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The 50 mg vial is reconstituted with 2 mL of bacteriostatic water, yielding a 25 mg/mL concentration (0.25 mg per unit on a 1 mL insulin syringe)

Attempting to reconstitute an unlicensed injectable compound obtained from an unregulated supplier carries serious risks, including microbial contamination, chemical degradation, and severe dosing errors

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This mechanism is sometimes described separately from the angiogenic pathway because it appears to involve protective signalling at the mucosal layer rather than vascularisation per se though the two are not mutually exclusive in research protocols