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Each batch undergoes independent analytical testing to verify: Compound identity Assay accuracy Purity confirmation Microbial safety Endotoxin levels Heavy metal screening Full batch traceability Research Use Limitation Used solely for in vitro experiments Not permitted for clinical trials involving humans Not permitted for human or veterinary administration Not permitted for investigational human use Independently analysed by Liquilabs s.r.o

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The degradation rate of the drugs was measured by observing the decrease in the area under the curve at the retention time of the drug

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At baseline and after one, three, six, and seven months, biological samples including blood, urine, and exfoliated buccal mucosal cells were collected