Absorption and safety of alendronate, a nitrogen-containing bisphosphonate, after intrapulmonary administration in rats

作者：Katsumi Hidemasa; Nakatani Maria; Sano Jun ichi; Abe Mari; Kusamori Kosuke; Kurihara Maki; Shiota Rika; Takashima Miki; Fujita Takuya; Sakane Toshiyasu; Hibi Toru; Yamamoto Akira^*

来源：International Journal of Pharmaceutics, 2010, 400(1-2): 124-130.

DOI：10.1016/j.ijpharm.2010.08.041

• Bisphosphonates
• Alendronate
• Pulmonary absorption
• Intrapulmonary administration
• Bone diseases

Alendronate, a nitrogen-containing bisphosphonate, has been used as a first-choice drug for the treatment of hypercalcemia and osteoporosis. In the present study, we examined the absorption and safety of alendronate after intrapulmonary administration in rats. The bioavailability (BA) of alendronate after intrapulmonary administration was 47% at a dose of 5 mg/kg, while the BA after oral administration was only 2.9% at a dose of 50 mg/kg in rats. Plasma calcium level, an index of the pharmacological effect of alendronate, was effectively reduced after intrapulmonary administration of alendronate. Furthermore, alendronate continuously reduced the increase in plasma calcium levels for 9 days after a single intrapulmonary administration in rats with 1 alpha-hydroxyvitamin-D(3)-induced hypercalcemia. Intrapulmonary administration of alendronate also effectively suppressed the decrease in bone mass in a rat model of osteoporosis. Alendronate significantly increased the activity of lactate dehydrogenase (LDH) in bronchoalveolar lavage fluid (BALF), indicating that pulmonary mucosal damage was induced by intrapulmonary administration of alendronate. However, co-administration of superoxide dismutase (SOD) with alendronate completely suppressed the alendronate-induced increase in LDH activity in BALF, while maintaining sufficient pulmonary absorption and therapeutic effects of alendronate in rats with alpha a-hydroxyvitamin-D(3)-induced hypercalcemia. These findings indicated that the lung is a promising, noninvasive alternative route for the delivery of alendronate in the treatment of bone diseases.

• 出版日期2010-11-15