RELATION BETWEEN CLINICAL EFFICACY AND PHARMACOKINETIC PARAMETERS AFTER SUBLINGUAL APOMORPHINE IN PARKINSONS-DISEASE

Apomorphine was administered sublingually in two single doses (0.3 and 0.6 mg/kg) to seven patients with idiopathic Parkinson's disease (PD) to assess the relation between clinical efficacy, dosage, and pharmacokinetic parameters of apomorphine. On day 1 and day 3, patients were given 0.3 mg/kg and 0.6 mg/kg of apomorphine, respectively (3 mg tablets). Before apomorphine administration and during the following 4 h, motor score was assessed by measuring tremor, akinesia scores, rising from a chair, and walking speed. The delay to turn on was not different between the two doses but after the 0.3 mg/kg dose, only three patients turned on, whereas all the patients treated with 0.6 mg/kg turned on. Apomorphine (0.3 mg/kg) induced a shorter duration of the ''on'' period than 0.6 mg/kg (0.3 mg/kg: 24.2 +/- 14.6 min; 0.6 mg/kg: 86.7 +/-14.9 min). The time to obtain the peak plasma concentration (t(max)) obtained with the two doses were not different (0.3 mg/kg: 31.5 +/- 3.4 min; 0.6 mg/kg: 38.3 +/- 2.8 min). Peak plasma concentrations (C(max)) and areas under the curve (AUC) were significantly higher after 0.6 mg/kg than 0.3 mg/kg (C(max): 0.3 mg/kg: 7.5 +/- 3.2 ng/ml; 0.6 mg/kg: 22.7 +/- 3.6 ng/ml; p < 0.01; AUC: 0.3 mg/kg: 929 +/- 109 ng/ml/min; 0.6 mg/kg: 2,277 +/- 209 ng/mt/min; p < 0.01). There was a significant linear correlation between the duration of therapeutic effect, AUC, and C(max) (r = 0.86, p < 0.01 for AUC; r = 0.63, p < 0.05 for C(max)). These results show that sublingual apomorphine could be of interest in the treatment of ''off'' phases in parkinsonian patients with motor fluctuations.