Esophageal transit of solid oral dosage forms – impact of different surface materials characterized in vitro and in vivo by MRI in healthy volunteers

IF 4.3 3区 医学 Q1 PHARMACOLOGY & PHARMACY
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Abstract

Acceptable swallowability and complete esophageal transit are decisive for the safe and effective administration of solid oral dosage forms. This applies in particular to the main user group of medicines, older adults, who often suffer from swallowing difficulties. It is well known that surface properties play an important role in this respect. In the past, this has led to the development of numerous coating formulations for tablets with improved swallowability. However, in vitro and especially in vivo data investigating a positive effect of different coating materials is limited. Therefore, we investigated coating materials being based on polyvinyl alcohol, hydroxypropyl methylcellulose, and a copolymer of methacrylate in respect to their influence on swallowability and esophageal transit of a tablet formulation. They were compared to uncoated tablets as well as to hard gelatin capsules. Three in vitro assays suitable for routine use in pharmaceutical development were performed: i.) Wettability test in artificial saliva; ii.) Swelling measurement in artificial saliva; iii.) Measurement of the adhesion between surface materials and a simulated mucosa surface. All three assays resulted in a differentiation of the surface materials. The coated tablets showed favorable behavior compared to uncoated tablets and hard gelatin capsules. To test the effect of the different materials in vivo, an intervention study was conducted. 36 adults were included and the likeliness of prolonged esophageal transit of (un-)coated tablets as well as a hard gelatin capsule of the same weight was objectively evaluated by means of magnetic resonance imaging. While hard gelatin capsules showed highest rates for prolonged esophageal transit, the tendency for adhesion was reduced for uncoated tablets, and least for coated tablets, i.e., prolonged esophageal transit in 22.2 %, 11.1 %, and ≤5.6 % of the cases, respectively. Further differentiation of the coating materials was not possible. Subjective evaluations of each participant with respect to subjective swallowability and esophageal transit did not correlate well with the objective measurements by means of magnetic resonance imaging. The use of coatings in general has a positive influence on esophageal transit. However, the selection of coating type seems to be of greater importance in respect to patients' oral perception of the dosage forms compared to their influence on the probability for prolonged esophageal transit.

Abstract Image

固体口服剂型的食道转运--不同表面材料对健康志愿者体外和体内磁共振成像的影响。
可接受的吞咽性和完全的食道转运对安全有效地服用固体口服剂型起着决定性作用。这一点尤其适用于药物的主要使用者群体--老年人,因为他们往往存在吞咽困难。众所周知,表面特性在这方面起着重要作用。因此,过去人们开发了许多可改善吞咽性的片剂包衣配方。然而,研究不同包衣材料积极作用的体外数据,尤其是体内数据非常有限。因此,我们研究了基于聚乙烯醇、羟丙基甲基纤维素和甲基丙烯酸酯共聚物的包衣材料对片剂吞咽性和食道转运的影响。将它们与无包衣片剂和硬明胶胶囊进行了比较。进行了三项适用于药物开发中常规使用的体外检测: i.)人工唾液湿润性测试; ii.)测量表面材料与模拟粘膜表面之间的粘附性。所有三项试验都对表面材料进行了区分。与无包衣片剂和硬明胶胶囊相比,包衣片剂表现良好。为了测试不同材料在体内的效果,我们进行了一项干预研究。研究对象包括 36 名成年人,并通过磁共振成像对(未)包衣药片和相同重量的硬明胶胶囊延长食道通过时间的可能性进行了客观评估。硬明胶胶囊的食管吞咽时间延长率最高,而无包衣片剂的粘附倾向较低,包衣片剂的粘附倾向最低,即分别有 22.2%、11.1% 和小于 5.6% 的病例出现食管吞咽时间延长。无法进一步区分包衣材料。每位受试者对主观吞咽性和食管通过性的主观评价与磁共振成像的客观测量结果并不十分相关。一般来说,涂层的使用会对食管转运产生积极影响。不过,与包衣对延长食管通过时间的可能性的影响相比,包衣类型的选择似乎对患者对剂型的口服感受更为重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.60
自引率
2.20%
发文量
248
审稿时长
50 days
期刊介绍: The journal publishes research articles, review articles and scientific commentaries on all aspects of the pharmaceutical sciences with emphasis on conceptual novelty and scientific quality. The Editors welcome articles in this multidisciplinary field, with a focus on topics relevant for drug discovery and development. More specifically, the Journal publishes reports on medicinal chemistry, pharmacology, drug absorption and metabolism, pharmacokinetics and pharmacodynamics, pharmaceutical and biomedical analysis, drug delivery (including gene delivery), drug targeting, pharmaceutical technology, pharmaceutical biotechnology and clinical drug evaluation. The journal will typically not give priority to manuscripts focusing primarily on organic synthesis, natural products, adaptation of analytical approaches, or discussions pertaining to drug policy making. Scientific commentaries and review articles are generally by invitation only or by consent of the Editors. Proceedings of scientific meetings may be published as special issues or supplements to the Journal.
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