| 查看: 390 | 回复: 0 | |||
iamlisheng木虫 (小有名气)
|
[求助]
药代动力学（医药专业）
|
|
12.3 Pharmacokinetics Absorption After single dose administration of REXULTI tablets, the peak plasma brexpiprazole concentrations occurred within 4 hours after administration; and the absolute oral bioavailability was 95%. Brexpiprazole steady-state concentrations were attained within 10-12 days of dosing. REXULTI can be administered with or without food. Administration of a 4 mg REXULTI tablet with a standard high fat meal did not significantly affect the Cmax or AUC of brexpiprazole. After single and multiple once daily dose administration, brexpiprazole exposure (Cmax and AUC) increased in proportion to the dose administered. In vitro studies of brexpiprazole did not indicate that brexpiprazole is a substrate of efflux transporters such as MDRI (P-gp) and BCRP. Distribution The volume of distribution of brexpiprazole following intravenous administration is high (1.56±0.42 L/kg), indicating extravascular distribution. Brexpiprazole is highly protein bound in plasma (greater than 99%) to serum albumin and a1-acid glycoprotein, and its protein binding is not affected by renal or hepatic impairment. Based on results of in vitro studies, brexpiprazole protein binding is not affected by warfarin, diazepam, or digitoxin. Elimination Metabolism Based on in vitro metabolism studies of brexpiprazole using recombinant human cytochrome P450 (CYP1A1, 1A2, 2A6, 2B6, 2C8, 2C9, 2C19, 2D6, 2E1, and 3A4), the metabolism of brexpiprazole was shown to be mainly mediated by CYP3A4 and CYP2D6. In vivo brexpirazole is metabolized primarily by CYP3A4 and CYP2D6 enzymes. After single- and multiple-dose administrations, brexpiprazole and its major metabolite, DM-3411, were the predominant drug moieties in the systemic circulation. At steady-state, DM-3411 represented 23% to 48% of brexpiprazole exposure (AUC) in plasma. DM-3411 is considered not to contribute to the therapeutic effects of brexpiprazole. Based on in vitro data, brexpiprazole showed little to no inhibition of CYP450 isozymes. Excretion Following a single oral dose of [14C]-labeled brexpiprazole, approximately 25% and 46% of the administered radioactivity was recovered in the urine and feces, respectively. Less than 1% of unchanged brexpiprazole was excreted in the urine and approximately 14% of the oral dose was recovered unchanged in the feces. Apparent oral clearance of a brexpiprazole oral tablet after once daily administration is 19.8 (±11.4) mL/h/kg. After multiple once daily administration of REXULTI, the terminal elimination half-lives of brexpiprazole and its major metabolite, DM-3411, were 91 hours and 86 hours, respectively. |
回复此楼» 猜你喜欢
售SCI一区文章，我:8 O5 51O 54,科目齐全
已经有4人回复
-
售SCI一区文章，我:8 O5 51O 54,科目齐全
已经有4人回复
-
售SCI一区文章，我:8 O5 51O 54,科目齐全
已经有5人回复
-
售SCI一区文章，我:8 O5 51O 54,科目齐全
已经有4人回复
-
售SCI一区文章，我:8 O5 51O 54,科目齐全
已经有6人回复
-
售SCI一区文章，我:8 O5 51O 54,科目齐全
已经有6人回复
-
售SCI一区文章，我:8 O5 51O 54,科目齐全
已经有6人回复
-
售SCI一区文章，我:8 O5 51O 54,科目齐全
已经有7人回复
-
售SCI一区文章，我:8 O5 51O 54,科目齐全
已经有7人回复
-
售SCI一区文章，我:8 O5 51O 54,科目齐全
已经有7人回复
10