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多功能纳米载体用于淋巴结转移的靶向药物递送和诊断应用:近期趋势和未来展望的综述。

Multifunctional nanocarriers for targeted drug delivery and diagnostic applications of lymph nodes metastasis: a review of recent trends and future perspectives.

机构信息

Department of Surgical Oncology, Hangzhou Cancer Hospital, Hangzhou, 310002, Zhejiang Province, China.

Department of Laboratory Medicine, Tiantai People's Hospital, Taizhou, 317200, Zhejiang Province, China.

出版信息

J Nanobiotechnology. 2023 Aug 2;21(1):247. doi: 10.1186/s12951-023-01990-4.


DOI:10.1186/s12951-023-01990-4
PMID:37528366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10394815/
Abstract

Lymph node metastasis is a frequent occurrence in a variety of tumour forms and poses an enormous challenge to cancer treatment. This process is critical to the development of the disease and is frequently linked to a poor prognosis. Over 90% of cancerous cells move through lymph nodes, making them important entry routes for the spread of cancer cells. The prognosis of cancer patients is significantly impacted by lymph node metastases, which also affects treatment choices. Targeting lymph node metastases presents numerous difficulties for conventional medication delivery techniques. It is still very difficult to selectively target cancer cells in lymph nodes without risking injury to healthy organs and unforeseen consequences. Additionally, systemic delivery of drugs is hampered by the slow flow rate of lymphatic vessels. Chemotherapeutic medicines' poor solubility and stability further reduce their effectiveness when taken orally. Additionally, the extracellular matrix that surrounds lymph node tumours is extensive, which makes it difficult for conventional pharmaceutical delivery systems to reach cancer cells. The development of nanocarriers for precise drug delivery to LNs has attracted a lot of interest to overcome these obstacles. Most solid tumours first spread through the lymphatic system, hence effective drug administration to these tissues is essential for better therapeutic results. Nanocarriers have several benefits, including the capacity to pass through barriers like blood-brain barriers and membranes to reach the lymphatic system. High medication dosages can be enclosed thanks to the physicochemical characteristics of nanocarriers, such as their higher surface-to-volume ratio. Additionally, ligands, antibodies, polymers, or biological molecules can be attached to nanocarrier surfaces to change their properties, allowing for the targeted delivery of lymph node epithelial cells. This use of nanocarriers for drug delivery maximizes on-target effects and related adverse effects while improving the effectiveness of medication delivery to target locations. More research and development in this field is needed to optimize nanocarrier design, increase targeting capabilities, and expand clinical applications for better cancer care.

摘要

淋巴结转移是多种肿瘤形式中常见的现象,对癌症治疗构成了巨大挑战。这个过程对疾病的发展至关重要,而且常常与预后不良有关。超过 90%的癌细胞通过淋巴结转移,因此淋巴结是癌细胞扩散的重要入口途径。淋巴结转移显著影响癌症患者的预后,也影响治疗选择。针对淋巴结转移存在许多困难,传统的药物输送技术很难实现。在不损害健康器官和出现不可预见后果的情况下,选择性地针对淋巴结中的癌细胞仍然非常困难。此外,由于淋巴管的流速较慢,药物的全身输送受到阻碍。化疗药物的溶解度和稳定性差,进一步降低了口服药物的疗效。此外,淋巴结肿瘤周围的细胞外基质广泛,这使得传统的药物输送系统难以到达癌细胞。为了克服这些障碍,开发用于精确向 LNs 输送药物的纳米载体引起了广泛关注。大多数实体瘤首先通过淋巴系统扩散,因此有效地向这些组织给药对于获得更好的治疗效果至关重要。纳米载体具有多种优势,包括能够穿透血脑屏障和膜等屏障到达淋巴系统。由于纳米载体的物理化学特性,如更高的表面积与体积比,可以包含更高的药物剂量。此外,可以将配体、抗体、聚合物或生物分子附着在纳米载体表面来改变其性质,从而实现对淋巴结上皮细胞的靶向输送。这种使用纳米载体进行药物输送最大限度地提高了靶向效果和相关的不良反应,同时提高了药物输送到目标部位的有效性。为了更好地进行癌症护理,需要在该领域进行更多的研究和开发,以优化纳米载体设计、提高靶向能力,并扩大临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65f/10394815/8cdebc88415f/12951_2023_1990_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65f/10394815/9472aaa6e2c8/12951_2023_1990_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65f/10394815/f2d37efca753/12951_2023_1990_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65f/10394815/8cdebc88415f/12951_2023_1990_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65f/10394815/9472aaa6e2c8/12951_2023_1990_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65f/10394815/f2d37efca753/12951_2023_1990_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65f/10394815/8cdebc88415f/12951_2023_1990_Fig3_HTML.jpg

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本文引用的文献

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