• 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

灰黄霉素在羟丙基纤维素/聚乙烯己内酰胺/十二烷基硫酸钠中的喷雾干燥无定形固体分散体:阐明十二烷基硫酸钠作为次要成分的多方面影响

Spray-Dried Amorphous Solid Dispersions of Griseofulvin in HPC/Soluplus/SDS: Elucidating the Multifaceted Impact of SDS as a Minor Component.

作者信息

Rahman Mahbubur, Ahmad Stephanie, Tarabokija James, Parker Nathaniel, Bilgili Ecevit

机构信息

Otto H. York Department of Chemical and Materials Engineering, New Jersey Institute of Technology, Newark, NJ 07102, USA.

出版信息

Pharmaceutics. 2020 Feb 25;12(3):197. doi: 10.3390/pharmaceutics12030197.

DOI:10.3390/pharmaceutics12030197
PMID:32106495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7150901/
Abstract

This study aimed to elucidate the impact of a common anionic surfactant, sodium dodecyl sulfate (SDS), along with hydroxypropyl cellulose (HPC) and Soluplus (Sol) on the release of griseofulvin (GF), a poorly soluble drug, from amorphous solid dispersions (ASDs). Solutions of 2.5% GF and 2.5%-12.5% HPC/Sol with 0.125% SDS/without SDS were prepared in acetone-water and spray-dried. The solid-state characterization of the ASDs suggests that GF-Sol had better miscibility and stronger interactions than GF-HPC and formed XRPD-amorphous GF, whereas HPC-based ASDs, especially the ones with a lower HPC loading, had crystalline GF. The dissolution tests show that without SDS, ASDs provided limited GF supersaturation (max. 250%) due to poor wettability of Sol-based ASDs and extensive GF recrystallization in HPC-based ASDs (max. 50%). Sol-based ASDs with SDS exhibited a dramatic increase in supersaturation (max. 570%), especially at a higher Sol loading, whereas HPC-based ASDs with SDS did not. SDS did not interfere with Sol's ability to inhibit GF recrystallization, as confirmed by the precipitation from the supersaturated state and PLM imaging. The favorable use of SDS in a ternary ASD was attributed to both the wettability enhancement and its inability to promote GF recrystallization when used as a minor component along with Sol.

摘要

本研究旨在阐明常见阴离子表面活性剂十二烷基硫酸钠(SDS)以及羟丙基纤维素(HPC)和固体分散体聚合物(Sol)对难溶性药物灰黄霉素(GF)从无定形固体分散体(ASD)中释放的影响。将2.5%的GF溶液以及含0.125% SDS/不含SDS的2.5%-12.5% HPC/Sol溶液在丙酮-水中配制并喷雾干燥。ASD的固态表征表明,GF-Sol比GF-HPC具有更好的混溶性和更强的相互作用,并形成了X射线粉末衍射无定形GF,而基于HPC的ASD,尤其是HPC含量较低的ASD,含有结晶GF。溶出试验表明,在没有SDS的情况下,由于基于Sol的ASD润湿性差以及基于HPC的ASD中GF大量重结晶(最大50%),ASD提供的GF过饱和度有限(最大250%)。含SDS的基于Sol的ASD过饱和度显著增加(最大570%),尤其是在Sol含量较高时,而含SDS的基于HPC的ASD则没有。如从过饱和状态沉淀和偏光显微镜成像所证实,SDS不干扰Sol抑制GF重结晶的能力。SDS在三元ASD中的良好应用归因于润湿性增强以及与Sol一起作为次要成分使用时它无法促进GF重结晶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/8a4643b0e58c/pharmaceutics-12-00197-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/67ce7c9f5f36/pharmaceutics-12-00197-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/1c332c16d437/pharmaceutics-12-00197-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/8607a9448bd2/pharmaceutics-12-00197-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/f2837000fae2/pharmaceutics-12-00197-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/d62aa1de810c/pharmaceutics-12-00197-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/0ed4feb0f642/pharmaceutics-12-00197-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/9dc67174845a/pharmaceutics-12-00197-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/ee85307d5add/pharmaceutics-12-00197-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/395c81d5defe/pharmaceutics-12-00197-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/8a4643b0e58c/pharmaceutics-12-00197-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/67ce7c9f5f36/pharmaceutics-12-00197-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/1c332c16d437/pharmaceutics-12-00197-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/8607a9448bd2/pharmaceutics-12-00197-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/f2837000fae2/pharmaceutics-12-00197-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/d62aa1de810c/pharmaceutics-12-00197-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/0ed4feb0f642/pharmaceutics-12-00197-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/9dc67174845a/pharmaceutics-12-00197-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/ee85307d5add/pharmaceutics-12-00197-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/395c81d5defe/pharmaceutics-12-00197-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/7150901/8a4643b0e58c/pharmaceutics-12-00197-g010.jpg

相似文献

1
Spray-Dried Amorphous Solid Dispersions of Griseofulvin in HPC/Soluplus/SDS: Elucidating the Multifaceted Impact of SDS as a Minor Component.灰黄霉素在羟丙基纤维素/聚乙烯己内酰胺/十二烷基硫酸钠中的喷雾干燥无定形固体分散体:阐明十二烷基硫酸钠作为次要成分的多方面影响
Pharmaceutics. 2020 Feb 25;12(3):197. doi: 10.3390/pharmaceutics12030197.
2
Synergistic and antagonistic effects of various amphiphilic polymer combinations in enhancing griseofulvin release from ternary amorphous solid dispersions.各种两亲性聚合物组合在增强三元无定形固体分散体中灰黄霉素释放方面的协同和拮抗作用。
Eur J Pharm Sci. 2020 Jul 1;150:105354. doi: 10.1016/j.ejps.2020.105354. Epub 2020 May 4.
3
Hybrid nanocrystal-amorphous solid dispersions (HyNASDs) as alternative to ASDs for enhanced release of BCS Class II drugs.用于增强 BCS 类 II 药物释放的混合纳米晶-无定形固体分散体(HyNASDs)替代 ASDs。
Eur J Pharm Biopharm. 2019 Dec;145:12-26. doi: 10.1016/j.ejpb.2019.10.002. Epub 2019 Oct 14.
4
Preparation and Characterization of Spray-Dried Hybrid Nanocrystal-Amorphous Solid Dispersions (HyNASDs) for Supersaturation Enhancement of a Slowly Crystallizing Drug.用于增强缓慢结晶药物过饱和度的喷雾干燥混合纳米晶体-无定形固体分散体(HyNASDs)的制备与表征
Nanomaterials (Basel). 2023 Aug 25;13(17):2419. doi: 10.3390/nano13172419.
5
Impact of Matrix Surface Area on Griseofulvin Release from Extrudates Prepared via Nanoextrusion.基质表面积对通过纳米挤压制备的挤出物中灰黄霉素释放的影响。
Pharmaceutics. 2021 Jul 7;13(7):1036. doi: 10.3390/pharmaceutics13071036.
6
Exploration of supersaturable lacidipine ternary amorphous solid dispersion for enhanced dissolution and in vivo absorption.探索拉西地平三元无定形固体分散体以提高溶解性能和体内吸收。
Eur J Pharm Sci. 2019 Nov 1;139:105043. doi: 10.1016/j.ejps.2019.105043. Epub 2019 Aug 12.
7
Nanoseeded Desupersaturation and Dissolution Tests for Elucidating Supersaturation Maintenance in Amorphous Solid Dispersions.用于阐明无定形固体分散体中过饱和维持的纳米晶种脱饱和与溶解试验
Pharmaceutics. 2023 Jan 30;15(2):450. doi: 10.3390/pharmaceutics15020450.
8
A comparative assessment of nanocomposites vs. amorphous solid dispersions prepared via nanoextrusion for drug dissolution enhancement.纳米复合体系与纳米挤出法制备的无定形固体分散体用于药物增溶的比较评估。
Eur J Pharm Biopharm. 2017 Oct;119:68-80. doi: 10.1016/j.ejpb.2017.06.003. Epub 2017 Jun 3.
9
Bottom-Up and Top-Down Approaches to Explore Sodium Dodecyl Sulfate and Soluplus on the Crystallization Inhibition and Dissolution of Felodipine Extrudates.上下求索:十二烷基硫酸钠和共聚维酮对非洛地平挤出物结晶抑制和溶出的影响
J Pharm Sci. 2018 Sep;107(9):2366-2376. doi: 10.1016/j.xphs.2018.04.025. Epub 2018 May 5.
10
Effect of Particle Size and Polymer Loading on Dissolution Behavior of Amorphous Griseofulvin Powder.粒径和聚合物载量对灰黄霉素无定形粉末溶解行为的影响。
J Pharm Sci. 2019 Jan;108(1):234-242. doi: 10.1016/j.xphs.2018.11.025. Epub 2018 Nov 22.

引用本文的文献

1
Co-Amorphous Solid Dispersion System for Improvement in Dissolution Profile of -(((1,4)-4-((6-fluorobenzo[]oxazol-2-yl)amino)cyclohexyl)methyl)-2-methylpropane-2-sulfonamide as a Neuropeptide Y5 Receptor Antagonist.用于改善作为神经肽Y5受体拮抗剂的-(((1,4)-4-((6-氟苯并恶唑-2-基)氨基)环己基)甲基)-2-甲基丙烷-2-磺酰胺溶出曲线的共无定形固体分散体系统。
Pharmaceutics. 2024 Oct 2;16(10):1293. doi: 10.3390/pharmaceutics16101293.
2
Curcumin-loaded soluplus® based ternary solid dispersions with enhanced solubility, dissolution and antibacterial, antioxidant, anti-inflammatory activities.基于Soluplus®的载姜黄素三元固体分散体,具有增强的溶解度、溶出度以及抗菌、抗氧化、抗炎活性。
Heliyon. 2024 Jul 14;10(14):e34636. doi: 10.1016/j.heliyon.2024.e34636. eCollection 2024 Jul 30.
3

本文引用的文献

1
Hybrid nanocrystal-amorphous solid dispersions (HyNASDs) as alternative to ASDs for enhanced release of BCS Class II drugs.用于增强 BCS 类 II 药物释放的混合纳米晶-无定形固体分散体(HyNASDs)替代 ASDs。
Eur J Pharm Biopharm. 2019 Dec;145:12-26. doi: 10.1016/j.ejpb.2019.10.002. Epub 2019 Oct 14.
2
Scale-up of pharmaceutical spray drying using scale-up rules: A review.采用放大规则放大制药喷雾干燥:综述。
Int J Pharm. 2019 May 1;562:271-292. doi: 10.1016/j.ijpharm.2019.03.047. Epub 2019 Mar 22.
3
Bottom-Up and Top-Down Approaches to Explore Sodium Dodecyl Sulfate and Soluplus on the Crystallization Inhibition and Dissolution of Felodipine Extrudates.
Investigation of Stabilized Amorphous Solid Dispersions to Improve Oral Olaparib Absorption.用于改善奥拉帕利口服吸收的稳定化无定形固体分散体的研究
Pharmaceutics. 2024 Jul 19;16(7):958. doi: 10.3390/pharmaceutics16070958.
4
Thermo-Structural Characterization of Phase Transitions in Amorphous Griseofulvin: From Sub-T Relaxation and Crystal Growth to High-Temperature Decomposition.非晶态灰黄霉素相变的热结构表征:从亚-T 弛豫和晶体生长到高温分解
Molecules. 2024 Mar 28;29(7):1516. doi: 10.3390/molecules29071516.
5
Advances in the development of amorphous solid dispersions: The role of polymeric carriers.非晶态固体分散体的发展进展:聚合物载体的作用。
Asian J Pharm Sci. 2023 Jul;18(4):100834. doi: 10.1016/j.ajps.2023.100834. Epub 2023 Aug 1.
6
Safety and Pharmaceutical Evaluation of a Novel Natural Polymer, Ocicum, as Solubility and Dissolution Enhancer in Solid Dispersion.一种新型天然聚合物罗勒(Ocicum)作为固体分散体中溶解度和溶出度增强剂的安全性和药学评价
Pharmaceuticals (Basel). 2022 Jul 14;15(7):869. doi: 10.3390/ph15070869.
7
Dry Dosage Forms of Add-Value Bioactive Phenolic Compounds by Supercritical CO-Assisted Spray-Drying.超临界 CO2 辅助喷雾干燥法制备增值生物活性酚类化合物的干法制剂。
Molecules. 2022 Mar 20;27(6):2001. doi: 10.3390/molecules27062001.
8
Development of spray-dried amorphous solid dispersions of tadalafil using glycyrrhizin for enhanced dissolution and aphrodisiac activity in male rats.使用甘草甜素制备他达拉非喷雾干燥无定形固体分散体以增强雄性大鼠的溶出度和壮阳活性
Saudi Pharm J. 2020 Dec;28(12):1817-1826. doi: 10.1016/j.jsps.2020.11.007. Epub 2020 Nov 21.
9
Improvement in the Oral Bioavailability and Efficacy of New Ezetimibe Formulations-Comparative Study of a Solid Dispersion and Different Micellar Systems.新型依折麦布制剂口服生物利用度和疗效的改善——固体分散体与不同胶束系统的对比研究
Pharmaceutics. 2020 Jul 2;12(7):617. doi: 10.3390/pharmaceutics12070617.
上下求索:十二烷基硫酸钠和共聚维酮对非洛地平挤出物结晶抑制和溶出的影响
J Pharm Sci. 2018 Sep;107(9):2366-2376. doi: 10.1016/j.xphs.2018.04.025. Epub 2018 May 5.
4
Polymer⁻Surfactant System Based Amorphous Solid Dispersion: Precipitation Inhibition and Bioavailability Enhancement of Itraconazole.基于聚合物-表面活性剂体系的无定形固体分散体:伊曲康唑的沉淀抑制与生物利用度提高
Pharmaceutics. 2018 Apr 24;10(2):53. doi: 10.3390/pharmaceutics10020053.
5
Investigation of Polymer/Surfactant Interactions and Their Impact on Itraconazole Solubility and Precipitation Kinetics for Developing Spray-Dried Amorphous Solid Dispersions.聚合物/表面活性剂相互作用及其对喷雾干燥无定形固体分散体中伊曲康唑溶解度和沉淀动力学影响的研究。
Mol Pharm. 2018 Mar 5;15(3):962-974. doi: 10.1021/acs.molpharmaceut.7b00902. Epub 2018 Feb 5.
6
A comparative assessment of nanocomposites vs. amorphous solid dispersions prepared via nanoextrusion for drug dissolution enhancement.纳米复合体系与纳米挤出法制备的无定形固体分散体用于药物增溶的比较评估。
Eur J Pharm Biopharm. 2017 Oct;119:68-80. doi: 10.1016/j.ejpb.2017.06.003. Epub 2017 Jun 3.
7
Amorphous-Amorphous Phase Separation in API/Polymer Formulations.药物活性成分/聚合物制剂中的非晶态-非晶态相分离
Molecules. 2017 Feb 15;22(2):296. doi: 10.3390/molecules22020296.
8
Comparison of solvent-wetted and kneaded l-sulpiride-loaded solid dispersions: Powder characterization and in vivo evaluation.溶剂湿润法和热熔挤出法制备的左旋舒必利固体分散体的比较:粉体表征及体内评价
Int J Pharm. 2016 Sep 10;511(1):351-358. doi: 10.1016/j.ijpharm.2016.07.006. Epub 2016 Jul 7.
9
Sodium Lauryl Sulfate Competitively Interacts with HPMC-AS and Consequently Reduces Oral Bioavailability of Posaconazole/HPMC-AS Amorphous Solid Dispersion.月桂醇硫酸酯钠与羟丙基甲基纤维素醋酸琥珀酸酯发生竞争性相互作用,从而降低泊沙康唑/羟丙基甲基纤维素醋酸琥珀酸酯无定形固体分散体的口服生物利用度。
Mol Pharm. 2016 Aug 1;13(8):2787-95. doi: 10.1021/acs.molpharmaceut.6b00391. Epub 2016 Jul 1.
10
Influence of spray drying and dispersing agent on surface and dissolution properties of griseofulvin micro and nanocrystals.喷雾干燥和分散剂对灰黄霉素微米和纳米晶体的表面及溶解性能的影响
Drug Dev Ind Pharm. 2016 Nov;42(11):1842-50. doi: 10.1080/03639045.2016.1178770. Epub 2016 May 4.