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SingleBioregulators

Bronchogen 20mg

Synthetic short bioregulator tetrapeptide Ala-Glu-Asp-Leu investigated in preclinical airway models and epigenetic regulation.

Mechanism

Bronchogen is proposed to penetrate cell nuclei and engage in sequence-preferential DNA interactions, stabilizing the double helix and modulating the expression of differentiation-associated genes within bronchial epithelial tissues.

Dosing

Preclinical documentation lists reference laboratory evaluation amounts starting at 100 mcg (approximately 1.5 units on a standard U-100 syringe at 6.67 mg/mL).

Reconstitution

Reconstituting a 20 mg vial with 3.0 mL of bacteriostatic water yields a clear peptide solution at an approximate concentration of 6.67 mg/mL.

Storage

Store the unmixed lyophilized powder refrigerated protected from light, and maintain the reconstituted liquid at 2 to 8 degrees Celsius without freezing.

Mix & measure Bronchogen 20mg

Pre-filled with this protocol's recommended BAC water and documented starting dose — edit any field to run your own numbers.

Mix & measure Bronchogen 20mg

Vial strength → BAC water → target dose

mL
Concentration6.67mg/mL
Draw volume0.015mL
On the syringe1.50units

Total doses in vial: 200.0

100u80u60u40u20u0

U-100 syringe: 100 units = 1 mL

Reconstitution math only — not dosing advice. U-100 syringe: 100 units = 1 mL. Advanced calculator →

Dosing Chart

Phase / Day(s)Dose & FrequencyVolume (U-100 units / mL)
Initial Reference Tier100 mcg laboratory reference1.5 units (0.015 mL)
Mid Reference Tier200 mcg laboratory reference3.0 units (0.03 mL)
Higher Reference Tier500 mcg laboratory reference7.5 units (0.075 mL)
Extended Reference Tier1.0 mg laboratory reference15.0 units (0.15 mL)

Reconstitution Steps

  1. 1

    Clean the rubber stoppers of both the Bronchogen vial and bacteriostatic water vial using sterile alcohol prep pads and permit them to air-dry completely.

  2. 2

    Draw exactly 3.0 mL of bacteriostatic water into a clean reconstituting syringe.

  3. 3

    Insert the needle at a slight angle through the vial septum, aiming the stream along the internal glass wall to prevent turbulent impact on the lyophilized powder.

  4. 4

    Allow the diluent to fully hydrate the peptide cake for approximately 30 to 60 seconds without agitating.

  5. 5

    Gently rotate and roll the vial between the palms until the solution is completely dissolved and transparent; do not shake or introduce foam.

  6. 6

    Confirm the reconstituted solution is clear, free of visible particles, and immediately place it in refrigerated storage at 2–8°C.

Supplies Needed

Peptide Vial

Peptide Vial

Contains 20 mg of lyophilized Bronchogen (Ala-Glu-Asp-Leu) powder for research analysis.

Insulin Syringes (U-100)

Insulin Syringes (U-100)

Calibrated 0.3 mL, 0.5 mL, or 1.0 mL syringes used to accurately draw very small liquid volumes.

Bacteriostatic Water

Bacteriostatic Water

Sterile diluent preserved with 0.9% benzyl alcohol required to solubilize 20 mg of peptide into 3 mL.

Alcohol Swabs

Alcohol Swabs

70% isopropyl alcohol wipes utilized to sanitize vial tops and contact points before each draw.

Why researchers study it

1

Bronchial epithelial cellular differentiation and repair

2

Experimental airway remodeling in animal models of COPD

3

Geroprotective pathways in aging respiratory tissues

4

Sequence-preferential DNA binding and epigenetic modulation

These describe what is being studied, not proven benefits, approved uses, or promised results.

Overview

Bronchogen is a synthetic tetrapeptide consisting of the amino acid sequence Ala-Glu-Asp-Leu (AEDL). Originating from the Russian bioregulator peptide research framework established by Vladimir Khavinson, this compound is specifically categorized as an airway and bronchial epithelium-targeted regulator. Scientific literature indicates that these low-molecular-weight peptides were developed to mimic the biological signals of native organ extracts, aiming to modulate tissue-specific cellular functions. Preclinical assessments in animal models and cell cultures suggest that Bronchogen influences the morphofunctional characteristics of respiratory tissues. In rodent models of experimental chronic obstructive pulmonary conditions, the peptide was reported to attenuate pathological airway remodeling and modulate inflammatory markers. In vitro experiments using bronchial epithelial cultures have demonstrated changes in differentiation markers and cellular proliferation, particularly in aged or stressed tissues. Despite its presence in specialized laboratory research and scientific publications, Bronchogen has not undergone human clinical trials and possesses no therapeutic approvals from regulatory authorities. All experimental data remain confined to non-clinical laboratory models, organotypic explants, and cell culture studies, where it serves primarily as a molecular probe for investigating peptide-nucleic acid interactions and respiratory cell biology.

References

  1. 1.Kuzubova et al., Bulletin of Experimental Biology and Medicine, 2015 — Modulating effect of peptide therapy on bronchial epithelium in rats with obstructive lung pathology
  2. 2.Titova et al., Rossiiskii Fiziologicheskii Zhurnal imeni I.M. Sechenova, 2017 — Anti-inflammatory and regenerative effect of peptide therapy in a model of obstructive lung pathology
  3. 3.Khavinson et al., Bulletin of Experimental Biology and Medicine, 2012 — Tissue-specific stimulation of cell differentiation during aging by synthetic peptides
  4. 4.Zakutskii et al., Advances in Gerontology, 2006 — Tissue-specific effects of synthetic bioregulators in young and old rat organotypic cultures
  5. 5.Fedoreyeva et al., Biochemistry (Moscow), 2011 — Nuclear penetration of short peptides and interaction with DNA sequences in HeLa cells
  6. 6.Monaselidze et al., Bulletin of Experimental Biology and Medicine, 2011 — Effect of the peptide Bronchogen on DNA thermostability and melting temperature
  7. 7.Fedoreyeva et al., Biochemistry (Moscow), 2017 — Regulation of gene expression by exogenous short peptides in Nicotiana tabacum cultures
  8. 8.Avolio et al., International Journal of Molecular Sciences, 2022 — Distinguishing synthetic bronchial bioregulators and inflammatory pathways in monocyte cultures
  9. 9.Khavinson, Neuroendocrinology Letters, 2002 — Theoretical foundations and history of short peptide bioregulators in aging

Supplies Needed

Suggested supplier

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