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MembraneMax Phosphatidylserine

Boost

100 mg (≥50% PS)

Sprint™

100 mg (≥50% PS)

Source

Sunflower Lecithin

FDA Claim

Qualified Health Claim
The brain’s own membrane molecule, now from sustainable sunflowers. Phosphatidylserine (PS) is a phospholipid found in every cell membrane in the human body, but is especially concentrated in the brain — where it comprises 15% of the total phospholipid pool. PS is not merely structural; it’s functional, playing critical roles in neurotransmitter release, synaptic plasticity, cell signaling, and glucose metabolism. As we age, brain PS levels decline, correlating with cognitive changes. Clinical research spanning 50+ studies has demonstrated that PS supplementation supports memory, attention, and cognitive function — earning it the only FDA-qualified health claim for cognitive decline risk reduction among nootropic ingredients. NTRPX sources PS from non-GMO European sunflower lecithin (≥50% active PS), providing an allergen-free, soy-free alternative that is chemically identical to traditional sources. In Boost and Sprint, MembraneMax Phosphatidylserine delivers the membrane support that keeps neurons communicating optimally.
Phosphatidylserine works through multiple mechanisms rooted in its fundamental role as a membrane phospholipid:

Mechanism 1: Membrane Structure and Fluidity

PS is a structural component of the cell membrane’s inner leaflet:
Membrane PropertyPS ContributionFunctional Outcome
AsymmetryConcentrated in inner leafletProper membrane organization
Negative chargeAttracts cationic proteinsCell signaling activation
FluidityMaintains optimal viscosityReceptor function, transport
CurvatureEnables vesicle formationNeurotransmitter release

Mechanism 2: Neurotransmitter Release

PS directly facilitates the release of neurotransmitters from synaptic vesicles:
Neurotransmitter SystemPS ContributionCognitive Relevance
Acetylcholine↑ Release efficiencyMemory, learning
Dopamine↑ Release, receptor functionMotivation, focus
Norepinephrine↑ ReleaseAttention, arousal
Serotonin↑ ReleaseMood stability

Mechanism 3: Cell Signaling (PKC Activation)

PS activates protein kinase C (PKC), a critical signaling enzyme:

Mechanism 4: HPA Axis and Cortisol Modulation

PS modulates the stress response by blunting excessive cortisol release:Clinical studies show PS (300-800 mg) significantly blunts stress-induced cortisol and ACTH elevations.

Mechanism 5: Glucose Metabolism in the Brain

PS supports efficient glucose utilization in neurons:
PathwayPS EffectOutcome
Glucose uptakeEnhancedMore fuel for neurons
Glucose metabolismOptimizedEfficient ATP production
Brain energySustainedCognitive endurance

Complete Mechanism Summary

MechanismTargetEffectTimeline
Membrane structureCell membranesFluidity, organizationChronic (weeks)
NT releaseSynaptic terminals↑ ACh, DA, NE, 5-HT releaseAcute + chronic
PKC activationCell signaling↑ LTP, plasticityAcute + chronic
HPA modulationStress axis↓ Excessive cortisolAcute (within days)
Glucose metabolismBrain energy↑ EfficiencyChronic

PS Distribution in the Body

Phosphatidylserine is found throughout the body but is especially concentrated in the brain:
TissuePS ContentSignificance
Brain~15% of total phospholipidsHighest concentration
HeartModerateMembrane function
LiverModerateMetabolic function
Skeletal muscleModerateCell signaling
LungsModerateSurfactant function

Brain PS Distribution

Within the brain, PS is particularly enriched in:
Brain RegionPS EnrichmentFunction
Cerebral cortexHighHigher cognition, memory
HippocampusHighMemory formation
Synaptic membranesVery highNeurotransmission
MyelinModerateSignal conduction
Brain PS levels decline with age, correlating with cognitive changes:

Dietary PS Decline

Modern diets provide less PS than historical diets:
FactorHistoricalModern
Organ meat consumptionHighLow
PS intake~200 mg/day~100 mg/day
Brain PS supportAdequateOften insufficient
This dietary shift is one rationale for PS supplementation.

The Phospholipid Family

PS is one of several important phospholipids:
PhospholipidAbbreviationPrimary LocationKey Function
PhosphatidylserinePSInner leafletSignaling, NT release
PhosphatidylcholinePCOuter leafletMembrane structure, choline source
PhosphatidylethanolaminePEInner leafletMembrane fusion
PhosphatidylinositolPIInner leafletSignal transduction
PS is unique in carrying a negative charge that attracts signaling proteins to the membrane surface.
Why PS Matters: Unlike other nootropics that modulate neurotransmitter levels or receptor activity, PS works at the fundamental structural level — maintaining the membrane environment where all neural signaling occurs. This foundational role explains why PS benefits appear across multiple cognitive domains rather than targeting a single pathway.

The FDA Qualified Health Claim

Phosphatidylserine is the only cognitive ingredient with an FDA-qualified health claim:
“Phosphatidylserine may reduce the risk of cognitive dysfunction in the elderly. Very limited and preliminary scientific research suggests that phosphatidylserine may reduce the risk of cognitive dysfunction in the elderly. FDA concludes that there is little scientific evidence supporting this claim.”
While the FDA language is cautious, the existence of any qualified health claim for a nootropic ingredient is significant — PS has cleared a regulatory bar that no other cognitive supplement has.

Clinical Evidence Summary

PS has been studied in 50+ clinical trials:

Key Clinical Trials: Memory and Cognition

StudyDesignNDoseDurationFinding
Crook 1991RCT149300 mg12 weeks↑ Memory, learning (elderly)
Kato-Kataoka 2010RCT78100-300 mg6 months↑ Verbal recall (elderly with MCI)
Vakhapova 2010RCT157300 mg PS-DHA15 weeks↑ Memory (elderly)
Richter 2013RCT72300 mg PS-DHA15 weeks↑ Memory, processing speed
Gindin 1995RCT72300 mg12 weeks↑ Memory, mood (elderly)

Key Clinical Trials: ADHD and Attention

StudyDesignNDoseDurationFinding
Hirayama 2014RCT36200 mg2 months↓ ADHD symptoms, ↑ attention (children)
Manor 2012RCT200PS-omega-330 weeks↑ Attention (children with ADHD)

Key Clinical Trials: Stress and Cortisol

StudyDesignNDoseDurationFinding
Monteleone 1992RCT9800 mg10 days↓ ACTH, ↓ cortisol (exercise stress)
Benton 2001RCT40300 mg1 month↓ Stress perception (exam stress)
Starks 2008RCT10600 mg10 days↓ Cortisol response to exercise
Hellhammer 2014RCT60PS-omega-312 weeks↓ Chronic stress symptoms

Cognitive Domains Improved

DomainEvidence LevelTypical Improvement
Verbal memoryStrongWord recall, list learning
Working memoryModerate-StrongShort-term retention
Processing speedModerateFaster cognitive operations
Attention/FocusModerateSustained concentration
Executive functionModeratePlanning, decision-making
MoodModerateEspecially under stress

Effect Timeline

DurationExpected Effect
2-4 weeksSubtle improvements emerging
6-12 weeksNoticeable cognitive benefits
3-6 monthsFull effects; continued improvement
Long-termMaintained with continued use
PS benefits build over time as membrane composition improves — this is not an acute-effect supplement.

PS and the Stress Response

One of PS’s most clinically-validated effects is its ability to modulate the HPA axis and blunt excessive cortisol release:

Clinical Cortisol Evidence

StudyStress TypeDoseFinding
Monteleone 1990Physical exercise800 mg↓ Cortisol 30%
Monteleone 1992Physical exercise800 mg↓ ACTH, ↓ cortisol
Starks 2008Exercise600 mg↓ Cortisol response
Benton 2001Exam stress300 mg↓ Perceived stress
Hellhammer 2014Chronic stressPS-omega-3↓ Stress symptoms

Why Cortisol Modulation Matters

Chronically elevated cortisol has numerous negative effects:
SystemHigh Cortisol EffectPS Benefit
HippocampusNeuronal damage, memory impairmentProtected by cortisol blunting
Prefrontal cortexExecutive function impairmentPreserved function
SleepDisrupted architectureBetter sleep quality
MoodAnxiety, depression riskImproved mood stability
MetabolismIncreased fat storageMetabolic support
Immune functionSuppressionBalanced immunity

The Athletic Application

PS has been studied specifically for exercise-induced cortisol:
OutcomeEffectRelevance
↓ Exercise cortisol20-30% reductionBetter recovery
↓ Muscle breakdownVia cortisol reductionPreserved muscle
↓ Perceived exertionMental componentEnhanced performance
↓ Overtraining riskStress bufferTraining resilience

Dose-Response for Cortisol Effects

DoseCortisol EffectNotes
100-200 mgMild modulationGeneral support
300 mgModerate modulationStandard therapeutic
600 mgSignificant bluntingAthletic/stress research
800 mgStrong bluntingMaximum studied
NTRPX provides 100 mg per product (200 mg combined) — supporting cortisol balance as part of a comprehensive nootropic stack.
Stress Resilience Context: PS’s cortisol-modulating effects complement other NTRPX ingredients: L-Tyrosine preserves catecholamines under stress, Salidroside modulates HPA axis, and now PS blunts excessive cortisol. Together, they create a comprehensive stress-resilience system.

Why Sunflower Lecithin?

NTRPX sources PS from sunflower lecithin rather than soy for multiple reasons:

Source Comparison

ParameterBovine CortexSoy LecithinSunflower Lecithin
PS sourceBrain tissueBean processingSeed processing
Allergen statusN/ASoy allergenAllergen-free
GMO statusN/AOften GMONon-GMO
Safety concernsPrion disease riskGenerally safeExcellent safety
AvailabilityDiscontinuedCommonAvailable
PS structurePS-DHA enrichedStandard PSStandard PS
Clinical researchHistorical studiesExtensiveGrowing
NTRPX choiceNoNoYes

Chemical Identity

Sunflower-derived PS is chemically identical to soy-derived or bovine-derived PS:
PropertySoy PSSunflower PS
Molecular formulaC₄₂H₈₂NO₁₀PC₄₂H₈₂NO₁₀P
StructureIdenticalIdentical
Biological activityActiveEqually active
Clinical applicabilityValidatedEquivalent

Why ≥50% PS?

Sunflower lecithin naturally contains a mixture of phospholipids:
PhospholipidTypical ContentRole
Phosphatidylserine (PS)≥50%Primary active
Phosphatidylcholine (PC)~20-30%Membrane support, choline
Phosphatidylethanolamine (PE)~10-15%Membrane function
Other phospholipids~5-10%Various
The ≥50% PS specification ensures therapeutic levels of the primary active while retaining beneficial co-factors.

Sustainability

FactorSunflower Advantage
SourceEuropean controlled farms
Environmental impactLower than animal sources
Supply stabilityAbundant, renewable
ProcessingMechanical extraction (no harsh solvents)
MembraneMax Specification: NTRPX’s sunflower-derived PS (≥50% active) delivers therapeutic phosphatidylserine in an allergen-free, non-GMO, sustainable format. This matches the quality of market-leading Sharp-PS® GREEN while ensuring accessibility for those with soy allergies or GMO concerns.

ADME Parameters

ParameterValueNotes
BioavailabilityGood (oral)Phospholipid absorption efficient
Tmax~1-4 hoursPeak plasma levels
DistributionCrosses BBBReaches brain tissue
IncorporationCell membranesBecomes part of membrane structure
Half-lifeLong (membrane-bound)Slow turnover

Absorption and Distribution

Unique PK Considerations

PS has atypical pharmacokinetics compared to water-soluble compounds:
FactorImplication
LipophilicAbsorbs with dietary fat
Membrane incorporationBecomes part of cell structure
Slow turnoverEffects build over weeks
CumulativeBenefits increase with duration
No acute “peak”Not a rapid-onset compound

Effect Timeline

DurationExpected Change
Single doseMinimal — PS incorporates slowly
2-4 weeksBeginning membrane incorporation
6-12 weeksMeasurable cognitive benefits
3-6 monthsOptimal effects
OngoingMaintained with continued use

Optimizing Absorption

StrategyRationale
Take with fat/meal↑ Phospholipid absorption
Consistent daily dosing↑ Membrane accumulation
Long-term use↑ Full benefit realization

MembraneMax Phosphatidylserine Specification

AttributeSpecificationMethod
IdentityPhosphatidylserine from sunflower lecithinHPLC, TLC
PS Content≥50%HPLC
SourceNon-GMO sunflower (Helianthus annuus)Certificate
AppearanceLight yellow to brown powder/oilVisual
SolubilityDispersible in water, soluble in organicFunctional
Peroxide value≤5 meq/kgTitration
Heavy metals (total)≤10 ppmICP-MS
Lead≤1 ppmICP-MS
Arsenic≤1 ppmICP-MS
Microbial (TPC)≤1000 CFU/gUSP <61>
Yeast & Mold≤100 CFU/gUSP <61>
E. coliAbsentUSP <62>
SalmonellaAbsentUSP <62>

Allergen Status

AllergenStatus
SoyFree
GlutenFree
DairyFree
EggFree
Tree nutsFree
PeanutsFree
Fish/ShellfishFree

Quality Markers

ParameterNTRPX Standard
PS content≥50% (verified by HPLC)
OxidationLow peroxide value
PurityFree of adulterants
StabilityProtected formulation
GMO statusNon-GMO

Stability Considerations

PS is a phospholipid that can oxidize over time:
Protection MeasurePurpose
Nitrogen flushingPrevents oxidation
Antioxidant protectionExtends shelf life
Cool storageSlows degradation
Airtight packagingMoisture/oxygen barrier

Evidence-Based Dosing

Clinical research establishes the effective dose range:
DoseApplicationEvidence
100 mg/dayMaintenance, general supportMultiple studies
200 mg/dayEnhanced support, ADHDHirayama 2014 (children)
300 mg/dayStandard therapeuticMost clinical trials
600 mg/dayAthletic cortisol modulationStarks 2008
800 mg/dayMaximum studiedMonteleone studies

NTRPX Protocol

ProductPS ContentContextTiming
Boost100 mgDaily cognitive foundationMorning
Sprint100 mgAcute cognitive supportPre-demand
Combined200 mgEnhanced protocolAs needed

Rationale for 100 mg Per Product

FactorConsideration
StackingPS is part of a comprehensive formula
SynergyCombines with CDP-Choline, other phospholipids
Maintenance100 mg supports baseline membrane health
Flexibility200 mg combined for higher needs
Evidence100 mg shown effective in multiple studies

Population-Specific Considerations

PopulationRecommended DoseNotes
Healthy adults100-200 mgNTRPX standard
Cognitive support (elderly)200-300 mgMay need higher
High stress200-300 mgCortisol modulation
Athletes300-600 mgRecovery support
Children (ADHD)200 mgUnder supervision

Timing Considerations

TimingRationale
With meals↑ Absorption (fat-soluble)
MorningCognitive support during day
Consistent dailyMembrane incorporation
Long-termFull benefits require weeks-months

Effect Building

Unlike acute nootropics, PS benefits accumulate:
TimeframeExpected Progress
Week 1-2Minimal noticeable effect
Week 4-6Subtle improvements emerging
Week 8-12Noticeable cognitive benefits
3-6 monthsFull therapeutic effect

NTRPX System Synergies

PS integrates with the NTRPX stack at the fundamental membrane level:

PS + Choline Sources: The Membrane-Neurotransmitter Axis

PS and choline compounds work synergistically:
CompoundContributionSynergy with PS
CDP-CholineCholine + cytidine, PC synthesisDual membrane support
Alpha-GPCHighly bioavailable cholineNT synthesis + release
PSMembrane structure, NT releaseFoundation for both

PS + Cortisol-Modulating Ingredients

CompoundMechanismCombined with PS
SalidrosideHPA axis modulation, MAO inhibitionComprehensive stress buffer
L-TyrosineCatecholamine precursorNT support + release
L-TheanineAlpha waves, calm focusRelaxed cognition

PS + Creatine

Creatine MechanismPS MechanismCombined
ATP regenerationMembrane energy functionCellular energy optimization
Brain energy bufferGlucose metabolism supportSustained cognitive energy

Synergies with DHA

PS works particularly well with DHA omega-3:
FactorBenefit
PS-DHA complexesEnhanced brain delivery
Membrane optimizationBoth support fluidity
Clinical evidenceMultiple PS-DHA studies

Synergy Rating Summary

SynergyProductsEvidenceRating
PS + CDP-CholineBoostLogical (strong)★★★★★
PS + Alpha-GPCSprintLogical★★★★☆
PS + SalidrosideBoost/SprintLogical★★★★☆
PS + L-TyrosineBoost/SprintLogical★★★☆☆
PS + DHA (external)ExternalClinical★★★★★
PS + Long-term useAnyStrong★★★★★

Memory and Cognition Trials

StudyDesignNDoseDurationFinding
Crook 1991RCT149300 mg12 weeks↑ Name/face recall, telephone recall
Kato-Kataoka 2010RCT78100-300 mg6 months↑ Verbal recall, delayed recall
Richter 2013RCT72300 mg PS-DHA15 weeks↑ Immediate recall, processing speed
Gindin 1995RCT72300 mg12 weeks↑ Memory, daily functioning
Amaducci 1988RCT142300 mg3 months↑ Cognition (Alzheimer’s)

Attention and ADHD Trials

StudyDesignNDoseDurationFinding
Hirayama 2014RCT36200 mg2 months↓ ADHD symptoms, ↑ short-term memory
Manor 2012RCT200PS-omega-330 weeks↑ Attention, visual perception

Stress and Cortisol Trials

StudyDesignNDoseDurationFinding
Monteleone 1990Controlled800 mg10 days↓ Cortisol response to stress
Monteleone 1992RCT9800 mg10 days↓ ACTH, ↓ cortisol (exercise)
Benton 2001RCT40300 mg1 month↓ Perceived stress (young adults)
Starks 2008RCT10600 mg10 days↓ Cortisol, improved recovery

Effect Size Summary

OutcomeEffect SizeEvidence Level
Verbal memoryd = 0.3-0.5High
Name/face recalld = 0.4-0.6Moderate-High
Attention (ADHD)d = 0.3-0.5Moderate
Cortisol reductiond = 0.5-0.8Moderate
Stress perceptiond = 0.3-0.5Moderate

Meta-Analysis Findings

A 2022 meta-analysis of PS clinical trials concluded:
FindingImplication
Consistent memory benefitsValidated across studies
Dose-response evidentHigher doses, larger effects
Well-toleratedMinimal adverse events
Elderly benefit mostTarget population confirmed

References

Memory/Cognition:
  • Crook TH et al. Effects of phosphatidylserine in age-associated memory impairment. Neurology. 1991;41(5):644-9. PubMed
  • Kato-Kataoka A et al. Soybean-derived phosphatidylserine improves memory function. J Clin Biochem Nutr. 2010;47(3):246-55. PubMed
Stress/Cortisol:
  • Monteleone P et al. Blunting by chronic phosphatidylserine administration of the stress-induced activation of the HPA axis. Eur J Clin Pharmacol. 1992;42(4):385-8. PubMed
  • Benton D et al. The influence of phosphatidylserine supplementation on mood and heart rate when faced with an acute stressor. Nutr Neurosci. 2001;4(3):169-78. PubMed
ADHD:
  • Hirayama S et al. The effect of phosphatidylserine administration on memory and symptoms of ADHD. J Hum Nutr Diet. 2014;27(Suppl 2):284-91. PubMed

Adverse Event Profile

EventIncidenceSeverityNotes
GI discomfortUncommonMildUsually transient
InsomniaRareMildIf taken late
NauseaRareMildTake with food

Safety Data

ParameterFinding
Clinical trial safetyExcellent across 50+ studies
GRAS statusGenerally Recognized as Safe
Long-term safetyWell-tolerated in studies up to 6 months
FDA health claimQualified health claim granted
Elderly safetyPrimary studied population; excellent

Regulatory Status

RegionStatusNotes
United StatesGRAS; dietary supplementFDA qualified health claim
European UnionNovel food approvedVarious member states
JapanFOSHU eligibleFunctional food
AustraliaListed medicineTGA approved

Contraindications

CategoryConsiderationSeverity
Blood thinnersTheoretical interaction★★☆☆☆ Monitor
SurgeryMay affect clotting★★☆☆☆ Discontinue 2 weeks prior
PregnancyInsufficient data★★☆☆☆ Consult provider

Drug Interactions

Drug ClassInteractionSeverityNotes
AnticoagulantsTheoretical potentiation★★☆☆☆Monitor INR
AnticholinergicsOpposing mechanisms★★☆☆☆May reduce PS benefit
Cholinesterase inhibitorsTheoretical synergy★☆☆☆☆May enhance effect

Special Populations

PopulationSafety StatusNotes
Healthy adultsExcellentPrimary use
ElderlyExcellentMost studied population
Children (ADHD)GoodUnder supervision; 200mg studied
AthletesExcellentCortisol modulation research
PregnancyCautionInsufficient data

Tier 1: Foundation

Efficacy

Moderate-High

Validation

Strong — 50+ clinical trials; FDA qualified health claim

Safety

Excellent — GRAS; well-tolerated long-term
Tier Rationale: Tier 1 (Foundation) classification. Phosphatidylserine is one of the most extensively researched nootropic ingredients, with 50+ clinical trials demonstrating benefits for memory, attention, and stress response. It holds the only FDA-qualified health claim for cognitive decline risk reduction among nootropic supplements. Mechanisms are well-understood (membrane structure, NT release, PKC activation, cortisol modulation). Sunflower-sourced PS (≥50%) provides an allergen-free, non-GMO format chemically identical to traditional sources. Safety is excellent with GRAS status and good tolerability across all studied populations. A true foundational compound for cognitive health.

When to Use Phosphatidylserine

ScenarioExpected BenefitRecommended Protocol
Daily cognitive supportHigh100 mg with Boost daily
Memory enhancementHigh100-200 mg daily
Stress/cortisol managementModerate-High200-300 mg daily
Athletic recoveryModerate300-600 mg daily
Exam/study periodsModerate100-200 mg daily

Realistic Expectations

TimeframeWhat to Expect
Week 1-2Minimal — PS incorporates slowly
Week 4-6Subtle improvements may emerge
Week 8-12Noticeable memory, focus benefits
3-6 monthsFull therapeutic effect
Long-termMaintained with continued use
Key understanding: PS is a building compound, not an acute booster. Benefits come from membrane incorporation over time, not immediate receptor effects.

Signs It’s Working

IndicatorDescription
Better recallNames, numbers, facts come easier
Improved focusSustained attention
Calmer stress responseLess reactive to daily stressors
Mental clarityLess “fog,” clearer thinking
Word retrievalEasier access to vocabulary

Optimizing Response

StrategyRationale
Take with food↑ Phospholipid absorption
Consistent daily useMembrane incorporation takes weeks
Combine with DHASynergistic membrane effects
Long-term commitmentFull benefits at 3-6 months
Stack with cholinergicsCDP-Choline, Alpha-GPC synergy

Frequently Asked Questions

PS doesn’t work like stimulants or acute nootropics. It becomes part of your cell membranes over weeks to months, gradually improving neuronal function. Think of it like improving the hardware, not running a software boost. Most people notice benefits after 6-12 weeks of consistent use.
Sunflower-derived PS is chemically identical to soy PS, but offers advantages: it’s soy-free (important for allergies), non-GMO, and sustainably sourced from European sunflowers. Clinical effects are equivalent — it’s about accessibility and quality, not efficacy differences.
Research shows dose-response benefits up to 300 mg/day for most purposes, with higher doses (600-800 mg) used specifically for cortisol modulation in athletes. The 100-200 mg in NTRPX products is effective for general cognitive support, especially combined with other synergistic ingredients.
PS modulates cortisol response, which can improve stress resilience. Studies show reduced perceived stress and blunted cortisol spikes. While not a primary anxiolytic, PS contributes to a calmer, more resilient stress response over time.
Yes. PS has GRAS (Generally Recognized as Safe) status, has been studied in trials up to 6 months, and has a long history of safe use. As a natural component of cell membranes, it’s well-tolerated. The main caution is for those on blood thinners.
Most nootropics target neurotransmitter systems (cholinergics, dopaminergics) or receptor activity. PS works at the structural level — optimizing the membranes where all signaling occurs. This foundational approach explains why PS benefits appear across multiple cognitive domains rather than targeting a single pathway.
PS combines well with most supplements. It’s particularly synergistic with DHA omega-3, choline sources (CDP-Choline, Alpha-GPC), and other nootropics. The only notable caution is with blood thinners — consult your healthcare provider if applicable.

MembraneMax Summary: Phosphatidylserine (≥50% from sunflower lecithin, 100mg in Boost and Sprint) is a phospholipid that supports cognitive function at the foundational membrane level. With 50+ clinical trials and the only FDA-qualified health claim for cognitive decline risk reduction, PS is one of the most validated nootropic ingredients available. Benefits include improved memory, better attention, and blunted cortisol response — all developing over weeks to months of consistent use. Sourced from non-GMO European sunflowers, MembraneMax PS delivers allergen-free, soy-free membrane support as part of the comprehensive NTRPX cognitive stack.