疏水离子配对使水溶性药物在聚合物胶束中共载

IF 10.5 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Armin Azadkhah Shalmani , Rasika Daware , Asmaa Said Elshafei , Federica De Lorenzi , Diana Moeckel , Eva M. Buhl , Barbara Mara Klinkhammer , Peter Boor , Srinivas Banala , Alina Adams , Fabian Kiessling , Gert Storm , Josbert M. Metselaar , Alexandros Marios Sofias , Yang Shi , Twan Lammers , Quim Peña , Tarun Ojha
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引用次数: 0

摘要

高分子胶束被广泛用于疏水药物的递送。然而,一些高效且广泛使用的抗癌药物是水溶性的,这使得它们在聚合物胶束中的(共)配方复杂化,而无需对其进行化学修饰。我们在这里探索疏水离子配对,以实现水溶性蒽环类化疗药物阿霉素和血管紧张素II受体拮抗剂替米沙坦(一种临床使用的降压药,与蒽环类药物联合使用已显示出有希望的(预)临床结果)的共同递送。我们发现阿霉素和替米沙坦的疏水离子配对促进了两种药物在π电子稳定的[PEG-b-p(HPMAm-Bz)]基聚合物胶束中的共包封。阿霉素的细胞毒活性被保留,与游离药物组合相比,双重载药胶束在体内表现出更强的抗肿瘤活性,同时也表现出良好的耐受性。综上所述,这项工作为疏水离子配对作为一种有前途的配方策略来促进多药物纳米医学和药物联合治疗提供了概念证明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hydrophobic ion pairing enables co-loading of water-soluble drugs in polymeric micelles

Hydrophobic ion pairing enables co-loading of water-soluble drugs in polymeric micelles

Hydrophobic ion pairing enables co-loading of water-soluble drugs in polymeric micelles
Polymeric micelles are widely used for the delivery of hydrophobic drugs. However, several highly potent and ubiquitously used anticancer drugs are water-soluble, complicating their (co-)formulation in polymeric micelles without having to chemically modify them. We here explore hydrophobic ion pairing to enable the co-delivery of the water-soluble anthracycline chemotherapy drug doxorubicin and the angiotensin II receptor antagonist telmisartan (a clinically used antihypertensive drug that has shown promising (pre-) clinical outcomes in combination with anthracyclines). We show that hydrophobic ion pairing of doxorubicin and telmisartan promotes the co-encapsulation of both drugs in π electron-stabilized [PEG-b-p(HPMAm-Bz)]-based polymeric micelles. The cytotoxic activity of doxorubicin is retained, and the dual drug-loaded micelles display enhanced antitumor activity in vivo as compared to the combination of the free drugs, while also exhibiting good tolerability. Taken together, this work provides proof-of-concept for hydrophobic ion pairing as a promising formulation strategy to promote multidrug nanomedicine and drug combination therapy.
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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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