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基于顺铂的脂质体纳米载体在肺癌治疗中的药物递送:最新进展和未来展望。

Cisplatin-based Liposomal Nanocarriers for Drug Delivery in Lung Cancer Therapy: Recent Progress and Future Outlooks.

机构信息

Nanotechnology Department, School of Advanced Technologies, Iran University of Science and Technology, Tehran, Iran.

Australasian Nanoscience and Nanotechnology Initiative (ANNI), Monash University LPO, Clayton, VIC 3168, Australia.

出版信息

Curr Pharm Des. 2024;30(36):2850-2881. doi: 10.2174/0113816128304923240704113319.

DOI:10.2174/0113816128304923240704113319
PMID:39051580
Abstract

In order to improve the treatment of lung cancer, this paper looks at the development of cisplatinbased liposomal nanocarriers. It focuses on addressing the drawbacks of conventional cisplatin therapy, including systemic toxicity, inadequate tumor targeting, and drug resistance. Liposomes, or spherical lipid vesicles, offer a potentially effective way to encapsulate cisplatin, enhancing its transport and minimizing harmful effects on healthy tissues. The article discusses many liposomal cisplatin formulations, including pH-sensitive liposomes, sterically stabilized liposomes, and liposomes coupled with specific ligands like EGFR antibodies. These novel formulations show promise in reducing cisplatin resistance, optimizing pharmacokinetics, and boosting therapeutic results in the two in vitro and in vivo models. They also take advantage of the Enhanced Permeability and Retention (EPR) effect in the direction of improved tumor accumulation. The study highlights the need for more investigation to move these liposomal formulations from experimental to clinical settings, highlighting their potential to offer less harmful and more effective cancer therapy alternatives.

摘要

为了改善肺癌的治疗效果,本文着眼于顺铂类脂质体纳米载体的发展。它专注于解决传统顺铂治疗的缺点,包括全身毒性、肿瘤靶向不足和耐药性。脂质体或球形脂质囊泡提供了一种封装顺铂的有效方法,可增强其输送并最大程度地减少对健康组织的有害影响。本文讨论了许多顺铂脂质体制剂,包括 pH 敏感脂质体、空间稳定脂质体和与特定配体(如 EGFR 抗体)偶联的脂质体。这些新型制剂在降低顺铂耐药性、优化药代动力学和提高两种体外和体内模型的治疗效果方面显示出前景。它们还利用了增强的通透性和保留(EPR)效应,以促进肿瘤的积累。该研究强调需要进一步研究,将这些脂质体制剂从实验环境推向临床环境,突出其提供毒性更低、更有效的癌症治疗替代方案的潜力。

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本文引用的文献

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Molecular targeted therapies for cutaneous squamous cell carcinoma: recent developments and clinical implications.皮肤鳞状细胞癌的分子靶向治疗:最新进展与临床意义
EXCLI J. 2024 Feb 27;23:300-334. doi: 10.17179/excli2023-6489. eCollection 2024.
2
Folate-modified liposomes mediate the co-delivery of cisplatin with miR-219a-5p for the targeted treatment of cisplatin-resistant lung cancer.叶酸修饰的脂质体介导顺铂与 miR-219a-5p 的共递送,用于顺铂耐药肺癌的靶向治疗。
BMC Pulm Med. 2024 Apr 1;24(1):159. doi: 10.1186/s12890-024-02938-6.
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Light-Responsive and Dual-Targeting Liposomes: From Mechanisms to Targeting Strategies.
iScience. 2024 Dec 26;28(1):111704. doi: 10.1016/j.isci.2024.111704. eCollection 2025 Jan 17.
光响应性和双靶向脂质体:从机制到靶向策略。
Molecules. 2024 Jan 30;29(3):636. doi: 10.3390/molecules29030636.
4
Exploring modified chitosan-based gene delivery technologies for therapeutic advancements.探索基于改性壳聚糖的基因传递技术以推动治疗学进展。
Int J Biol Macromol. 2024 Mar;260(Pt 2):129581. doi: 10.1016/j.ijbiomac.2024.129581. Epub 2024 Jan 22.
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Nanomaterials-assisted photothermal therapy for breast cancer: State-of-the-art advances and future perspectives.纳米材料辅助光热疗法治疗乳腺癌:最新进展与未来展望。
Photodiagnosis Photodyn Ther. 2024 Feb;45:103959. doi: 10.1016/j.pdpdt.2023.103959. Epub 2024 Jan 14.
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Co-encapsulation of fisetin and cisplatin into liposomes: Stability considerations and in vivo efficacy on lung cancer animal model.将非瑟酮和顺铂共同包封于脂质体中:稳定性考虑因素及对肺癌动物模型的体内疗效。
Int J Pharm. 2024 Feb 15;651:123744. doi: 10.1016/j.ijpharm.2023.123744. Epub 2023 Dec 23.
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