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    §HealingResearch protocol

    LL-37.

    LL-37 (also known as CAP-18) is a 37-amino-acid cationic antimicrobial peptide derived from the C-terminal of human cathelicidin (hCAP18)[1]. It is the only known human cathelicidin, exhibiting bro...

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    Calculated-volume support unavailable

    This selected cited guide does not contain one unambiguous vial, per-event amount, cadence, and diluent set. No value was inferred from general library metadata. Review the cited table below before creating a private Research Use Only record.

    Cited protocol & reconstitution guide

    Source-backed reference fields by phase, including any volume fields authored in the cited guide.

    Starting range (community subQ)

    100-200 mcg/day

    Units / volume4–8 units (0.04–0.08 mL)

    Commonly reported cluster (community subQ)

    100-250 mcg per day

    Units / volume4–10 units (0.04–0.10 mL)

    Upper range cited (community subQ)

    Up to 500 mcg/day

    Units / volume20 units (0.20 mL)

    Overview

    Overview

    LL-37 (also known as CAP-18) is a 37-amino-acid cationic antimicrobial peptide derived from the C-terminal of human cathelicidin (hCAP18)[1]. It is the only known human cathelicidin, exhibiting broad-spectrum antibacterial activity and immune-modulating properties[2][3]. This educational protocol presents a once-daily subcutaneous approach using a practical dilution for clear insulin-syringe measurements. Reconstitute: Add 3.0 mL bacteriostatic water → ~1.67 mg/mL concentration. Typical daily r

    Category
    Healing
    Routes
    subcutaneous

    Mechanism

    LL-37

    Mechanism of action

    Mechanism of action

    LL-37 exerts both direct and indirect antimicrobial effects. Its amphipathic, cationic α-helical structure (net +6 charge) allows it to preferentially bind and disrupt negatively charged microbial membranes [2] . Beyond direct killing, LL-37 modulates host immunity: in murine sepsis models, it induced neutrophils to release microvesicles rich in antimicrobial proteins, lowering bacterial burden and improving survival [3] . LL-37 can also bind bacterial lipopolysaccharide (LPS) and block its interaction with CD14/TLR4, reducing endotoxin-triggered TNF release and neutrophil apoptosis [2] . These combined mechanisms help explain its potential in infection control and tissue-repair contexts.

    Key research findings
    • 01

      Identity: LL-37 is the only human cathelicidin-derived antimicrobial peptide (37 residues beginning with two leucines), processed from the hCAP18 precursor; it is an endogenous component of innate immunity.

    • 02

      In vitro: broad antimicrobial activity (bacteria, some fungi and viruses) is reported, attributed largely to disruption of microbial membranes.

    • 03

      In vitro / animal model: well-documented immunomodulatory roles, including chemotaxis of immune cells, modulation of inflammatory signaling, and wound-related angiogenesis.

    • 04

      In vitro / animal model: wound studies report involvement in re-epithelialization and tissue-repair processes.

    • 05

      In vitro / observational research: context-dependent roles are described, with elevated LL-37 associated with certain inflammatory skin conditions, illustrating that effects are concentration- and context-dependent.

    Primary source: LL-37 has a large, well-established preclinical research base (extensive in vitro and animal studies) as an endogenous human host-defense peptide with antimicrobial and immunomodulatory roles. Synthetic LL-37 and analogs are studied as research materials, but clinical translation of administered LL-37 remains early.

    Researched Effects

    Researched benefits

    Areas of active research and investigation. Results may vary and are based on preclinical or early clinical data.

    ✨

    In chronic venous leg ulcers (which often lack endogenous LL-37), topical treatment with synthetic LL-37 significantly accelerated healing rates compared to placebo[4].

    ✨

    In diabetic foot ulcer trials, LL-37 cream improved granulation tissue formation and wound closure[5].

    ✨

    Broad-spectrum antimicrobial action helps clear infections; in experimental sepsis models, LL-37 treatment reduced bacterial loads and mortality[3].

    Protocol Reference

    Protocol reference

    Research Use Only. PeptiJournal supports private research documentation and calculation support. It does not provide medical advice, human-use directions, or claims of safety or effectiveness.
    subcutaneous

    Commonly cited research range: 50–400 mcg, daily.

    Reference figures reported in the research literature — not a dosing recommendation. For interactive vial math and scheduling, see the Calculator and Schedule tabs.

    Cited protocol & reconstitution guide

    Source-backed reference fields by phase, including any volume fields authored in the cited guide.

    Starting range (community subQ)

    100-200 mcg/day

    Units / volume4–8 units (0.04–0.08 mL)

    Commonly reported cluster (community subQ)

    100-250 mcg per day

    Units / volume4–10 units (0.04–0.10 mL)

    Upper range cited (community subQ)

    Up to 500 mcg/day

    Units / volume20 units (0.20 mL)

    Titration protocol

    1. StartStart
      100-200 mcg/day

      Once daily, often 5 days/week

    2. 2-4 week blockBuild
      100-250 mcg per day

      Once daily, often 5 days on with 2 days off, for a 2-4 week block

    3. Upper rangeBuild
      Up to 500 mcg/day

      Once daily

    4. CycleMaintenance
      -

      2-4 weeks on, then a break. Short block: 2-3 weeks on / 2+ weeks off (most common); standard block: 4 weeks on / 2-4 weeks off

    Storage & Handling

    Storage requirements(typical for most peptides)

    ❄️
    Lyophilized (powder)
    -20°C (frozen)

    Can be stored for extended periods. Protect from moisture.

    🧊
    Reconstituted
    2-8°C (refrigerated)

    Store in refrigerator door. Never freeze after reconstitution.

    ⏱️
    Stability window
    28-30 days after reconstitution

    Label vials with reconstitution date. Discard if cloudy.

    Reconstitution steps

    1. 01🌡️Sanitize: wipe the vial stopper and BAC water stopper with an alcohol swab
    2. 02🧴Draw 2 mL bacteriostatic water into a sterile syringe — this 5 mg vial yields 2.5 mg/mL.
    3. 03💉Add slowly: let the water run down the inside wall of the vial, not straight onto the powder
    4. 04💧Dissolve gently: swirl, do not shake; wait until the solution is clear
    5. 05🔄Inspect: solution should be clear and colorless; discard if cloudy or particulate
    6. 06🏷️Store cold: refrigerate the reconstituted vial at 2-8 °C (35.6-46.4 °F) and keep it out of light
    7. 07❄️Use promptly: LL-37 degrades in solution, so use within its refrigerated window rather than storing for weeks
    8. 08💉Important: This guide is for educational purposes only and is not medical advice. For research use only. Not for human consumption.

    Additional storage notes

    Lyophilized

    Store at −20 °C (−4 °F) in dry, dark conditions; stable ~24 months.

    Reconstituted

    Refrigerate at 2–8 °C (35.6–46.4 °F) for up to 4 weeks; frozen at −20 °C (−4 °F) for up to 6 months.

    Allow vials to reach room temperature before opening to reduce condensation uptake.

    Clinical Evidence

    Clinical evidence

    Extensively researched in innate-immunity and wound-healing models for both antimicrobial and immunomodulatory activity.

    LL-37 has a large, well-established preclinical research base (extensive in vitro and animal studies) as an endogenous human host-defense peptide with antimicrobial and immunomodulatory roles. Synthetic LL-37 and analogs are studied as research materials, but clinical translation of administered LL-37 remains early.

    1. 01Identity: LL-37 is the only human cathelicidin-derived antimicrobial peptide (37 residues beginning with two leucines), processed from the hCAP18 precursor; it is an endogenous component of innate immunity.
    2. 02In vitro: broad antimicrobial activity (bacteria, some fungi and viruses) is reported, attributed largely to disruption of microbial membranes.
    3. 03In vitro / animal model: well-documented immunomodulatory roles, including chemotaxis of immune cells, modulation of inflammatory signaling, and wound-related angiogenesis.
    4. 04In vitro / animal model: wound studies report involvement in re-epithelialization and tissue-repair processes.
    5. 05In vitro / observational research: context-dependent roles are described, with elevated LL-37 associated with certain inflammatory skin conditions, illustrating that effects are concentration- and context-dependent.

    Evidence maturity varies by compound; much peptide research is preclinical (in vitro or animal-model). Where human data are limited, findings should be read as research observations, not clinical conclusions.

    References

    Literature references

    Published research articles and sources related to LL-37.

    1. 01
      DiVA Portal / Wound Repair and Regeneration — Evaluation of LL-37 in healing of hard-to-heal venous leg ulcers: multicentric RCT View Source
    2. 02
      Journal of Immunology (PMC) — Little peptide, big effects: the role of LL-37 in inflammation and autoimmune disease View Source
    3. 03
      Innate Immunity (PMC) — Antimicrobial peptide LL-37 ameliorates a murine sepsis model via microvesicle release from neutrophils View Source
    4. 04
      Wound Repair and Regeneration (PMC) — Evaluation of LL-37 in healing of hard-to-heal venous leg ulcers: a multicentric prospective RCT View Source
    5. 05
      Archives of Dermatological Research (PMC) — Efficacy of LL-37 cream in enhancing healing of diabetic foot ulcer: a randomized double-blind controlled trial View Source
    6. 06
      Pure Lab Peptides — LL-37 (CAP-18) 5 mg product page (purity, storage, and batch documentation) View Source
    7. 07
      Bachem Knowledge Center — Handling and storage guidelines for peptides View Source
    8. 08
      CDC One & Only Campaign — One needle, one syringe, only one time (injection safety) View Source
    9. 09
      Johns Hopkins Arthritis Center — How to give a subcutaneous injection (site selection, rotation) View Source
    10. 10
      PubMed / Journal of Steroid Biochemistry — Vitamin D and the antimicrobial peptide cathelicidin (LL-37) View Source
    11. 11
      MedlinePlus (NIH) — Subcutaneous (SQ) injections: patient instructions View Source
    12. 12
      CDC — Vaccine administration: subcutaneous injection (angle/site; no aspiration) View Source
    13. 13
      NCBI Bookshelf — Best practices for injection (asepsis, preparation, and administration) View Source
    14. 14
      Clinical Pharmacology & Therapeutics (PMC) — Subcutaneous drug injection review: pharmacologic considerations View Source
    Search PubMed for LL-37

    Observed Effects

    Observed effects in cited research

    Reported
    • Generally well tolerated; occasional mild injection-site reactions (redness, itch) may occur with subcutaneous administration.

    Research Considerations

    Research considerations

    Research Use Only - not for human or veterinary therapeutic use. Current evidence is limited to in vitro and/or animal-model research; human data are minimal or absent. Consult a licensed healthcare professional for any clinical decisions.

    Factors noted in the research literature; not patient-specific medical advice.

    Regulatory Status

    Regulatory status

    RUO

    Research Use Only. PeptiJournal supports private research documentation and calculation support. It does not provide medical advice, human-use directions, or claims of safety or effectiveness.

    Comparisons

    Comparisons

    CompoundMechanismRouteStatus
    LL-37thisThe sole human cathelicidin-derived cationic antimicrobial peptide (37 residues), studied for broad-spectrum antimicrobial activity, immune modulation, and roles in wound healing and angiogenesis.subcutaneousInvestigational / RUO
    MGFA splice variant of IGF-1 (IGF-1Ec) produced in response to mechanical stress; its unique C-terminal E-peptide is studied for activation of muscle satellite cells and tissue repair.subcutaneousInvestigational / RUO
    PEG MGFA pegylated form of mechano growth factor designed for extended stability and systemic half-life; the C-terminal E-peptide is studied for satellite-cell activation and muscle repair.subcutaneousInvestigational / RUO
    PNC-27A synthetic peptide combining an HDM-2-binding domain with a membrane-penetrating sequence, studied for selective membrane disruption of cancer cells displaying surface HDM-2.subcutaneousInvestigational / RUO
    TB-500Upregulates actin, promotes cell migration, reduces inflammation, and stimulates wound healing and tissue repair.subcutaneous, intramuscularInvestigational / RUO
    MazdutideA long-acting dual agonist of GLP-1 and glucagon receptors, combining GLP-1 appetite/glycemic signaling with glucagon-mediated energy expenditure.subcutaneousInvestigational / RUO
    Melanotan IIA synthetic non-selective melanocortin receptor agonist (including MC1R and MC4R) studied for stimulation of melanogenesis (skin pigmentation) and central melanocortin-mediated activity.subcutaneousInvestigational / RUO

    Attributes shown for research comparison only; not a statement of efficacy or therapeutic equivalence.

    FAQ

    Frequently asked questions

    Research-use notice

    Research Use Only. This educational content and calculation support is intended for private research documentation. It does not provide medical advice, human-use directions, or claims of safety or effectiveness.

    Cited guide source: View source

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