Pharmacokinetics, side effects, dosage forms, drug interactions of curcu-mine

This review presents current data on the pharmacokinetics, side effects, dosage forms and interactions of curcumin. Curcumin, the major bioactive component of turmeric, has low bioavailability due to its low water solubility, rapid metabolism in the liver and rapid excretion from the body. The main pathways of curcumin metabolism are described, including its reduction and subsequent conjugation with glucuronic acid and sulphates. Side effects of curcumin such as hyperoxaluria, iron deficiency anaemia, hepatotoxicity, arrhythmias, allergic reactions and potential carcinogenic properties are discussed. Various dosage forms of curcumin developed to enhance its bioavailability are discussed, including liposomes, nanoparticles, hydrogels and phytosomes. Particular attention is given to the drug interactions of curcumin with chemotherapeutic agents such as 5-fluorouracil, vincristine, gemcitabine, adriamycin and cisplatin, as well as with hypolipidaemic agents, antiaggregants and anticoagulants. These data highlight the need for further studies to optimise the therapeutic use of curcumin and minimise its side effects.

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Publication Details

Journal
Experimental and Clinical Gastroenterology
Published
2025-03-06
DOI
https://doi.org/10.31146/1682-8658-ecg-229-9-147-160
Primary Topic
Curcumin's Biomedical Applications
Type
article
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article

Pharmacokinetics, side effects, dosage forms, drug interactions of curcu-mine

Evgeny Pokushalov, Михаил В. Хвостов, M. F. Novikova, E. V. Shrayner et al.
1 links
Experimental and Clinical Gastroenterology
Curcumin's Biomedical Applications
article

Pharmacokinetics, side effects, dosage forms, drug interactions of curcu-mine

Evgeny Pokushalov, Михаил В. Хвостов, M. F. Novikova, E. V. Shrayner, K. M. Nikolaychuk, Т. Г. Толстикова, А. И. Хавкин, D. A. Lukichev, A. S. Veremenko, I. D. Levchenko, E. E. Vergunova, A. S. Tumas, P. Ya. Platonova, D. A. Kudlai, D. A. Sergeev, Alla V. Pavlova
article en

Abstract

This review presents current data on the pharmacokinetics, side effects, dosage forms and interactions of curcumin. Curcumin, the major bioactive component of turmeric, has low bioavailability due to its low water solubility, rapid metabolism in the liver and rapid excretion from the body. The main pathways of curcumin metabolism are described, including its reduction and subsequent conjugation with glucuronic acid and sulphates. Side effects of curcumin such as hyperoxaluria, iron deficiency anaemia, hepatotoxicity, arrhythmias, allergic reactions and potential carcinogenic properties are discussed. Various dosage forms of curcumin developed to enhance its bioavailability are discussed, including liposomes, nanoparticles, hydrogels and phytosomes. Particular attention is given to the drug interactions of curcumin with chemotherapeutic agents such as 5-fluorouracil, vincristine, gemcitabine, adriamycin and cisplatin, as well as with hypolipidaemic agents, antiaggregants and anticoagulants. These data highlight the need for further studies to optimise the therapeutic use of curcumin and minimise its side effects.

Experimental and Clinical Gastroenterology(9)
Belgorod National Research University (RU), Sechenov University (RU), Novosibirsk State University (RU), Lomonosov Moscow State University (RU), Institute of Chemical Biology and Fundamental Medicine (RU), Novosibirsk Institute of Organic Chemistry (RU), Ministry of Health of the Russian Federation (RU), Siberian Branch of the Russian Academy of Sciences (RU), Medical Technologies (Czechia) (CZ)
Openalex Percentile: Top 97%
Curcumin's Biomedical Applications
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