阻滞似乎尤为重要,这可能是长效普萘洛尔具有独立于其改善依从性潜力的治疗优势的主要适应症。