Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 May 10:381:113586.
doi: 10.1016/j.jconrel.2025.113586. Epub 2025 Mar 1.

Transdermal delivery of ultradeformable cationic liposomes complexed with miR211-5p (UCL-211) stabilizes BRAFV600E+ melanocytic nevi

Affiliations

Transdermal delivery of ultradeformable cationic liposomes complexed with miR211-5p (UCL-211) stabilizes BRAFV600E+ melanocytic nevi

Tanya Chhibber et al. J Control Release. .

Abstract

Small non-coding RNAs (e.g., siRNA, miRNA) are involved in a variety of melanocyte-associated skin conditions and act as drivers for alterations in gene expression within melanocytes. These molecular changes can potentially affect the cellular stability of melanocytes and promote their oncogenic transformation. Thus, small RNAs can be considered as therapeutic targets for these conditions, however, their transdermal delivery to the melanocytes through the epidermal barrier is challenging. We synthesized and extensively evaluated ultradeformable cationic liposome (UCLs) carriers complexed with synthetic microRNAs (miR211-5p; UCL-211) for transdermal delivery to melanocytes. UCL-211 complexes were characterized for their physicochemical properties, encapsulation efficiency, and deformability, which revealed a significant advantage over conventional liposomal carriers. Increased expression of miR211-5p stabilizes melanocytic nevi and keeps them in a growth-arrested state. We did a comprehensive assessment of cellular delivery, and biological activity of the miR211-5p carried by UCL-211 in vitro and their permeation through the epidermis of intact skin using ex vivo human skin tissue explants. We also demonstrated, in vivo, that transdermal delivery of miR211-5p by topical application of UCL-211 stabilized BRAFV600E+ nevi melanocytes in a benign nevi state.

Keywords: Melanocytes; Melanocytic nevi; Transdermal delivery; Ultradeformable cationic liposomes; miRNA delivery.

PubMed Disclaimer

Conflict of interest statement

Declaration of competing interest The authors have no competing interests to declare.

Update of

Similar articles

References

    1. Yamaguchi Y and Hearing VJ, Melanocytes and their diseases. Cold Spring Harbor perspectives in medicine, 2014. 4(5): p. a017046. - PMC - PubMed
    1. Cichorek M, et al., Skin melanocytes: biology and development. Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii, 2013. 30(1): p. 30–41. - PMC - PubMed
    1. Fitzpatrick TB and Breathnach A, The epidermal melanin unit system. Dermatologische Wochenschrift, 1963. 147: p. 481–489. - PubMed
    1. Casalou C, et al., Loss of ‘epidermal melanin unit’integrity in human skin during melanoma-genesis. Frontiers in oncology, 2022. 12: p. 878336. - PMC - PubMed
    1. Domingues B, et al., Melanoma treatment in review. ImmunoTargets and therapy, 2018: p. 35–49. - PMC - PubMed

LinkOut - more resources