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卟啉/金属卟啉及其共轭物:一个有前景的药物递送平台。

Porphyrin/metalloporphyrin and their conjugates: a promising platform for drug delivery.

作者信息

Iqbal Dure Najaf, Khaliq Sohail, Mehdi Muhammad Zaeem, Mughram Mohammed H Al, Ahmed Mahmood

机构信息

Department of Chemistry, The University of Lahore, Lahore, 53700, Pakistan.

Department of Chemistry, Division of Science and Technology, University of Education, College Road, Lahore, Pakistan.

出版信息

Mol Divers. 2025 Jul 15. doi: 10.1007/s11030-025-11289-1.

DOI:10.1007/s11030-025-11289-1
PMID:40663246
Abstract

Porphyrins and metalloporphyrins are emerging as versatile platforms for advanced drug delivery due to their unique structural, photophysical, and coordination properties. These macrocyclic compounds, known for their chemical stability and capacity to chelate various metal ions, address critical challenges in drug delivery, including poor solubility, non-specific toxicity, and limited control over drug release. This review explores synthetic strategies for porphyrins and their metal complexes, including classical and green methods, and highlights their therapeutic applications through diverse nanocarrier systems, such as gold nanoparticles, cyclodextrin conjugates, mesoporous silica, liposomes, and metal-organic frameworks. These systems offer stimuli-responsive, targeted, and synergistic therapeutic functionalities-especially in cancer therapy-by combining chemotherapy with photodynamic or sonodynamic modalities. Despite their promise, limitations persist, including scalability issues, potential metal toxicity, and insufficient long-term biocompatibility data. The review outlines future directions, advocating for AI-driven design, sustainable synthesis, and expanded applications beyond oncology, emphasizing the need for systematic comparative studies and clinical translation efforts.

摘要

卟啉和金属卟啉因其独特的结构、光物理和配位性质,正成为先进药物递送的多功能平台。这些大环化合物以其化学稳定性和螯合各种金属离子的能力而闻名,解决了药物递送中的关键挑战,包括溶解度差、非特异性毒性和药物释放控制有限。本文综述了卟啉及其金属配合物的合成策略,包括经典方法和绿色方法,并通过多种纳米载体系统,如金纳米颗粒、环糊精缀合物、介孔二氧化硅、脂质体和金属有机框架,突出了它们的治疗应用。这些系统通过将化疗与光动力或声动力模式相结合,提供刺激响应、靶向和协同治疗功能,特别是在癌症治疗中。尽管它们前景广阔,但仍存在局限性,包括可扩展性问题、潜在的金属毒性和长期生物相容性数据不足。本文综述概述了未来的方向,倡导人工智能驱动的设计、可持续合成以及肿瘤学以外的扩展应用,强调了系统比较研究和临床转化努力的必要性。

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本文引用的文献

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Green chemistry: Modern therapies using nanocarriers for treating rare brain cancer metastasis from colon cancer.绿色化学:利用纳米载体治疗结肠癌罕见脑转移的现代疗法。
SLAS Discov. 2025 Mar;31:100213. doi: 10.1016/j.slasd.2025.100213. Epub 2025 Jan 16.
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Precisely Tailoring Molecular Structure of Doxorubicin Prodrugs to Enable Stable Nanoassembly, Rapid Activation, and Potent Antitumor Effect.精确调整阿霉素前药的分子结构以实现稳定的纳米组装、快速激活和强大的抗肿瘤效果。
Pharmaceutics. 2024 Dec 11;16(12):1582. doi: 10.3390/pharmaceutics16121582.
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Remineralization and bacterial inhibition of early enamel caries surfaces by carboxymethyl chitosan lysozyme nanogels loaded with antibacterial drugs.
载有抗菌药物的羧甲基壳聚糖溶菌酶纳米凝胶对早期釉质龋表面的再矿化及细菌抑制作用
J Dent. 2025 Jan;152:105489. doi: 10.1016/j.jdent.2024.105489. Epub 2024 Nov 29.
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Metal-organic frameworks in drug delivery: engineering versatile platforms for therapeutic applications.金属有机框架在药物递送中的应用:构建用于治疗的多功能平台
RSC Adv. 2024 Sep 23;14(41):30201-30229. doi: 10.1039/d4ra04441j. eCollection 2024 Sep 18.
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Targeting tumor-associated macrophages with nanocarrier-based treatment for breast cancer: A step toward developing innovative anti-cancer therapeutics.基于纳米载体的乳腺癌治疗靶向肿瘤相关巨噬细胞:迈向开发创新抗癌疗法的一步。
Heliyon. 2024 Aug 30;10(18):e37217. doi: 10.1016/j.heliyon.2024.e37217. eCollection 2024 Sep 30.
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Enhanced anticancer activity of silver doped zinc oxide magnetic nanocarrier loaded with sorafenib for hepatocellular carcinoma treatment.载有索拉非尼的银掺杂氧化锌磁性纳米载体增强了对肝癌的抗癌活性。
Sci Rep. 2024 Jul 5;14(1):15538. doi: 10.1038/s41598-024-65235-6.
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RSC Adv. 2024 Jul 1;14(29):20837-20855. doi: 10.1039/d4ra02277g. eCollection 2024 Jun 27.
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A single-dose, randomized, open-label, four-period, crossover equivalence trial comparing the clinical similarity of the proposed biosimilar rupatadine fumarate to reference Wystamm in healthy Chinese subjects.一项单剂量、随机、开放标签、四周期、交叉等效性试验,比较拟用生物类似药富马酸卢帕他定与参比制剂Wystamm在健康中国受试者中的临床相似性。
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Mol Pharm. 2024 Feb 5;21(2):609-621. doi: 10.1021/acs.molpharmaceut.3c00749. Epub 2024 Jan 8.