# A Randomized, Double‐Blind, Two‐Treatment, Two‐Period, Crossover Study Investigating the Systemic Bioavailability of a Novel Cocrystal Ubiquinol Formulation Compared with a Ubiquinone Formulation in Healthy Adults

**Authors:** Xuefeng Mei, Bingqing Zhu, Kshitij Soni, Kishore Kasaraneni, Nirav Panchal

PMC · DOI: 10.1002/cpdd.70042 · 2026-03-06

## TL;DR

This study shows that a new ubiquinol formulation has better absorption in the body than a traditional ubiquinone formulation in healthy adults.

## Contribution

The study introduces a novel cocrystal ubiquinol formulation with significantly higher systemic bioavailability compared to ubiquinone.

## Key findings

- The test ubiquinol formulation showed 2.20 times higher peak plasma concentration than the ubiquinone reference.
- The ubiquinol formulation had 2.01 times higher AUC0–t and 3.43 times higher AUC0–∞ compared to ubiquinone.
- No adverse events were reported for either formulation in the small pilot study.

## Abstract

Coenzyme Q10 (CoQ10) is a naturally occurring biochemical cofactor found in all human cell membranes in two interconvertible forms: oxidized ubiquinone and reduced ubiquinol. Clinical studies indicate that different CoQ10 formulations have different absorption rates, highlighting research comparing their systemic bioavailability. This study compared the oral bioavailability of cocrystal formulation soft gels (test product), a novel ubiquinol formulation, and ubiquinone formulation (reference product) in a randomized, double‐blind, two‐period crossover study with 12 healthy subjects under fasting conditions. The secondary objective of this study was to evaluate the safety and tolerability of the ubiquinol formulation. The pharmacokinetic analyses indicated that the test ubiquinol formulation demonstrated substantially higher relative systemic bioavailability compared with the ubiquinone reference. The geometric mean ratios (test/reference) for baseline‐corrected peak plasma concentration (Cmax) and area under the curve from zero to last quantifiable time (AUC0–t) were 2.20 and 2.01, respectively, with 90% confidence intervals of 1.59–3.04 and 1.51–2.70. The geometric mean ratio for AUC from time zero to infinity (AUC0–∞) was 3.43 (90% CI: 1.47–8.00). No adverse events were reported in this small pilot study for either of the formulations. These findings demonstrate that ubiquinol has a better systemic bioavailability than ubiquinone, supporting the novel formulation's potential as a promising alternative to traditional CoQ10 supplements.

## Linked entities

- **Chemicals:** Coenzyme Q10 (PubChem CID 5281915), ubiquinol (PubChem CID 9962735)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, F2R (coagulation factor II thrombin receptor) [NCBI Gene 2149] {aka CF2R, HTR, PAR-1, PAR1, TR}
- **Diseases:** mitochondrial diseases (MESH:D028361), alcoholism (MESH:D000437), dyslipidemia (MESH:D050171), inflammation (MESH:D007249), mitochondrial cytopathy (MESH:C540770), diseases (MESH:D004194), cardiovascular or neurodegenerative disorders (MESH:D019636), malignancy (MESH:D009369), Endothelial dysfunction (MESH:D014652), diabetes (MESH:D003920), substance abuse (MESH:D019966), cardiovascular, hepatic, renal, gastrointestinal, neurological, psychiatric, or other (MESH:D001523), polycystic ovarian syndrome (MESH:D011085), swallowing difficulties (MESH:D003680), insulin resistance (MESH:D007333), fibromyalgia (MESH:D005356), cardiovascular disease (MESH:D002318), diabetic neuropathy (MESH:D003929), hypersensitivity (MESH:D004342), muscle pain (MESH:D063806), muscle symptoms (MESH:D009135), congestive heart failure (MESH:D006333), type 2 diabetes (MESH:D003924), chronic illnesses (MESH:D002908), migraines (MESH:D008881)
- **Chemicals:** ammonium formate (MESH:C030544), T (MESH:D014316), CoQ10 (MESH:C024989), nicotinamide (MESH:D009536), water (MESH:D014867), nitric oxide (MESH:D009569), xanthine (MESH:D019820), sodium (MESH:D012964), K2EDTA (-), R (MESH:D001120), minerals (MESH:D008903), 1-propanol (MESH:D000433), Ubiquinone (MESH:D014451), nitrogen oxides (MESH:D009589), lipid (MESH:D008055), reactive oxygen species (MESH:D017382), Ubiquinol (MESH:C003741), glucose (MESH:D005947), p-benzoquinone (MESH:C004532), alcohol (MESH:D000438)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12965043/full.md

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Source: https://tomesphere.com/paper/PMC12965043