SCIENTIFIC REVIEW · BIOCHEMISTRY · NUTRACEUTICAL SCIENCE

TELOLAB™: Biological Efficacy
of a MultiMechanism
Geroprotective Extract

Antioxidant, Anti-Inflammatory, Telomere Extension, and Selective Anti-Cancer Activity in Validated Laboratory Models

PRIMARY INSTITUTION
Kasetsart University

AFFILIATED INSTITUTION
Maejo University-Phrae Campus

DEPARTMENT
Biochemistry

EXTRACT CLASS
Geroprotective Nutraceutical

ABSTRACT
TELOLAB™ is a proprietary multi-component nutraceutical extract comprising 9 medicinal plant botanicals and 1 algal species. It has undergone systematic laboratory evaluation across four primary biological dimensions. Key findings include: (1) Reduction of reactive oxygen species (ROS) by 10.55% in RAW 264.7 macrophage cells (DCFH-DA assay, p<0.01) with dose-dependent yeast survival under H₂O₂ oxidative challenge; (2) Selective cytokine modulation: IL-6 suppression of 73.65%, TNF-α reduction of 40.17%, and IL-10 upregulation of 32.42% (ELISA, LPS-stimulated model); (3) Telomere length extension in HeLa cells of +58.5% at 125 µg/mL (qRT-PCR, ΔΔCq method, p<0.001); (4) Selective cytotoxicity against MCF-7 breast cancer cells at IC₅₀ = 87.78 µg/mLwith normal cell viability maintained above 80% at equivalent concentrations. These results establish TELOLAB™ as a synergistic, multi-target geroprotective agent with strong laboratory evidence supporting its biological validity.

Keywords: TELOLAB™ · geroprotective nutraceutical · antioxidant · anti-inflammatory · telomere extension · selective cytotoxicity · Nrf2 pathway · Sirtuin activation · multi-mechanism synergy

73.65%

IL-6 Reduction
(Anti-inflammatory)

+58.5%

Telomere Length
Extension in HeLa Cells

87.75

IC₅₀ µg/mL
MCF-7 Breast Cancer

>80%

Normal Cell
Viability Maintained

FOUR-MECHANISM BIOLOGICAL PROFILE

How TELOLAB™ Acts on the Biology of Aging

TELOLAB™ interrupts the aging cascade at four molecularly distinct and interconnected targets —
a multi-mechanism architecture that no single-compound supplement can replicate

Antioxidant Activity
NRF2 / ROS PATHWAY
TELOLAB™ activates the Nrf2 transcription factor — the master cellular antioxidant switch — inducing SOD, CAT, HO-1, and NQO1 enzymes. Active contributors include Astragalus membranaceus, Vitis sp., astaxanthin from Haematococcus pluvialis, and additional proprietary co-actives within the matrix.
10.55%
ROS reduction in RAW 264.7 macrophage cells at 500 µg/mL (DCFH-DA, p<0.01)
Dose-dep.
S. cerevisiae survival under H₂O₂ oxidative stress (in vivo model)

Anti-Inflammatory
NF-ΚB / CYTOKINE REGULATION
Bidirectional cytokine modulation: simultaneously suppresses pro-inflammatory IL-6 and TNF-α while upregulating anti-inflammatory IL-10 — achieving immune homeostasis rather than immune suppression. Uniquely important as IL-6 drives telomere shortening via STAT3 pathway.

73.65%
IL-6 suppression (ELISA, LPS-stimulated RAW 264.7, p<0.001)
40.17%
TNF-α reduction at equivalent conditions
+32.42%
IL-10 upregulation — anti-inflammatory immune balance

Telomere Extension

TERT / TELOMERASE ACTIVATION
Demonstrated telomere length extension in HeLa cells via two synergistic pathways: (1) Direct telomerase activation — cycloastragenol and astragaloside IV from A. membranaceus increase TERT mRNA expression; (2) Indirect protection — reduced ROS and IL-6 slow oxidative telomeric DNA damage. Measured by qRT-PCR ΔΔCq method (gold standard).
+58.5%
Telomere length increase in HeLa cells at 125 µg/mL (qRT-PCR, p<0.001)
Dual
Direct (TERT) + Indirect (oxidative protection) mechanism
Selective Anti-Cancer
PI3K/AKT/MTOR · STAT3 · APOPTOSIS
TELOLAB™ demonstrates selective cytotoxicity against 5 human cancer cell lines while maintaining >80% normal cell viability at equivalent concentrations. Mechanisms include PI3K/AKT/mTOR, MAPK/ERK, STAT3 inhibition and apoptosis induction. Multi-pathway inhibition reduces potential for drug resistance.

 

87.78
IC₅₀ µg/mL against MCF-7 breast cancer (MTT Assay, 72h)
>80%
Normal RAW 264.7 cell viability at equivalent concentrations

MULTITARGET SYNERGY

Why Four Mechanisms Are Stronger Than One

The biological aging cascade operates as an interconnected loop — not a linear progression. TELOLAB™ is uniquely designed to interrupt this loop at multiple points simultaneously, creating a virtuous cycle that counters each hallmark of cellular aging.Critically, the anti-inflammatory and antioxidant effects directly amplify the telomere extension effect — and all three together reduce the oncogenic signaling environment that promotes cancer growth.Type your paragraph hereType your paragraph here

ANTI-INFLAMMATORY — IL-6 SUPPRESSION

73.65%

IL-6 is both a key inflammatory cytokine and a direct activator of STAT3, which drives cancer proliferation and telomere shortening simultaneously. TELOLAB™'s IL-6 suppression therefore delivers triple-pathway benefit in a single mechanism.

ELISA · LPS-stimulated RAW 264.7 · n=3 independent experiments · p<0.001

TELOMERE EXTENSION — HELA CELLS

58.5%

The largest single-dose telomere extension result in this formula class, achieved at 125 µg/mL via dual mechanism (direct TERT activation + oxidative DNA protection). The dose-dependent relationship confirms specificity of effect.

qRT-PCR (ΔΔCq method) · 24h incubation · Gold-standard telomere measurement · p<0.001

PROPRIETARY FORMULA

Multi-Botanical Synergy Matrix

TELOLAB™ is a proprietary concert of medicinal plant extracts and a select algal species — engineered so that each bioactive compound reinforces the others. The formula's power is not in any single ingredient, but in the convergence of their mechanisms on the same anti-aging cascade.

The complete botanical index is held under trade-secret protection. What we share publicly is the architecture — the four pathway pillars, representative signature actives, and the quantified synergistic outcomes validated at Kasetsart University and Maejo University-Phrae Campus.

PILLAR · 01

Antioxidant Defence

Multi-compartment ROS quenching — mitochondrial, membrane, and nuclear — activating the Nrf2 master antioxidant switch and its downstream enzymes (SOD, CAT, HO-1, NQO1).

NRF2 AXIS · −10.55% ROS

PILLAR · 02

Anti-Inflammatory Modulation

NF-κB pathway suppression and balanced cytokine regulation — reducing pro-inflammatory signals while simultaneously up-regulating anti-inflammatory IL-10.

NF-ΚB ↓ · IL-6 −73.65%

PILLAR · 03

Telomere & Telomerase

Direct TERT mRNA up-regulation combined with oxidative DNA protection — a dual mechanism producing the largest single-dose telomere extension yet observed in this formula class.

TERT ↑ · TELOMERE +58.5%

PILLAR · 04

Selective Anti-Cancer Activity

STAT3 dephosphorylation, apoptosis induction, and Ras oncogene inhibition — achieving cytotoxicity against cancer cell lines while preserving >80% normal-cell viability.

MCF-7 IC₅₀ · 87.78 ΜG/ML

SIGNATURE ACTIVES · PUBLICLY DISCLOSED

·  Astragalus membranaceus — traditionally documented telomerase support via cycloastragenol; anchor of the telomere pillar.
·  Haematococcus pluvialis (algae) — source of astaxanthin, the highest-potency mitochondrial antioxidant in the food spectrum.
·  Vitis vinifera — resveratrol & OPC proanthocyanidins; SIRT1 longevity-gene activation.
·  Curcuma longa — curcumin; comprehensive NF-κB / COX-2 / STAT3 pathway modulation.Type your paragraph here

ADDITIONAL PROPRIETARY EXTRACTS


+ Six additional botanical extracts

Selected for anti-inflammatory cascade completion, neuroprotection, telomerase modulation, and selective anti-cancer activity. Identities retained under trade-secret.

The complete 10-component formulation, extraction ratios, and co-active pairings constitute TELOLAB™ proprietary intellectual property. All results published in this document were validated on the full, unaltered formula — no single component is independently marketed.

Why  Synergy Matters

No single plant — not even the most studied longevity compound — simultaneously elevates telomerase activity, suppresses NF-κB, and induces selective cancer-cell apoptosis at the same dose window. TELOLAB™'s multi-botanical matrix resolves this limitation by design: each compound contributes a distinct mechanism, yet all converge on four overlapping molecular pathways. The quantified outcomes below are measured on the composite formula — not additive predictions.

4

CONVERGENT
PATHWAYS

10

BOTANICAL
COMPONENTS

8

VALIDATED
ASSAY ENDPOINTS

2

INDEPENDENT
UNIVERSITIES

LABORATORY-VERIFIED DATA

Quantified Biological Results

All results from independent, replicated laboratory assays using standardised validated methodologies

10.55%

ROS Reduction in RAW 264.7 Macrophage Cells

DCFH-DA Assay · 500 µg/mL · p<0.01

73.65%

IL-6 Suppression in LPS-Stimulated Cells

ELISA · n=3 independent experiments · p<0.001

40.17%

TNF-α Reduction at Equivalent Concentration

ELISA · LPS-stimulated model · p<0.01

+32.42%

IL-10 Upregulation — Anti-inflammatory Balance

ELISA · Demonstrates immunomodulation, not immunosuppression

+58.5%

Telomere Length Extension in HeLa Cells

qRT-PCR (ΔΔCq) · 125 µg/mL · 24h · p<0.001

87.78

IC₅₀ µg/mL — MCF-7 Breast Cancer (MTT, 72h)

Comparable to purified B. monnieri (72–75 µg/mL in literature)

+7.47%

Macrophage Phagocytic Activity Enhancement

500 µg/mL · Innate immune activation · p<0.05

>80%

Normal Cell Viability at Anti-Cancer Concentrations

RAW 264.7 viability — confirms selective cytotoxicity profile

BIOCHEMICAL ARCHITECTURE

Molecular Pathway Integration

TELOLAB™'s four mechanisms are not independent
they share overlapping molecular targets, creating a self-reinforcing anti-aging cascade

ACADEMIC & SCIENTIFIC VALIDATION

Laboratory Evaluation Infrastructure

TELOLAB™'s biological efficacy data is grounded in validated laboratory methodologies
consistent with international standards in nutraceutical and pharmacological research

🎓  Kasetsart University

Department of Biochemistry
· Primary Research Institution

Primary evaluation laboratory for TELOLAB™ biological efficacy studies. Kasetsart University
is one of Thailand's premier research institutions with internationally recognized biochemistry and pharmacological science programs.

PRIMARY RESEARCH INSTITUTION

🔬 Maejo University

Department of Biochemistry
· Affiliated Research Site

Affiliated research site contributing validated laboratory data. Maejo University's agricultural and life science research infrastructure provides validated supplementary analytical capacity for complex botanical formulations.

AFFILIATED RESEARCH INSTITUTION

📊 Validated Assay                Methodology

Gold-Standard Laboratory Protocols

Primary evaluation laboratory for TELOLAB™ biological efficacy studies. Kasetsart University
is one of Thailand's premier research institutions with internationally recognized biochemistry and pharmacological science programs.

PRIMARY RESEARCH INSTITUTION

       BIOLOGICAL                       ASSAY METHOD                      CELL / MODEL SYSTEM                             KEY RESULT                          STATISTICAL                      EVIDENCE
       DIMENSION                                                                                                                                                                                                                                  SIGNIFICANC                    LEVEL

Antioxidant (ROS)

DCFH-DA
Fluorescence

RAW 264.7 Macrophage

−10.55% ROS

p < 0.01

In vitro + in vivo

Anti-inflammatory (IL-6)

Sandwich ELISA

LPS-stimulated RAW 264.7

−73.65% IL-6

p < 0.001

In vitro

Anti-inflammatory (TNF-α)

Sandwich ELISA

LPS-stimulated RAW 264.7

−40.17% TNF-α

p < 0.01

In vitro

Immunomodulation (IL-10)

Sandwich ELISA

LPS-stimulated RAW 264.7

+32.42% IL-10

p < 0.05

In vitro

Telomere Extension

qRT-PCR (ΔΔCq)

HeLa Cells (cervical)

+58.5% at 125 µg/mL

p < 0.001

In vitro

Anti-Cancer (MCF-7)

MTT Cytotoxicity

MCF-7 Breast Cancer

IC₅₀ = 87.78 µg/mL

p < 0.05

In vitro

Normal Cell Safety

MTT Viability

RAW 264.7 Normal

>80% viability

p < 0.05

In vitro

Innate Immunity

Phagocytosis Assay

Macrophage Phagocytic Activity

+7.47% at 500 µg/mL

p < 0.05

In vitro

PROPRIETARY TRADEMARK EXTRACT

The TELOLAB™ name, formulation composition, and associated biological efficacy claims are subject to trademark protection. Unauthorized reproduction of the name or formula is prohibited.

TRADEMARK & INTELLECTUAL PROPERTY

TELOLAB™ — Protected Proprietary Extract

TELOLAB™ represents a novel, proprietary botanical combination with a specific, validated biological profile. The trademark protects both the name and the associated composition and claims — establishing exclusive commercial rights to the TELOLAB™ geroprotective extract brand.This website (www.telolab.info) serves as the official scientific reference for TELOLAB™, providing evidence-based documentation of the extract's biological mechanisms, laboratory-validated efficacy data, and compositional profile for regulatory, licensing, and academic purposes.

TRADEMARK NAME PROTECTION

The designation "TELOLAB™" is a registered trademark. All use of the name in commercial or formulation contexts requires explicit licensing authorization.

FORMULA COMPOSITION REFERENCE

The 10-component botanical profile described herein constitutes the TELOLAB™ proprietary formulation. Independent replication of this specific combination without authorization is a trademark infringement.

BIOLOGICAL CLAIMS DOCUMENTATION

All biological efficacy claims associated with TELOLAB™ are documented on this reference site and supported by laboratory data from Kasetsart University and Maejo University-Phrae Campus.

LICENSING & FORMULATION INQUIRY

For licensing of the TELOLAB™ trademark for use in nutraceutical formulations, supplement products, or clinical research, contact our licensing team via the inquiry form below.

SCIENTIFIC REFERENCES

Literature & Research Citations

All biological efficacy data for TELOLAB™ is supported by peer-reviewed scientific
literature and direct laboratory evaluation reports. Key references below.

01
 
Primary Research Document: "Evaluation of the Antioxidant, Anti-Inflammatory, and Anticancer Properties of TELOLAB™." Department of Biochemistry, Kasetsart University & Maejo University-Phrae Campus. Internal Laboratory Evaluation Report.

ullamcorper mattis, pulvinar dapibus leo.

02
 
Blackburn, E.H., Greider, C.W., Szostak, J.W. (2009). Telomeres and Telomerase. Nobel Prize in Physiology or Medicine. The Nobel Foundation, Stockholm.
03
 
Howitz, K.T., et al. (2003). Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan. Nature, 425(6954), 191–196. [Resveratrol / SIRT1 pathway — basis of Vitis extract component]
04
 
Fauce, S.R., et al. (2008). Telomerase-based pharmacologic enhancement of antiviral function of human CD8+ T lymphocytes. Journal of Immunology, 181(10), 7400–7406. [Cycloastragenol / TERT activation pathwa
05
 
Itoh, K., et al. (2010). Discovery of the negative regulator of Nrf2, Keap1: a historical overview. Free Radical Biology and Medicine, 88, 2–8. [Nrf2 antioxidant pathway — activated by TELOLAB™ botanicals]
06
 
Aggarwal, B.B., & Harikumar, K.B. (2009). Potential therapeutic effects of curcumin, the anti-inflammatory agent, against neurodegenerative, cardiovascular, pulmonary, metabolic, autoimmune and neoplastic diseases. International Journal of Biochemistry & Cell Biology, 41(1), 40–59.
07
 
Dimri, G.P., et al. (1995). A biomarker that identifies senescent human cells in culture and in aging skin in vivo. PNAS, 92(20), 9363–9367. [Cellular senescence — reversed by telomere extension]
08
 
Hanahan, D., & Weinberg, R.A. (2011). Hallmarks of cancer: The next generation. Cell, 144(5), 646–674. [Cancer hallmarks addressed by TELOLAB™'s anti-cancer mechanism panel]
09
 
Furman, D., et al. (2019). Chronic inflammation in the etiology of disease across the life span. Nature Medicine, 25, 1822–1832. [Inflammaging — directly targeted by TELOLAB™'s IL-6 / TNF-α suppression]
10
 
López-Otín, C., et al. (2013). The hallmarks of aging. Cell, 153(6), 1194–1217. [Foundational framework for geroprotective nutraceutical design — all 9 hallmarks addressed by TELOLAB™]

Disclaimer: The biological efficacy data presented on this website is derived from in vitro laboratory evaluations conducted at Kasetsart University and Maejo University-Phrae Campus. These findings represent laboratory evidence and should not be interpreted as clinical claims for the prevention, treatment, or cure of any disease in humans. In vivo animal studies and human clinical trials are required for full regulatory substantiation of health claims. This website serves as a scientific reference for trademark documentation purposes.

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