Natural biodegradable polymer-based microneedles for controlled drug delivery: a rational design framework and translational perspectives.

IF 2.9 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Khaled E Abuelella, Nermin M Sheta
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引用次数: 0

Abstract

Microneedle (MN) technology has emerged as a promising minimally invasive platform for transdermal drug delivery, enabling efficient transport of therapeutic agents across the stratum corneum while improving patient compliance. In recent years, natural biodegradable polymers have gained increasing attention in microneedle fabrication due to their biocompatibility, biodegradability, and functional versatility. This review provides a comprehensive overview of recent advances in natural polymer-based microneedle systems, including material selection, fabrication strategies, and mechanisms of controlled drug release. Importantly, beyond conventional descriptive analysis, this work introduces a rational design framework that systematically integrates therapeutic objectives, polymer properties, mechanical performance, and release kinetics to guide the development of optimized microneedle platforms. The review further addresses key translational challenges, including mechanical limitations, manufacturing scalability, stability concerns, and regulatory considerations. In addition, emerging trends such as stimuli-responsive systems, nanocarrier integration, and personalized drug delivery approaches are discussed. Notably, data-driven strategies, including artificial intelligence (AI) and machine learning, are highlighted as promising tools for predicting system performance, optimizing formulation parameters, and accelerating the development of next-generation microneedle-based drug delivery systems. Overall, this work shifts the paradigm from empirical formulation toward a predictive, engineering-driven design strategy, offering valuable insights to advance the clinical translation of smart microneedle technologies.

天然可生物降解聚合物微针控制药物输送:一个合理的设计框架和翻译的观点。
微针(MN)技术已经成为一种有前途的经皮给药的微创平台,使治疗药物能够有效地穿过角质层,同时提高患者的依从性。近年来,天然生物可降解聚合物因其生物相容性、生物可降解性和功能多功能性而在微针制造中受到越来越多的关注。本文综述了天然聚合物微针系统的最新进展,包括材料选择、制造策略和药物控释机制。重要的是,在传统的描述性分析之外,这项工作引入了一个合理的设计框架,该框架系统地集成了治疗目标、聚合物特性、机械性能和释放动力学,以指导优化微针平台的开发。该综述进一步解决了关键的转化挑战,包括机械限制、制造可扩展性、稳定性问题和监管考虑。此外,还讨论了刺激反应系统、纳米载体整合和个性化给药方法等新兴趋势。值得注意的是,包括人工智能(AI)和机器学习在内的数据驱动策略被强调为预测系统性能、优化配方参数和加速下一代微针给药系统开发的有前途的工具。总的来说,这项工作将范式从经验公式转向预测,工程驱动的设计策略,为推进智能微针技术的临床转化提供了有价值的见解。
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
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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