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The Role of Platelet Homeostasis in a Novel Topical PRP Formulation

Authors :
Lawrence A. Rheins
Shaun Wooten
Robert S. Kellar
Zoe Diana Draelos
Source :
Journal of Drugs in Dermatology. 19:1215-1218
Publication Year :
2020
Publisher :
SanovaWorks, 2020.

Abstract

Background Topical platelet-rich plasma (PRP) must demonstrate stability to insure biologic activity in aesthetic medicine. Objective The objective of this research was to evaluate the role of platelet homeostasis in a novel PRP topical cosmetic formulation to provide facial appearance improvement. Methods The stability of the topical PRP formulation was evaluated in vitro followed by clinical in vivo testing. The in vitro evaluation examined platelet stability and morphology over a 90-day period within the preservative cosmetic base utilizing ELISA and light microscopy (LM)/scanning electron microscopy (SEM). The in vivo clinical study enrolled 20 subjects in a 120-day double blind split face study to evaluate the effect of 5n7x concentrated PRP compared to 2n3x concentrated PRP on facial photoaging. Cosmetic effect was evaluated by the subject and the dermatologist investigator on a 5-point ordinal scale at baseline, week 8, and week 16. Results 90-day stability for the topical PRP formulation was verified via ELISA and LM/SEM. ELISA showed the PRP was more inactive than control conditions via analyte concentration curves (PDGF-AB, EGF, and P-Selectin). LM/SEM demonstrated the PRP had less aggregation/activation over time within the cosmetic base and that refrigeration is superior to room-temperature storage thus delaying full platelet degranulation. The in vivo clinical study demonstrated parity between 20ml and 60ml PRP in terms of clinical efficacy. Conclusion Platelets remain viable for up to 90 days in a refrigerated cosmetic vehicle with demonstrated topical clinical PRP facial benefits. PRP kits of 20ml and 60ml volumes for topical PRP are equally efficacious. J Drugs Dermatol. 2020;19(12): doi:10.36849/JDD.2020.5495.

Details

ISSN :
15459616
Volume :
19
Database :
OpenAIRE
Journal :
Journal of Drugs in Dermatology
Accession number :
edsair.doi.dedup.....4916d33c31a797949d144963b595fa32