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[依曲替酯、阿维A及13-顺式阿维A的药代动力学:血药浓度导向临床应用的新结果及优势]

[Pharmacokinetics of etretinate, acitretin and 13-cis-acitretin: new results and advantages of blood level oriented clinical use].

作者信息

Gollnick H, Rinck G, Bitterling T, Orfanos C E

机构信息

Universitäts-Hautklinik und Poliklinik, Klinikum Steglitz der Freien Universität Berlin.

出版信息

Z Hautkr. 1990 Jan;65(1):40-50.

PMID:2139274
Abstract

Plasma concentrations of etretinate (E), acitretin (A) and 13-cis-acitretin (13-cis A) were measured using a reverse phase HPLC assay in patients with psoriasis during 24h after the first dose (0.8 mg/kg) and after 3 weeks (group A), and in a second group with various skin diseases (B) under long-term treatment after 3 months. Group A (n = 8) showed median peak plasma concentration levels (Cmax) 578 ng/ml for E. and 161 ng/ml for A 4h after dosing (tmax). The plasma concentration profile of 13-cis A. was plateau-like with Cmax-levels of 138 ng/ml after 4 to 10 hours. In group B treated with 0.3 to 0.4 mg/kg etretinate a trend to increased Cmax-values with 123 ng/ml for E., 44 ng/ml for A. and, more pronounced, 210 ng/ml for 13-cis A. occurred (steady state). In a third group C (n = 17) it was found that after an eight month treatment free period measurements of the 13-cis A. plasma concentration are more sensitive than that of E. or A. Comparing the pharmacokinetics in two patients with the same clinical conditions under E. and A., resp., two fold higher Cmax-values of A. after A. were found than for A. after E. However, 13-cis A. values were higher after E. than after A. Our observations have shown that the metabolisation of A. to 13-cis A. may be disturbed and the clinical efficacy may appear only after dramatic increase of the oral doses. Routine monitoring of plasma concentration profiles of oral retinoids and their metabolites under short or long-term treatment enable us to early identify and understand better the so-called "non-responders", either due to a disturbed metabolism of retinoids or to non-compliance. Furthermore, monitoring of 13-cis A in plasma after cessation of treatment with E. or A. in women in childbearing age seems to be more sensitive than measurement of plasma levels of E. or A. These measurements are helpful for defining the strategy of oral retinoid therapy and for reliable information of females who wish to become pregnant after interrupting the drug.

摘要

采用反相高效液相色谱法测定了银屑病患者在首剂(0.8mg/kg)后24小时及3周后(A组),以及另一组患有各种皮肤病且长期治疗3个月后的患者(B组)血浆中阿维A酯(E)、阿维A(A)和13 - 顺式阿维A(13 - 顺式A)的浓度。A组(n = 8)给药后4小时(达峰时间tmax),E的血浆峰浓度中位数(Cmax)为578ng/ml,A为161ng/ml。13 - 顺式A的血浆浓度曲线呈平台状,4至10小时后Cmax水平为138ng/ml。在接受0.3至0.4mg/kg阿维A酯治疗的B组中,出现了Cmax值升高的趋势,E为123ng/ml,A为44ng/ml,13 - 顺式A更为明显,为210ng/ml(稳态)。在第三组C(n = 17)中发现,在停药8个月后,13 - 顺式A血浆浓度的测量比E或A更敏感。比较两名临床情况相同但分别接受E和A治疗的患者的药代动力学,发现服用A后A的Cmax值比服用E后高两倍。然而,服用E后13 - 顺式A的值比服用A后高。我们的观察表明,A向13 - 顺式A的代谢可能受到干扰,临床疗效可能仅在口服剂量大幅增加后才会出现。在短期或长期治疗过程中对口服维甲酸及其代谢物的血浆浓度曲线进行常规监测,使我们能够早期识别并更好地理解所谓的“无反应者”,其原因要么是维甲酸代谢紊乱,要么是依从性差。此外,在育龄妇女停止使用E或A治疗后,监测血浆中的13 - 顺式A似乎比测量E或A的血浆水平更敏感。这些测量有助于确定口服维甲酸治疗策略,并为希望在停药后怀孕的女性提供可靠信息。

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