Akhtar Naseem, Mohammed Hamdoon A, Yusuf Mohammed, Al-Subaiyel Amal, Sulaiman Ghassan M, Khan Riaz A
Department of Pharmaceutics, College of Dentistry & Pharmacy, Buraydah Private Colleges, P.O. Box 31717, Buraydah 51418, Qassim, Saudi Arabia.
Department of Medicinal Chemistry & Pharmacognosy, College of Pharmacy, Qassim University, Buraydah 51452, Qassim, Saudi Arabia.
Nanomaterials (Basel). 2022 Oct 20;12(20):3686. doi: 10.3390/nano12203686.
Considerable efforts have been directed towards development of nano-structured carriers to overcome the limitations of anticancer drug, doxorubicin's, delivery to various cancer sites. The drug's severe toxicity to cardio and hepatic systems, low therapeutic outcomes, inappropriate dose-demands, metastatic and general resistance, together with non-selectivity of the drug have led to the development of superparamagnetic iron oxide nanoparticles (SPIONs)-based drug delivery modules. Nano-scale polymeric co-encapsulation of the drug, doxorubicin, with SPIONs, the SPIONs surface end-groups' cappings with small molecular entities, as well as structural modifications of the SPIONs' surface-located functional end-groups, to attach the doxorubicin, have been achieved through chemical bonding by conjugation and cross-linking of natural and synthetic polymers, attachments of SPIONs made directly to the non-polymeric entities, and attachments made through mediation of molecular-spacer as well as non-spacer mediated attachments of several types of chemical entities, together with the physico-chemical bondings of the moieties, e.g., peptides, proteins, antibodies, antigens, aptamers, glycoproteins, and enzymes, etc. to the SPIONs which are capable of targeting multiple kinds of cancerous sites, have provided stable and functional SPIONs-based nano-carriers suitable for the systemic, and in vitro deliveries, together with being suitable for other biomedical/biotechnical applications. Together with the SPIONs inherent properties, and ability to respond to magnetic resonance, fluorescence-directed, dual-module, and molecular-level tumor imaging; as well as multi-modular cancer cell targeting; magnetic-field-inducible drug-elution capacity, and the SPIONs' magnetometry-led feasibility to reach cancer action sites have made sensing, imaging, and drug and other payloads deliveries to cancerous sites for cancer treatment a viable option. Innovations in the preparation of SPIONs-based delivery modules, as biocompatible carriers; development of delivery route modalities; approaches to enhancing their drug delivery-cum-bioavailability have explicitly established the SPIONs' versatility for oncological theranostics and imaging. The current review outlines the development of various SPIONs-based nano-carriers for targeted doxorubicin delivery to different cancer sites through multiple methods, modalities, and materials, wherein high-potential nano-structured platforms have been conceptualized, developed, and tested for, both, in vivo and in vitro conditions. The current state of the knowledge in this arena have provided definite dose-control, site-specificity, stability, transport feasibility, and effective onsite drug de-loading, however, with certain limitations, and these shortcomings have opened the field for further advancements by identifying the bottlenecks, suggestive and plausible remediation, as well as more clear directions for future development.
为克服抗癌药物阿霉素向不同癌症部位递送的局限性,人们付出了巨大努力来开发纳米结构载体。该药物对心脏和肝脏系统的严重毒性、低治疗效果、不合适的剂量需求、转移性和普遍耐药性,以及药物的非选择性,促使了基于超顺磁性氧化铁纳米颗粒(SPIONs)的药物递送模块的发展。通过天然和合成聚合物的共轭和交联进行化学键合、将SPIONs直接连接到非聚合物实体上、通过分子间隔物介导的连接以及几种化学实体的非间隔物介导的连接,实现了药物阿霉素与SPIONs的纳米级聚合物共包封、用小分子实体对SPIONs表面端基进行封端,以及对SPIONs表面定位的功能端基进行结构修饰以连接阿霉素。此外,诸如肽、蛋白质、抗体、抗原、适体、糖蛋白和酶等部分与能够靶向多种癌位点的SPIONs之间的物理化学键合,提供了适用于全身和体外递送以及其他生物医学/生物技术应用的稳定且功能性的基于SPIONs的纳米载体。连同SPIONs的固有特性、对磁共振的响应能力、荧光导向的双模块和分子水平肿瘤成像能力、多模块癌细胞靶向能力、磁场诱导的药物洗脱能力,以及SPIONs的磁力测量引导下到达癌症作用部位的可行性,使得对癌症部位进行传感、成像以及药物和其他有效载荷递送以用于癌症治疗成为一个可行的选择。基于SPIONs的递送模块作为生物相容性载体在制备方面的创新、递送途径方式的发展、提高其药物递送兼生物利用度的方法,已明确确立了SPIONs在肿瘤治疗诊断学和成像方面的多功能性。本综述概述了通过多种方法、方式和材料开发的各种基于SPIONs的纳米载体,用于将阿霉素靶向递送至不同癌症部位,其中高潜力的纳米结构平台已在体内和体外条件下进行了概念化、开发和测试。该领域目前的知识状态提供了确定的剂量控制、位点特异性、稳定性、运输可行性和有效的现场药物卸载,但存在一定局限性,这些缺点通过识别瓶颈、提出暗示性和合理的补救措施以及更明确的未来发展方向,为进一步的进步开辟了领域。