Advances in the delivery of anticancer drugs by nanoparticles and chitosan-based nanoparticles

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics: X Pub Date : 2024-08-28 DOI:10.1016/j.ijpx.2024.100281
Jarmila Prieložná , Veronika Mikušová , Peter Mikuš
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Abstract

Cancer is the leading cause of death globally, and conventional treatments have limited efficacy with severe side effects. The use of nanotechnology has the potential to reduce the side effects of drugs by creating efficient and controlled anticancer drug delivery systems. Nanoparticles (NPs) used as drug carriers offer several advantages, including enhanced drug protection, biodistribution, selectivity and, pharmacokinetics. Therefore, this review is devoted to various organic (lipid, polymeric) as well as inorganic nanoparticles based on different building units and providing a wide range of potent anticancer drug delivery systems. Within these nanoparticulate systems, chitosan (CS)-based NPs are discussed with particular emphasis due to the unique properties of CS and its derivatives including non-toxicity, biodegradability, mucoadhesivity, and tunable physico-chemical as well as biological properties allowing their alteration to specifically target cancer cells. In the context of streamlining the nanoparticulate drug delivery systems (DDS), innovative nanoplatform-based cancer therapy pathways involving passive and active targeting as well as stimuli-responsive DDS enhancing overall orthogonality of developed NP-DDS towards the target are included. The most up-to-date information on delivering anti-cancer drugs using modern dosage forms based on various nanoparticulate systems and, specifically, CSNPs, are summarised and evaluated concerning their benefits, limitations, and advanced applications.

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利用纳米颗粒和壳聚糖基纳米颗粒递送抗癌药物的研究进展
癌症是导致全球死亡的主要原因,而传统疗法疗效有限,副作用严重。使用纳米技术有可能通过创建高效、可控的抗癌药物输送系统来减少药物的副作用。纳米颗粒(NPs)作为药物载体具有多种优势,包括增强药物保护、生物分布、选择性和药代动力学。因此,本综述将专门讨论基于不同构建单元的各种有机(脂质、聚合物)和无机纳米颗粒,它们提供了多种有效的抗癌药物递送系统。在这些纳米颗粒系统中,重点讨论了基于壳聚糖(CS)的纳米粒子,因为壳聚糖及其衍生物具有独特的特性,包括无毒性、生物降解性、粘附性、可调整的物理化学和生物特性,允许改变它们以特异性靶向癌细胞。在简化纳米颗粒给药系统(DDS)方面,包括基于纳米平台的创新癌症治疗途径,涉及被动和主动靶向以及刺激响应式 DDS,增强了所开发的 NP-DDS 对靶点的整体正交性。总结并评估了基于各种纳米颗粒系统(特别是 CSNPs)的现代剂型用于递送抗癌药物的最新信息,包括其优点、局限性和先进应用。
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来源期刊
International Journal of Pharmaceutics: X
International Journal of Pharmaceutics: X Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.60
自引率
0.00%
发文量
32
审稿时长
24 days
期刊介绍: International Journal of Pharmaceutics: X offers authors with high-quality research who want to publish in a gold open access journal the opportunity to make their work immediately, permanently, and freely accessible. International Journal of Pharmaceutics: X authors will pay an article publishing charge (APC), have a choice of license options, and retain copyright. Please check the APC here. The journal is indexed in SCOPUS, PUBMED, PMC and DOAJ. The International Journal of Pharmaceutics is the second most cited journal in the "Pharmacy & Pharmacology" category out of 358 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
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