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活动性肺结核患者中利福平与异烟肼的肠道通透性及吸收不良情况

Intestinal permeability and malabsorption of rifampin and isoniazid in active pulmonary tuberculosis.

作者信息

Pinheiro Valéria G F, Ramos Lysiane M A, Monteiro Helena S A, Barroso Elizabeth C, Bushen Oluma Y, Façanha Mônica C, Peloquin Charles A, Guerrant Richard L, Lima Aldo A M

机构信息

Clinical Research Unit & Institute of Biomedicine/Center for Global Health, Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Fortaleza, CE, Brazil.

出版信息

Braz J Infect Dis. 2006 Dec;10(6):374-9. doi: 10.1590/s1413-86702006000600003.

Abstract

Low antimycobacterial drug concentrations have been observed in tuberculosis (TB) patients under treatment. The lactulose/mannitol urinary excretion test (L/M), normally used to measure intestinal permeability, may be useful to assess drug absorption. The objective of this research was to study intestinal absorptive function and bioavailability of rifampin and isoniazid in TB patients. A cross sectional study was done with 41 patients and 28 healthy controls, using the L/M test. The bioavailabilities of rifampin (R) and isoniazid (H) were evaluated in 18 patients receiving full doses. Urinary excretion of mannitol and lactulose, measured by HPLC, was significantly lower in TB patients. The serum concentrations of the drugs were below the expected range for R (8-24 mcg/mL) or H (3-6 mcg/mL) in 16/18 patients. Analyzing the drugs individually, 12/18 patients had low serum concentrations of R, 13/18 for H and 8/18 for both drugs. We suggest that there is a decrease in the functional absorptive area of the intestine in TB patients, which would explain the reduced serum concentrations of antituberculosis drugs. There is a need for new approaches to improve drug bioavailability in TB patients.

摘要

在接受治疗的肺结核(TB)患者中观察到抗分枝杆菌药物浓度较低。通常用于测量肠道通透性的乳果糖/甘露醇尿排泄试验(L/M),可能有助于评估药物吸收情况。本研究的目的是研究肺结核患者中利福平及异烟肼的肠道吸收功能和生物利用度。采用L/M试验对41例患者和28名健康对照者进行了一项横断面研究。对18例接受全剂量药物治疗的患者评估了利福平(R)和异烟肼(H)的生物利用度。通过高效液相色谱法测定,肺结核患者中甘露醇和乳果糖的尿排泄量显著降低。在16/18例患者中,药物的血清浓度低于R(8-24 mcg/mL)或H(3-6 mcg/mL)的预期范围。单独分析药物时,12/18例患者的R血清浓度较低,13/18例患者的H血清浓度较低,8/18例患者的两种药物血清浓度均较低。我们认为,肺结核患者肠道的功能性吸收面积减少,这可以解释抗结核药物血清浓度降低的原因。需要新的方法来提高肺结核患者的药物生物利用度。

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