The Palatability of Lopinavir and Ritonavir Delivered by an Innovative Freeze-Dried Fast-Dissolving Tablet Formulation.

IF 1.1 Q4 INFECTIOUS DISEASES AIDS Research and Treatment Pub Date : 2018-01-17 eCollection Date: 2018-01-01 DOI:10.1155/2018/5908167
David W Pittman, Alexandra M Brantly, Alexandra L Drobonick, Hannah T King, Daniel C Mesta, Caroline G Richards, Manjari Lal, Manshun Lai
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Abstract

Negative hedonic sensory qualities of HIV antiretroviral drugs often reduce patient adherence particularly in pediatric populations requiring oral consumption. This study examines the palatability of an innovative delivery mechanism utilizing a freeze-drying-in-blister approach to create fast-dissolving tablets (FDTs) containing a fixed-dose combination of lopinavir and ritonavir (LPV/r). Consumption patterns of solutions during brief-access and long-term testing and baby foodstuff consumption were analyzed to evaluate the orosensory detection and avoidance of placebo FDTs containing no LPV/r (FDT-) and FDTs containing LPV/r (FDT+). Rats showed no change in consumption patterns for the placebo FDT- compared with control solutions. Rats can detect but do not avoid FDT+ at body-weight-adjusted dosages in both brief-access (30-s) and long-term (23 h) consumption tests. There is an aversive response to concentrated doses of FDT+ during brief-access tests that cannot be masked by 25% sucrose. However, the strongest FDT+ concentration was not rejected when mixed with 50 g of applesauce, banana sauce, or rice cereal baby foodstuffs. The averseness of the FDT+ was associated with the presence of LPV/r and not the FDT- formulation itself. The novel FDT formulation appears to be a palatable delivery mechanism for oral antiretroviral pharmaceuticals especially when mixed with baby foodstuffs.

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以创新型冷冻干燥速溶片剂给药的洛匹那韦和利托那韦的适口性
艾滋病抗逆转录病毒药物的负感官特性往往会降低患者的依从性,尤其是在需要口服的儿童群体中。本研究探讨了一种创新给药机制的适口性,该机制采用泡罩冷冻干燥法制成含洛匹那韦和利托那韦固定剂量组合片剂(LPV/r)的速溶片剂(FDTs)。分析了大鼠在短暂接触和长期测试期间的溶液摄入模式以及婴儿食品摄入模式,以评估大鼠对不含 LPV/r 的安慰剂 FDT(FDT-)和含 LPV/r 的 FDT(FDT+)的口感官检测和回避情况。与对照组溶液相比,大鼠食用安慰剂 FDT- 的模式没有变化。在短暂摄入(30 秒)和长期摄入(23 小时)的测试中,大鼠都能检测到按体重调整剂量的 FDT+,但不会避开它。在短暂摄入测试中,大鼠对高浓度剂量的 FDT+ 会产生厌恶反应,而 25% 的蔗糖无法掩盖这种反应。然而,当与 50 克苹果酱、香蕉酱或大米谷物婴儿食品混合时,最强浓度的 FDT+ 不会被排斥。FDT+ 的排斥性与 LPV/r 的存在有关,而与 FDT- 配方本身无关。新型 FDT 制剂似乎是口服抗逆转录病毒药物的一种适口给药机制,尤其是在与婴儿食品混合时。
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来源期刊
AIDS Research and Treatment
AIDS Research and Treatment INFECTIOUS DISEASES-
CiteScore
3.10
自引率
0.00%
发文量
13
审稿时长
18 weeks
期刊介绍: AIDS Research and Treatment is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies focused on all aspects of HIV and AIDS, from the molecular basis of disease to translational and clinical research. In addition, articles relating to prevention, education, and behavior change will be considered
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