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    Silicon (Orthosilicic Acid)

    Also known as: orthosilicic acid, choline-stabilized orthosilicic acid (ch-OSA), choline-stabilised orthosilicic acid, CS-OSA, OSA-VC

    Randomized trials of choline‑stabilised orthosilicic acid (ch‑OSA) report increased markers of type I collagen formation (PINP) versus calcium and vitamin D alone at 6 mg and 12 mg Si daily over 12 months, without clear dose response and without significant lumbar spine BMD change. A 12‑week trial in knee osteoarthritis found no effect in the overall population but a benefit on symptoms and cartilage biomarkers in men. A small peri‑implantitis trial reported stabilisation of peri‑implant bone measures and less mucosal recession versus placebo after surgery. Short pharmacokinetic work shows appreciable plasma and urinary appearance of Si after an OSA‑vanillin dose.

    Last reviewed: 2026-10-14 · 5 indexed studies

    Evidence Score
    61/100
    Support bone healthSupport connective tissue / joint healthSupport mucosal and implant site healing
    Data Completeness3/4 · 75%
    Evidence ScoreDosageSafetyLinked Studies

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    Overview

    Oral orthosilicic acid (often stabilised with choline or vanillin) has been trialled as a dietary silicon source to support markers of bone and connective tissue health. Human trials report effects on biochemical markers of bone collagen and some measures of bone or peri‑implant tissue stability, but clinical benefits on bone mineral density are not established.

    Mechanism & Function

    Mechanism of Action

    Silicon in the form of orthosilicic acid is proposed to support collagen synthesis and connective tissue matrix metabolism, which could translate to effects on bone collagen markers and tissue integrity. The human trials measured biochemical markers consistent with this pathway but do not establish clinical outcomes such as fracture risk reduction.

    Physiological Role

    Potential cofactor or substrate in collagen and extracellular matrix formation; involved in bone and connective tissue metabolism.

    Primary Pathways

    Collagen synthesis / extracellular matrix metabolismBone remodelling markers

    Performance / Health Relevance

    Limited for athletic performance; any relevance is indirect through connective tissue or bone health rather than acute ergogenic effects.

    Evidence Review

    Overall61/100
    Human Clinical62/100
    Meta-Analysis50/100
    Mechanistic70/100
    Real-World48/100
    Safety80/100

    Compare Choline Forms

    4 choline forms are indexed. Bioavailability, clinical evidence, and best-use cases differ meaningfully between them.

    FormEvidence
    Silicon (Orthosilicic Acid)This page

    Oral orthosilicic acid formulations showed measurable increases in plasma and urinary Si over 6 h, indicating absorption; stabilised forms (choline or vanillin complexes) aim to limit polymerisation and improve bioavailability.

    61/100
    Alpha-GPC

    Superior choline bioavailability vs CDP-choline or choline bitartrate

    78/100
    Choline (Choline Bitartrate)

    Choline bitartrate is well-absorbed, but significant first-pass metabolism can limit its systemic bioavailability for direct cholinergic effects compared to more advanced forms like CDP-choline or Alpha-GPC.

    60/100
    Citicoline

    Near-complete oral absorption; hydrolysed to choline and cytidine before crossing the blood-brain barrier.

    45/100
    Open full side-by-side comparison

    Practical Use & Dosage

    Minimum Effective Dose
    Approximately 6 mg elemental Si daily showed effects on a bone formation marker in a 12‑month RCT.
    Optimal Range
    Not established; trials used 3–12 mg Si/day (ch‑OSA).
    Upper / Caution Level
    Not established from provided abstracts.
    Timing
    Dosing schedules in trials were daily; one peri‑implantitis trial used twice daily capsules for 1 year.
    Best Format
    Choline‑stabilised orthosilicic acid (ch‑OSA) or orthosilicic acid complexes (e.g. vanillin‑stabilised) as oral capsules.
    Bioavailability
    Oral orthosilicic acid formulations showed measurable increases in plasma and urinary Si over 6 h, indicating absorption; stabilised forms (choline or vanillin complexes) aim to limit polymerisation and improve bioavailability.
    Absorption Considerations
    Orthosilicic acid can polymerise in concentrated or non‑neutral pH solutions; stabilised complexes were used in trials to preserve monomeric, absorbable Si.

    Safety & Interactions

    Side Effects

    • •No ch‑OSA related adverse events reported in the cited long‑term RCTs

    Who Should Avoid

    • •People with known hypersensitivity to product excipients (e.g. choline preparations)

    Monitoring

    Standard biochemical safety parameters remained within normal range in the reported 12‑month trial; no routine specific monitoring indicated in the provided abstracts.

    Frequently Asked Questions

    Auto-generated from indexed evidence — dosage, safety, interactions, and more.

    When is Silicon (Orthosilicic Acid) typically used or indicated?

    Silicon (Orthosilicic Acid) is most commonly used for: Support bone health, Support connective tissue / joint health, Support mucosal and implant site healing. Potential cofactor or substrate in collagen and extracellular matrix formation; involved in bone and connective tissue metabolism.

    How does Silicon (Orthosilicic Acid) work?

    Silicon in the form of orthosilicic acid is proposed to support collagen synthesis and connective tissue matrix metabolism, which could translate to effects on bone collagen markers and tissue integrity. The human trials measured biochemical markers consistent with this pathway but do not establish clinical outcomes such as fracture risk reduction.

    What is the recommended dose of Silicon (Orthosilicic Acid)?

    The optimal range is Not established; trials used 3–12 mg Si/day (ch‑OSA).. with a minimum effective dose of Approximately 6 mg elemental Si daily showed effects on a bone formation marker in a 12‑month RCT.. Best taken: Dosing schedules in trials were daily; one peri‑implantitis trial used twice daily capsules for 1 year.. Upper / caution level: Not established from provided abstracts..

    What are the side effects of Silicon (Orthosilicic Acid)?

    Reported side effects include: No ch‑OSA related adverse events reported in the cited long‑term RCTs. Monitoring: Standard biochemical safety parameters remained within normal range in the reported 12‑month trial; no routine specific monitoring indicated in the provided abstracts.

    Who should avoid Silicon (Orthosilicic Acid)?

    Silicon (Orthosilicic Acid) is generally not recommended for: People with known hypersensitivity to product excipients (e.g. choline preparations).

    How strong is the evidence for Silicon (Orthosilicic Acid)?

    Evidence level: Moderate (overall score 61/100), based on 5 indexed studies on SuppIndex.

    Research & References (5)

    Choline-stabilized orthosilicic acid supplementation as an adjunct to calcium/vitamin D3 stimulates markers of bone formation in osteopenic females: a randomized, placebo-controlled trial.

    RCT2008
    PubMed

    12‑month double‑blind RCT in osteopenic women receiving calcium (1000 mg) and vitamin D3 (20 µg) plus ch‑OSA at doses providing 3, 6 or 12 mg Si/day or placebo; assessed bone turnover markers and BMD.

    The effect of choline-stabilized orthosilicic acid in patients with peri-implantitis: an exploratory randomized, double-blind, placebo controlled study.

    RCT2021
    PubMed

    Exploratory randomized, double‑blind, placebo‑controlled study in patients with peri‑implantitis; patients had surgical treatment and then took CS‑OSA or placebo twice daily for 1 year; clinical and CBCT bone measures assessed.

    A 12-week randomized, double-blind, placebo-controlled multicenter study of choline-stabilized orthosilicic acid in patients with symptomatic knee osteoarthritis.

    RCT2017
    PubMed

    12‑week multicentre, double‑blind RCT in 211 patients with knee osteoarthritis randomised to ch‑OSA or placebo; primary outcome WOMAC pain; secondary outcomes included WOMAC subscales and cartilage biomarkers CTX‑II and COMP.

    Digestive absorption of silicon, supplemented as orthosilicic acid-vanillin complex.

    RCT2015
    PubMed

    Single‑centre, double‑blind, cross‑over RCT in 14 healthy subjects comparing an orthosilicic acid‑vanillin complex (OSA‑VC) to placebo; plasma and urinary Si measured over 6 h to assess absorption and excretion.

    Silicon Supplementation for Bone Health: An Umbrella Review Attempting to Translate from Animals to Humans.

    Systematic Review2024
    PubMed

    2024 umbrella review attempting to summarise silicon supplementation studies across species and translate to humans; assessed ranges of silicon intakes and effects on bone and mineral metabolism.

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    Other top-rated ingredients in Minerals.

    Research Overview

    Moderate Evidence
    5Total Studies
    4Human Trials
    0Meta-Analyses
    2024Latest Study
    0Animal / In Vitro
    0Athlete Studies
    Primary data sourceClinical Patients
    Pooled evidence (meta-analysis / systematic review)Yes

    Cite this ingredient

    One-click citation export in APA, MLA, Chicago, BibTeX, or HTML. The URL below is stable and safe to link.

    Stable URL

    https://thesuppindex.com/ingredients/silicon-orthosilicic-acid

    SuppIndex. (2026). Silicon (Orthosilicic Acid): Evidence summary, dosage and clinical studies. Retrieved October 16, 2026, from https://thesuppindex.com/ingredients/silicon-orthosilicic-acid

    Based on 5 indexed studies · Evidence level: Moderate.

    Goal Ratings

    General Health
    Recovery

    Stack Compatibility

    Was administered alongside calcium and vitamin D in at least one trial; interactions with common supplements were not reported in the provided studies.

    Calcium + vitamin D