Challenges and Strategies for Topical and Transdermal Delivery of Bioactive Peptides.

IF 3 4区 医学 Q2 PHARMACOLOGY & PHARMACY Critical Reviews in Therapeutic Drug Carrier Systems Pub Date : 2022-01-01 DOI:10.1615/CritRevTherDrugCarrierSyst.2021038141
Antonio Jiménez-Rodríguez, Daniela Guardado-Félix, Marilena Antunes-Ricardo
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引用次数: 7

Abstract

Bioactive peptides have gained the attention and interest of researchers and the industry for their therapeutic effects and high specificity, thus reducing the risks of side effects and making them an attractive alternatives in developing new biopharmaceuticals or cosmeceuticals. Nevertheless, their incorporation into formulations and administration presents challenges such as low stability under different storage conditions and gastrointestinal degradation after oral delivery. Likewise, the parenteral route is an invasive method that is painful and therefore reduces patient compliance. Topical delivery of bioactive peptides is a painless noninvasive alternative to reduce peptide degradation, exert local effects in the applied area, and improve patient compliance. In this review, we discuss the physicochemical properties of peptides and the mechanisms involved in their degradation. In addition, the most important aspects of skin structure and skin permeation routes, and the requirements for topical and transdermal drug delivery are also discussed in this article. Finally, nanocarrier development advances for the topical delivery of peptides (water-in-oil-in-water emulsions, microemulsions, nanoparticles, solid lipid nanoparticles, liposomes, niosomes, and microneedles) and other strategies, such as metal complexation, cell-penetrating peptides, and synthetic modification, are also reviewed. All these topics consider the perspective of their effect to improve skin permeability to peptides and their stability over time during storage.

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生物活性肽局部和透皮递送的挑战和策略。
生物活性肽因其具有良好的治疗效果和高特异性,降低了副作用的风险,成为开发新型生物制药或药妆品的一个有吸引力的替代方案,已引起研究人员和业界的关注和兴趣。然而,将其纳入制剂和给药面临挑战,如在不同储存条件下的低稳定性和口服给药后的胃肠道降解。同样,肠外途径是一种侵入性方法,是痛苦的,因此降低了患者的依从性。生物活性肽的局部递送是一种无痛、无创的替代方法,可以减少肽的降解,在应用区域发挥局部作用,提高患者的依从性。在这篇综述中,我们讨论了多肽的物理化学性质及其降解机制。此外,本文还讨论了最重要的皮肤结构和皮肤渗透途径,以及局部和透皮给药的要求。最后,综述了用于局部递送多肽的纳米载体的发展进展(水包油乳液、微乳液、纳米颗粒、固体脂质纳米颗粒、脂质体、乳质体和微针)以及其他策略,如金属络合、细胞穿透肽和合成修饰。所有这些主题都考虑了它们对改善皮肤对肽的渗透性及其在储存期间的稳定性的影响。
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来源期刊
CiteScore
5.50
自引率
18.50%
发文量
27
审稿时长
>12 weeks
期刊介绍: Therapeutic uses of a variety of drug carrier systems have significant impact on the treatment and potential cure of many chronic diseases, including cancer, diabetes mellitus, psoriasis, parkinsons, Alzheimer, rheumatoid arthritis, HIV infection, infectious diseases, asthma, and drug addiction. Scientific efforts in these areas are multidisciplinary, involving the physical, biological, medical, pharmaceutical, biological materials, and engineering fields. Articles concerning this field appear in a wide variety of journals. With the vast increase in the number of articles and the tendency to fragment science, it becomes increasingly difficult to keep abreast of the literature and to sort out and evaluate the importance and reliability of the data, especially when proprietary considerations are involved. Abstracts and noncritical articles often do not provide a sufficiently reliable basis for proper assessment of a given field without the additional perusal of the original literature. This journal bridges this gap by publishing authoritative, objective, comprehensive multidisciplinary critical review papers with emphasis on formulation and delivery systems. Both invited and contributed articles are subject to peer review.
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