A single equivalent dose, randomized, parallel design pharmacokinetic study to evaluate the Comparative bioavailability of Vitamin C vs. Liposomal Vitamin C.
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This study compared the bioavailability of Liposomal Vitamin C (T1 - Haroutine Vitamin C) and Standard Vitamin C (T2) in a randomized, single-dose, fasting trial. Key pharmacokinetic parameters were analyzed to measure absorption and retention.
Absorption and Metrics
Absorption (Cmax and Tmax):
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Cmax (Maximum Plasma Concentration):
- T1 (Liposomal): 6.10 ± 2.75 μg/mL
- T2 (Standard): 6.68 ± 3.14 μg/mL
- % Difference: T1 was 8.68% lower than T2.
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Tmax (Time to Reach Cmax):
- T1: 3.50 hours
- T2: 3.25 hours
- T1 still demonstrated slightly delayed absorption compared to T2.
Retention (AUC and Half-Life):
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AUCinf (Total Drug Exposure Over Time):
- T1: 157.31 ± 204.51 μg·h/mL
- T2: 92.22 ± 67.34 μg·h/mL
- % Difference: T1 had 70.58% higher total exposure than T2.
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Thalf (Half-Life):
- T1: 28.99 ± 32.78 hours
- T2: 14.91 ± 14.55 hours
- % Difference: T1 had a 94.45% longer retention time than T2.
Statistical Insights:
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Consistency and Elimination:
- After removing outliers, T1 still exhibited a slower elimination rate (Kel: 0.0428 vs. 0.1468 for T2), indicating sustained release.
- The variability (CV) for T1's AUCinf remained high (130%), while T2's AUCinf variability was reduced to 73%.
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Outcome:
- T1's superiority in total exposure and retention was maintained, supporting its suitability for sustained therapeutic effects.
- T2's slight advantage in Cmax remained, indicating quicker but less durable absorption.
Inferences:
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Enhanced Retention with Liposomal Vitamin C:
- T1 consistently showed higher AUCinf and Thalf, indicating prolonged absorption and therapeutic presence.
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Implications of Lower Cmax:
- While T1's peak plasma concentration was slightly lower than T2, its sustained levels over time could better support applications requiring steady Vitamin C availability.
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Improved Consistency for Standard Vitamin C:
- Removing outliers reduced variability for T2, enhancing its reliability in achieving higher peak concentrations.
Conclusion:
After excluding outliers, Liposomal Vitamin C (T1) continues to exhibit superior retention and total exposure metrics compared to Standard Vitamin C (T2). These findings affirm T1's potential for long-term benefits, such as immune support or skin health. However, T2 may remain a better option for immediate needs due to its higher Cmax. Further research across broader populations is recommended to confirm these results.