Selank Dosage Guide: Nasal & Injection Protocol
Educational reference for Selank dosage protocols via intranasal, subcutaneous, and sublingual routes. Covers the synthetic tuftsin analog discussed in Russian clinical research for anxiolytic and nootropic properties.
Medical Disclaimer
This guide is for educational and informational purposes only. It is not medical advice. Dosages described reflect ranges discussed in published research and clinical practice literature — they are not recommendations. Always consult a licensed healthcare provider before using any peptide. Legality and availability vary by jurisdiction.
Overview
Selank (Thr-Lys-Pro-Arg-Pro-Gly-Pro) is a synthetic analog of the naturally occurring immunomodulatory peptide tuftsin, developed at the Institute of Molecular Genetics of the Russian Academy of Sciences. It was designed by adding a Pro-Gly-Pro sequence to the C-terminus of tuftsin to improve metabolic stability. Selank is approved in Russia as an anxiolytic nasal spray (0.15% solution, marketed under the brand name Selank) and has been studied for its effects on anxiety, cognitive function, and immune modulation. Research by Zozulya et al. (2008) described its anxiolytic effects as comparable to benzodiazepines without the sedation, dependence potential, or cognitive impairment associated with that drug class. Selank is also reported in research literature to modulate the expression of brain-derived neurotrophic factor (BDNF) and influence serotonergic, noradrenergic, and dopaminergic systems.
Dosing Protocols
Intranasal Spray Protocol
The most commonly discussed route, matching the approved Russian pharmaceutical formulation (0.15% nasal spray). Each spray delivers approximately 75–100 mcg. Administered into each nostril. The Russian clinical protocol describes 14-day courses that may be repeated after a 1–2 week break. No reconstitution required for pre-made nasal spray formulations.
Subcutaneous Injection Protocol
An alternative route discussed in research literature for potentially higher bioavailability compared to intranasal administration. Injectable Selank requires reconstitution from lyophilized powder. Less commonly used than the nasal route. Administered in the abdominal area or upper arm. For educational reference only — not a medical recommendation.
Sublingual Protocol
Sublingual administration is discussed as an alternative to injection that avoids first-pass metabolism. The solution is held under the tongue for 60–90 seconds before swallowing. Bioavailability is expected to be intermediate between intranasal and subcutaneous routes. Less clinical data exists for this route compared to intranasal delivery.
Reconstitution & Storage
| Vial sizes | 5 mg lyophilized powder (for injectable preparation) |
| Recommended water volume | 2 mL bacteriostatic water (BAC water) |
| Storage | Refrigerate at 2–8°C after reconstitution. Do not freeze. |
| Stability once reconstituted | Use within 30 days of reconstitution. Pre-made nasal spray formulations may have different stability profiles — follow manufacturer guidelines. |
Use our reconstitution calculator to determine exact syringe units for your dose.
Cycle Guidance
The Russian clinical protocol describes Selank use in courses of 14 days, which may be repeated after a 1–2 week break. Some research protocols discuss extended use of up to 4 weeks per cycle. Unlike benzodiazepines, Selank is not reported to produce physical dependence or withdrawal symptoms in the available research literature. However, cycling is generally recommended to maintain receptor sensitivity and assess ongoing need. Some research discusses using Selank situationally (as needed for acute stress or cognitive demand) rather than in fixed cycles.
Stacking Considerations
- Selank and Semax are frequently discussed together in nootropic research contexts. Both are Russian-developed peptides with complementary mechanisms — Selank primarily anxiolytic, Semax primarily stimulatory and neuroprotective.
- Some protocols discuss combining Selank with DSIP (Delta Sleep-Inducing Peptide) for anxiety management alongside sleep optimization.
- Selank is discussed as a non-sedating alternative to benzodiazepines that may complement adaptogenic compounds such as ashwagandha or rhodiola rosea.
- In immune-support contexts, Selank's tuftsin-derived immunomodulatory properties are discussed alongside Thymosin Alpha-1.
Potential Side Effects
- Nasal irritation or mild burning sensation — reported with intranasal administration, typically transient
- Fatigue or mild sedation — occasionally reported, particularly at higher doses
- Headache — infrequently reported
- Mild allergic reactions — rare; discontinue if hypersensitivity occurs
- Taste disturbance — a metallic or unusual taste may occur with intranasal or sublingual administration
- Generally well-tolerated — the Russian clinical literature describes a favorable safety profile with minimal adverse effects
Contraindications & Cautions
- Known hypersensitivity to Selank, tuftsin, or any component of the formulation
- Pregnancy or breastfeeding — insufficient safety data in these populations
- Active nasal infections or severe rhinitis — may impair intranasal absorption and cause additional irritation
- Individuals on immunosuppressive therapy — Selank's immunomodulatory effects may interfere with immunosuppression protocols
- Children — limited safety data in pediatric populations
Related
References
- Selank (specific anxiolytic): results of clinical study of its anxiolytic activity (2008) — PubMed
- Immunomodulating effects of Selank: in vitro studies on human peripheral blood cells (2008) — PubMed
- The effect of Selank on the BDNF gene expression in the hippocampus and frontal cortex of rats (2011) — PubMed
- Anxiolytic effect of Selank and its metabolites tuftsin and Pro-Gly-Pro (2008) — PubMed