Effect of Vehicle Composition on the Preparation of Different Types of Dapsone Crystals for Topical Drug Delivery

聚乙二醇 水合物 结晶 化学 PEG比率 溶剂 水溶液 化学工程 作文(语言) 渗透(战争) 共晶 粒径 活性成分 Crystal(编程语言) 材料科学 色谱法 有机化学 分子 氢键 生物信息学 语言学 哲学 财务 物理化学 运筹学 计算机科学 工程类 经济 生物 程序设计语言
作者
Bianca da Costa Bernardo Port,Gabriela Schneider Rauber,Débora Fretes Argenta,Mihails Arhangelskis,Carlos Eduardo Maduro de Campos,Adaı́lton J. Bortoluzzi,Thiago Caon
出处
期刊:Molecular Pharmaceutics [American Chemical Society]
卷期号:19 (7): 2164-2174 被引量:1
标识
DOI:10.1021/acs.molpharmaceut.2c00031
摘要

Topical formulations composed of API-pure crystals have been increasingly studied, especially in regards to the impact of particle size in penetration efficiency. Less attention, however, has been devoted to the solid-state properties of drugs delivered to the skin. In this study, we address the effect of formulation composition on the crystal form existing in topical products. Dapsone (DAP) gel formulations were prepared by mixing an organic solution containing DAP with an aqueous solution containing polymers and preservatives. The organic solvent was chosen as ethoxydiglycol (DEGEE), polyethylene glycol (PEG), or 1-methyl-2-pirrolidone (MPR) to assess the impact of composition on DAP crystal form. Such solvent variations resulted in different particulate matter. In terms of crystalline nature, the presence of DEGEE in formulations induced the crystallization of DAP hydrate, while PEG cocrystal and a mixture of hydrate and MPR solvate crystallized from the same amounts of PEG and MPR, respectively. Microscopic analysis of the gels showed heterogeneous particles with different characteristics. The behavior of gels after application to the skin was also tested. Interestingly, the different formulations seemed to accumulate in different regions of the skin. This could be the result of the effect of vehicle composition/excipients on the characteristics of the skin, such as hydration. The site-specific accumulation, however, was more pronounced in crystal-loaded gels as opposed to blank formulations. These results indicate that future studies should consider the effect of formulation composition on the API crystal form landscape as part of the strategies used to successfully target drug delivery to the skin.
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