Microdermabrasion with Calcium Hydrogen Phosphate for Enhancing Skin Permeation of Lidocaine-tetracaine Eutectic Microemulsion Gel.

IF 4.3 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Ying Chen, Yuye Yang, Jin Su, Yuanxin Ji, Bingning Liu, Yan Chen, Yihan Peng, Xinghuang Cai, Huixian Zhang, Mei Dong, Qingsong Wang, Chunmeng Sun, Zhigui Su
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Abstract

Background: Transdermal drug delivery (TDD) offers a convenient administration for treating local or systemic diseases. However, the dense "brick-mortar" structure of the stratum corneum hinders the skin permeation of most of bioactive molecules, which highly constrained the application of TDD.

Methods: This study analyzed stratum corneum disruption and enhanced permeation by gently rubbing calcium hydrogen phosphate (Chp) particles of varying sizes on skin. Enhanced anesthetic efficacy of Chp-containing microemulsion gel (MG) loaded with lidocaine-tetracaine eutectic was evaluated in guinea pigs using a needle-prick model.

Results: Using Chp as dermabrasion particle could effectively disrupt the barrier of stratum corneum after applying gently rubbing on the skin, which resulted in increasing skin permeation of both FITC, FITC-Dextran4000 and MG loaded with lidocaine-tetracaine eutectic. The enhanced skin permeation depended not only on the increase of particle size and amount of Chp in the MG, but also on the increase of rubbing pressure and duration after being applied to the skin, finally shortening the onset time and improving the efficacy of local anesthetics.

Conclusions: The incorporation of Chp into the topical formulation, followed by rubbing them on the skin with appropriate pressure and a certain duration, can significantly disrupt the stratum corneum, enhance drug permeation through the skin, and shorten the onset time of local anesthetics. This study provided a potential strategy for improving the skin permeation with well tolerance, which could be further used to expand the range of bioactive molecules for TDD.

磷酸氢钙微磨皮增强利多卡因-丁卡因共晶微乳凝胶的皮肤渗透性。
背景:经皮给药(TDD)为局部或全身性疾病的治疗提供了方便的给药方法。然而,角质层致密的“砖砂浆”结构阻碍了大多数生物活性分子的皮肤渗透,这极大地限制了TDD的应用。方法:本研究通过在皮肤上轻轻摩擦不同大小的磷酸氢钙颗粒,分析其对角质层的破坏和增强渗透的作用。在豚鼠针刺模型中,研究了载利多卡因-丁卡因共混剂的chp微乳凝胶(MG)增强麻醉效果。结果:Chp作为磨皮颗粒轻揉皮肤后,可有效破坏角质层的屏障,使FITC、FITC- dextran4000和负载利多卡因共晶MG的皮肤渗透性均增加。皮肤渗透的增强不仅取决于MG中Chp颗粒大小和用量的增加,还取决于敷于皮肤后摩擦压力和时间的增加,最终缩短了起效时间,提高了局麻药的疗效。结论:将Chp加入外用制剂中,以适当的压力和一定的时间在皮肤上摩擦,可明显破坏角质层,增强药物在皮肤中的渗透,缩短局麻药起效时间。本研究提供了一种具有良好耐受性的改善皮肤渗透的潜在策略,可进一步用于扩大TDD生物活性分子的范围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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