Effect of Garcinia kola on Atorvastatin Dissolution Profile: An Indication for Possible Drug-Drug Interactions After Oral Administration

A. Adegbola, S. Igbinoba, E. Adebisi, B. Omotoso, J. Soyinka
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Abstract

Background: Herb-drug interactions are of growing concern due to the widespread use of herbal supplements alongside medications.  These interactions can affect therapeutic outcomes. Understanding and identifying specific interactions is crucial for ensuring safe and  effective medication use. Objective: This study investigated the impact of Garcinia kola, a common food supplement, on the dissolution of atorvastatin tablets.Methods: The dissolution profiles of atorvastatin tablets were investigated alone and in the presence of varying concentrations of G. Kola  by mixing 1, 2, or 4g of G. Kola powder respectively with the dissolution medium. Samplings were performed at predetermined time  points (10, 20, 30, 45 and 60 minutes) and the amount of atorvastatin dissolved was measured using a validated HPLC method.  Statistical analyses were conducted to assess the significance of the observed differences.Results: The percentages of atorvastatin released in dissolution medium without G. kola were 31.38±11.81,46.02±8.73, 72.23±33.30,  63.55±27.10, 82.54±31.12% across the sampling time points. Whereas the percentage of drug released were 17.01±7.33, 27.02±8.42,  34.70±13.90, 39.74±13.53, 28.47±11.78% in the presence of 1g G. kola; 12.44±5.89, 11.87±1.51, 23.33±5.18, 27.33±8.50, 52.49±11.66% in the  presence of 2g G. kola and 2.28±3.53, 4.94±7.21, 7.26±9.01, 4.68±7.37, 6.86±8.70% in the presence of 4g G. kola. There was a statistically  significant difference in the amount of drug dissolved in conditions studied.Conclusion: There was a significant change in the dissolution profile of atorvastatin with increasing concentrations of G. kola. This  suggests a need to establish the impact of G. kola on the disposition of atorvastatin in vivo. 
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加西可拉对阿托伐他汀溶解曲线的影响:口服后可能发生药物间相互作用的迹象
背景:由于草药补充剂与药物的广泛使用,草药与药物之间的相互作用日益受到关注。 这些相互作用会影响治疗效果。了解和识别特定的相互作用对于确保安全有效用药至关重要。研究目的本研究调查了一种常见的食物补充剂--加西可拉对阿托伐他汀片剂溶出度的影响:方法:将 1 克、2 克或 4 克哥拉粉末分别混入溶解介质中,研究阿托伐他汀片剂单独和在不同浓度的哥拉存在下的溶解情况。在预定的时间点(10、20、30、45 和 60 分钟)进行取样,并使用经过验证的 HPLC 方法测量阿托伐他汀的溶解量。 进行统计分析以评估观察到的差异的显著性:在不含哥拉的溶解培养基中,阿托伐他汀在各取样时间点的释放率分别为 31.38±11.81、46.02±8.73、72.23±33.30、63.55±27.10、82.54±31.12%。而在 1g G. kola 存在的情况下,药物释放率分别为 17.01±7.33、27.02±8.42、34.70±13.90、39.74±13.53、28.47±11.78%;在 1g G. kola 存在的情况下,药物释放率分别为 12.44±5.89、11.87±1.在 2g G. kola 存在下,分别为 12.44±5.89、11.87±1.51、23.33±5.18、27.33±8.50、52.49±11.66%;在 4g G. kola 存在下,分别为 2.28±3.53、4.94±7.21、7.26±9.01、4.68±7.37、6.86±8.70%。在所研究的条件下,药物溶解量的差异有统计学意义:结论:阿托伐他汀的溶解度随哥拉浓度的增加而发生了明显变化。这表明有必要确定葛根对阿托伐他汀体内处置的影响。
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