Neugebauer G, Akpan W, Stemmle B, Jaeger H, Mosberg H, Lutz D
Boehringer Mannheim GmbH, Clinical Pharmacology, FRG.
Int J Clin Pharmacol Ther Toxicol. 1989 Jan;27(1):34-8.
From the in vitro release-rate constant of a new sustained-release (SR) preparation of 40 mg isosorbide-5-mononitrate, the concentration-time profile in healthy subjects could be excellently predicted. Therapeutically, effective concentrations of 100 ng/ml were achieved within 20 min and lasted up to a maximum of 15.6 h. The decline of concentrations below this value thereafter, guarantees the absence of tolerance development in chronic therapy. In a three-period change-over study, two other commercial SR preparations exhibited only 79% and 53% of the bioavailability of the new formulation, which was significant in both cases. Compared with literature data, the absolute bioavailability of the new form should lie in the order of at least 85%.
根据新的40毫克单硝酸异山梨酯缓释制剂的体外释放速率常数,能够很好地预测健康受试者体内的浓度-时间曲线。在治疗上,20分钟内就能达到100纳克/毫升的有效浓度,且最长可持续15.6小时。此后浓度降至该值以下,可确保在长期治疗中不会产生耐受性。在一项三期交叉研究中,另外两种市售缓释制剂的生物利用度仅为新制剂的79%和53%,两种情况均具有显著性差异。与文献数据相比,新剂型的绝对生物利用度至少应在85%左右。