由环糊精金属有机框架和环糊精纳米海绵组成的复合载体形成的水凝胶改善了姜黄素的局部递送。

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Songting Li , Meng Long , Jiaqi Li , Yongtai Zhang , Nianping Feng , Zhicheng Zhang
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引用次数: 0

摘要

姜黄素(Curcumin, CUR)在局部治疗方面具有很高的应用前景,但水不溶性是影响其药性的主要挑战之一,而传统的脂质纳米载体受载药量低、添加剂多和工艺复杂的限制。本研究构建了环糊精金属有机骨架(γ-CD-MOF)和环糊精纳米海绵(β-CDNS)复合载体,其中γ-CD-MOF的载药量为13.9%,水溶性提高267.1倍,且β-CDNS具有生物黏附性,进一步提高了药物的溶解度。复合载体(γ-CD-MOF@β-CDNS)显著改善了CUR的体外释放和透皮渗透,其有限的吸水性能和优异的生物粘附性为局部给药治疗高渗出性疾病创造了优势,可防止患处因配方中的水分反吸收而恶化病情。因此,这种复合载体为解决不溶性药物的局部递送提供了新的选择,并为CUR的临床应用提供了一个有希望的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Improved topical delivery of curcumin by hydrogels formed by composite carriers integrated with cyclodextrin metal-organic frameworks and cyclodextrin nanosponges

Improved topical delivery of curcumin by hydrogels formed by composite carriers integrated with cyclodextrin metal-organic frameworks and cyclodextrin nanosponges
Curcumin (CUR) is highly promising for topical therapeutic applications, but water-insolubility is one of the major challenges plaguing its drugability, while conventional lipid nanocarriers are limited by low drug-carrying capacity, many additives, and complex processes. In the current work, we constructed a composite carrier integrated with cyclodextrin metal-organic framework (γ-CD-MOF) and cyclodextrin nanosponge (β-CDNS), in which the γ-CD-MOF had 13.9 % drug loading and 267.1-fold increase in solubility in water for CUR, and the β-CDNS showed bioadhesion and further increasing drug solubility. The composite carrier (γ-CD-MOF@β-CDNS) significantly improved the in vitro release and transdermal permeation of CUR, and its limited water absorption properties and excellent bioadhesion create an advantage in the local administration of the drug for treating diseases with high exudate, which prevents the affected area from deteriorating the condition by counter-absorption of water from the formulation. Thus, this composite carrier contributes a new option to address the local delivery of insoluble drugs and offers a promising strategy for the clinical application of CUR.
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来源期刊
International Journal of Pharmaceutics: X
International Journal of Pharmaceutics: X Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.60
自引率
0.00%
发文量
32
审稿时长
24 days
期刊介绍: International Journal of Pharmaceutics: X offers authors with high-quality research who want to publish in a gold open access journal the opportunity to make their work immediately, permanently, and freely accessible. International Journal of Pharmaceutics: X authors will pay an article publishing charge (APC), have a choice of license options, and retain copyright. Please check the APC here. The journal is indexed in SCOPUS, PUBMED, PMC and DOAJ. The International Journal of Pharmaceutics is the second most cited journal in the "Pharmacy & Pharmacology" category out of 358 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
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