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A Novel Oral Syringe for Dosing and Administration of Multiparticulate Formulations: Acceptability Study in Preschool and School Children

机译:一种用于剂量和施用多颗粒制剂的新型口腔注射器:学龄前儿童的可接受性研究

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摘要

The popularity of multiparticulate formulations (MPs) as a paediatric dosage form continues to increase. MPs comprise of multiple small units that are easy-to-swallow. Currently, MPs are commonly manufactured into unit doses that are either swallowed whole or opened prior to administration. While this is an acceptable approach, dosing is envisioned to be optimised with a “standard” paediatric device which can better harness the flexible dosing potential of MPs. We evaluated a novel oral syringe (SympfinyTM, HS Design, Morristown, NJ, USA) that is being developed as a tool to dispense and administer MPs to children. Forty children, 4–12 years old, received 0.5, 1.2, and 2.0 mL doses of placebo MPs using the oral syringe with spring water or a drink of choice to complete sample intake. Acceptability was recorded as those able to completely swallow the dose and participants also rated dose acceptability on a 5-point scale. The ability to completely swallow the dose decreased as dose volume increased; the smallest dose was completely swallowed by 87.5% (35/40) children, and 69.4% (27/39) of children confirmed their willingness to take the sample as a daily medicine. Larger doses, 1.2 and 2.0 mL, gave values of 55% and 57.5% for the doses completely swallowed and 58.8% and 51.72% for willingness to take the sample as a daily medicine, respectively. Use of a drink of choice showed no increase in swallowability as compared with water. The novel oral syringe being developed is an appropriate device for dispensing doses flexibly and administering neutral tasting MPs directly to the mouth in the lower dose range without the need for a co-administration vehicle in children aged 4–12 years.
机译:多颗粒制剂(MPS)作为儿科剂型的普及继续增加。 MPS包括多个小单位,易于吞咽。目前,MPS通常制造成单位剂量,在给药前吞服或打开。虽然这是一种可接受的方法,但可以设想给药以通过“标准”小儿装置进行优化,这可以更好地利用MPS的柔性给药潜力。我们评估了一种新颖的口腔注射器(SympfinyTM,HS Design,Morristown,NJ,USA),它是被开发的作为一种分配和管理MPS的工具。四十个孩子,4-12岁,收到0.5,1.2和2.0毫升的安慰剂MPS使用口腔注射器,泉水或饮料选择样品摄入。可接受性被记录为能够完全吞下剂量和参与者的可接受性以及在5分尺寸上额定剂量可接受性。随着剂量的增加,可以完全吞下剂量的能力降低;最小的剂量被87.5%(35/40)儿童完全吞下,69.4%(27/39)儿童证实了他们将样品作为日常药物服用。较大的剂量,1.2和2.0ml,为剂量完全吞下的剂量为55%和57.5%,愿意分别将样品作为日药作为日药的58.8%和51.72%。与水相比,使用饮料的选择表明,无吞咽性不会增加。正在开发的新型口腔注射器是一种适当的装置,用于灵活地分配剂量,并将中性品尝MPS直接施用于较低剂量范围内的口腔,而不需要在4-12岁的儿童中进行共同给药载体。

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