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Sold for laboratory use only, it is not an approved drug and has no established human dose
To evaluate if 0.04% MMC application at the ostium enhances the outcome of non-endoscopic endonasal dacryocystorhinostomy (NEED) in individuals with primary acquired nasolacrimal duct obstruction (PANDO)
The neuroprotective and systemic repair signaling mechanisms warrant investigationbut only with materials meeting pharmaceutical-grade standards, not cosmetic formulations diluted below bioactive thresholds
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