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阿奇霉素在囊性纤维化患者长期治疗期间血浆、血液、多形核中性粒细胞和痰液中的药代动力学。

Pharmacokinetics of azithromycin in plasma, blood, polymorphonuclear neutrophils and sputum during long-term therapy in patients with cystic fibrosis.

作者信息

Wilms E B, Touw D J, Heijerman H G M

机构信息

The Hague Central Hospital Pharmacy, Escamplaan 900, The Hague, The Netherlands.

出版信息

Ther Drug Monit. 2006 Apr;28(2):219-25. doi: 10.1097/01.ftd.0000195617.69721.a5.

Abstract

Chronic therapy with the macrolide antibiotic azithromycin (AZM) is widely practiced in the treatment of patients with cystic fibrosis (CF) and chronic lung infection with Pseudomonas aeruginosa. Azithromycin dosage is variable, based on published studies, and not supported by pharmacokinetic data. This study describes the pharmacokinetics of the long-term administration of AZM (500 mg per day) in CF patients. AZM concentrations were quantified in the plasma, blood, isolated polymorphonuclear neutrophils (PMNNs), and sputum of 8 adult CF patients. The AZM distribution t1/2 was 0.1 hours in plasma. The (mean +/- standard deviation) elimination t(1/2) was 102 +/- 20 hours in plasma, 180 +/- 68 hours in blood, and 289 +/- 166 hours in PMNNs. The C(max) of AZM was 0.67 +/- 0.31 mg/L in plasma and 2.01 +/- 0.74 mg/L in blood, of which 1.44 +/- 0.69 mg/L was found in PMNNs. In sputum the concentration of AZM ranged from 12 to 53 mg/L and was still detectable at concentrations in the range 4 to 27 mg/L 10 days after the last dose. On average, the concentration in PMNNs was 2100 times the C(plasma) 24 hours after dosing AZM. These results confirm the accumulation of AZM in PMNNs. The authors conclude that sputum levels are elevated far above plasma and blood concentrations. The long t(1/2) in blood and PMNNs and the slow decrease in sputum levels indicate a less frequent dosing schedule (for instance once weekly) should be studied in future clinical trials of AZM in patients with cystic fibrosis.

摘要

大环内酯类抗生素阿奇霉素(AZM)的长期治疗在囊性纤维化(CF)患者以及铜绿假单胞菌慢性肺部感染患者的治疗中被广泛应用。根据已发表的研究,阿奇霉素的剂量各不相同,且缺乏药代动力学数据的支持。本研究描述了CF患者长期服用AZM(每日500毫克)的药代动力学情况。对8名成年CF患者的血浆、血液、分离的多形核中性粒细胞(PMNNs)和痰液中的AZM浓度进行了定量分析。AZM在血浆中的分布半衰期为0.1小时。(平均值±标准差)消除半衰期在血浆中为102±20小时,在血液中为180±68小时,在PMNNs中为289±166小时。AZM的C(max)在血浆中为0.67±0.31毫克/升,在血液中为2.01±0.74毫克/升,其中在PMNNs中为1.44±0.69毫克/升。痰液中AZM的浓度范围为12至53毫克/升,在最后一剂后10天,浓度在4至27毫克/升范围内仍可检测到。平均而言,服用AZM 24小时后,PMNNs中的浓度是血浆C(plasma)的2100倍。这些结果证实了AZM在PMNNs中的蓄积。作者得出结论,痰液中的水平远高于血浆和血液浓度。血液和PMNNs中的长半衰期以及痰液水平的缓慢下降表明,在未来阿奇霉素治疗囊性纤维化患者的临床试验中,应研究给药频率更低的方案(例如每周一次)。

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