FOOD–DRUG INTERACTION AND THEIR CLINICAL IMPLICATIONS: SELECTED INVESTIGATIONS

Authors

  • M. ABD ELGADIR Department of Food Science and Human Nutrition, College of Agriculture and Veterinary Medicine, Qassim University, Saudi Arabia

DOI:

https://doi.org/10.22159/ijpps.2019v11i3.25930

Keywords:

Food-drug interaction, Medication, Clinical implications, Clinical practice

Abstract

Food-drug interactions occur as a result of pharmacokinetic or pharmacodynamics mechanisms. Pharmacokinetic mechanisms include what the body does to a drug while Pharmacodynamics mechanisms involve what drugs do to the body. Many types of food have been shown to influence metabolism and the absorption of drugs. Large numbers of drugs are produced and introduced yearly. The interaction between Food and drug may cause negative effects in the nutritional status of the patient as well as safety and efficacy of drug therapy. Due to the possibility of unexpected or poor outcomes, generally, food-drug interactions, in this case, should be avoided. As the good clinical practice, drugs taken by mouth must be absorbed either through the lining of the stomach or the small intestine. Reduction in the absorbance of a drug might be influenced by the presence of food in the digestive tract. The avoidance of such interactions could be possible if the drug is taken 1 hour before or 2 h after eating the food. The effects of several types of food such as milk or milk products, grapefruit and grapefruit juice, bananas, oranges, legumes, fermented meats and pickled fish and some nutrient elements such as calcium, potassium, magnesium, iron, zinc, and vitamin K are highlighted in this paper including their clinical implications.

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Author Biography

M. ABD ELGADIR, Department of Food Science and Human Nutrition, College of Agriculture and Veterinary Medicine, Qassim University, Saudi Arabia

Associate Professor, College of Agriculture and Veterinary Medicine. Qassim University , Saudi Arabia

References

Frankel EH. Basic concepts. In: Handbook of food-drug interactions. McCabe BJ, Frankel EH, Wolfe JJ. (Eds.) CRC Press: Boca Raton; 2003. p. 2.

Ayo JA, Agu H, Madaki I. Food and drug interactions: its side effects. Nutr Food Sci 2005;35:243–52.

Jith PK, Kumar A, Joy AC. A prospective study of drug-drug interactions and adverse drug reactions among stroke patients in a tertiary care hospital. Asian J Pharm Clin Res 2016;9:100–4.

Hansten PD. Appendix II: important interactions and their mechanisms. In: Katzung BG. Editor. 09th edn. Basic and Clinical Pharmacology, McGraw hill, Boston; 2004. p. 1110.

Schmidt LE, Dalhoff K. Food-drug interactions. Drugs 2002;62:1481–502.

Lin L, Wang M, Tsai T. Food-drug interaction of (−)-epigallocatechin-3-gallate on the pharmacokinetics of irinotecan and the metabolite SN-38. Chem Biol Interact 2008;174:177–82.

Uwai Y, Ozeki Y, Isaka T, Honjo H, Iwamoto K. Inhibitory effect of caffeic acid on human organic anion transporters hOAT1 and hOAT3: a novel candidate for food-drug interaction. Drug Metabol Pharm 2011;5:486–93.

Bushra R, Aslam N, Khan AY. Food-drug interactions. Oman Med J 2011;26:77–83.

Boullata JI, Pharm DR, Hudson LM. Drug-nutrient interactions: a broad view with implications for practice. J Acad Nutr Diet 2012;112:506–17.

Egashira K, Sasaki H, Higuchi S, Ieiri I. Food-drug interaction of tacrolimus with pomelo, ginger, and turmeric juice in rats. Drug Metabol Pharm 2012;27:242–7.

Won CS, Nicholas H Oberlies, Mary F Paine. Mechanisms underlying food-drug interactions: inhibition of intestinal metabolism and transport. Pharm Ther 2012;136:186–201.

De Boer A, Florence Van Hunsel, Aalt Bast. Adverse food-drug interactions. Regul Toxicol Pharm 2015;73:859–65.

Mouly S, Lloret Linares C, Sellier P, Sene D, Bergmann J. Is the clinical relevance of drug-food and drug-herb interactions limited to grapefruit juice and Saint-John’s Worth? Pharm Res 2017;118:82–92.

Di Minno A, Frigerio B, Spadarella G, Ravani A, Sansaro D, Amato M, Kitzmiller JP, et al. Old and new oral anticoagulants: food, herbal medicines and drug interactions. Blood Rev 2017;31:193–203.

Pasko P, Rodacki T, Domagała Rodacka, Palimonka RK, Marcinkowska M, Owczarek D. Second generation H1-antihistamines interaction with food and alcohol-a systematic review. Biomed Pharm 2017;93:27–39.

Wang N, Zhu C, Zhang X, Zhai X, Lu Y. Food-drug interactions involving multiple mechanisms: a case study with an effect of capsaicin on the pharmacokinetics of irinotecan and its main metabolites in rat. J Funct Foods 2018;40:292–8.

Ashak R, Kousalya K, Senthil NB, Valentina P. An outlook on the mechanisms of drug interactions with other drugs, fruits, herbs and their preventive measures. Asian J Pharm Clin Res 2016;9:10–8.

Davit BM, Conner DP. Food effects on drug bioavailability. In: Krishna R, Yu L. eds. Biopharmaceutics applications in drug development. New York, NY: Springer; 2008. p. 317–35.

FDA. US Food and Drug Administration. Guidance for industry: Food-effect bioavailability and fed equivalence studies. Food Drug Administration: Rockville, MD, December; 2002. Available from: http://www.fda.gov/downloads/Drugs/Guidance Compliance Regulatory Information Guidances/ucm070241.pdf. [Last accessed on 25 Jan 2018].

Amidon GL, Lennern Ås H, Shah VP, Crison JR. A theoretical basis for a biopharmaceutics drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res 1995;12:413–20.

Wu CY, Benet LZ. Predicting drug disposition via application of BCS: Transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system. Pharm Res 2005;22:11–23.

Yang Y, Faustino PJ, Volpe DA, Ellison CD, Lyon RC, Yu LX. Biopharmaceutics classification of selected–blockers: solubility and permeability class membership. Mol Pharm 2007;4:608–14.

Custodio JM, Wu CY, Benet LZ. Predicting drug disposition, absorption/elimination/transporter interplay and the role of food on drug absorption. Adv Drug Delivery Rev 2008;60:717–33.

Holt GA. Food and drug interactions. Chicago. Precept Press; 1998. p. 293.

Zikria J, Goldman R, Ansell J. Cranberry juice and warfarin: when bad publicity trumps science. Am J Med 2010;123:384–92.

Dresser GK, Bailey DG, Leake BF, Schwarz UI, Dawson PA, Freeman DJ, et al. Fruit juices inhibit organic anion transporting polypeptide-mediated drug uptake to decrease the oral availability of fexofenadine. Clin Pharmacol Ther 2002;71:11–20.

Bailey DG, Dresser GK, Bend JR. Bergamottin, lime juice and red wine as inhibitors of CYP3A4 activity: Comparison with grapefruit juice. Clin Pharmacol Ther 2003;73:529–37.

Rebello S, Zhao S, Hariry S, Dahlke M, Alexander N, Vapurcuyan A, et al. Intestinal OATP1A2 inhibition as a potential mechanism for the effect of grapefruit juice on aliskiren pharmacokinetics in healthy subjects. Eur J Clin Pharmacol 2012;68:697–708.

Greenblatt DJ. Analysis of drug interactions involving fruit beverages and organic anion–transporting polypeptides. J Clin Pharmacol 2009;49:1403–7.

Komperda KE. Potential interaction between pomegranate juice and warfarin. Pharmacotherapy 2009;29:1002–6.

Tapaninen T, Neuvonen PJ, Niemi M. Grapefruit juice greatly reduces the plasma concentrations of the OATP2B1 and CYP3A4 substrate aliskiren. Clin Pharmacol Ther 2010;88:339–42.

Ho PC, Saville DJ, Coville PF, Wanwimolruk S. Content of CYP3A4 inhibitors, naringin, naringenin and bergapten in grapefruit and grapefruit juice products. Pharm Acta Helv 2000;74:379–85.

Ross SA, Ziska DS, Zhao K, ElSohly MA. Variance of common flavonoids by brand of grapefruit juice. Fitoterapia 2000;71:154–61.

De Castro WV, Mertens Talcott S, Rubner A, Butterweck V, Derendorf H. Variation of flavonoids and furanocoumarins in grapefruit juices: a potential source of variability in grapefruit juice–drug interaction studies. J Agric Food Chem 2006;54:249–55.

Wanwimolruk S, Marquez PV. Variations in the content of active ingredients causing drug interactions in grapefruit juice products sold in california. Drug Metabol Drug Interact 2006;21:233–43.

Brill S, Zimmermann C, Berger K, Drewe J, Gutmann H. In vitro interactions with repeated grapefruit juice administration-to peel or not to peel? Planta Med 2009;75:332–35.

Neuhofel AL, Wilton JH, Victory JM, Hejmanowsk LG, Amsden GW. Lack of bioequivalence of ciprofloxacin when administered with calcium-fortified orange juice: a new twist on an old interaction. J Clin Pharmacol 2002;42:461–6.

Wallace AW, Victory JM, Amsden GW. Lack of bioequivalence when levofloxacin and calcium-fortified orange juice are coadministered to healthy volunteers. J Clin Pharmacol 2003;43:539–44.

Lilja JJ, Juntti Patinen L, Neuvonen PJ. Orange juice substantially reduces the bioavailability of the beta-adrenergic–blocking agent celiprolol. Clin Pharmacol Ther 2004a;75:184–90.

Lilja JJ, Juntti Patinen L, Neuvonen PJ. Effects of regular consumption of grapefruit juice on the pharmacokinetics of simvastatin. Br J Clin Pharmacol 2004b;58:56–60.

Hagenbuch B, Gui C. Xenobiotic transporters of the human organic anion transporting polypeptides (OATP) family. Xenobiotica 2008;38:778–801.

Imanaga J, Kotegawa T, Imai H, Tsutsumi K, Yoshizato T, Ohyama T, et al. The effects of the SLCO2B1 c.1457C>T polymorphism and apple juice on the pharmacokinetics of fexofenadine and midazolam in humans. Pharm Genom 2011;21:84–93.

Mougey EB, Feng H, Castro M, Irvin CG, Lima JJ. Absorption of montelukast is transporter-mediated: a common variant of OATP2B1 is associated with reduced plasma concentrations and poor response. Pharm Genom 2009;19:129–38.

Ieiri I, Doi Y, Maeda K, Sasaki T, Kimura M, Hirota T, et al. Microdosing clinical study: pharmacokinetic, pharmacogenomic (SLCO2B1), and interaction (grapefruit juice) profiles of celiprolol following the oral microdose and therapeutic dose. J Clin Pharmacol 2011;52:1078–89.

Ming X, Knight BM, Thakker DR. Vectorial transport of fexofenadine across caco–2 cells: involvement of apical uptake and basolateral efflux transporters. Mol Pharm 2011;8:1677–86.

Glaeser H, Bailey DG, Dresser GK, Gregor JC, Schwarz UI, McGrath JS, et al. Intestinal drug transporter expression and the impact of grapefruit juice in humans. Clin Pharmacol Ther 2007;81:362–70.

Mandery K, Bujok K, Schmidt I, Keiser M, Siegmund W, Balk B, et al. Influence of the flavonoids apigenin, kaempferol, and quercetin on the function of organic anion transporting polypeptides 1A2 and 2B1. Biochem Pharmacol 2010; 80:1746–53.

Zlotogorski A, Dayan A, Dayan D, Chaushu G, Salo T, Vered M. Nutraceuticals as new treatment approaches for oral cancer: II. Green tea extracts and resveratrol. Oral Oncol 2013;49:502–6.

Shahidi F, Ambigaipalan P. Phenolics and polyphenolics in foods, beverages and spices: antioxidant activity and health effects-a review. J Funct Foods 2015;18:820–97.

Harrington L, Cris Gonzales C. Food and drug interactions in critically ill adults. Crit Care Nurs Clin North Am 2004; 16:501–8.

Min KJ, Kwon TK. Anticancer effects and molecular mechanisms of epigallocatechin–3–gallate. Int Med Res 2014;3:16–24.

Shirakami Y, Shimizu M, Moriwaki H. Cancer chemoprevention with green tea catechins: from bench to bed. Curr Drug Targets 2012;13:1842–57.

Zaveri NT. Green tea and its polyphenolic catechins: medicinal uses in cancer and noncancer applications. Life Sci 2006; 78:2073–80.

Roth M, Timmermann BN, Hagenbuch B. Interactions of green tea catechins with organic anion–transporting polypeptides. Drug Metab Dispos 2011;39:920–6.

Fuchikami H, Satoh H, Tsujimoto M, Ohdo S, Ohtani H, Sawada Y. Effects of herbal extracts on the function of human organic anion–transporting polypeptide OATP–B. Drug Metab Dispos 2006;34:577–82.

Published

01-03-2019

How to Cite

ELGADIR, M. A. “FOOD–DRUG INTERACTION AND THEIR CLINICAL IMPLICATIONS: SELECTED INVESTIGATIONS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 11, no. 3, Mar. 2019, pp. 1-5, doi:10.22159/ijpps.2019v11i3.25930.

Issue

Section

Review Article(s)