کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2480066 1556164 2016 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The molecular assembly of the ionic liquid/aliphatic carboxylic acid/aliphatic amine as effective and safety transdermal permeation enhancers
ترجمه فارسی عنوان
ترکیب مولکولی متیل آلیفاتیک / آمین کربوکسیلیک اسید / آلیفاتیک یونی به عنوان افزایش دهنده های نفوذ موثر و ایمنی ترانسدورال
کلمات کلیدی
ترکیبات آمفیکاتیک، طیف سنجی مادون قرمز، ارزیابی آسیب، مایعات یونی، مونتاژ مولکولی، تقویت کننده نفوذ پوست
موضوعات مرتبط
علوم پزشکی و سلامت داروسازی، سم شناسی و علوم دارویی اکتشاف دارویی
چکیده انگلیسی

In spite of numerous advantages, transdermal drug delivery systems are unfeasible for most drugs because of the barrier effect of the stratum corneum. Ionic liquids were recently used to enhance transdermal drug delivery by improving drug solubility. In the present study, safe and effective ionic liquids for transdermal absorption were obtained as salts generated by a neutralization reaction between highly biocompatible aliphatic carboxylic acids (octanoic acid or isostearic acid) and aliphatic amines (diisopropanolamine or triisopropanolamine) (Medrx Co., Ltd., 2009). The mechanism of skin permeability enhancement by ionic liquids was investigated by hydrophilic phenol red and hydrophobic tulobuterol. Further, the skin permeation enhancing effect was remarkably superior in the acid excess state rather than the neutralization state. Infrared absorption spectrum analysis confirmed that ionic liquids/aliphatic carboxylic acid/aliphatic amine are coexisting at all mixing states. In the acid excess state, ionic liquids interact with aliphatic carboxylic acids via hydrogen bonds. Thus, the skin permeation enhancing effect is not caused by the ionic liquid alone. The “liquid salt mixture,” referred to as a complex of ingredients coexisting with ionic liquids, forms a molecular assembly incorporating hydrophilic drug. This molecular assembly was considered an effective and safety enhancer of transdermal drug permeation.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Journal of Pharmaceutical Sciences - Volume 86, 30 April 2016, Pages 75–83
نویسندگان
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