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Peptide

Reference library

Educational peptide reference — research use only.

Research & educational use only

For laboratory and educational research only. Not for human or veterinary consumption. This is not medical advice. Always follow applicable laws and consult qualified professionals.

The calculator performs unit math for research reference. It must not be used to plan or guide dosing in humans or animals. Verify all figures independently in your lab protocol.

Liraglutide

A GLP-1 receptor agonist studied in diabetes and obesity research.

Half-life (approx.)
~13 h (approx., subQ)
Diluent
Pre-mixed pen
Common vials
3, 6 mg

Half-life figures are literature approximations for educational reference — not pharmacokinetic advice.

Overview

Liraglutide is a daily GLP-1 receptor agonist with 97% homology to native GLP-1, studied in diabetes and obesity trials (Victoza/Saxenda). Research compares its efficacy and GI side-effect profile to newer weekly analogs. Once-daily acylated GLP-1 analog with LEADER cardiovascular outcome data.

Structure & identity

GLP-1(7-37) analog with C16 fatty-acid side chain

Status: FDA-approved (Victoza, Saxenda).

Mechanism

Liraglutide activates GLP-1 receptors with fatty-acid mediated albumin binding, prolonging half-life for once-daily subcutaneous dosing in published trials.

Acylated GLP-1 analog with albumin binding for once-daily DPP-4-resistant receptor activation. Albumin binding via C16 fatty-acid side chain extends half-life versus native GLP-1.

Studies & clinical programs

  • LEADER cardiovascular outcomes(Phase 3)

    Type 2 diabetes with high CV risk

    • Cardiovascular safety and MACE endpoints evaluated in long-term follow-up.

    Source: LEADER trial

  • SCALE obesity program(Phase 3)

    Adults with overweight or obesity

    • Daily GLP-1 dosing with C16 acylation for albumin binding documented weight-loss endpoints.

Research models in literature

  • LEADER CV trial
  • SCALE obesity program

Literature highlights

  • Acylated GLP-1 analog studied in LEADER cardiovascular and SCALE obesity programs.
  • Once-daily albumin-binding extends half-life versus native GLP-1 in PK trials.
  • HbA1c, weight, and CV outcome endpoints well characterized in published trials.

Key targets & pathways

GLP-1 receptorLEADER trial endpointsSatiety signaling

Research areas

GLP-1 agonistDaily dosingDiabetesObesity

Routes in research literature

Subcutaneous

Also known as

VictozaSaxenda

Stability & storage phases

PhaseConditionGuidance
LyophilizedSealed vial, refrigerated (2–8 °C)Intact lyophilized cake or powder is typically stable for months to years per published stability data; protect from moisture, light, and repeated freeze-thaw of the dry vial.
ReconstitutedBacteriostatic water (0.9% benzyl alcohol), refrigeratedMost aqueous peptide solutions remain usable for approximately 2–4 weeks refrigerated; verify published stability data and label with reconstitution date.
Working aliquotsPre-drawn syringes or microtubes, frozen (−20 °C)Aliquot promptly after mixing to limit freeze-thaw cycles on the main vial; thaw once and use to reduce protease-mediated degradation.

Stability windows are formulation-dependent — verify published data and your lab SOP.

Reconstitution reference table

Vial (mg)Diluent (mL)mcg/mLUnits @ 100 mcgUnits @ 250 mcgUnits @ 500 mcg
30.56000.01.74.28.3
60.512000.00.82.14.2

U-100 insulin syringe scale (100 units = 1 mL). Illustrative only — not dosing guidance.

Reconstitution steps

  1. Allow vial to reach room temperature (15–30 min)
  2. Swab rubber stopper with alcohol prep pad
  3. Draw calculated bacteriostatic water into syringe
  4. Inject diluent slowly down vial wall — do not spray directly onto cake
  5. Gently swirl until fully dissolved — do not shake vigorously
  6. Label with date, concentration, and diluent volume
  7. Refrigerate and use within your lab stability window

Often supplied pre-mixed; research powder formulations vary.

Laboratory record checklist

  • Compound identity recorded in lab notebook (name, lot, preparation date)
  • Analytical identity cross-checked against published sequence or structure
  • Potency or concentration documented from analytical certificate when available
  • Purity or HPLC data filed when provided with research material
  • Appearance noted: intact lyophilized cake or uniform powder
  • Sterility / endotoxin report archived when available
  • Storage temperature applied immediately per published stability guidance