College of Pharmacy, University of Arizona, 1703 E. Mabel St, Tucson, Arizona 85721, USA.
AAPS PharmSciTech. 2010 Mar;11(1):168-73. doi: 10.1208/s12249-009-9371-6. Epub 2010 Jan 26.
Potential efficacy of zileuton, a 5-LOX inhibitor, was evaluated for the reduction of pulmonary adenomas in the A/J murine model when administered via nose-only inhalation. Development of pulmonary adenomas was induced with benzo(a)pyrene. Animals were treated with a zileuton solution (5 mg/mL in 85:15 ethanol/water) either twice weekly or five times a week via nose-only inhalation; The placebo solution (85:15 EtOH/H2O, no active) was also evaluated. Dose delivered was calculated to be 1.2 mg/kg per exposure for each zileuton group. After 20 weeks of treatment, surface tumors were enumerated and histologically assessed. A significant reduction in tumor count was noted for both the twice weekly administration (40%) and the five times a week administration (59%). The data also showed a significant reduction for the group, which received the placebo (approximately 58%). The treatment groups were also found to have an impact on the histological stages of adenoma development.
5-脂氧合酶抑制剂齐留通通过鼻内吸入给药在 A/J 小鼠模型中降低肺腺癌的潜在疗效进行了评估。用苯并(a)芘诱导肺腺癌的发展。动物用齐留通溶液(5mg/ml 于 85:15 乙醇/水中)通过鼻内吸入每周两次或每周五次进行治疗;也评估了安慰剂溶液(85:15 EtOH/H2O,无活性)。每个齐留通组的给药剂量计算为每次暴露 1.2 毫克/千克。经过 20 周的治疗,表面肿瘤进行计数和组织学评估。每周两次给药(40%)和每周五次给药(59%)均显著降低肿瘤计数。数据还表明,接受安慰剂的组(约 58%)也有显著减少。治疗组还发现对腺瘤发展的组织学阶段有影响。