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α-生育酚和 DMSO 溶液中浓缩卡巴他赛的局部药物递送。

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

机构信息

School of Chemical Engineering and Technology, Key Laboratory of Systems Bioengineering (Ministry of Education), Frontiers Science Center for Synthetic Biology (Ministry of Education), State Key Laboratory of Chemical Engineering, Tianjin University, Tianjin, 300350, P. R. China.

Skin Barrier Research Group, Faculty of Pharmacy, Charles University, Akademika Heyrovského 1203, Hradec Králové, 50005, Czech Republic.

出版信息

Adv Sci (Weinh). 2023 Oct;10(29):e2302658. doi: 10.1002/advs.202302658. Epub 2023 Aug 9.

DOI:10.1002/advs.202302658
PMID:37555802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10582425/
Abstract

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 . 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 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 ), tumor growth is significantly suppressed compared to lower concentration groups (0, 25, or 50 mg mL 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.

摘要

局部化疗方法与某些皮肤癌的治疗相关。本研究观察到卡巴他赛(CTX),一种广谱第二代紫杉烷细胞毒性药物,可以在浓度超过 100mg/mL 的 α-生育酚中溶解。二维核磁共振(NMR)分析和分子动力学(MD)用于研究这种现象。向 α-生育酚/CTX 溶液中添加 30%二甲亚砜(DMSO)可提高其工作粘度,并增强 CTX 在体外透过人体皮肤的渗透作用(24 小时内超过 5μg/cm),而当 CTX 单独溶解在 α-生育酚中时,则无法检测到药物渗透。在经皮水分流失测定中,CTX 在 30%DMSO 中的 α-生育酚中引起的屏障损伤是可逆的,在制剂从皮肤表面去除 8 小时后即可恢复。用携带 A431 人鳞状细胞癌皮肤癌异种移植物的裸鼠评估局部 CTX 制剂的抗肿瘤功效。与低浓度组(0、25 或 50mg/mL CTX)相比,局部应用浓缩 CTX 溶液(75mg/mL)可显著抑制肿瘤生长。总之,这些发现表明,使用 DMSO 和 α-生育酚溶剂的局部 CTX 递送值得进一步研究,作为治疗皮肤恶性肿瘤的一种方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/c09201c28a54/ADVS-10-2302658-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/a4a3db3bc0fd/ADVS-10-2302658-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/73cd0631ad99/ADVS-10-2302658-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/fc584c9486c3/ADVS-10-2302658-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/b514b2a8673a/ADVS-10-2302658-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/d8b8e9c91d23/ADVS-10-2302658-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/ec5137bd9105/ADVS-10-2302658-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/22380a9a0505/ADVS-10-2302658-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/c09201c28a54/ADVS-10-2302658-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/a4a3db3bc0fd/ADVS-10-2302658-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/73cd0631ad99/ADVS-10-2302658-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/fc584c9486c3/ADVS-10-2302658-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/b514b2a8673a/ADVS-10-2302658-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/d8b8e9c91d23/ADVS-10-2302658-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/ec5137bd9105/ADVS-10-2302658-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/22380a9a0505/ADVS-10-2302658-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c95/10582425/c09201c28a54/ADVS-10-2302658-g005.jpg

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