Langtry H D, Spencer C M
Adis International Limited, Auckland, New Zealand.
Drugs. 1997 May;53(5):867-84. doi: 10.2165/00003495-199753050-00013.
Nisoldipine coat-core is an extended-release once-daily formulation of a dihydropyridine calcium antagonist effective in the treatment of chronic stable angina pectoris. With immediate-release formulations of nisoldipine, plasma drug concentrations that produce therapeutic effects result rapidly, but are not sustained and do not maintain the effects throughout a 12-hour dosage interval. In contrast, with nisoldipine coat-core, a gradual increase in plasma nisoldipine concentrations occurs over 12 hours and therapeutic concentrations are then maintained for the duration of a 24-hour dosage interval. In dosages of 10 to 60 mg once daily, nisoldipine coat-core controls symptoms of angina and improves exercise-induced signs of ischaemia in patients with stable angina. Compared with placebo, daily nisoldipine coat-core doses of > or = 20 mg provide statistically significant increases in total exercise time and time to produce angina and a trend towards an increase in the time to produce 1 mm ST segment depression, in exercise tests conducted approximately 23 hours postdose. When administered in 20 and 40 mg daily doses, nisoldipine coat-core produces improvements in exercise test parameters that are similar to those seen with amlodipine 5 or 10 mg/day or regular-release or sustained-release (SR) diltiazem 240 mg/day. The frequency of daily angina attacks and consumption of short-acting nitrates are also reduced by nisoldipine to a similar extent to that observed with these other agents. After longer term (1 year) administration of 10 to 60 mg daily, improvements in exercise test parameters are maintained, with equivalent anti-ischaemic efficacy seen in patients receiving nisoldipine coat-core alone or with background nitrate or beta-blocker therapy. Adverse events associated with nisoldipine coat-core are typical of the dihydropyridine class of calcium antagonists, with peripheral oedema and headache being most common. Nisoldipine coat-core appears to be associated with fewer deaths than placebo, notably in the DEFIANT-II (Doppler Flow and Echocardiography in Functional Cardiac Insufficiency: Assessment of Nisoldipine Therapy II) study, where only 1 death occurred with nisoldipine compared with 7 in the placebo group. Nisoldipine should not be taken during phenytoin therapy. In addition, grapefruit juice should be avoided during nisoldipine therapy and nisoldipine should not be taken concurrently with high-fat meals. Thus, the coat-core formulation of nisoldipine appears to have overcome the limitations of the shorter duration of action of immediate-release nisoldipine. Nisoldipine coat-core is well tolerated and once-daily administration produces a long duration of effective anti-ischaemic relief in patients with chronic stable angina pectoris.
尼索地平包芯片是一种二氢吡啶类钙拮抗剂的缓释制剂,每日服用一次,对治疗慢性稳定型心绞痛有效。对于尼索地平的速释制剂,产生治疗效果的血浆药物浓度迅速出现,但无法持续,且不能在12小时的给药间隔内维持疗效。相比之下,尼索地平包芯片在12小时内血浆尼索地平浓度逐渐升高,然后在24小时的给药间隔内维持治疗浓度。每日剂量为10至60毫克时,尼索地平包芯片可控制稳定型心绞痛患者的心绞痛症状,并改善运动诱发的缺血体征。与安慰剂相比,每日服用尼索地平包芯片剂量≥20毫克时,在给药后约23小时进行的运动试验中,总运动时间、出现心绞痛的时间有统计学显著增加,且出现1毫米ST段压低的时间有增加趋势。每日服用20毫克和40毫克剂量时,尼索地平包芯片改善运动试验参数的效果与氨氯地平每日5毫克或10毫克或普通释放或缓释地尔硫䓬每日240毫克相似。尼索地平还可将每日心绞痛发作频率和短效硝酸盐的消耗量降低到与这些其他药物相似的程度。长期(1年)每日服用10至60毫克后,运动试验参数的改善得以维持,单独服用尼索地平包芯片或联合使用硝酸酯类或β受体阻滞剂进行背景治疗的患者,抗缺血疗效相当。与尼索地平包芯片相关的不良事件是二氢吡啶类钙拮抗剂的典型不良反应,外周水肿和头痛最为常见。尼索地平包芯片的死亡人数似乎比安慰剂少,尤其是在DEFIANT-II(功能性心力衰竭中的多普勒血流和超声心动图:尼索地平治疗评估II)研究中,尼索地平组仅发生1例死亡,而安慰剂组有7例。苯妥英治疗期间不应服用尼索地平。此外,尼索地平治疗期间应避免饮用葡萄柚汁,且不应与高脂肪餐同时服用。因此,尼索地平的包芯片制剂似乎克服了尼索地平速释制剂作用持续时间较短的局限性。尼索地平包芯片耐受性良好,每日一次给药可在慢性稳定型心绞痛患者中产生长时间有效的抗缺血缓解作用。