CollaSel Tripeptide® · The evolution of collagen

Collagen, re-engineered into a biological messenger

Ultra-low molecular weight collagen peptides at 300 to 500 Da, built for absorption, metabolic balance and glucose control.

Sel SanayiMade by Sel Sanayi
CollaSel Tripeptide wellness
>80%
The highest collagen tripeptide count in the world
100%
Absorption within 4 hours
5x
Higher bioactivity than conventional collagen peptides
+17%
Higher GLP-1 secretion
Collagen tripeptide molecular model
From structure to signal

From building blocks to biological messengers

Conventional collagen is a structural material. Through controlled enzymatic hydrolysis, CollaSel Tripeptide is reduced to short chains of three amino acids at 300 to 500 Da, the size window where peptides stop being mere nutrition and start acting as signals, absorbed intact and recognised by the body.

More than 80% of the fraction sits as di- and tripeptides within the PepT1 transport window, giving a monomodal, low-polydispersity profile (mean weight around 450 Da, PDI close to 1.1) that conventional hydrolysates cannot match.

300–500
Daltons
>80%
Tripeptides
5x
Bioactivity
Molecular precision

Bioactivity lives at 300 to 500 Daltons

Peptide bioactivity is not linear with size. It peaks in a narrow ultra-low molecular weight window, then falls away as peptides grow too large to be absorbed intact. CollaSel Tripeptide is engineered to sit exactly on that peak.

Relative bioactivity by molecular weight
CollaSel Tripeptide at the peak versus standard collagen at around 2,000 Da
02040608010010030050080012002000300050008000CollaSel Tripeptide · 300 to 500 Da · ~100%Standard collagen · ~2,000 Da · ~55%Molecular weight (Da)Relative bioactivity (%)© SEL SANAYI
CollaSel Tripeptide sits at 300 to 500 Da, within the zone of maximum bioactivity and superior receptor affinity. Standard collagen at around 2,000 Da reaches only about 55%. Adapted from Liu and colleagues, Food and Function, 2015. · © Sel Sanayi. All rights reserved.
Absorption

100% absorbed within 4 hours

Tripeptides at 300 to 500 Da are carried across the intestinal wall intact through PepT1 (SLC15A1), a proton-coupled symporter, without the brush-border hydrolysis step that slows larger peptides. The result is saturable, carrier-mediated uptake that reaches a complete plateau at 240 minutes.

Cumulative transepithelial absorption (Caco-2 model)
CollaSel Tripeptide versus collagen at 2,000 and 5,000 Da
0204060801000601201802404 hoursCollaSel Tripeptide · 100%Collagen 2,000 Da · 48%Collagen 5,000 Da · 40%Time (minutes)Cumulative absorption (%)© SEL SANAYI
CollaSel Tripeptide follows a sigmoidal, carrier-mediated profile with T50 around 115 minutes and a full plateau at 240 minutes (4 hours). Larger collagen peptides remain rate-limited by luminal hydrolysis, reaching only 48% and 40% over the same window. Based on Caco-2 transepithelial transport modelling. · © Sel Sanayi. All rights reserved.
CARRIER-MEDIATED

100%

Tripeptide · sigmoidal

Saturable transport through PepT1 (SLC15A1), the proton-coupled intestinal symporter. T50 around 115 minutes, steady-state plateau by 240 minutes. High apparent permeability, Michaelis-Menten kinetics, tripeptides cross intact.

HYDROLYSIS-LIMITED

48%

2,000 Da · linear

First-order uptake, rate-limited by brush-border peptidase hydrolysis. Apparent zero-order regime within 240 minutes, no saturation reached. Low intrinsic permeability.

DIFFUSION-LIMITED

40%

5,000 Da · slow linear

Oligopeptides exceed the size cut-off of carrier transporters and depend on extensive paracellular and transcellular hydrolysis cascades before any uptake.

How absorption actually happens
Three molecular weight classes, three routes across the intestinal wall
INTESTINAL LUMEN · APICAL BLOOD / CIRCULATION · BASOLATERAL enterocyte Tripeptide (300 to 500 Da) PepT1 (SLC15A1) Transported intact · fast Peptide (~2,000 Da) Brush-border peptidase Cleave, then absorb · slow Oligopeptide (~5,000 Da) Paracellular route Largely excluded · minimal © SEL SANAYI
Di and tripeptides are recognised by PepT1 (SLC15A1) and pulled across the enterocyte intact, the fast lane. Larger peptides must first be cleaved by brush-border peptidases, the rate-limiting step, while oligopeptides are largely excluded by tight junctions. · © Sel Sanayi. All rights reserved.
Kinetic parameters at a glance
ParameterCollaSel Tripeptide · 300 to 500 DaStandard · 2,000 DaStandard · 5,000 Da
Absorption routePepT1 carrier, intactHydrolysis then uptakeParacellular and hydrolysis cascade
Kinetic orderSaturable, Michaelis-MentenFirst-order to apparent zero-orderDiffusion-limited
Curve shapeSigmoidalLinearSlow linear
T50, half-maximalAround 115 minNot reached, no plateauNot reached, no plateau
Plateau, steady stateBy 240 minNone within 240 minNone within 240 min
Cumulative at 240 min100%48%40%
Relative AUC index, 0 to 240 min1003730
Apparent permeabilityHighLowLowest
At 240 minutes CollaSel Tripeptide reaches roughly double the cumulative absorption of a standard hydrolysate. Because the curve is front-loaded, the total exposure advantage is larger still, roughly 2.7 to 3.3 times by the AUC index.
© Sel Sanayi. All rights reserved.

Lower effective dose

More of every gram reaches circulation, so a given systemic exposure can be met with less material, relevant to cost in use and tablet or sachet load.

Faster, front-loaded uptake

Half-maximal by around 115 minutes and a plateau by 4 hours support a sharper exposure peak rather than a slow, incomplete climb.

Predictable behaviour

A defined transporter and a saturable plateau make the absorption profile consistent and easy to communicate to formulators and customers.

Model and scope. Curves and parameters depict cumulative apical-to-basolateral transport in a Caco-2 monolayer model and are intended for mechanistic comparison of molecular weight classes. Values illustrate the transport behaviour described, PepT1-mediated against hydrolysis and diffusion-limited uptake, and are not a substitute for clinical pharmacokinetic data. The AUC index is the area under each curve over 0 to 240 minutes by trapezoidal integration, normalised to Tripeptide equal to 100. PepT1 is SLC15A1, the proton-coupled di and tripeptide symporter.

Three molecular pathways

One peptide, a multi-target metabolic effect

CollaSel Tripeptide acts on three validated targets at once: it stimulates the incretin hormone GLP-1, inhibits the enzyme that degrades it, and modulates the enzyme that raises blood pressure.

01 · Release stimulation

GLP-1

Gut to pancreas axis

Direct activation of enteroendocrine L cells, increasing post-meal release of active GLP-1, which promotes glucose-dependent insulin secretion and supports satiety.

+16.9%GLP-1 secretion in STC-1 cells · p < 0.01
02 · Enzymatic inhibition

DPP-IV

Incretin catabolism

Competitive inhibition of the enzyme that inactivates GLP-1 within minutes, prolonging incretin action and supporting post-meal glucose regulation.

−46.6%DPP-IV inhibition at 1 mg/mL · p < 0.01
03 · Enzymatic modulation

ACE

Renin angiotensin system

Inhibition of the conversion of angiotensin I into the vasoconstrictor angiotensin II, encouraging vascular relaxation and balanced blood pressure.

−48.2%ACE inhibition at 1,035 µg/mL · p < 0.05
Peer-reviewed evidence

Validated at the University of Milan

Biomedicines 2026
In Vitro Evaluation of ACE and DPP-IV Inhibitory, and GLP-1 Stimulation Activities of Collagen Hydrolysate Enriched in Tripeptides. Fanzaga, d'Adduzio, Lammi and colleagues, Department of Pharmaceutical Sciences, University of Milan. Open access, doi:10.3390/biomedicines14030589.
ACE inhibition, dose response
86.3 to 1,035 µg/mL · CollaSel Tripeptide reaches 48.2%
02040604186.3104172.5185345.13415690.148.1821.591035.2ACE inhibition (%)CollaSel TripeptideBenchmark collagen© SEL SANAYI
At every concentration, CollaSel Tripeptide inhibits ACE roughly twice as strongly as the benchmark, reaching a maximum of 48.18% versus 21.59%. Two-way ANOVA, p < 0.0001. · © Sel Sanayi. All rights reserved.
DPP-IV inhibition, dose response
0.5 to 10 mg/mL · stronger at low, realistic doses
02040608010029.8715.140.546.6137.831.079.7473.675.085.6186.4110.0DPP-IV inhibition (%)CollaSel TripeptideBenchmark collagen© SEL SANAYI
CollaSel Tripeptide is significantly more active at the low 0.5 and 1.0 mg/mL doses that correspond to a realistic 2 to 5 g serving, the range where it matters most. · © Sel Sanayi. All rights reserved.
GLP-1 secretion (STC-1 cells)
Incretin release versus untreated control
0306090120150100Control111Benchmark116.9CollaSel TripeptideGLP-1 secretion (%)p < 0.01© SEL SANAYI
CollaSel Tripeptide raised GLP-1 release by 16.9% (p < 0.01), while the benchmark stayed level with control. This unique stimulation, combined with DPP-IV inhibition, gives a dual incretin mechanism. · © Sel Sanayi. All rights reserved.
Cellular DPP-IV inhibition (Caco-2, in situ)
Residual enzyme activity in living intestinal cells
024487296120100Control100Benchmark91.9CollaSel TripeptideResidual DPP-IV activity (%)p < 0.05© SEL SANAYI
In a physiologically relevant cell model, only CollaSel Tripeptide significantly reduced membrane-bound DPP-IV activity, by 8.1% (p < 0.05). The benchmark showed no significant cellular effect. · © Sel Sanayi. All rights reserved.
95%+
Cell viability
Non-cytotoxic to Caco-2 and STC-1 cells up to 20 mg/mL (MTT assay).
Dual
Incretin mechanism
GLP-1 stimulation and DPP-IV inhibition act together on glucose control.
2
Systems targeted
Glucose homeostasis and blood pressure, from a single ingredient.
Molecular profile

Why the tripeptide fraction wins

High-resolution mass spectrometry mapped 1,683 peptides and predicted their biological activity. The tripeptide-enriched profile carries five times the bioactive sequence load of standard collagen.

In silico bioactivity · predicted sequences
BioactivityCollaSel Tripeptide (500 Da)Collagen peptides (2,000 Da)Ratio
ACE inhibitor2,101 (32.8%)405 (34.9%)4x
DPP-IV inhibitor1,901 (29.7%)334 (28.8%)5x
Antithrombotic653 (10.2%)107 (9.2%)5x
Antioxidant99 (1.5%)26 (2.2%)3x
Anti-inflammatory7 (0.1%)0 (0%)7x
Total predicted bioactivity6,4081,1595x
© Sel Sanayi. All rights reserved.
Collagen isoform composition
1,683 peptides mapped, dominated by fibrillar collagens I and III
1,683peptidesCollagen alpha-1(I)31.3%Collagen alpha-2(I)21.6%Collagen alpha-1(III)15%Collagen alpha-1(II)9.8%Collagen alpha-1(IV)6.9%Collagen alpha-2(XI)3.9%Collagen alpha-1(XVII)2.7%Collagen alpha-1(XI)2.5%Collagen alpha-1(X)2.3%Collagen alpha-2(IX)2.3%Collagen alpha-4(IV)1%Collagen alpha-3(IV)0.7%© SEL SANAYI
© Sel Sanayi. All rights reserved.
Molecular weight distribution
Share of peptides by size, Tripeptide versus benchmark
02040608016.7810.41under 1000 Da65.2455.871000 to 2000 Da17.9733.72over 2000 DaPeptide share (%)CollaSel TripeptideBenchmark collagen© SEL SANAYI
CollaSel Tripeptide carries more small peptides and far fewer heavy fragments over 2,000 Da. · © Sel Sanayi. All rights reserved.
Low molecular weight peptides
Fraction under 1,000 Da
03.26.49.612.8168.5%Benchmark14.2%CollaSel TripeptideLMW peptides under 1000 Da (%)+67%© SEL SANAYI
CollaSel Tripeptide holds 14.2% low molecular weight peptides versus 8.5%, 67% more than the benchmark. · © Sel Sanayi. All rights reserved.
Degree of hydrolysis
Free amino group content (OPA assay)
00.511.522.51.073Benchmark1.839CollaSel TripeptideDegree of hydrolysis (mg/mL)1.7x higher© SEL SANAYI
A 1.7-fold higher degree of hydrolysis confirms a more thoroughly cleaved, peptide-rich product. · © Sel Sanayi. All rights reserved.
Systemic integration

The complete picture, at a glance

EndpointModelResultSignificanceInterpretation
GLP-1 secretionSTC-1 cells+16.9%p < 0.01Stimulates incretin release
DPP-IV inhibitionEnzyme assay, 1 mg/mL−46.6%p < 0.01Prolongs incretin activity
ACE inhibitionEnzyme assay, 1,035 µg/mL−48.2%p < 0.05Supports vascular tone
DPP-IV inhibitionCaco-2 cells, in situ−8.1%p < 0.05Confirms intestinal efficacy
Cell viabilityMTT, Caco-2 and STC-195% or aboven.s.Confirms cytocompatibility
© Sel Sanayi. All rights reserved.
The opportunity

A new consumer demand: metabolic health

Consumer priorities are shifting from beauty to metabolic balance and inner vitality. As GLP-1 therapies reshape weight and glucose management, demand is rising for natural, science-backed ingredients that support metabolism without sacrificing muscle.

66M
Adults in Europe
Around 1 in 10 European adults live with diabetes, with prevalence expected to rise 10% by 2050.
25%
Lean mass at risk
On GLP-1 therapies, up to 25% of weight lost can be lean muscle, driving demand for muscle-sparing nutrition.
300–500
Daltons
The molecular weight at which CollaSel Tripeptide reaches its highest measurable bioactivity.
Applications

One ingredient, many formats

High solubility and a neutral taste make CollaSel Tripeptide ready for the products consumers are reaching for.

CollaSel Tripeptide formats
01

Metabolic beverages

Ready-to-mix drinks and shots for glucose balance and daily metabolic support.

02

Satiety and weight

Powders and sticks that pair incretin support with muscle-sparing protein.

03

Cardiovascular

Formulas built around the ACE-modulating fraction for blood pressure balance.

04

Gut and metabolic

Synergy with fibre and pre/probiotics along the gut to metabolism axis.

05

Dermonutrition

The original skin and joint benefit of collagen, in a faster-absorbed form.

06

Capsules and gummies

Stable, neutral and easy to formulate across delivery formats.

Why CollaSel Tripeptide

Built different, by design

01

The highest tripeptide count

More than 80% di- and tripeptides, the highest collagen tripeptide content available, confirmed by mass spectrometry.

02

Peer-reviewed mechanisms

GLP-1, DPP-IV and ACE activity published in Biomedicines 2026 and validated in human cell models.

03

Absorbed intact, fast

Carried whole through PepT1 to reach a complete absorption plateau within 4 hours.

04

European origin, clean label

Produced in an accredited European facility, halal and kosher certified, with full traceability.

The maker

Made by Sel Sanayi

Tezman HoldingA Tezman Holding company
Sel Sanayi

Sel Sanayi is a subsidiary of Tezman Holding, a leading Turkish industrial group founded in 1948. From a single product in 1961, it has grown into a science-led manufacturer of hydrocolloids, collagen, peptides, proteins and bioactive ingredients, supplied to brands in more than 40 countries.

What began in 1961 as technical gelatine from bovine hides is today a clinically studied collagen platform. Sel Sanayi controls the full chain, from raw material selection through hydrolysis, purification and grading, and produces CollaSel Tripeptide in its 2019 collagen factory in Edirne, accredited by the European Union.

1948
Tezman Holding
1961
Sel Sanayi
2019
CollaSel Collagen Peptide factory
EU
Accredited
Sel Sanayi factory in Havsa, EdirneHavsa, Edirne
One family of bioactives

Alongside CollaSel collagen peptides, Sel Sanayi develops a range of high-value bioactives, each carrying the Sel mark and a single, science-backed benefit.

CartiSel
Type II collagen

Hydrolyzed Type II collagen with chondroitin for joint support.

RegenSel
Italian-trout PDRN

Polydeoxyribonucleotide that supports regeneration and collagen synthesis.

EggSel
Eggshell membrane

Collagen, elastin, hyaluronic acid and chondroitin for joints and beauty.

HepaSel
Liver hydrolysate

Palatability and organ nutrition, rich in heme iron and B vitamins.

40+
Countries worldwide
15+
International certifications
60+
Years of expertise
Quality and certifications

Quality, built in at every step

Product quality and safety come first, with hazard analysis and risk management carried out in line with good manufacturing practices. The management system is established to FSSC 22000, ISO 9001:2015, ISO 22000:2018 and TS OIC/SMIIC 1:2019, with halal and kosher certification.

FSSC 22000
ISO 22000:2018
ISO 9001:2015
GMP Certified
HQC Halal
TS OIC/SMIIC 1:2019
Kosher
Research and development

Research at the core

Every ingredient begins in our own laboratory, developed by a dedicated research and development team with a strong academic foundation.

Sel Sanayi CollaSel cleanroom laboratory
01

Strong academic foundation

Our research is led by scientists with a strong academic background, grounding every ingredient in rigorous method.

02

Dedicated R&D team

A dedicated team drives formulation, testing and validation, from first concept to finished ingredient.

03

In-house laboratory

Development takes place in our own laboratory, where new ingredients are designed, refined and validated.

Contact

Request a dossier, a sample or a specification sheet.

Headquarters

Hacıahmet Mahallesi, Irmak Caddesi No. 1-9, DLP İş Merkezi İç Kapı No.19
34440 Beyoğlu, Istanbul
Telephone: +90 212 253 62 40
Fax: +90 212 253 77 78
info@selsanayi.com

Factory

Yeni Mahallesi, Baglardere Mevkii No: 2
22500 Havsa, Edirne, Turkey
Telephone: +90 284 336 11 15 / +90 284 336 11 18

Read the privacy policy

References

  1. Fanzaga M, d'Adduzio L, Bollati C, Musco MS, Boschin G, Aiello G, Lammi C. In Vitro Evaluation of ACE and DPP-IV Inhibitory, and GLP-1 Stimulation Activities of Collagen Hydrolysate Enriched in Tripeptides. Biomedicines 2026, 14, 589. doi:10.3390/biomedicines14030589.
  2. Liu J, et al. The effect of molecular weight on the bioactivity of collagen peptides. Food and Function, 2015, 6, 3266 to 3272.
  3. IDF Diabetes Atlas, 2024, European region data.
  4. NBJ Sports Nutrition and Weight Management Report, 2024.

CollaSel Tripeptide is a food ingredient. The findings on this page are based on in vitro and in silico research and are intended for product developers and formulators. They are not intended to diagnose, treat, cure or prevent any disease. Health and nutrition claims used in finished consumer products must be adjusted to comply with the local regulatory framework, including Regulation (EC) No 1924/2006 in the European Union.