Advances in paclitaxel nanoformulations: A systematic review of in vivo therapeutic efficacy and safety enhancements

IF 10.5 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Salma Seyam, Batoul Alallam, Nurdianah Harif Fadzilah, Erazuliana Abd Kadir
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引用次数: 0

Abstract

Paclitaxel (PTX) is a broad-spectrum anticancer compound which nowadays used as the most common chemotherapeutic agent against many forms of cancer. The application of this compound is difficult because of its limited solubility, recrystallisation upon dilution, and cosolvent-induced toxicity. As a way to overcome these hindrances, nanotechnology could offer solutions by enabling specific and selective delivery of the drug to target sites while also increasing the drug half-life and lowering its toxicity. Nanoparticles (NPs) are capable of enhancing antitumour effects while demonstrating minimal toxicity in normal tissues, as well as building up in the tissue, potentially linked to enhanced permeability and retention. A trend analysis of literature on the latest advancements in nanomaterials developed for PTX delivery was conducted through a bibliometric approach. This review focused on the enhancement of PTX anticancer therapeutic effects and reduction of its toxicity by the nanoformulations (NFs). A total of 2712 papers published between 2018 and 2023 were screened on the development of nanomaterials for PTX delivery. The data were gathered from the ScienceDirect, Scopus, and PubMed databases. Sixty-six in vivo studies have been included in the qualitative synthesis assessment. Most of the studies revealed superior therapeutic efficiency of the PTX NFs compared to the free PTX treatment, as presented in the reported animal studies using rodent cancer models. These outcomes were generally accomplished through static and dynamic targeting to specific tumour environment. This review also highlights the therapeutic importance of PTX nanomaterials across different types of cancer rodent models, including data on their toxicity and safety. PTX NFs could serve as a safer and efficient alternative for conventional PTX cancer treatment by improving the drug's delivery and safety, thus providing new avenues for PTX-based cancer treatment and management.

Abstract Image

紫杉醇纳米制剂的进展:体内治疗效果和安全性增强的系统综述
紫杉醇(PTX)是一种广谱抗癌化合物,目前作为最常用的化疗药物用于治疗多种形式的癌症。该化合物的应用是困难的,因为它的溶解度有限,稀释后重结晶,以及共溶剂诱导的毒性。作为克服这些障碍的一种方法,纳米技术可以提供解决方案,使药物能够特异性和选择性地递送到目标位点,同时还可以增加药物的半衰期并降低其毒性。纳米颗粒(NPs)能够增强抗肿瘤作用,同时在正常组织中显示最小的毒性,以及在组织中积聚,可能与增强渗透性和保留性有关。通过文献计量学方法对用于PTX递送的纳米材料的最新进展进行了趋势分析。本文综述了纳米制剂增强PTX抗癌作用和降低其毒性的研究进展。2018年至2023年间发表的2712篇关于PTX递送纳米材料开发的论文被筛选。数据收集自ScienceDirect、Scopus和PubMed数据库。66项体内研究已纳入定性合成评估。大多数研究显示,与游离PTX治疗相比,PTX NFs的治疗效果更好,这在使用啮齿动物癌症模型的动物研究中得到了证实。这些结果通常通过对特定肿瘤环境的静态和动态靶向来实现。本综述还强调了PTX纳米材料在不同类型癌症啮齿动物模型中的治疗重要性,包括其毒性和安全性的数据。通过改善PTX的药物传递和安全性,PTX NFs可以作为传统PTX癌症治疗的更安全有效的替代方案,从而为PTX为基础的癌症治疗和管理提供新的途径。
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
Journal of Controlled Release
Journal of Controlled Release 医学-化学综合
CiteScore
18.50
自引率
5.60%
发文量
700
审稿时长
39 days
期刊介绍: The Journal of Controlled Release (JCR) proudly serves as the Official Journal of the Controlled Release Society and the Japan Society of Drug Delivery System. Dedicated to the broad field of delivery science and technology, JCR publishes high-quality research articles covering drug delivery systems and all facets of formulations. This includes the physicochemical and biological properties of drugs, design and characterization of dosage forms, release mechanisms, in vivo testing, and formulation research and development across pharmaceutical, diagnostic, agricultural, environmental, cosmetic, and food industries. Priority is given to manuscripts that contribute to the fundamental understanding of principles or demonstrate the advantages of novel technologies in terms of safety and efficacy over current clinical standards. JCR strives to be a leading platform for advancements in delivery science and technology.
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