Superior Bioavailability of a Novel Curcumin Formulation in Healthy Humans Under Fasting Conditions

Background Despite its broad range of biological activities, use of curcumin is limited because of poor bioavailability. Here we report a novel curcumin formulation, Curcuwin Ultra+ (CU+), with superior bioavailability as compared to 95% turmeric extract (TUR 1800). Methods A randomized, double-blin...

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Published inAdvances in therapy Vol. 39; no. 5; pp. 2128 - 2138
Main Authors Kothaplly, Sudhakar, Alukapally, Shankar, Nagula, Nagaraju, Maddela, Rambabu
Format Journal Article
LanguageEnglish
Published Cheshire Springer Healthcare 01.05.2022
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ISSN0741-238X
1865-8652
1865-8652
DOI10.1007/s12325-022-02081-w

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Summary:Background Despite its broad range of biological activities, use of curcumin is limited because of poor bioavailability. Here we report a novel curcumin formulation, Curcuwin Ultra+ (CU+), with superior bioavailability as compared to 95% turmeric extract (TUR 1800). Methods A randomized, double-blind, three-treatment, crossover oral bioavailability study was conducted in 24 healthy volunteers under fasting conditions. Subjects received a single dose of CU+ 250 mg, 500 mg and 1900 mg of TUR1800 as per randomization schedule and blood samples were collected at 4 h and 0 h before dosing, and 0.5, 1, 2, 3, 4, 5, 6, 8, 10, 12, 24 h post dose. Total curcuminoids were measured as curcumin, demethoxycurcumin, bisdemethoxycurcumin, and tetrahydrocurcumin using a validated LC–MS/MS method. Results CU+ achieved a significantly higher ( p  < 0.05) maximum plasma concentration ( C max ) and total systemic exposure (AUC 0–6 and AUC 0–12 ) for total curcuminoids as compared to TUR 1800. We observed 101 and 100 times higher C max respectively for 250 and 500 mg doses of CU+ as compared to 1900 mg of TUR1800. Similarly, AUC 0–6 was 144 and 149 times higher whereas AUC 0–12 was 99 and 113 times higher respectively for 250 and 500 mg doses of CU+ as compared to 1900 mg dose of TUR1800. Further, CU+ showed 40% faster absorption ( p  < 0.05). No safety issues were observed. Conclusion CU+, which is designed for increased absorption and protection of curcuminoids from intestinal degradation, demonstrated superior bioavailability as compared to TUR1800 at considerably smaller doses. Additional clinical studies will help to demonstrate the impact of its increased bioavailability on efficacy. Clinical Trial Registration CTRI/2020/10/028508 (Clinical Trials Registry—India).
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ISSN:0741-238X
1865-8652
1865-8652
DOI:10.1007/s12325-022-02081-w