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Simplifying the delivery of melanocytes and keratinocytes for the treatment of vitiligo using a chemically defined carrier dressing

Version 2 2024-03-12, 15:18
Version 1 2024-03-01, 10:08
journal contribution
posted on 2024-03-12, 15:18 authored by Paula EvesPaula Eves, Nial A. Bullet, David Haddow, Alison J. Beck, Christopher Layton, Louise Way, Alex G. Shard, David J. Gawkrodger, Sheila MacNeil
<p>Obtaining pigmentary function in autologous skin grafts is a current challenge for burn surgeons as is developing reliable robust grafting strategies for patients with vitiligo and piebaldism. In this paper, we present the development of a simple methodology for delivering cultured keratinocytes and melanocytes to the patient that is of low risk for the patient but also user friendly for the surgeon. In this study, we examined the ability of keratinocytes and melanocytes to transfer from potential cell carriers under different media conditions to an in vitro human wound bed model. The number of melanocytes transferred, their location within the neoepidermis, and their ability to pigment were evaluated as preclinical end points. Two inert substrates (polyvinyl chloride and silicone sheets) and three candidate plasma-polymerized coatings with controlled surface chemistry deposited on these substrates were explored. Two media for expansion of cells, Greens, currently used clinically (but which contains fetal calf serum), and a serum-free alternative, M2 (melanocyte medium), were explored. Reproducible transfer of physiologically relevant numbers of melanocytes capable of pigmentation from the coculture of melanocytes and keratinocytes was obtained using either Greens medium or M2 medium, and a silicone carrier pretreated with 20% carboxylic acid deposited by plasma polymerization. © 2008 The Society for Investigative Dermatology.</p>

History

School affiliated with

  • University of Lincoln (Historic Research Outputs)

Publication Title

Journal of Investigative Dermatology

Volume

128

Issue

6

Pages/Article Number

1554-1564

Publisher

Elsvier

ISSN

0022-202X

eISSN

1523-1747

Date Submitted

2017-04-21

Date Accepted

2007-10-27

Date of First Publication

2008-06-01

Date of Final Publication

2008-06-01

Date Document First Uploaded

2017-04-21

ePrints ID

26986