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临床试验/NCT07694401
NCT07694401已完成不适用

Metabolic Profiling of Acesulfame Potassium After Coca-Cola Zero Sugar Consumption in Healthy Adults

Czech University of Life Sciences Prague1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2023年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
10
试验地点
1
主要终点
Urinary concentration of acesulfame potassium (Ace-K)

研究概览

简要总结

Consumption of beverages containing non-nutritive sweeteners has increased worldwide, but limited information is available regarding the short-term urinary excretion of acesulfame potassium (Ace-K) and the acute metabolic response following consumption of commercially available beverages. This study investigates the urinary pharmacokinetics of Ace-K and the acute urinary metabolomic response after consumption of 500 mL of Coca-Cola Zero Sugar in healthy adults. Participants complete two study arms under free-living conditions: Coca-Cola Zero Sugar and still water (control), separated by a one-month washout period. Urine samples are collected before beverage consumption and repeatedly over the subsequent 24 hours. Proton nuclear magnetic resonance (¹H NMR) spectroscopy is used to quantify Ace-K and other urinary metabolites. The study aims to determine the urinary appearance and elimination kinetics of Ace-K and to identify metabolic changes associated with Coca-Cola Zero Sugar consumption compared with water.

详细描述

Non-nutritive sweeteners (NNS) are widely used as sugar substitutes in reduced-calorie foods and beverages. Among these, acesulfame potassium (Ace-K) is extensively incorporated into commercially available soft drinks because of its high sweetening potency, thermal stability, and minimal caloric contribution. Following oral ingestion, Ace-K is rapidly absorbed and excreted predominantly unchanged in urine, making it a promising biomarker of NNS consumption and dietary exposure. However, limited information is available regarding the urinary pharmacokinetics of Ace-K following consumption of commercially formulated beverages under free-living conditions.

Proton nuclear magnetic resonance (¹H NMR) spectroscopy enables simultaneous quantitative analysis of exogenous compounds and endogenous metabolites in complex biological samples. By applying the same analytical platform to both the intervention beverage and sequential urine samples, this study investigates the relationship between the ingested dose of Ace-K and its urinary excretion profile while simultaneously evaluating short-term metabolic responses following Coca-Cola Zero Sugar consumption.

This non-randomized, within-subject controlled study compares the urinary metabolomic response after consumption of Coca-Cola Zero Sugar with that observed following consumption of still water. The study aims to characterize the urinary appearance and elimination kinetics of Ace-K, quantify pharmacokinetic parameters including time to peak concentration and urinary elimination half-life, and explore acute changes in urinary metabolite profiles associated with Coca-Cola Zero Sugar consumption using quantitative ¹H NMR metabolomics.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy adults aged 18 to 60 years
  • Able and willing to provide written informed consent
  • Willing to consume 500 mL of Coca-Cola Zero Sugar and 500 mL of still water during separate study periods
  • Willing to collect urine samples before and during the 24 hours after each intervention according to the study instructions
  • Willing to avoid foods and beverages containing non-nutritive sweeteners for 48 hours before each study period

排除标准

  • Younger than 18 years or older than 60 years
  • Current smoker
  • Known kidney disease or metabolic disease
  • Regular use of prescription medications
  • Use of antibiotics in last 3 months
  • Consumption of foods or beverages containing non-nutritive sweeteners within 48 hours before either study period
  • Unable or unwilling to comply with the study procedures or urine collection schedule

研究组 & 干预措施

Coca-Cola Zero Sugar

Experimental

Participants consumed 500 mL of Coca-Cola Zero Sugar with breakfast. Spot urine samples were collected before beverage consumption and repeatedly over the subsequent 24-hour period for metabolomic and pharmacokinetic analyses using proton nuclear magnetic resonance (¹H NMR) spectroscopy.

干预措施: Coca-Cola Zero Sugar (Other)

Still Water

Active Comparator

Participants consumed 500 mL of still water with breakfast following a one-month washout period. Spot urine samples were collected before beverage consumption and repeatedly over the subsequent 24-hour period using the same sampling schedule as the Coca-Cola Zero Sugar arm.

干预措施: Still water (Other)

结局指标

主要结局

Urinary concentration of acesulfame potassium (Ace-K)

时间窗: Baseline and up to 24 hours after beverage consumption

Quantitative measurement of urinary acesulfame potassium (Ace-K) concentration following consumption of 500 mL Coca-Cola Zero Sugar compared with still water, determined by quantitative proton nuclear magnetic resonance (¹H NMR) spectroscopy and used to characterize urinary excretion kinetics.

Creatinine-normalized urinary acesulfame potassium (Ace-K) concentration (µM/mM creatinine)

时间窗: Baseline and each scheduled urine collection over 24 hours following beverage consumption.

Quantitative measurement of urinary acesulfame potassium (Ace-K) concentration following consumption of 500 mL Coca-Cola Zero Sugar and still water, determined by quantitative proton nuclear magnetic resonance (¹H NMR) spectroscopy. Concentrations will be normalized to urinary creatinine and reported at each scheduled urine collection time point.

次要结局

  • Urinary metabolomic profile(Baseline and up to 24 hours after beverage consumption)
  • Creatinine-normalized urinary metabolite concentrations (µM/mM creatinine)(Baseline and each scheduled urine collection over 24 hours following beverage consumption.)

研究者

发起方
Czech University of Life Sciences Prague
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jaroslav Havlik

Associate Professor

Czech University of Life Sciences Prague

研究点 (1)

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