Department of Biopharmaceutics and Pharmaceutical Technology, Institute of Pharmacy, University of Greifswald, Felix-Hausdorff-Straße 3, 17489 Greifswald, Germany.
Department of Pharmaceutical Biology, Institute of Pharmacy, University of Greifswald, Felix-Hausdorff-Straße 1, 17489 Greifswald, Germany.
Eur J Pharm Biopharm. 2018 Jun;127:443-452. doi: 10.1016/j.ejpb.2018.03.011. Epub 2018 Mar 27.
Improving our knowledge about human gastrointestinal physiology and its impact on oral drug delivery is crucial for the development of new therapies and effective drug delivery systems. The aim of this study was to develop an in vivo tool to determine gastric emptying of water by administration of a caffeine as a tracer substance followed by subsequent saliva caffeine analysis. For this purpose, 35 mg of caffeine were given to six healthy volunteers after a 10 h overnight together with 240 mL of tap water either on a fasted stomach or 30 min after the high-caloric, high-fat breakfast recommended for bioavailability/bioequivalence (BA/BE) studies. Caffeine was administered in form of an ice capsule in order to omit the contamination of the oral cavity with caffeine. Parallel to saliva sampling, magnetic resonance imaging (MRI) was applied in order to validate this novel approach. After administration of the ice capsule, MRI measurements were performed every 2 min for the first 20 min followed by further measurements after 25, 30, 35, 40, 50 and 60 min. Saliva samples were collected always 1 min after the MRI measurement in supine position in the MRI scanner and continued for further 240 min. The caffeine concentration in saliva was quantified after liquid-liquid extraction by a validated HPLC/MS-MS method. The obtained MRI data revealed a fast emptying of the co-administered water within 10 to 50 min in the fasted state and likewise in the fed state. Salivary caffeine kinetics showed a C from 150 to 400 ng/mL with a t from 20 to 90 min. MRI data were normalized by setting the maximum emptied volume to 100% and the salivary caffeine kinetics were normalized by setting C to 100%. In order to compare the results obtained by the MRI and the saliva method, the normalized data for each volunteer was correlated based on a linear regression. In the fasted state the mean slope for six comparisons was 0.9114 ± 0.1500 and the mean correlation coefficient was 0.912 ± 0.055. In the fed state, a mean slope of 0.8326 ± 0.1630 and a mean correlation coefficient of 0.887 ± 0.047 were obtained. Based on these results, we could show that salivary caffeine concentrations are suitable to describe the emptying of water as a non-caloric liquid from the fasted and the fed stomach. The presented technique provides a straight-forward, inexpensive and noninvasive method to assess gastric emptying of hydrophilic liquids, which can be broadly used in oral biopharmaceutics. Possible applications are the characterization of real-life conditions, specific populations (e.g. elderly people) and the better understanding of the contribution of gastric emptying to pharmacokinetic profiles of orally administered drugs.
提高我们对人类胃肠道生理学及其对口服药物传递影响的认识,对于开发新的治疗方法和有效的药物传递系统至关重要。本研究旨在开发一种体内工具,通过给予咖啡因作为示踪物质来确定水的胃排空情况,随后对唾液中的咖啡因进行分析。为此,将 35mg 咖啡因给予 6 名健康志愿者,在禁食状态下或在推荐用于生物利用度/生物等效性 (BA/BE) 研究的高热量高脂肪早餐后 30 分钟,同时给予 240ml 自来水。咖啡因以冰胶囊的形式给予,以避免口腔受到咖啡因的污染。同时进行磁共振成像 (MRI) 以验证这种新方法。在给予冰胶囊后,在最初的 20 分钟内每 2 分钟进行一次 MRI 测量,然后在 25、30、35、40、50 和 60 分钟后进行进一步测量。在 MRI 测量后 1 分钟内,志愿者以仰卧位在 MRI 扫描仪中采集唾液样本,并在接下来的 240 分钟内继续采集。通过经验证的 HPLC/MS-MS 方法对唾液中的咖啡因进行液液萃取后定量。获得的 MRI 数据显示,在禁食状态和进食状态下,共同给予的水在 10 至 50 分钟内快速排空。唾液中的咖啡因动力学表现为 C 从 150 到 400ng/mL,t 从 20 到 90 分钟。通过将最大排空体积设置为 100%对 MRI 数据进行归一化,并将唾液中的咖啡因动力学数据设置为 C=100%进行归一化。为了比较 MRI 和唾液方法获得的结果,基于线性回归,对每个志愿者的归一化数据进行了相关性分析。在禁食状态下,6 次比较的平均斜率为 0.9114±0.1500,平均相关系数为 0.912±0.055。在进食状态下,平均斜率为 0.8326±0.1630,平均相关系数为 0.887±0.047。基于这些结果,我们可以表明唾液中的咖啡因浓度适合描述禁食和进食胃中的水作为无热量液体的排空情况。所提出的技术提供了一种直接、廉价且非侵入性的方法来评估亲水性液体的胃排空情况,该方法可广泛用于口服生物药剂学。可能的应用包括描述真实生活条件、特定人群(例如老年人)的特征以及更好地了解胃排空对口服药物药代动力学特征的贡献。