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经皮给药系统:增强皮肤渗透性的方法及其评价

Transdermal Drug Delivery Systems: Methods for Enhancing Skin Permeability and Their Evaluation.

作者信息

Bakhrushina Elena O, Shumkova Marina M, Avdonina Yana V, Ananian Arsen A, Babazadeh Mina, Pouya Ghazaleh, Grikh Viktoria V, Zubareva Irina M, Kosenkova Svetlana I, Krasnyuk Ivan I, Krasnyuk Ivan I

机构信息

A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow 119048, Russia.

出版信息

Pharmaceutics. 2025 Jul 20;17(7):936. doi: 10.3390/pharmaceutics17070936.


DOI:10.3390/pharmaceutics17070936
PMID:40733144
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12300492/
Abstract

Transdermal drug delivery (TDD) is an increasingly important non-invasive method for administering active pharmaceutical ingredients (APIs) through the skin barrier, offering advantages such as improved therapeutic efficacy and reduced systemic side effects. As demand increases for patient-friendly and minimally invasive treatment options, TDD has attracted substantial attention in research and clinical practice. This review summarizes recent advances enhancing skin permeability through chemical enhancers (e.g., ethanol, fatty acids, terpenes), physical (e.g., iontophoresis, microneedles, sonophoresis), and nanotechnological methods (e.g., liposomes, ethosomes, solid lipid nanoparticles, and transferosomes). A comprehensive literature analysis, including scientific publications, regulatory guidelines, and patents, was conducted to identify innovative methods and materials used to overcome the barrier properties of the stratum corneum. Special emphasis was placed on in vitro, ex vivo, and in vivo evaluation techniques for such as Franz diffusion cells for assessing drug permeation and skin interactions. The findings highlight the importance of active physical methods, passive nanostructured systems, and chemical penetration enhancers. In conclusion, integrating multiple analytical techniques is essential for the rational design and optimization of effective transdermal drug delivery systems.

摘要

经皮给药(TDD)是一种日益重要的非侵入性给药方法,可通过皮肤屏障输送活性药物成分(API),具有提高治疗效果和减少全身副作用等优点。随着对患者友好型和微创治疗方案的需求增加,经皮给药在研究和临床实践中受到了广泛关注。本综述总结了通过化学促进剂(如乙醇、脂肪酸、萜类化合物)、物理方法(如离子导入、微针、超声导入)和纳米技术方法(如脂质体、醇质体、固体脂质纳米粒和传递体)提高皮肤渗透性的最新进展。通过对科学出版物、监管指南和专利等进行全面的文献分析,以确定用于克服角质层屏障特性的创新方法和材料。特别强调了体外、离体和体内评估技术,如用于评估药物渗透和皮肤相互作用的弗兰兹扩散池。研究结果突出了主动物理方法、被动纳米结构系统和化学渗透促进剂的重要性。总之,整合多种分析技术对于合理设计和优化有效的经皮给药系统至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c49a/12300492/19d111560d23/pharmaceutics-17-00936-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c49a/12300492/30d9f195be06/pharmaceutics-17-00936-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c49a/12300492/b41632d54558/pharmaceutics-17-00936-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c49a/12300492/19d111560d23/pharmaceutics-17-00936-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c49a/12300492/30d9f195be06/pharmaceutics-17-00936-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c49a/12300492/b41632d54558/pharmaceutics-17-00936-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c49a/12300492/19d111560d23/pharmaceutics-17-00936-g003.jpg

相似文献

[1]
Transdermal Drug Delivery Systems: Methods for Enhancing Skin Permeability and Their Evaluation.

Pharmaceutics. 2025-7-20

[2]
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Curr Drug Deliv. 2017

[3]
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[4]
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[5]
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[6]
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[7]
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Ther Deliv. 2025-2

[8]
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[9]
4'-OH as the Action Site of Lipids and MRP1 for Enhanced Transdermal Delivery of Flavonoids.

ACS Appl Mater Interfaces. 2023-3-22

[10]
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Curr Opin Pharmacol. 2025-8

本文引用的文献

[1]
Advances in Transdermal Drug Delivery Systems and Clinical Applications in Inflammatory Skin Diseases.

Pharmaceutics. 2025-6-6

[2]
A Novel Natural Penetration Enhancer for Transdermal Drug Delivery: In Vitro/In Vivo Evaluation and Penetration Enhancement Mechanism.

Pharmaceutics. 2025-2-14

[3]
Skin penetration enhancers: Mechanistic understanding and their selection for formulation and design.

Drug Deliv Transl Res. 2025-2-21

[4]
METTL3-modified exosomes from adipose-derived stem cells enhance the proliferation and migration of dermal fibroblasts by mediating m6A modification of CCNB1 mRNA.

Arch Dermatol Res. 2025-2-15

[5]
Drug Release and Dermal Drug Permeation Studies of Selected Commercial Benzoyl Peroxide Topical Formulations: Correlation Between Human and Porcine Skin Models.

Mol Pharm. 2025-3-3

[6]
Microneedles as transdermal drug delivery system for enhancing skin disease treatment.

Acta Pharm Sin B. 2024-12

[7]
Intratracheal Administration of Itraconazole-Loaded Hyaluronated Glycerosomes as a Promising Nanoplatform for the Treatment of Lung Cancer: Formulation, Physiochemical, and In Vivo Distribution.

Pharmaceutics. 2024-11-10

[8]
Skin Structure, Physiology, and Pathology in Topical and Transdermal Drug Delivery.

Pharmaceutics. 2024-10-31

[9]
Augmented glycerosomes as a promising approach against fungal ear infection: Optimization and microbiological, and assessments.

Int J Pharm X. 2024-10-22

[10]
Towards the understanding of the IVPT results variability-Development, verification and validation of the PBPK model of caffeine in vitro human skin permeation.

Eur J Pharm Sci. 2025-1-1

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