• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

与无定形固体分散体相比,无水槲皮素与聚合物物理混合物具有更高的溶解度。

Superior solubility of anhydrous quercetin and polymer physical mixtures compared to amorphous solid dispersions.

作者信息

Ma Xu, Su Hong, Liu Yongming, Chen Fenghua, Xue Rongrong

机构信息

College of Chemistry and Materials Science, Fujian Normal University Fuzhou 350117 Fujian China.

School of Resources and Chemical Engineering, Sanming University Sanming 365004 Fujian China

出版信息

RSC Adv. 2025 Mar 27;15(12):9348-9358. doi: 10.1039/d4ra08796h. eCollection 2025 Mar 21.

DOI:10.1039/d4ra08796h
PMID:40151530
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11947903/
Abstract

Quercetin (QUE) is a functional flavonoid molecule with low water solubility. The study of its amorphous solid dispersions (ASDs) is still insufficient. This work reveals that the solubility of the physical mixtures of anhydrous QUE and polymers (PVP or soluplus) is better than that of the ASDs of QUE and the corresponding polymers. Gel-like phase separation occurring during the QUE ASDs dissolution process (weak in ASDs with PVP and strong in ASDs with soluplus) reduces the driving force for QUE release, which makes research on the QUE ASDs insufficient, and can be avoided in the QUE physical mixtures with polymers. Combination of metastable polymorph and polymer is a feasible strategy for improving the solubility of poorly water-soluble molecules whose ASDs encounter the gel-like phase separation.

摘要

槲皮素(QUE)是一种水溶性低的功能性黄酮类分子。对其无定形固体分散体(ASD)的研究仍不充分。这项工作表明,无水QUE与聚合物(PVP或尤特奇)物理混合物的溶解度优于QUE与相应聚合物的ASD。QUE的ASD溶解过程中发生的凝胶状相分离(在与PVP的ASD中较弱,在与尤特奇的ASD中较强)降低了QUE释放的驱动力,这使得对QUE的ASD研究不足,而在QUE与聚合物的物理混合物中可以避免这种情况。亚稳多晶型物与聚合物的组合是提高ASD遇到凝胶状相分离的难溶性分子溶解度的可行策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6511/11947903/a54451555273/d4ra08796h-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6511/11947903/464c3fda548a/d4ra08796h-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6511/11947903/e3df628480d8/d4ra08796h-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6511/11947903/1287a3959e06/d4ra08796h-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6511/11947903/a54451555273/d4ra08796h-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6511/11947903/464c3fda548a/d4ra08796h-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6511/11947903/e3df628480d8/d4ra08796h-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6511/11947903/1287a3959e06/d4ra08796h-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6511/11947903/a54451555273/d4ra08796h-f4.jpg

相似文献

1
Superior solubility of anhydrous quercetin and polymer physical mixtures compared to amorphous solid dispersions.与无定形固体分散体相比,无水槲皮素与聚合物物理混合物具有更高的溶解度。
RSC Adv. 2025 Mar 27;15(12):9348-9358. doi: 10.1039/d4ra08796h. eCollection 2025 Mar 21.
2
Quercetin amorphous solid dispersions prepared by hot melt extrusion with enhanced solubility and intestinal absorption.通过热熔挤出技术制备的槲皮素无定形固体分散体,提高了溶解度和肠道吸收。
Pharm Dev Technol. 2020 Apr;25(4):472-481. doi: 10.1080/10837450.2019.1709502. Epub 2020 Jan 7.
3
The Amorphous Quercetin/ Hydroxypropylmethylcellulose Acetate Succinate Solid Dispersions Prepared by Co-Precipitation Method to Enhance Quercetin Dissolution.共沉淀法制备无定形槲皮素/羟丙甲纤维素醋酸琥珀酸酯固体分散体以提高槲皮素溶出度。
J Pharm Sci. 2021 Sep;110(9):3230-3237. doi: 10.1016/j.xphs.2021.05.004. Epub 2021 May 15.
4
Solid dispersion of quercetin in cellulose derivative matrices influences both solubility and stability.槲皮素在纤维素衍生物基质中的固体分散体影响其溶解度和稳定性。
Carbohydr Polym. 2013 Feb 15;92(2):2033-40. doi: 10.1016/j.carbpol.2012.11.073. Epub 2012 Dec 3.
5
Surfactant-free amorphous solid dispersion with high dissolution for bioavailability enhancement of hydrophobic drugs: a case of quercetin.无表面活性剂的高溶解性无定形固体分散体提高疏水性药物生物利用度:以槲皮素为例。
Drug Dev Ind Pharm. 2021 Jan;47(1):153-162. doi: 10.1080/03639045.2020.1862173.
6
Insights into the Dissolution Mechanism of Ritonavir-Copovidone Amorphous Solid Dispersions: Importance of Congruent Release for Enhanced Performance.利托那韦-共聚维酮无定形固体分散体的溶解机制研究:一致释放对于增强性能的重要性。
Mol Pharm. 2019 Mar 4;16(3):1327-1339. doi: 10.1021/acs.molpharmaceut.8b01261. Epub 2019 Feb 5.
7
Combining amorphous solid dispersions for improved kinetic solubility of posaconazole simultaneously released from soluble PVP/VA64 and an insoluble ammonio methacrylate copolymer.将无定形固体分散体结合,以同时提高可溶 PVP/VA64 和不溶性氨甲丙烯酸酯共聚物释放的泊沙康唑的动力学溶解度。
Eur J Pharm Sci. 2019 May 15;133:79-85. doi: 10.1016/j.ejps.2019.03.012. Epub 2019 Mar 16.
8
Phase Behavior of Ritonavir Amorphous Solid Dispersions during Hydration and Dissolution.利托那韦无定形固体分散体在水合和溶解过程中的相行为。
Pharm Res. 2017 Dec;34(12):2842-2861. doi: 10.1007/s11095-017-2265-5. Epub 2017 Sep 27.
9
Patterns of drug release as a function of drug loading from amorphous solid dispersions: A comparison of five different polymers.作为无定形固体分散体载药量函数的药物释放模式:五种不同聚合物的比较
Eur J Pharm Sci. 2020 Dec 1;155:105514. doi: 10.1016/j.ejps.2020.105514. Epub 2020 Aug 15.
10
Water-Resistant Drug-Polymer Interaction Contributes to the Formation of Nano-Species during the Dissolution of Felodipine Amorphous Solid Dispersions.水稳定性药物-聚合物相互作用有助于非洛地平无定形固体分散体溶解过程中纳米物种的形成。
Mol Pharm. 2022 Aug 1;19(8):2888-2899. doi: 10.1021/acs.molpharmaceut.2c00250. Epub 2022 Jun 27.

本文引用的文献

1
The bioavailability, absorption, metabolism, and regulation of glucolipid metabolism disorders by quercetin and its important glycosides: A review.槲皮素及其重要糖苷调节糖脂代谢紊乱的生物利用度、吸收、代谢和调控:综述。
Food Chem. 2024 Nov 15;458:140262. doi: 10.1016/j.foodchem.2024.140262. Epub 2024 Jun 27.
2
Drug-drug co-amorphous systems: An emerging formulation strategy for poorly water-soluble drugs.药物共无定形系统:一种用于提高难溶性药物溶解度的新兴制剂策略。
Drug Discov Today. 2024 Feb;29(2):103883. doi: 10.1016/j.drudis.2024.103883. Epub 2024 Jan 14.
3
Quercetin: A Potential Polydynamic Drug.
槲皮素:一种潜在的多动态药物。
Molecules. 2023 Dec 17;28(24):8141. doi: 10.3390/molecules28248141.
4
Stability Challenges of Amorphous Solid Dispersions of Drugs: A Critical Review on Mechanistic Aspects.药物无定形固体分散体的稳定性挑战:机制方面的批判性综述。
Crit Rev Ther Drug Carrier Syst. 2024;41(3):45-94. doi: 10.1615/CritRevTherDrugCarrierSyst.2023039877.
5
Recent Advances in Co-Former Screening and Formation Prediction of Multicomponent Solid Forms of Low Molecular Weight Drugs.低分子量药物多组分固体形式的共成型剂筛选与晶型预测的最新进展
Pharmaceutics. 2023 Aug 22;15(9):2174. doi: 10.3390/pharmaceutics15092174.
6
Navigating the Complex Solid Form Landscape of the Quercetin Flavonoid Molecule.探索槲皮素类黄酮分子复杂的固体形态格局
Cryst Growth Des. 2023 Jul 13;23(8):6034-6045. doi: 10.1021/acs.cgd.3c00584. eCollection 2023 Aug 2.
7
The Raman Active Vibrations of Flavone and Quercetin: The Impact of Conformers and Hydrogen Bonding on Fingerprint Modes.黄酮和槲皮素的喇曼活性振动:构象和氢键对指纹模式的影响。
J Phys Chem A. 2023 Feb 16;127(6):1387-1394. doi: 10.1021/acs.jpca.2c06718. Epub 2023 Feb 3.
8
Pharmaceutical amorphous solid dispersion: A review of manufacturing strategies.药物非晶态固体分散体:制备策略综述
Acta Pharm Sin B. 2021 Aug;11(8):2505-2536. doi: 10.1016/j.apsb.2021.05.014. Epub 2021 Jun 5.
9
Ingredients with anti-inflammatory effect from medicine food homology plants.具有药食同源植物抗炎作用的成分。
Food Chem. 2022 Jan 30;368:130610. doi: 10.1016/j.foodchem.2021.130610. Epub 2021 Aug 10.
10
The Amorphous Quercetin/ Hydroxypropylmethylcellulose Acetate Succinate Solid Dispersions Prepared by Co-Precipitation Method to Enhance Quercetin Dissolution.共沉淀法制备无定形槲皮素/羟丙甲纤维素醋酸琥珀酸酯固体分散体以提高槲皮素溶出度。
J Pharm Sci. 2021 Sep;110(9):3230-3237. doi: 10.1016/j.xphs.2021.05.004. Epub 2021 May 15.