Component

Fractional absorption of administered lycopene

Fractional absorption of administered lycopene. Species, exposure and limitations are retained in each linked claim.

2 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What acts on it

  1. Modeled bioavailability did not differ between cis lycopene, 24.5% ± 6%, and all-trans lycopene, 23.2% ± 8%.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/lycopene-research/26561629.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682", "start_char": 0, "end_char": 2207, "text_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682"}
    experimental_model
    Stable-isotope tracer and seven-compartment kinetic modeling
    exposure
    10.2 mg carbon-13 lycopene, 82% all-trans and 18% cis
    limitations
    Small study; model-dependent pool estimates; formulation differs from food-matrix comparisons.
    nutrient_topic
    Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
    organism
    Human, eight healthy adults
    plain_language
    Cis forms were not universally better absorbed under these conditions.
    primary_references
    [lycopene-p26561629] Compartmental and noncompartmental modeling of ¹³C-lycopene absorption, isomerization, and distribution kinetics in healthy adults. (2015). https://pubmed.ncbi.nlm.nih.gov/26561629/ DOI: 10.3945/ajcn.114.103143
    tissue_or_cell_type
    Plasma over 28 days and modeled tissue pools

    Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 208–219

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Stable-isotope tracer and seven-compartment kinetic modeling · source_derived_draft · unverified_draft

    ### lycopene-isomer-absorption-null Modeled bioavailability did not differ between cis lycopene, 24.5% ± 6%, and all-trans lycopene, 23.2% ± 8%. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Cis forms were not universally better absorbed under these conditions. organism: Human, eight healthy adults tissue_or_cell_type: Plasma over 28 days and modeled tissue pools experimental_model: Stable-isotope tracer and seven-compartment kinetic modeling limitations: Small study; model-dependent pool estimates; formulation differs from food-matrix comparisons. exposure: 10.2 mg carbon-13 lycopene, 82% all-trans and 18% cis evidence_span: {"source_cache": "artifacts/lycopene-research/26561629.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682", "start_char": 0, "end_char": 2207, "text_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682"} [lycopene-p26561629] Compartmental and noncompartmental modeling of ¹³C-lycopene absorption, isomerization, and distribution kinetics in healthy adults. (2015). https://pubmed.ncbi.nlm.nih.gov/26561629/ DOI: 10.3945/ajcn.114.103143
    Complete structured claim and evidence
  2. Mean fractional lycopene absorption was 23% ± 6% in the human carbon-13 tracer experiment.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/lycopene-research/26561629.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682", "start_char": 0, "end_char": 2207, "text_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682"}
    experimental_model
    Stable-isotope tracer and seven-compartment kinetic modeling
    exposure
    10.2 mg carbon-13 lycopene, 82% all-trans and 18% cis
    limitations
    Small study; model-dependent pool estimates; formulation differs from food-matrix comparisons.
    nutrient_topic
    Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
    organism
    Human, eight healthy adults
    plain_language
    Only part of an oral dose reached the body in this study.
    primary_references
    [lycopene-p26561629] Compartmental and noncompartmental modeling of ¹³C-lycopene absorption, isomerization, and distribution kinetics in healthy adults. (2015). https://pubmed.ncbi.nlm.nih.gov/26561629/ DOI: 10.3945/ajcn.114.103143
    tissue_or_cell_type
    Plasma over 28 days and modeled tissue pools

    Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 195–206

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Stable-isotope tracer and seven-compartment kinetic modeling · source_derived_draft · unverified_draft

    ### lycopene-tracer-absorption Mean fractional lycopene absorption was 23% ± 6% in the human carbon-13 tracer experiment. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Only part of an oral dose reached the body in this study. organism: Human, eight healthy adults tissue_or_cell_type: Plasma over 28 days and modeled tissue pools experimental_model: Stable-isotope tracer and seven-compartment kinetic modeling limitations: Small study; model-dependent pool estimates; formulation differs from food-matrix comparisons. exposure: 10.2 mg carbon-13 lycopene, 82% all-trans and 18% cis evidence_span: {"source_cache": "artifacts/lycopene-research/26561629.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682", "start_char": 0, "end_char": 2207, "text_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682"} [lycopene-p26561629] Compartmental and noncompartmental modeling of ¹³C-lycopene absorption, isomerization, and distribution kinetics in healthy adults. (2015). https://pubmed.ncbi.nlm.nih.gov/26561629/ DOI: 10.3945/ajcn.114.103143
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards