Synthetic and Natural Polymeric Drug Delivery Systems - A Comprehensive Overview of Polycaprolactone and Glucan Particles

IF 0.5 Q4 ENGINEERING, BIOMEDICAL Journal of Biomimetics, Biomaterials and Biomedical Engineering Pub Date : 2023-02-14 DOI:10.4028/p-ns8294
N. Bernardi, Sandra Jesus, O. Borges
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引用次数: 1

Abstract

The small size and large surface area of nano and microparticles are interesting properties for drug delivery, hypothetically capable of overcoming some limitations of conventional therapeutic medicine and diagnostic agents. Although their features are highly influenced by the polymer characteristics, these particles are known for encapsulating high amounts of drugs, improving their stability and bioavailability and enabling different administration routes. Among synthetic polymers, polycaprolactone (PCL) nanoparticles are widely studied in drug delivery due to the polymer excellent biocompatibility and degradability and for its ability to blend with other polymers. On its turn, among natural polymers, glucan has been emerging as a promising candidate for drug delivery particularly due to structure forming abilities and its immunomodulatory effects. Under the safe-by-design approach for the development of polymeric particles, this review encloses a comprehensive summary of production methods, physicochemical characteristics and immunotoxicity profiles of PCL and glucan particles developed for drug delivery.
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合成和天然聚合物给药系统——聚己内酯和葡聚糖颗粒综述
纳米和微米颗粒的小尺寸和大表面积是药物递送的有趣特性,假设能够克服传统治疗药物和诊断剂的一些局限性。尽管它们的特性受到聚合物特性的高度影响,但众所周知,这些颗粒包封了大量药物,提高了它们的稳定性和生物利用度,并实现了不同的给药途径。在合成聚合物中,聚己内酯(PCL)纳米颗粒因其优异的生物相容性和降解性以及与其他聚合物共混的能力而在药物递送中得到广泛研究。反过来,在天然聚合物中,葡聚糖已成为一种很有前途的药物递送候选物,特别是由于其结构形成能力及其免疫调节作用。根据聚合物颗粒开发的安全设计方法,本综述全面总结了用于药物递送的PCL和葡聚糖颗粒的生产方法、物理化学特性和免疫毒性特征。
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CiteScore
1.40
自引率
14.30%
发文量
73
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