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Topical Drug Delivery of Concentrated Cabazitaxel in an α‐Tocopherol and DMSO Solution

Topical chemotherapy approaches are relevant for certain skin cancer treatments. This study observes that cabazitaxel (CTX), a broad‐spectrum second‐generation taxane cytotoxic agent, can be dissolved in α‐tocopherol at high concentrations exceeding 100 mg mL(−1). 2D nuclear magnetic resonance (NMR)...

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Autores principales: Sun, Boyang, Paraskevopoulos, Georgios, Min, Jiwei, Rossdeutcher, Robert, Ghosh, Sanjana, Quinn, Breandan, Lin, Meng‐Hsuan, Sarkar, Debanjan, Sukumaran, Dinesh, Wang, Yuefei, Vávrová, Kateřina, Lovell, Jonathan F., Zhang, Yumiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582425/
https://www.ncbi.nlm.nih.gov/pubmed/37555802
http://dx.doi.org/10.1002/advs.202302658
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author Sun, Boyang
Paraskevopoulos, Georgios
Min, Jiwei
Rossdeutcher, Robert
Ghosh, Sanjana
Quinn, Breandan
Lin, Meng‐Hsuan
Sarkar, Debanjan
Sukumaran, Dinesh
Wang, Yuefei
Vávrová, Kateřina
Lovell, Jonathan F.
Zhang, Yumiao
author_facet Sun, Boyang
Paraskevopoulos, Georgios
Min, Jiwei
Rossdeutcher, Robert
Ghosh, Sanjana
Quinn, Breandan
Lin, Meng‐Hsuan
Sarkar, Debanjan
Sukumaran, Dinesh
Wang, Yuefei
Vávrová, Kateřina
Lovell, Jonathan F.
Zhang, Yumiao
author_sort Sun, Boyang
collection PubMed
description Topical chemotherapy approaches are relevant for certain skin cancer treatments. This study observes that cabazitaxel (CTX), a broad‐spectrum second‐generation taxane cytotoxic agent, can be dissolved in α‐tocopherol at high concentrations exceeding 100 mg mL(−1). 2D nuclear magnetic resonance (NMR) analysis and molecular dynamics (MD) are used to study this phenomenon. The addition of 30% dimethyl sulfoxide (DMSO) to the α‐tocopherol/CTX solution improves its working viscosity and enhances CTX permeation through human skin in vitro (over 5 µg cm(−2) within 24 h), while no detectable drug permeates when CTX is dissolved in α‐tocopherol alone. In a transepidermal water loss assay, the barrier impairment induced by CTX in 30% DMSO in α‐tocopherol, but not in pure DMSO, is reversible 8 h after the formulation removal from the skin surface. Antitumor efficacy of the topical CTX formulation is evaluated in nude mice bearing A431 human squamous carcinoma skin cancer xenografts. With topical application of concentrated CTX solutions (75 mg mL(−1)), tumor growth is significantly suppressed compared to lower concentration groups (0, 25, or 50 mg mL(−1) CTX). Taken together, these findings show that topical delivery of CTX using a DMSO and α‐tocopherol solvent warrants further study as a treatment for skin malignancies.
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spelling pubmed-105824252023-10-19 Topical Drug Delivery of Concentrated Cabazitaxel in an α‐Tocopherol and DMSO Solution Sun, Boyang Paraskevopoulos, Georgios Min, Jiwei Rossdeutcher, Robert Ghosh, Sanjana Quinn, Breandan Lin, Meng‐Hsuan Sarkar, Debanjan Sukumaran, Dinesh Wang, Yuefei Vávrová, Kateřina Lovell, Jonathan F. Zhang, Yumiao Adv Sci (Weinh) Research Articles Topical chemotherapy approaches are relevant for certain skin cancer treatments. This study observes that cabazitaxel (CTX), a broad‐spectrum second‐generation taxane cytotoxic agent, can be dissolved in α‐tocopherol at high concentrations exceeding 100 mg mL(−1). 2D nuclear magnetic resonance (NMR) analysis and molecular dynamics (MD) are used to study this phenomenon. The addition of 30% dimethyl sulfoxide (DMSO) to the α‐tocopherol/CTX solution improves its working viscosity and enhances CTX permeation through human skin in vitro (over 5 µg cm(−2) within 24 h), while no detectable drug permeates when CTX is dissolved in α‐tocopherol alone. In a transepidermal water loss assay, the barrier impairment induced by CTX in 30% DMSO in α‐tocopherol, but not in pure DMSO, is reversible 8 h after the formulation removal from the skin surface. Antitumor efficacy of the topical CTX formulation is evaluated in nude mice bearing A431 human squamous carcinoma skin cancer xenografts. With topical application of concentrated CTX solutions (75 mg mL(−1)), tumor growth is significantly suppressed compared to lower concentration groups (0, 25, or 50 mg mL(−1) CTX). Taken together, these findings show that topical delivery of CTX using a DMSO and α‐tocopherol solvent warrants further study as a treatment for skin malignancies. John Wiley and Sons Inc. 2023-08-09 /pmc/articles/PMC10582425/ /pubmed/37555802 http://dx.doi.org/10.1002/advs.202302658 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Sun, Boyang
Paraskevopoulos, Georgios
Min, Jiwei
Rossdeutcher, Robert
Ghosh, Sanjana
Quinn, Breandan
Lin, Meng‐Hsuan
Sarkar, Debanjan
Sukumaran, Dinesh
Wang, Yuefei
Vávrová, Kateřina
Lovell, Jonathan F.
Zhang, Yumiao
Topical Drug Delivery of Concentrated Cabazitaxel in an α‐Tocopherol and DMSO Solution
title Topical Drug Delivery of Concentrated Cabazitaxel in an α‐Tocopherol and DMSO Solution
title_full Topical Drug Delivery of Concentrated Cabazitaxel in an α‐Tocopherol and DMSO Solution
title_fullStr Topical Drug Delivery of Concentrated Cabazitaxel in an α‐Tocopherol and DMSO Solution
title_full_unstemmed Topical Drug Delivery of Concentrated Cabazitaxel in an α‐Tocopherol and DMSO Solution
title_short Topical Drug Delivery of Concentrated Cabazitaxel in an α‐Tocopherol and DMSO Solution
title_sort topical drug delivery of concentrated cabazitaxel in an α‐tocopherol and dmso solution
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582425/
https://www.ncbi.nlm.nih.gov/pubmed/37555802
http://dx.doi.org/10.1002/advs.202302658
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