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硝苯地平在血浆和龈沟液中的分布与药物性牙龈增生的关系。

Disposition of nifedipine in plasma and gingival crevicular fluid in relation to drug-induced gingival overgrowth.

作者信息

Ellis J S, Seymour R A, Monkman S, Idle J R

机构信息

Department of Restorative Dentistry, Dental School, University of Newcastle upon Tyne, England.

出版信息

J Periodontal Res. 1993 Sep;28(5):373-8. doi: 10.1111/j.1600-0765.1993.tb01081.x.

Abstract

The present study investigates the relationship between the pharmacokinetic variables of nifedipine with the incidence and severity of gingival overgrowth in 9 adult male patients medicated with the drug for at least 6 months. Five of the patients had experienced significant gingival changes and were thus designated "responders". The remaining four patients exhibited no gingival overgrowth, and thus acted as a control. A baseline periodontal examination (plaque scores, bleeding index and gingival overgrowth assessment) was carried out on each patient, and confined to the upper and lower anterior teeth. Serial blood and gingival crevicular fluid samples were collected over an eight-hour investigation period. Samples were analyzed for nifedipine by gas chromatography. No significant difference (p > 0.05) was seen between responders and non-responders with regard to drug therapy, periodontal parameters or plasma pharmacokinetics of nifedipine. Nifedipine was detected in the gingival crevicular fluid of seven subjects (all responders, and two non-responders). The peak concentration of nifedipine in crevicular fluid was 15-90 fold greater than levels observed in plasma.

摘要

本研究调查了9名成年男性患者服用硝苯地平至少6个月后,其药代动力学变量与牙龈增生的发生率和严重程度之间的关系。其中5名患者出现了明显的牙龈变化,因此被指定为“反应者”。其余4名患者未出现牙龈增生,因此作为对照。对每位患者进行了基线牙周检查(菌斑评分、出血指数和牙龈增生评估),检查范围限于上下前牙。在8小时的调查期内采集了系列血液和龈沟液样本。通过气相色谱法分析样本中的硝苯地平。在药物治疗、牙周参数或硝苯地平的血浆药代动力学方面,反应者和非反应者之间未观察到显著差异(p>0.05)。在7名受试者的龈沟液中检测到了硝苯地平(均为反应者,还有2名非反应者)。龈沟液中硝苯地平的峰值浓度比血浆中观察到的水平高15至90倍。

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