基于纳米颗粒的银屑病局部给药系统的最新进展。

IF 3.9 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Ritwik Mitra, Dinesh Kumar Sharma, Arnab Ghosh, Sahil Senapati
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引用次数: 0

摘要

慢性自身免疫性皮肤病牛皮癣(PSO)的典型特征是皮肤细胞过度增殖,在皮肤表面形成厚厚的、红色和鳞状斑块。由于瘙痒和疼痛,这些斑块可能会让患有这种疾病的人感到不舒服。牛皮癣的治疗方法是减轻炎症,缓解症状,减缓过多皮肤细胞的增殖。银屑病的传统治疗方法,包括局部皮质类固醇、全身免疫抑制剂和生物制剂,经常面临患者依从性差、全身毒性、皮肤渗透有限和药物吸收效率低下等问题。然而,纳米技术驱动的药物传递系统通过增强药代动力学和药效学特性提供了显著的改进。这些系统确保靶向和持续的药物释放,同时最大限度地减少脱靶效应,代表了一种有前途的PSO治疗新方法。本文讨论了各种纳米颗粒药物载体,已开发,以提高透皮和局部给药。这些载体包括脂质体、乳质体、转移体、脂质体、树状大分子、纳米乳液、固体脂质纳米颗粒、纳米凝胶、银纳米颗粒、金纳米颗粒、纳米海绵、纳米胶囊和纳米晶体。这些纳米载体改善了药物在角质层的渗透,促进了表皮和真皮层中药物库的形成,并使药物扩散得到控制。这延长了治疗作用,同时减少了全身暴露。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent advancements in nanoparticle-based topical drug delivery systems for psoriasis treatment.

Chronic autoimmune skin disorder known as psoriasis (PSO) is typified by the excessive proliferation of skin cells, which develops thick, red and scaly patches on the skin's surface. These patches may be uncomfortable for people with this illness due to their itching and soreness. Treatments for psoriasis try to lessen inflammation, ease symptoms and slow the proliferation of too many skin cells. Traditional treatment methods for psoriasis, including topical corticosteroids, systemic immunosuppressant and biologics, often struggle with issues like poor patient adherence, systemic toxicity, limited skin penetration and inefficient drug absorption. However, nanotechnology-driven drug delivery systems offer a significant improvement by enhancing pharmacokinetic and pharmacodynamics properties. These systems ensure targeted and sustained drug release while minimising off-target effects, representing a promising new approach to PSO treatment. This article discusses various nano particulate drug carriers that have been developed to enhance transdermal and topical drug delivery. These carriers include liposomes, niosomes, transfersomes, ethosomes, dendrimers, nanoemulsions, solid lipid nanoparticles, nanogels, silver nanoparticles, gold nanoparticles, nanosponges, nanocapsules and nanocrystals. These nanocarriers improve the permeation of drugs across the stratum corneum, facilitate the formation of depots in the epidermis and dermis and enable controlled drug diffusion. This prolongs therapeutic action while reducing systemic exposure.

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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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