About RejuvaTech
An innovation-driven platform company specializing in patent-protected longevity chemistry, advanced absorption systems, and scalable GMP integration.
Our Strategic Focus
RejuvaTech’s objectives are centered on advancing protected longevity chemistry and scalable delivery architectures that address structural limitations in current supplement formats.
We focus on:
• Stabilizing and enhancing next-generation NAD⁺ precursor systems
• Engineering multimodal bioavailability platforms
• Developing cost-efficient, scalable synthesis pathways
• Supporting structured GMP integration and regulatory positioning
Our goal is to enable premium-tier product architectures grounded in defensible intellectual property and measurable performance differentiation.
Regenerative & Telomere Support Platform
RejuvaTech has developed a patent-pending triterpenoid composition and delivery framework designed to address structural limitations in regenerative compound bioavailability.
This platform combines optimized triterpenoid synthesis pathways with advanced nanocarrier and self-nanoemulsifying delivery systems (SNEDDS) to improve systemic exposure and cellular uptake. The architecture is designed to support telomerase modulation, structural cellular integrity, inflammatory balance, and oxidative stress resilience — key domains within the longevity and regenerative health landscape.
Importantly, our synthesis and delivery integration enables scalable manufacturing while reducing cost inefficiencies commonly associated with high-purity triterpenoid production. The result is a protected regenerative platform engineered for commercial viability, differentiation, and integration across premium wellness portfolios.
We stand out at RejuvaTech by consistently pushing the boundaries of biochemistry, delivering safe, effective, and transformative tools that integrate seamlessly into daily life. With us, our customers aren’t just choosing a supplement—they’re investing in our forward-thinking approach to wellness, fueled by our expertise, innovation, and deep passion for improving quality of life at every stage.
This platform forms the foundation for both systemic and dermal applications, including next-generation skin health formulations positioned to exceed traditional retinoid-based performance profiles.
Scientific Foundation & Platform Evolution
Since 2015, RejuvaTech has operated as a research-driven development platform focused on longevity chemistry, regenerative compound systems, and advanced delivery architecture.
Our work integrates contemporary peer-reviewed research with applied formulation science, emphasizing plant-derived bioactives, NAD⁺ precursor evolution, and telomere-supportive compound classes. Rather than relying on isolated ingredients, we focus on structural improvement — enhancing stability, systemic exposure, and delivery precision through engineered architectures.
Our triterpenoid composition platform reflects this approach, combining optimized synthesis with nanocarrier and SNEDDS delivery systems to support dermal and systemic regenerative applications. Parallel to this work, our NAD⁺-related research has progressed from first-generation nicotinamide riboside formulations to stabilized next-generation precursor systems engineered for improved intracellular conversion efficiency.
Throughout this evolution, our objective has remained consistent: to develop protected, scalable, and commercially viable chemistry platforms capable of supporting premium wellness portfolios with measurable performance differentiation.
Scientific Integration, Manufacturing Interface & Scalable Production Architecture
Platform Integration & Commercial Deployment
RejuvaTech operates at the intersection of protected chemistry development and structured commercial integration.
Beyond platform innovation, we provide formulation architecture, excipient strategy, and process-transfer documentation designed to support seamless deployment within established GMP manufacturing environments. Our integration model includes stability guidance, optimized blending protocols, and delivery-system compatibility analysis to reduce scale-up variability and accelerate commercialization timelines.
Our expertise spans precursor stabilization, triterpenoid synthesis optimization, and multimodal absorption systems, including nanocarrier and self-nanoemulsifying architectures engineered for systemic exposure enhancement.
Rather than functioning as a traditional supplement consultancy, RejuvaTech supports strategic partners with platform-level integration — enabling efficient transition from protected scientific innovation to scalable, premium-tier product deployment.
Detailed technical documentation and process frameworks are available under confidentiality agreement.
Longevity Chemistry & Regenerative Platform Research
Bret M. Lee - Chief Scientist
Bret M. Lee is a biochemist and longevity researcher with more than four decades of experience in chemistry, cellular biology, and applied health science.
As Chief Scientist of RejuvaTech, he leads research focused on protected longevity precursor systems, regenerative triterpenoid platforms, and advanced bioavailability architectures. His work centers on stabilizing and enhancing bioactive compound classes to improve intracellular performance, systemic exposure, and commercial scalability.
Mr. Lee’s expertise in natural product chemistry and structural optimization has guided the development of multiple patent-pending platforms, including next-generation NAD⁺ precursor compositions and integrated nanocarrier delivery systems. His research approach combines mechanistic cellular understanding with practical formulation science, bridging laboratory innovation with structured commercialization pathways.
Clinical Research Oversight & Translational Validation
Dr. Santiago T. Pena, Jr. - V.P. VSU
Dr. Santiago T. Peña, Jr. is an academic leader and biotechnology researcher with extensive experience in clinical study design, translational research, and institutional research governance.
As Vice President for Research, Extension, and Innovation at Visayas State University, Dr. Peña oversees multidisciplinary research initiatives, including biotechnology and health-focused programs. His leadership role provides structured oversight for clinical research development, protocol design, data management, and institutional compliance frameworks.
Within RejuvaTech’s research program, Dr. Peña will play a critical role in supervising clinical trial planning and execution across multiple intellectual property platforms, ensuring scientific rigor, ethical compliance, and data integrity. His involvement supports the transition of protected chemistry platforms from preclinical modeling to formal clinical validation.
Technology Transfer, Synthesis Oversight & Supply Chain Governance
Ms. Alice Sun, M.S. Chemistry, MBA, M.S. Economics & Management
Alice Sun serves as Director of Technology Transfer and oversees synthesis coordination, precursor sourcing, and manufacturing integration across RejuvaTech’s compound platforms.
With advanced training in chemistry and management, she manages the structured transfer of protected compositions — including stabilized NRH architectures and triterpenoid systems — from laboratory development to scaled manufacturing environments. Her role includes procurement oversight of critical analogs and precursors, vendor qualification, and alignment of synthesis protocols with GMP production partners.
Ms. Sun’s interdisciplinary background in chemistry, business, and economic systems supports disciplined cost management, supply chain resilience, and scalable production architecture — ensuring that RejuvaTech’s protected platforms can transition efficiently from innovation to commercial deployment.
