Altamura A C, Melorio T, Invernizzi G, Colacurcio F, Gomeni R
Psychopharmacology (Berl). 1983;81(4):281-5. doi: 10.1007/BF00427563.
Dose kinetics and side effects of viloxazine (VLX) in 16 healthy volunteers (range age 25-90 years) were studied after single oral administration of 200 mg of VLX. Significant differences in peak plasma values (P less than 0.01), t1/2 (P less than 0.01) and Cl/F (P less than 0.05) were found between subjects under 50 and over 60 years. Positive correlations were found between age and peak plasma values (P less than 0.05), age and AUC (P less than 0.01). No correlations were found between age, t1/2 and Cl/F, due to the high interindividual variability in pharmacokinetic profiles. Total reported and observed side effects scores were higher overall in subjects under 50 years than over 60 years and were inversely correlated to AUC (P less than 0.05). Drowsiness was inversely related to the age of subjects (P less than 0.05). Our data support the importance of single dose kinetic studies, particularly for new antidepressants, in relation to age, both to emphasize differences in pharmacokinetic profiles and to predict side effects during chronic treatment.
在16名健康志愿者(年龄范围25 - 90岁)单次口服200毫克维洛沙嗪(VLX)后,对其剂量动力学和副作用进行了研究。发现50岁以下和60岁以上受试者之间的血浆峰值(P < 0.01)、t1/2(P < 0.01)和Cl/F(P < 0.05)存在显著差异。年龄与血浆峰值之间存在正相关(P < 0.05),年龄与AUC之间存在正相关(P < 0.01)。由于药代动力学特征存在高度个体间变异性,年龄、t1/2和Cl/F之间未发现相关性。总体而言,报告和观察到的副作用总评分在50岁以下受试者中高于60岁以上受试者,且与AUC呈负相关(P < 0.05)。嗜睡与受试者年龄呈负相关(P < 0.05)。我们的数据支持单剂量动力学研究的重要性,特别是对于新型抗抑郁药,与年龄相关,既强调药代动力学特征的差异,又预测长期治疗期间的副作用。