Quercetin + Fisetin (Senolytic Protocol) — Research Protocol

⚠️ RESEARCH SUMMARY — NOT A TREATMENT PROTOCOL. Discuss all findings with your healthcare provider.

Quercetin (often combined with dasatinib as D+Q) and fisetin are among the most studied senolytic agents. Published research has investigated intermittent dosing regimens. Dosing regimens in published literature vary. This page summarizes published research protocols. It is not a guide for self-treatment. Discuss any treatment decisions with your physician.

Research Dosing (from Published Studies)

ContextDoseRouteFrequencyNotes
D+Q senolytic (research context)Dosing regimens in published literature vary — consult the cited studies for detailsOralSee cited trialKirkland/Mayo published research investigated intermittent regimens. Published studies have investigated various dosing approaches using a brief-exposure approach targeting senescent cells.
Fisetin senolytic (AFFIRM trial)Dosing regimens in published literature vary — consult the cited studies for detailsOralSee cited trialAFFIRM trial investigated specific regimens. Bioavailability is low — enhanced formulations under development. See cited trial for specific details.
Quercetin alone (anti-inflammatory research)Dosing regimens in published literature vary — consult the cited studies for detailsOralSee cited studiesResearch has also investigated non-senolytic anti-inflammatory applications of quercetin. Published studies have investigated various dosing approaches.

Pharmacokinetics

Quercetin: bioavailability 3-17%. Half-life 3-5 hours. Fisetin: very low oral bioavailability (<10%). Both are rapidly glucuronidated and sulfated. Fat-soluble — absorption improved with dietary fat.

Safety Profile

Quercetin: well tolerated up to 1000mg/day. Mild GI upset possible. Fisetin: limited human safety data at senolytic doses. D+Q: dasatinib component carries hematologic toxicity risk at chronic doses, mitigated by intermittent protocol.

Contraindications

Monitoring Parameters

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