Orubu Samuel, Kendall Richard A, Sheng Yucheng, Tuleu Catherine
Department of Biomedical Engineering, College of Engineering, Boston University, Boston, MA 02215, USA.
Department of Pharmaceutics, UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London WC1N 1AX, UK.
Pharmaceutics. 2022 Feb 15;14(2):420. doi: 10.3390/pharmaceutics14020420.
Milk is often used as a dispersion medium for medicines administration in young children but its taste-masking ability is unknown. A human taste panel was conducted to assess the potential of infant formula milk (Aptamil 1) to mask the taste of two model WHO priority medicines, zinc sulfate and paracetamol, manufactured as dispersible tablets. Simultaneously, the palatability of powder blends of the tablet platforms was assessed. Twenty healthy adult volunteers performed a swirl-and-spit assessment of placebos and API-containing blends in either a lactose-based or a mannitol-based dispersible tablet platform, reconstituted in 10 mL of either water or Aptamil 1. Eighteen samples were rated for aversion using a 100-mm Visual Analogue Scale, grittiness using a 5-point Likert scale, and "acceptability-as-a-medicine" evaluated as: "Would you find this sample acceptable to swallow as a medicine?" with binary answers of Yes/No. The API-containing formulations were more aversive than the placebos; the paracetamol-containing samples being more aversive than zinc sulfate samples. The platforms themselves were not aversive. Non-gritty samples had four-fold greater odds of being acceptable as a medicine. Aptamil 1 masked the taste of zinc sulfate in the mannitol-based formulation but did not mask the taste of paracetamol in either platform, suggesting a limited taste-masking ability, which may be API and formulation dependent.
牛奶常被用作幼儿给药的分散介质,但其掩味能力尚不清楚。进行了一项人体味觉测试,以评估婴儿配方奶粉(爱他美1段)对两种世界卫生组织重点示范药物——硫酸锌和对乙酰氨基酚(制成可分散片剂)的掩味潜力。同时,对片剂平台的粉末混合物的适口性进行了评估。20名健康成年志愿者对基于乳糖或甘露醇的可分散片剂平台中的安慰剂和含活性成分的混合物进行了搅拌和吐出评估,这些混合物用10毫升水或爱他美1段进行重构。使用100毫米视觉模拟量表对18个样品的厌恶程度进行评分,使用5点李克特量表对沙砾感进行评分,并将“作为药物的可接受性”评估为:“你会觉得这个样品作为药物吞咽是可以接受的吗?”,答案为是/否。含活性成分的制剂比安慰剂更难吃;含对乙酰氨基酚的样品比硫酸锌样品更难吃。片剂平台本身不难吃。无沙砾感的样品作为药物可接受的几率高出四倍。爱他美1段在基于甘露醇的制剂中掩盖了硫酸锌的味道,但在任何一个平台中都没有掩盖对乙酰氨基酚的味道,这表明其掩味能力有限,这可能取决于活性成分和制剂。