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Protocol Reference
Animal data only

BPC-157 protocol

BPC-157 (Body Protection Compound 157). The published work on this compound is animal or cell-culture research. No human dosing schedule exists to cite.

Category
Healing & Repair
Common vials
10, 20 mg
Half-life
Not established in humans
Route in the literature
Subcutaneous or oral in animal work
Evidence level
Animal data only

Protocol overview

Research area
Tissue-healing and cytoprotective models
Evidence
Animal and cell studies only; no human trials
Dosing in the literature
10 ng/kg to 10 μg/kg once daily in rodent models
Reconstitution
1 to 2 mL per 10 mg vial gives 10 or 5 mg/mL
Storage
Lyophilized cold and dark; reconstituted at 2 to 8 °C

How BPC-157 works

A synthetic pentadecapeptide derived from a sequence found in human gastric juice. Rodent work reports accelerated tendon, muscle and gut healing, with effects on angiogenesis and nitric-oxide signalling proposed as mechanisms.

BPC-157 dosing — what the literature actually supports

Animal data only. This is the single most important thing to know about BPC-157: despite how widely it is discussed, there are no published human clinical trials establishing a dose. The entire evidence base is rodent work, where amounts are given in micrograms per kilogram of rat and administered by routes that do not map onto human use. Any human schedule you see quoted — including the widely circulated microgram-per-kilogram figures — is an extrapolation somebody performed, not a measured human amount from a trial.

We publish a schedule when there is a citable human source and we say so when there is not. Filling this space with a number nobody measured would make the page look more complete and be worth less than nothing to you.

What the published studies actually administered

These are the amounts that appear in the actual published work, reported as published. They are animal doses and cell-culture concentrations, not human protocols.

WorkAmount usedRouteContext
Rodent injury models (Sikiric group, dozens of papers)10 ng/kg or 10 μg/kg, typically once dailyIntraperitoneal, intragastric, or topical by modelThe two canonical doses repeated across the gut, tendon, muscle and vessel studies
Tendon fibroblast work (Chang 2011)ng/mL to μg/mL in culture mediumIn vitroConcentrations in a dish, not doses in a body
About the figures you see elsewhere: the 200 to 800 mcg daily "protocols" circulating on retailer and community pages trace back to scaling the rat 10 μg/kg dose to human bodyweight. That conversion assumes allometric scaling holds, that the injection route matches the study route, and that rat and human pharmacokinetics are interchangeable. None of those have been tested, which is why we report the extrapolation as an extrapolation instead of printing it as a schedule.

Reconstitution and measurement

This part is arithmetic and does not depend on the evidence level. Concentration is vial size divided by the bacteriostatic water you add. Draw volume is your target amount divided by that concentration. Units are draw volume times 100, because a U-100 syringe reads 100 units per millilitre. Common vials for BPC-157: 10, 20 mg.

  1. Wipe the stoppers of both vials with an alcohol swab and let them dry.
  2. Draw the bacteriostatic water with a sterile syringe and inject it slowly down the inside wall of the peptide vial — never straight onto the powder.
  3. Swirl gently until the solution is clear. Do not shake; foaming and agitation damage peptides.
  4. Label the vial with the date and concentration, and refrigerate at 2–8 °C protected from light.

Worked example at the calculator defaults: 10 mg + 2 mL of bacteriostatic water = 5 mg/mL, so on a U-100 insulin syringe 1 unit = 50 mcg of BPC-157. Change either input and the calculator redoes this for you.

Open the BPC-157 calculator → Unit converter

Storage and stability

Dry powder
Cold, dark and dry. Lyophilized peptide is the stable form — keep it that way until you intend to use it.
After reconstitution
Refrigerate at 2–8 °C, protect from light, and plan around a limited window. Do not freeze a reconstituted vial — freeze-thaw damages peptides.
Mixing
Run bacteriostatic water down the inside wall of the vial rather than onto the powder, then swirl. Never shake.
Inspect before use
A clear solution is expected. Cloudiness or particles mean discard, not use.

Full storage guide → · Cloudy solution?

Supplies math

Whatever amounts your research uses, the planning arithmetic is the same. The calculator runs all of this per compound.

Vials
Doses per vial = vial size in mg divided by your per-dose amount in mg. A 10 vial at 500 mcg per dose is 20 doses; scale for your own numbers.
Syringes
One sterile U-100 insulin syringe per injection, plus roughly 10% spares for bent tips and mis-draws. Daily protocols run 30 or 31 per month.
Bacteriostatic water
1 to 3 mL per vial reconstituted. A single 10 mL bottle covers 3 to 10 vials, so one bottle usually outlasts several vials.
Alcohol swabs
Two per injection: one for the vial stopper, one for the site. A 100-count box covers about 7 weeks of daily work.

Subcutaneous technique and practical notes

General best practice from clinical injection guidance — the same fundamentals nurses are taught, none of it specific to any compound.

Fresh sterile syringe, every time
Reusing needles dulls the tip, hurts more, and is the easiest contamination route. Dispose of used syringes in a sharps container, not the bin.
Rotate sites
Abdomen (5 cm clear of the navel), thighs, upper arms. Rotating systematically prevents localised irritation and lipohypertrophy.
Slow and steady
Pinch a skinfold, insert at 45–90°, inject slowly, and wait a few seconds before withdrawing. Subcutaneous injections are not aspirated.
Write it down
Log the date, amount and site. A record is the only way to keep any research protocol consistent — and the first thing to review if anything looks off.

Reported effects

  • Rodent models consistently report accelerated healing of tendon, ligament, muscle and gut injuries — this is the core of the literature, and it is animal data.
  • Anti-inflammatory and cytoprotective activity reported across preclinical injury models.
  • No human safety data from controlled trials.
  • Rodent studies consistently report a wide therapeutic window with little observed toxicity, which is not the same as human safety.
  • In 2022 BPC-157 was added to prohibited-substance monitoring in sport, which is worth knowing if you are tested.

The part that isn't a peptide

None of the literature above was run on a background of poor sleep and no protein. Whatever the research question, these variables move outcomes more reliably than any compound on this site.

  • Tendon and muscle models in the literature pair the compound with controlled loading — tissue adapts to progressive load, and no rodent study used bed rest as the protocol.
  • Protein intake and overall energy availability set the ceiling on any repair process being studied.
  • Sleep is when most tissue-repair signalling happens; it is the cheapest variable in the whole model.
  • For an actual injury, a qualified clinician and a rehab plan are the intervention with human evidence behind them.

Sourcing BPC-157

Whatever you are working with, the documentation matters more than the price. Ask for a batch certificate of analysis whose lot number matches the vial you actually receive — a COA for a different batch tells you nothing about yours.

BPC-157 at Summit Research Supply → Grade a COA first

Summit is the supplier we feature and an affiliate link. Our COA checklist applies the same way to any vendor.

Sources and further reading

  • Sikiric P, et al. Stable gastric pentadecapeptide BPC 157: novel therapy in gastrointestinal tract. Current Pharmaceutical Design, 2011. — find on PubMed
  • Chang CH, et al. The promoting effect of pentadecapeptide BPC 157 on tendon healing involves tendon outgrowth, cell survival, and cell migration. Journal of Applied Physiology, 2011. — find on PubMed
  • Seiwerth S, et al. BPC 157 and blood vessels. Current Pharmaceutical Design, 2014. — find on PubMed
  • Vukojevic J, et al. Rat inferior caval vein occlusion and BPC 157 (vascular recruitment). Vascular Pharmacology, 2018. — find on PubMed

Broader literature searches:

For laboratory research use only. This page documents what the published literature reports about BPC-157. It is not a recommendation, not a treatment plan, and not medical advice. Compounds referenced are sold strictly as research chemicals and are not for human or veterinary use. Some supplier links are affiliate links and may earn us a commission. This never affects tier placement or review conclusions.
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