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研发一种新型阿仑膦酸钠(一种含氮双膦酸盐)透皮贴剂,用于治疗骨质疏松症。

Development of a novel transdermal patch of alendronate, a nitrogen-containing bisphosphonate, for the treatment of osteoporosis.

机构信息

Department of Biopharmaceutics, Kyoto Pharmaceutical University, Yamashina-ku, Kyoto, Japan.

出版信息

J Bone Miner Res. 2010 Dec;25(12):2582-91. doi: 10.1002/jbmr.147. Epub 2010 Jun 7.

Abstract

Bisphosphonates are widely used for the treatment and prevention of bone diseases, including Paget disease, hypercalcemia of malignancy, and postmenopausal osteoporosis. In this study, we developed a novel transdermal patch of alendronate, a nitrogen-containing bisphosphonate, for the treatment of bone diseases. The maximum permeation fluxes of alendronate through rat and human skin after application of this patch were 1.9 and 0.3 µg/cm(2) per hour, respectively. The bioavailability (BA) of alendronate in rats was approximately 8.3% after the application of alendronate patch and approximately 1.7% after oral administration. These results indicated that the transdermal permeation of alendronate using this patch system was sufficient for the treatment of bone diseases. The plasma calcium level was effectively reduced after application of the alendronate patch in 1α-hydroxyvitamin D(3) -induced hypercalcemia model rats. The alendronate patch also effectively suppressed the decrease in bone mass in model rats with osteoporosis. Modest alendronate-induced erythema of rat skin was observed after application of the alendronate patch. Incorporation of butylhydroxytoluene in the alendronate patch almost completely suppressed this alendronate-induced skin damage while maintaining the transdermal permeation and pharmacologic effects of alendronate. These findings indicate that our novel transdermal delivery system for alendronate is a promising approach to improve compliance and quality of life of patients in the treatment of bone diseases.

摘要

双膦酸盐被广泛用于治疗和预防骨疾病,包括 Pagets 病、恶性高钙血症和绝经后骨质疏松症。在这项研究中,我们开发了一种新型的阿仑膦酸钠(一种含氮的双膦酸盐)透皮贴剂,用于治疗骨疾病。该贴剂应用于大鼠和人体皮肤后,阿仑膦酸钠的最大渗透通量分别为 1.9 和 0.3μg/cm(2)/小时。阿仑膦酸钠在大鼠中的生物利用度(BA)约为贴剂应用后 8.3%,口服给药后约为 1.7%。这些结果表明,该贴剂系统中阿仑膦酸钠的透皮渗透足以治疗骨疾病。在 1α-羟基维生素 D(3)诱导的高钙血症模型大鼠中,应用阿仑膦酸钠贴剂后可有效降低血浆钙水平。阿仑膦酸钠贴剂还可有效抑制骨质疏松症模型大鼠的骨量减少。在应用阿仑膦酸钠贴剂后,大鼠皮肤出现适度的阿仑膦酸钠诱导红斑。在阿仑膦酸钠贴剂中加入丁羟甲苯可完全抑制这种阿仑膦酸钠引起的皮肤损伤,同时保持阿仑膦酸钠的透皮渗透和药理作用。这些发现表明,我们新型的阿仑膦酸钠透皮给药系统有望提高骨疾病治疗患者的依从性和生活质量。

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