Surface engineering of nanocarriers with polymer coatings: materials, strategies, functional outcomes, and clinical translation.

IF 2.9 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Hassan Gamal Mostafa, Nermin M Sheta, Michael M Farag, Rania Moataz El-Dahmy, Sally A Abdel Halim
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引用次数: 0

Abstract

Polymer coating of nanocarriers has emerged as a powerful strategy to improve the performance of advanced drug delivery systems by enhancing stability, bioavailability, targeting capability, and therapeutic efficiency. Surface functionalization with biocompatible polymers can significantly modify the physicochemical and biological behavior of nanoparticles, enabling improved interaction with biological barriers and controlled drug release profiles. This review provides a comprehensive overview of the most widely used polymers for nanocarrier surface modification, including chitosan, alginate, hyaluronic acid, polyethylene glycol (PEG), methacrylate copolymers, pectin, dextran, and poly-L-lysine. The mechanisms by which these polymers enhance nanocarrier functionality are discussed in detail. In addition, the review summarizes commonly employed coating techniques such as adsorption, covalent conjugation, layer-by-layer assembly, and polymer grafting, highlighting their influence on nanoparticle characteristics and therapeutic performance. Particular emphasis is placed on the pharmaceutical outcomes associated with polymer-coated nanocarriers, including improved drug stability, enhanced bioavailability, site-specific targeting, and prolonged circulation time. Finally, the major scientific, manufacturing, safety, and regulatory challenges that limit the clinical translation of polymer-coated nanocarrier systems are critically discussed. Overall, polymer surface engineering represents a promising approach for the development of next-generation nanomedicines, although further advances in large-scale manufacturing, standardized characterization, and regulatory frameworks are required to facilitate their successful clinical and commercial implementation.

高分子涂层纳米载体的表面工程:材料、策略、功能结果和临床转化。
纳米载体的聚合物包被已成为一种强有力的策略,通过增强稳定性、生物利用度、靶向性和治疗效率来改善先进药物递送系统的性能。生物相容性聚合物的表面功能化可以显著改变纳米颗粒的物理化学和生物行为,从而改善与生物屏障的相互作用并控制药物释放。本文综述了目前应用最广泛的纳米载体表面改性聚合物,包括壳聚糖、海藻酸盐、透明质酸、聚乙二醇(PEG)、甲基丙烯酸酯共聚物、果胶、葡聚糖和聚l -赖氨酸。详细讨论了这些聚合物增强纳米载体功能的机理。此外,综述了常用的涂层技术,如吸附、共价偶联、层层组装和聚合物接枝,重点介绍了它们对纳米颗粒特性和治疗性能的影响。特别强调与聚合物包被纳米载体相关的药物结果,包括改善药物稳定性,增强生物利用度,位点特异性靶向和延长循环时间。最后,对限制聚合物包被纳米载体系统临床转化的主要科学、制造、安全和监管挑战进行了批判性讨论。总的来说,聚合物表面工程代表了下一代纳米药物开发的一种有前途的方法,尽管需要在大规模制造、标准化表征和监管框架方面取得进一步进展,以促进其成功的临床和商业实施。
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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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