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PRUVN Announces Human Clinical Trial Findings on the Impact of Max International RiboCeine™ Supplementation on Serum Glutathione Levels - 25th April 2024

PRUVN Human Clinical Trial on RiboCeine™ and Serum Glutathione Levels
A human clinical trial conducted by PRUVN Research LLC has provided important evidence on the impact of Max International’s patented RiboCeine supplementation on serum glutathione levels.
This double-blind placebo-controlled study was ethically approved and involved 40 participants aged between 38 and 60 who were randomly assigned to receive either a daily 250 mg dose of RiboCeine™ or a placebo over a four-week period. Serum glutathione levels were measured before and after supplementation using a standard spectrophotometric assay.

Key Findings from the Trial

  • Participants in the placebo group experienced a decrease in serum glutathione levels over the course of the study.

  • The group receiving RiboCeine showed a significant 26.6 % increase in serum glutathione levels overall.

  • The effect was especially notable in the older age group (51-60), where serum glutathione increased by 64.7 %.

  • These results suggest that RiboCeine can effectively elevate glutathione levels in humans with pronounced benefits seen in mature adults.

While this preliminary study highlights promising trends in supporting the body’s natural antioxidant capacity more research with larger participant numbers is recommended to further validate the findings.

This study marks a significant step in translating decades of preclinical research into meaningful evidence of RiboCeine’s role in enhancing glutathione production in real-world settings.

 

Dr Herbert T Nagasawa explains about The Science of Riboceine™
 
RiboCeine
For many decades scientists and medical professionals have recognised Glutathione as the body’s most powerful internal defender. It functions as the master antioxidant and a key detoxifier produced naturally within our cells. However, under constant oxidative stress and with advancing age particularly from around 40 the body’s ability to generate sufficient Glutathione begins to decline.

Earlier approaches such as N-acetyl-cysteine (NAC) provided partial support yet came with clear limitations. This changed with a major scientific breakthrough led by the late Dr Herbert T Nagasawa. His work resulted in the development of RiboCeine a patented compound designed to deliver Cysteine to cells with greater efficiency allowing the body to naturally increase its own Glutathione production in a more effective and sustainable way.

Max International is the proud holder of the United States Patent for RiboCeine. This innovation is supported by decades of scientific research plus real world application, making it one of the most advanced Glutathione supporting technologies available today.

RiboCeine represents a smarter approach to cellular protection detoxification and long term wellness from within.

 

Scientifically Proven and Patented Technology
RiboCeine is a scientifically engineered molecule created from Ribose and Cysteine both of which are naturally present in the body. After consumption RiboCeine is efficiently absorbed into the bloodstream where it delivers these critical nutrients directly into the cells. This targeted delivery supports the body’s natural production of Glutathione while also supplying Ribose an essential component in the formation of ATP the primary energy currency of every cell.

In multiple scientific comparisons RiboCeine has consistently demonstrated superior performance when measured against other Glutathione supporting approaches. To date it has been featured in more than 60 peer reviewed scientific studies many of which were supported by the National Institutes of Health plus other respected research institutions. These studies reinforce both its effectiveness and its innovative design.

Explore the Science Behind RiboCeine™
Gain access to an extensive body of knowledge including over 60 published studies focused on RiboCeine. These studies explain how RiboCeine functions at the cellular level to enhance the body’s own Glutathione production. Its unique mechanism of action ensures that essential building blocks are delivered directly into cells distinguishing it clearly from conventional supplementation methods.

Independent peer reviewed research published on trusted third party scientific platforms allows you to examine the evidence firsthand. These validated findings highlight RiboCeine’s proven ability to elevate Glutathione levels strengthen cellular defences and support overall cellular health.

 
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  2. Roberts, J.C.; Francetic, D.J.; Zera, R.T. L-cysteine prodrug protects against cyclophosphamide urotoxicity without compromising therapeutic activity. Cancer Chemotherapy and Pharmacology 1991, 28, 166-170.
  3. Roberts, J.C.; Francetic, D.J. Time course for the elevation of glutathione in numerous organs of L1210-bearing CDF1 mice given the L-cysteine prodrug, RibCys. Toxicology Letters, 1991, 59, 245-251.
  4. Roberts, J.C.; Francetic, D.J. Mechanisms of Chemoprotection by RibCys, a Thiazolidine Prodrug of L cysteine. Med. Chem. Res., 1991, 1, 213-219.
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  7. Roberts, J.C.; Francetic, D.J.; Zera, R.T. Chemoprotection against Cyclophosphamide-Induced Urotoxicity: Comparison of Nine Thiol Protective Agents. AntiCancer Research, 1994, 14, 389-396.
  8. Carroll, M.P.; Zera, R.T.; Roberts, J.C.; Schlafmann, S.E.; Feeny, D.A.; Johnston, G.R.; West, M.A.; Bubrick, M.P. Efficacy of Radioprotective Agents in Preventing Small and Large Bowel Radiation Injury. Dis. Colon Rectum, 1995, 38(7), 716-722.
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  16. Waldren, C.A.; Vannais, D.B.; Ueno A.M. A role for long-lived radicals (LLR) in radiation-induced mutation and persistent chromosomal instability: counteraction by Ascorbate and RibCys but not DMSO. Mutation Research. 2004, 551:255-265.
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  32. Medubi L.J., Ama C., Medubi O.O., Onwosu N.C., Lawal O.R., Osinubi A.A.A. D-Ribose-L-Cysteine-Rich Supplement Attenuates Doxorubicin-Induced Impaired Spermatogenesis, Testicular Steroidogenesis and Redox Status in Sprague-Dawley Rats. African Journal of Biomedical Research. 2019(22):179-185.
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  35. Emokpae O, Ben-Azu B, Ajayi AM, Umukoro S. D-Ribose-L-Cysteine enhances memory task, attenuates oxidative stress and acetyl-cholinesterase activity in scopolamine amnesic mice. Drug Dev Res. 2020;1-9
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  52. Ogunlade, B., Gbotolorun, S.C., Ogunlade, A.A. D-ribose-L-cysteine modulates lead acetate-induced hematobiochemical alternations, hormonal imbalance, and ovarian toxicity in adult female Wistar rats. Drug and Chemical Toxicology. 2022 45(4), 1606-1613.
  53. Adekomi,D.A, Olajide, O.J., Adewale, O.O., Okesina, A.A., Fatoki, J.O., Falana, B.A. Adeniyi, T.D., Adegoke A.A., Ojo, W.A., Alabi, S.O. D-ribose-L-Cysteine exhibits neuroprotective activity through inhibition of oxido-behavioral dysfunctions and modulated activities of neurotransmitters in the cerebellum of Juvenile mice exposed to ethanol. Drug Chem. Toxicol. 2022 June 20:1-11.
  54. Mega, O.O., Edesiri, T.P., Victor, E., Kingsley, N.E., Rume, R.A., Faith, F.Y., Simon, O.I., Oghenetega, B.O., Agbonito-Chijiokwu, E. d-ribose- l-cysteine abrogates testicular maladaptive responses induced by polychlorinated bisphenol intoxication in rats via activation of the mTOR signaling pathway mediating inhibition of apoptosis, inflammation, and oxidonitrergic flux. J. Biochem Mol. Toxicol. 2022 July 13, e23161.
  55. Ojetola, A.A., Asiwe, J.N., Adeyemi, W.J., Ogundipe, D.J., Fasanmade, A.A. Dietary Supplementation with D-Ribose-L-Cysteine Prevents Hepatic Stress and Pro-Inflammatory Responses in Male Wistar Rats Fed a High-Fructose High-Fat Diet. Pathophysiology 2022, 29, 631-639.
 
 
 

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