Oral delivery of ivermectin using a fast dissolving oral film: Implications for repurposing ivermectin as a pharmacotherapy for alcohol use disorder

被引:11
|
作者
Yardley, Megan M. [1 ]
Huynh, Nhat [2 ]
Rodgers, Kathleen E. [2 ]
Alkana, Ronald L. [3 ]
Davies, Daryl L. [2 ]
机构
[1] Univ Calif Los Angeles, Dept Psychol, Los Angeles, CA 90095 USA
[2] Univ So Calif, Sch Pharm, Titus Family Dept Clin Pharm & Pharmaceut Econ &, Los Angeles, CA 90033 USA
[3] Univ So Calif, Sch Pharm, Dept Pharmacol & Pharmaceut Sci, Los Angeles, CA 90033 USA
关键词
Medications development; Alcoholism therapy; Drug repositioning; Drug delivery; CHLORIDE CHANNEL; UNITED-STATES; DEPENDENCE; RECEPTORS; GAVAGE;
D O I
10.1016/j.alcohol.2015.03.006
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Individuals suffering from an alcohol-use disorder (AUD) constitute a major health concern. Preclinical studies in our laboratory show that acute and chronic intraperitoneal (i.p.) administration of ivermectin (IVM) reduces alcohol intake and preference in mice. To enable clinical investigation to use IVM for the treatment of an AUD, development of an oral formulation that can be used in animals as well as longterm preclinical toxicology studies are required. The present work explores the use of a promising alternative dosage form of IVM, fast-dissolving oral films (Cure Pharmaceutical (R)), to test the efficacy and safety of oral IVM in conjunction with alcohol exposure. We tested the effect of IVM (0.21 mg) using a fast-dissolving oral film delivery method on reducing 10% v/v alcohol (10E) intake in female C57BL/6 mice using a 24-h access two-bottle choice paradigm for 6 weeks (5 days per week). Differences in ethanol intake, preference for ethanol, water intake, fluid intake, food intake, changes in mouse and organ weights, as well as histological changes to kidney, liver, and brain were analyzed. The IVM group drank significantly less ethanol over the 30-day period compared to the placebo (blank strip) and the no-treatment groups. Organ weights did not differ between the groups. Histological evaluation showed no differences in the brain and kidney between groups. In the liver, there was a slight increase in the incidence of microvesicular fatty and degenerative changes of the animals receiving the thin strips. No overt hepatocellular necrosis or perivascular inflammation was noted. Overall, these data support the use of this novel method of oral drug delivery for longer-term studies and should facilitate FDA required preclinical testing that is necessary to repurpose IVM for treatment of an AUD. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:553 / 559
页数:7
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