用于局部应用的赛鲁替尼的制剂前评估:利用 MALDI 成像和 LC-MS/MS 进行皮肤分布和光降解分析。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Edith Nicol,Bernard Do,Marina Vignes,Maxime Annereau,Muriel Paul,Pierre Wolkenstein,David Touboul,Philippe-Henri Secretan
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引用次数: 0

摘要

了解药物在皮肤内的行为,尤其是光敏化合物的行为,对于开发有效、安全的局部疗法至关重要。本研究采用基质辅助激光解吸/电离质谱成像(MALDI-MSI)和液相色谱-质谱联用(LC-MS/MS)技术研究了用于治疗1型神经纤维瘤病(NF1)的MEK抑制剂赛鲁米尼的皮肤渗透性和光稳定性。在使用凝胶制剂时,皮肤切片中的色瑞替尼含量最高,这表明要想获得更高的药物渗透性,凝胶制剂比膏霜制剂更可取。我们的研究还发现,色瑞替尼可在体外皮肤切片中发生光降解,并产生一种主要降解产物,其降解可能是由氢抽取引发的。MALDI-MSI结果显示,赛鲁替尼及其降解产物集中在皮肤附属物中,表明这些结构可能是药物贮库,有可能延长药物的保留时间和疗效。这项研究表明,MALDI-MSI 与 LC/MS-MS 的结合可极大地促进光敏化合物在皮肤中命运的表征,而这是开发化合物特异性光保护措施的必要前提。它还将为治疗 NF1 的创新局部给药策略铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preformulation evaluation of selumetinib for topical application: skin distribution and photodegradation analysis using MALDI imaging and LC-MS/MS.
Understanding drug behavior within the skin, especially for photosensitive compounds, is crucial for developing effective and safe topical therapies. This study employs Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry Imaging (MALDI-MSI) and Liquid Chromatography-Mass Spectrometry (LC-MS/MS) to investigate the skin permeation and photostability of selumetinib, a MEK inhibitor used in treating type 1 neurofibromatosis (NF1). The highest amounts of selumetinib in the skin sections were obtained when using the gel formulation, suggesting that it is to be preferred to cream formulations to achieve higher permeation of the drug. Our study also revealed that selumetinib is amenable to photodegradation in ex vivo skin explants, and yields one main degradation product, whose degradation is likely triggered by hydrogen abstraction. MALDI-MSI results showed selumetinib and its degradation product concentrate in skin appendages, indicating these structures might serve as drug reservoirs, potentially prolonging retention and efficacy. This study demonstrates that combining MALDI-MSI with LC/MS-MS can highly contribute to the characterization of the fate of photosensitive compounds in the skin, an essential prerequisite to the development of compound-specific photoprotective measures. It will also pave the way for innovative topical delivery strategies for NF1 treatment.
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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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