IGF-1 LR3 (1 mg Vial) Dosage Protocol
IGF-1 LR3 (Long R3 Insulin-like Growth Factor-1) is a synthetic analog of human IGF-1 with two structural modifications: an N-terminal 13-amino acid extension and a glutamate-to-arginine substitution at position 3. These changes dramatically reduce IGF-1 binding protein affinity, extending the half-life from ~10 minutes to approximately 20β30 hours.
β‘ Quickstart Highlights
Dosing & Reconstitution Guide
Route: Subcutaneous or IM | Frequency: Once daily during active cycle
| Protocol | Dose Per Day | U-100 Units | Volume | Notes |
|---|---|---|---|---|
| Conservative | 20β40 mcg/day | 2β4 units | 0.02β0.04 mL | Use 30-unit syringe for precision |
| Standard | 50β80 mcg/day | 5β8 units | 0.05β0.08 mL | Common research range |
| Advanced | 80β100 mcg/day | 8β10 units | 0.08β0.10 mL | Upper research limit; monitor glucose |
Reconstitution Steps
- Draw 1.0 mL bacteriostatic water into a sterile syringe.
- Inject slowly down the inside glass wall of the vial; avoid foaming.
- Gently swirl until dissolved. Do not shake.
- Label with reconstitution date. Refrigerate at 2β8Β°C; use within 28 days.
Supplies Planning
| Item | 4-Week Cycle (50 mcg/day) | 6-Week Cycle |
|---|---|---|
| IGF-1 LR3 vials (1 mg each) | 2 vials | 3 vials |
| Insulin syringes (30-unit) | 28 | 42 |
| Bacteriostatic water (10 mL) | 1 Γ 10 mL | 1 Γ 10 mL |
| Alcohol swabs | 1 Γ 100-pack | 1 Γ 100-pack |
Mechanism of Action
IGF-1 LR3 is a recombinant analog of insulin-like growth factor 1, modified with an N-terminal 13-amino acid extension (the 'Long' component) and a Glu-3βArg substitution (the 'R3' component). These modifications dramatically reduce the binding affinity of IGF-1 to its six binding proteins (IGFBPs), which in natural IGF-1 sequester approximately 99% of circulating IGF-1 in an inactive bound form. By reducing IGFBP binding, IGF-1 LR3 remains in free, biologically active form for much longer β extending the half-life from ~10 minutes (native IGF-1) to approximately 20β30 hours.
IGF-1 LR3 acts directly at IGF-1 receptors and insulin receptors in muscle, bone, and other tissues, promoting amino acid uptake, protein synthesis, satellite cell activation (muscle stem cells), and anti-catabolism. Unlike GH secretagogues which work upstream through the pituitary, IGF-1 LR3 acts at the downstream effector level β bypassing the GH axis entirely.
Research Findings & Safety Profile
- Extended half-life (20β30 hr) vs natural IGF-1 (~10 min) due to dramatically reduced IGFBP binding.
- Promotes muscle protein synthesis, satellite cell activation, and anti-catabolism in preclinical models.
- Hypoglycemia risk: IGF-1 LR3 has significant insulin-receptor cross-activity. Monitor blood glucose; do not administer without access to fast-acting carbohydrates.
- Potential for abnormal tissue growth with chronic supraphysiological dosing β not suitable for extended continuous cycles.
- Typical research cycles: 4β6 weeks maximum; extended use increases hypoglycemia and tissue proliferation risk.
- WADA prohibited. Not FDA approved for any indication in this form.
Storage
| State | Temperature | Duration | Notes |
|---|---|---|---|
| Lyophilized | β20Β°C (β4Β°F) | Up to 24 months | Dry, dark conditions |
| Reconstituted | 2β8Β°C (35β46Β°F) | Up to 28 days | Avoid freeze-thaw; protect from light |