Local vasoregulative interventions impact drug concentrations in the skin after topical laser-assisted delivery.

5-fluorouracil fractional ablative CO2 laser in vivo skin optical coherence tomography topical laser-assisted drug delivery

Journal

Lasers in surgery and medicine
ISSN: 1096-9101
Titre abrégé: Lasers Surg Med
Pays: United States
ID NLM: 8007168

Informations de publication

Date de publication:
12 2022
Historique:
revised: 09 05 2022
received: 01 03 2022
accepted: 09 05 2022
pubmed: 21 5 2022
medline: 16 12 2022
entrez: 20 5 2022
Statut: ppublish

Résumé

The ability of ablative fractional lasers (AFL) to enhance topical drug uptake is well established. After AFL delivery, however, drug clearance by local vasculature is poorly understood. Modifications in vascular clearance may enhance AFL-assisted drug concentrations and prolong drug dwell time in the skin. Aiming to assess the role and modifiability of vascular clearance after AFL-assisted delivery, this study examined the impact of vasoregulative interventions on AFL-assisted 5-fluorouracil (5-FU) concentrations in in vivo skin. 5-FU uptake was assessed in intact and AFL-exposed skin in a live pig model. After fractional CO Compared to intact skin, AFL facilitated a prompt peak in 5-FU delivery that remained elevated up to 4 hours (1500 μm: 1.5 vs. 31.8 ng/ml [1 hour, p = 0.002]; 5.3 vs. 14.5 ng/ml [4 hours, p = 0.039]). However, AFL's impact was transient, with 5-FU concentrations comparable to intact skin at later time points. Overall, vasoregulative intervention with brimonidine or PDL led to significantly higher peak 5-FU concentrations, prolonging the drug's dwell time in the skin versus AFL delivery alone. As such, brimonidine and PDL led to twofold higher 5-FU concentrations than AFL alone in both skin layers by 1 hour (e.g., 500 μm: 107 ng/ml [brimonidine]; 96.9 ng/ml [PDL], 46.6 ng/ml [AFL alone], p ≤ 0.024), and remained significantly elevated at 4 hours (p ≤ 0.024). A similar pattern was observed for epinephrine, although trends remained nonsignificant (p ≥ 0.09). Prolonged 5-FU delivery was provided by PDL, resulting in sustained drug deposition compared to AFL alone at both 48 and 72 hours in the superficial skin layer (p ≤ 0.024). Supporting drug delivery findings, OCT revealed that increases in local blood flow after AFL were mitigated in test areas also exposed to PDL, brimonidine, or epinephrine, with PDL providing the greatest, sustained reduction in flow over 48 hours. Vasoregulative intervention in conjunction with AFL-assisted delivery enhances and prolongs 5-FU deposition in in vivo skin.

Identifiants

pubmed: 35593006
doi: 10.1002/lsm.23558
pmc: PMC9675883
mid: NIHMS1808254
doi:

Substances chimiques

Fluorouracil U3P01618RT
Brimonidine Tartrate 4S9CL2DY2H
Epinephrine YKH834O4BH

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1288-1297

Subventions

Organisme : NIBIB NIH HHS
ID : P41 EB015903
Pays : United States

Informations de copyright

© 2022 The Authors. Lasers in Surgery and Medicine published by Wiley Periodicals LLC.

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Auteurs

Emily Wenande (E)

Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Department of Dermatology, Bispebjerg Hospital, University of Copenhagen, Copenhagen NV, Denmark.

Sarat Chandra Gundavarapu (SC)

Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Joshua Tam (J)

Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Department of Dermatology, Harvard Medical School, Boston, Massachusetts, USA.

Brijesh Bhayana (B)

Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Carina N Thomas (CN)

Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

William A Farinelli (WA)

Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Benjamin J Vakoc (BJ)

Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Department of Dermatology, Harvard Medical School, Boston, Massachusetts, USA.

R Rox Anderson (RR)

Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Department of Dermatology, Harvard Medical School, Boston, Massachusetts, USA.

Merete Haedersdal (M)

Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Department of Dermatology, Bispebjerg Hospital, University of Copenhagen, Copenhagen NV, Denmark.

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Classifications MeSH