• 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

[芒果苷磷脂复合物自微乳化药物传递系统的处方研究]

[Study on prescription of self-microemulsifying drug delivery system of mangiferin phospholipid complex].

作者信息

Xuan Xiao-yu, Wang Ya-jing, Tian Hui, Pi Jia-xin, Sun Shi-zhen, Zhang Wei-ling

机构信息

Tianjin University of Traditional Chinese Medicine, Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China.

出版信息

Zhong Yao Cai. 2012 Sep;35(9):1508-11.

PMID:23451508
Abstract

OBJECTIVE

To study formulation of self-microemulsifying drug delivery system (SMEDDS) of mangiferin phospholipid complex and improve dissolution and bioavailability of mangiferin.

METHODS

Ternary phase diagram was applied to optimize the prescription of self-microemulsifying drug delivery system of mangiferin phospholipid complex, and the best recipe was selected by comprehensive evaluation of the speed of microemulsifying, microemulsion size and electric potential.

RESULTS

The optimum formulation of SMEDDS was composed of IPM-Cremphor EL35-labrasol = 2 : 4.8 : 3.2.

CONCLUSION

Self-microemulsifying drug delivery system of mangiferin phospholipid complex can effectively improve the dissolution of Mangiferin.

摘要

目的

研究芒果苷磷脂复合物自微乳化给药系统(SMEDDS)的处方,提高芒果苷的溶出度和生物利用度。

方法

应用三元相图优化芒果苷磷脂复合物自微乳化给药系统的处方,并通过对微乳化速度、微乳液粒径和电位的综合评价筛选出最佳处方。

结果

SMEDDS的最佳处方为IPM-聚氧乙烯蓖麻油EL35-月桂酰基聚氧乙烯甘油酯=2:4.8:3.2。

结论

芒果苷磷脂复合物自微乳化给药系统可有效提高芒果苷的溶出度。

相似文献

1
[Study on prescription of self-microemulsifying drug delivery system of mangiferin phospholipid complex].[芒果苷磷脂复合物自微乳化药物传递系统的处方研究]
Zhong Yao Cai. 2012 Sep;35(9):1508-11.
2
A Self-microemulsifying Drug Delivery System (SMEDDS) for a Novel Medicative Compound Against Depression: a Preparation and Bioavailability Study in Rats.一种用于新型抗抑郁药物化合物的自微乳化药物递送系统(SMEDDS):大鼠体内的制备及生物利用度研究
AAPS PharmSciTech. 2015 Oct;16(5):1051-8. doi: 10.1208/s12249-014-0280-y. Epub 2015 Feb 6.
3
Effects of spray-drying and choice of solid carriers on concentrations of Labrasol® and Transcutol® in solid self-microemulsifying drug delivery systems (SMEDDS).喷雾干燥和固体载体选择对固体自微乳药物传递系统(SMEDDS)中 Labrasol® 和 Transcutol® 浓度的影响。
Molecules. 2013 Jan 2;18(1):545-60. doi: 10.3390/molecules18010545.
4
[Studies on self-microemulsifying drug preparations of total flavones of Hippophae rhamnoides].[沙棘总黄酮自微乳化药物制剂的研究]
Zhongguo Zhong Yao Za Zhi. 2009 Jan;34(1):43-6.
5
[Design and in vitro evaluation of self-microemulsifying drug delivery systems for piroxicam].
Yao Xue Xue Bao. 2008 Apr;43(4):415-20.
6
Preparation and In Vitro/In Vivo Evaluation of Puerarin Solid Self-Microemulsifying Drug Delivery System by Spherical Crystallization Technique.采用球形结晶技术制备葛根素固体自微乳化药物传递系统及其体外/体内评价
AAPS PharmSciTech. 2016 Dec;17(6):1336-1346. doi: 10.1208/s12249-015-0469-8. Epub 2015 Dec 22.
7
Self-microemulsifying smaller molecular volume oil (Capmul MCM) using non-ionic surfactants: a delivery system for poorly water-soluble drug.使用非离子表面活性剂的自微乳化小分子体积油(Capmul MCM):一种难溶性药物的给药系统。
Drug Dev Ind Pharm. 2012 Jul;38(7):883-92. doi: 10.3109/03639045.2011.631548. Epub 2011 Nov 16.
8
Formulation and Evaluation of a Self-microemulsifying Drug Delivery System Containing Bortezomib.含硼替佐米的自微乳化药物递送系统的制剂与评价
Chem Pharm Bull (Tokyo). 2016;64(8):1108-17. doi: 10.1248/cpb.c16-00035.
9
Enhancement of oral bioavailability of fenofibrate by solid self-microemulsifying drug delivery systems.固体自微乳药物传递系统增强非诺贝特的口服生物利用度。
Drug Dev Ind Pharm. 2013 Sep;39(9):1431-8. doi: 10.3109/03639045.2012.719903. Epub 2012 Oct 9.
10
Preparation and evaluation of valsartan by a novel semi-solid self-microemulsifying delivery system using Gelucire 44/14.使用Gelucire 44/14通过新型半固体自微乳化给药系统制备和评价缬沙坦。
Drug Dev Ind Pharm. 2016 Oct;42(10):1545-52. doi: 10.3109/03639045.2016.1151034. Epub 2016 Mar 4.

引用本文的文献

1
Novel Carbon Dots Derived from Significantly Improve the Solubility and Bioavailability of Mangiferin.源自[具体物质]的新型碳点显著提高了芒果苷的溶解度和生物利用度。 (注:原文中“Significantly Improve the Solubility and Bioavailability of Mangiferin”前缺少具体物质,翻译时补充了[具体物质],以便句子意思完整)
Int J Nanomedicine. 2024 Apr 20;19:3611-3622. doi: 10.2147/IJN.S456053. eCollection 2024.
2
Pharmacological properties of mangiferin: bioavailability, mechanisms of action and clinical perspectives.山竹堿素的药理学特性:生物利用度、作用机制和临床前景。
Naunyn Schmiedebergs Arch Pharmacol. 2024 Feb;397(2):763-781. doi: 10.1007/s00210-023-02682-4. Epub 2023 Sep 1.
3
Plant-derived natural products for drug discovery: current approaches and prospects.
用于药物发现的植物源天然产物:当前方法与前景
Nucleus (Calcutta). 2022;65(3):399-411. doi: 10.1007/s13237-022-00405-3. Epub 2022 Oct 18.
4
Solubility, Antioxidation, and Oral Bioavailability Improvement of Mangiferin Microparticles Prepared Using the Supercritical Antisolvent Method.超临界抗溶剂法制备芒果苷微粒的溶解度、抗氧化性及口服生物利用度改善
Pharmaceutics. 2020 Jan 22;12(2):90. doi: 10.3390/pharmaceutics12020090.
5
Discovery and Current Status of Evaluation System of Bioavailability and Related Pharmaceutical Technologies for Traditional Chinese Medicines--Flos Lonicerae Japonicae--Fructus Forsythiae Herb Couples as an Example.中药生物利用度及相关制药技术评价体系的发现与现状——以金银花-连翘药对为例
Int J Mol Sci. 2015 Dec 4;16(12):28812-40. doi: 10.3390/ijms161226132.