靶向口腔黏膜:新出现的药物传递平台和糖胺聚糖的治疗潜力。

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Bruno Špiljak, Maja Somogyi Škoc, Iva Rezić Meštrović, Krešimir Bašić, Iva Bando, Ivana Šutej
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引用次数: 0

摘要

口腔粘膜靶向给药系统(DDS)的研究正在迅速发展,越来越重视提高生物利用度和精确靶向,同时克服口腔环境独特的解剖和生理障碍。尽管取得了相当大的进展,但酶降解、有限的粘膜渗透和溶解度问题等挑战仍然阻碍着治疗的成功。最近的进展集中在创新配方策略上,包括纳米颗粒和仿生系统,以提高给药效率和全身吸收。同时,智能和刺激反应材料正在出现,提供动态的,环境敏感的药物释放概况。一个特别有前途的领域涉及到糖胺聚糖的应用,这是一类天然衍生的多糖,具有良好的生物相容性、粘接性能和水凝胶形成能力。这些材料不仅增加了药物在粘膜部位的停留时间,而且还实现了控制释放动力学,从而改善了治疗效果。然而,关键的研究空白仍然存在:标准化,临床意义的黏附/渗透测定和强大的体内外相关性仍然缺乏;GAGs的长期稳定性、批次一致性和明确的监管分类(药物、器械或组合)继续阻碍扩大和转化。以患者为中心的性能——适口性、口感、谨慎的可穿戴性——以及与标准护理相比的头对头试验,也需要系统的评估来指导采用。总的来说,基于gag的膜、水凝胶和纳米工程载体的进步使得口腔粘膜给药成为精确局部和选择性全身治疗的现实近期选择,前提是该领域解决了标准化、稳定性、监管和可用性障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Targeting the Oral Mucosa: Emerging Drug Delivery Platforms and the Therapeutic Potential of Glycosaminoglycans.

Targeting the Oral Mucosa: Emerging Drug Delivery Platforms and the Therapeutic Potential of Glycosaminoglycans.

Targeting the Oral Mucosa: Emerging Drug Delivery Platforms and the Therapeutic Potential of Glycosaminoglycans.

Targeting the Oral Mucosa: Emerging Drug Delivery Platforms and the Therapeutic Potential of Glycosaminoglycans.

Research into oral mucosa-targeted drug delivery systems (DDS) is rapidly evolving, with growing emphasis on enhancing bioavailability and precision targeting while overcoming the unique anatomical and physiological barriers of the oral environment. Despite considerable progress, challenges such as enzymatic degradation, limited mucosal penetration, and solubility issues continue to hinder therapeutic success. Recent advancements have focused on innovative formulation strategies-including nanoparticulate and biomimetic systems-to improve delivery efficiency and systemic absorption. Simultaneously, smart and stimuli-responsive materials are emerging, offering dynamic, environment-sensitive drug release profiles. One particularly promising area involves the application of glycosaminoglycans, a class of naturally derived polysaccharides with excellent biocompatibility, mucoadhesive properties, and hydrogel-forming capacity. These materials not only enhance drug residence time at the mucosal site but also enable controlled release kinetics, thereby improving therapeutic outcomes. However, critical research gaps remain: standardized, clinically meaningful mucoadhesion/permeation assays and robust in vitro-in vivo correlations are still lacking; long-term stability, batch consistency of GAGs, and clear regulatory classification (drug, device, or combination) continue to impede scale-up and translation. Patient-centric performance-palatability, mouthfeel, discreet wearability-and head-to-head trials versus standard care also require systematic evaluation to guide adoption. Overall, converging advances in GAG-based films, hydrogels, and nanoengineered carriers position oral mucosal delivery as a realistic near-term option for precision local and selected systemic therapies-provided the field resolves standardization, stability, regulatory, and usability hurdles.

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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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