Hines Rochelle M, Khumnark Matthew, Macphail Ben, Hines Dustin J
Department of Psychology, University of Nevada Las Vegas, Las Vegas, NV, United States.
Rapid Dose Therapeutics, Burlington, ON, Canada.
Front Pharmacol. 2019 Sep 10;10:983. doi: 10.3389/fphar.2019.00983. eCollection 2019.
Route of administration is well-known to impact factors ranging from absorption and distribution, up through the subjective effects of active ingredients. Different routes of administration confer specific advantages, such as more rapid absorption resulting from intravenous injection, or increased convenience with oral administration, but a combination of both rapid and convenient delivery is highly desirable. QuickStrip™ was designed as a rapidly dissolving thin film matrix that contains active ingredients, which may be promising for rapid and convenient delivery the oral mucosa. To assess the delivery of QuickStrip™, we administered the well-characterized active ingredient caffeine to mice and compared QuickStrip™ to standard oral gavage delivery at an equivalent dose of 20 mg kg. Using HPLC assessment of serum concentrations of caffeine, we found that QuickStrip™ delivery resulted in higher serum levels of caffeine at 1, 10, and 30 min following administration compared to gavage. QuickStrip™ also produced greater bioavailability compared to gavage, as demonstrated by area under the curve analysis. Caffeine delivered by QuickStrip™ produced robust behavioral activation of locomotion, consistent with gavage caffeine. Electroencephalographic (EEG) assessment of central nervous system effects demonstrated that both gavage and QuickStrip™ caffeine produced suppression of delta and theta, consistent with prior literature on the effects of caffeine. In addition, QuickStrip™ produced a more rapid onset of EEG suppression, supporting the more rapid absorption demonstrated in the serum studies. Collectively, these studies suggest that QuickStrip™ may provide a balance between convenience and rapid onset, offering new options for delivery of therapeutics.
给药途径对从吸收、分布到活性成分主观效应等一系列因素都有显著影响。不同的给药途径具有特定的优势,例如静脉注射可实现更快的吸收,口服给药则更加方便,但兼具快速和便捷的给药方式是非常理想的。速溶条(QuickStrip™)被设计成一种含有活性成分的快速溶解薄膜基质,有望实现对口腔黏膜的快速便捷给药。为了评估速溶条(QuickStrip™)的给药效果,我们给小鼠施用了特征明确的活性成分咖啡因,并将速溶条(QuickStrip™)与标准口服灌胃给药进行比较,给药剂量均为20毫克/千克。通过高效液相色谱法(HPLC)测定血清中咖啡因的浓度,我们发现与灌胃给药相比,速溶条(QuickStrip™)给药后1分钟、10分钟和30分钟时血清中的咖啡因水平更高。曲线下面积分析表明,速溶条(QuickStrip™)的生物利用度也高于灌胃给药。速溶条(QuickStrip™)递送的咖啡因能引发明显的行为性运动激活,与灌胃咖啡因的效果一致。对中枢神经系统效应的脑电图(EEG)评估表明,灌胃和速溶条(QuickStrip™)递送的咖啡因均能抑制δ波和θ波,这与先前关于咖啡因作用的文献一致。此外,速溶条(QuickStrip™)能更快地引发脑电图抑制,这支持了血清研究中显示的更快吸收。总的来说,这些研究表明速溶条(QuickStrip™)可能在便利性和起效速度之间取得平衡,为治疗药物的递送提供了新的选择。