Scope of this article
This content is not diagnosis, prescribing, personal risk assessment or a treatment plan. Sources may be limited to a particular product, device, task, indication or study group.
This translation is provided for general access and has no recorded medical-language review.
Editorial general information — not a clinical-review record
Published: Updated: Publisher: Dr. Murat Toktamışoğlu
Particle count or CD9/CD63 positivity does not demonstrate an intended biological function. A potency assay should measure a defined mechanism-related activity with suitable controls and across lots; a laboratory response is not a guarantee of clinical benefit in people.
This translation has no recorded clinical or medical-language review.
If a product claims wound healing, inflammatory modulation or collagen activity, the assay should be biologically related to that specific claim. Cell proliferation, migration, enzyme activity and signaling changes are different endpoints. When the intended mechanism is unclear, selecting one easy marker may not demonstrate meaningful potency.
Positive and negative controls, a vehicle control, dose-response, repeatability, sensitivity, specificity and a lot acceptance range are needed. Function after storage or freeze-thaw also requires testing. One positive research experiment is not a routine lot-release method, and a changed assay needs bridging between old and new results.
More collagen marker in a cell culture does not establish visible facial change, dose, durability or safety in people. Route, barrier, immunity and a co-procedure may change the outcome. A potency certificate does not replace clinical trials or authorization. Do not turn laboratory findings into product promises when product-specific human evidence is absent.
This content is not diagnosis, prescribing, personal risk assessment or a treatment plan. Sources may be limited to a particular product, device, task, indication or study group.
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Foppiani JA et al. · 2025
Scope and limitations: Interpret this source only within the exact product, device, method, indication and study population it names. It does not establish personal suitability, Turkish authorization, a universal protocol or a guaranteed outcome; consult the full source and current local information.
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Austin GK, Struble SL, Quatela VC · 2022
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Sanyal RD, Fabi SG · 2024
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U.S. Food and Drug Administration (FDA) · 2025
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Pour Mohammad A et al. · 2023
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Mirza HN, Mirza FN, Khatri KA · 2021
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U.S. Food and Drug Administration (FDA) · 2023
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Editorial source — not a signed clinical review
V. V. T. Nguyen et al. · 2020
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PMDA Science Board authors · 2024
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International Society for Extracellular Vesicles consensus authors · 2024
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Editorial source — not a signed clinical review