• 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

Relative bioavailability of danazol in dogs from liquid-filled hard gelatin capsules.

作者信息

Erlich L, Yu D, Pallister D A, Levinson R S, Gole D G, Wilkinson P A, Erlich R E, Reeve L E, Viegas T X

机构信息

Apotex Pharmaceuticals, Weston, Ont. M9L2Y6, Canada.

出版信息

Int J Pharm. 1999 Mar 1;179(1):49-53. doi: 10.1016/s0378-5173(98)00386-x.

DOI:10.1016/s0378-5173(98)00386-x
PMID:10053201
Abstract

Danazol was dissolved in non-aqueous mixtures containing either polyethylene glycol 400 or polysorbate 80, and filled into hard gelatin capsules at 50 mg concentrations. The bioavailability of these formulations was compared with commercial danazol capsules in a two-way crossover study using young female beagle dogs. Both formulations showed greater oral bioavailability when compared with either the 100 or 200 mg commercial brand of danazol. The bioavailability of the polyethylene glycol 400 and polysorbate 80 formulations was enhanced 3.7 and 15.8 times, respectively, when compared at the 100 mg dose level.

摘要

相似文献

1
Relative bioavailability of danazol in dogs from liquid-filled hard gelatin capsules.
Int J Pharm. 1999 Mar 1;179(1):49-53. doi: 10.1016/s0378-5173(98)00386-x.
2
Supersaturation produces high bioavailability of amorphous danazol particles formed by evaporative precipitation into aqueous solution and spray freezing into liquid technologies.过饱和使得通过蒸发沉淀到水溶液中以及喷雾冷冻成液技术形成的无定形达那唑颗粒具有高生物利用度。
Drug Dev Ind Pharm. 2006 Jun;32(5):559-67. doi: 10.1080/03639040500529176.
3
Increasing the proportional content of surfactant (Cremophor EL) relative to lipid in self-emulsifying lipid-based formulations of danazol reduces oral bioavailability in beagle dogs.在达那唑的自乳化脂质基制剂中,相对于脂质增加表面活性剂(聚氧乙烯蓖麻油)的比例会降低比格犬的口服生物利用度。
Pharm Res. 2007 Apr;24(4):748-57. doi: 10.1007/s11095-006-9194-z. Epub 2007 Feb 15.
4
Non-linear increases in danazol exposure with dose in older vs. younger beagle dogs: the potential role of differences in bile salt concentration, thermodynamic activity, and formulation digestion.在老年比格犬与年轻比格犬中,达那唑暴露量随剂量呈非线性增加:胆汁盐浓度、热力学活性和制剂消化差异的潜在作用。
Pharm Res. 2014 Jun;31(6):1536-52. doi: 10.1007/s11095-013-1260-8. Epub 2014 Jan 30.
5
Bioavailability enhancement of a poorly water-soluble drug by solid dispersion in polyethylene glycol-polysorbate 80 mixture.通过在聚乙二醇 - 聚山梨酯80混合物中形成固体分散体来提高难溶性药物的生物利用度。
Int J Pharm. 2004 Jan 9;269(1):251-8. doi: 10.1016/j.ijpharm.2003.09.002.
6
An in vitro digestion test that reflects rat intestinal conditions to probe the importance of formulation digestion vs first pass metabolism in Danazol bioavailability from lipid based formulations.一项反映大鼠肠道状况的体外消化试验,以探究制剂消化与首过代谢对基于脂质的制剂中达那唑生物利用度的重要性。
Mol Pharm. 2014 Nov 3;11(11):4069-83. doi: 10.1021/mp500197b. Epub 2014 Sep 29.
7
Evaluation of the impact of surfactant digestion on the bioavailability of danazol after oral administration of lipidic self-emulsifying formulations to dogs.给犬口服脂质自乳化制剂后,评估表面活性剂消化对达那唑生物利用度的影响。
J Pharm Sci. 2008 Feb;97(2):995-1012. doi: 10.1002/jps.21246.
8
'Stealth' lipid-based formulations: poly(ethylene glycol)-mediated digestion inhibition improves oral bioavailability of a model poorly water soluble drug.“隐形”脂质制剂:聚乙二醇介导的消化抑制作用提高了模型难溶性药物的口服生物利用度。
J Control Release. 2014 Oct 28;192:219-27. doi: 10.1016/j.jconrel.2014.07.037. Epub 2014 Jul 22.
9
Effect of food and a monoglyceride emulsion formulation on danazol bioavailability.食物和甘油单酯乳剂配方对达那唑生物利用度的影响。
J Clin Pharmacol. 1993 Apr;33(4):381-6. doi: 10.1002/j.1552-4604.1993.tb04673.x.
10
Susceptibility to lipase-mediated digestion reduces the oral bioavailability of danazol after administration as a medium-chain lipid-based microemulsion formulation.作为中链脂质基微乳制剂给药后,对脂肪酶介导消化的敏感性降低了达那唑的口服生物利用度。
Pharm Res. 2004 Aug;21(8):1405-12. doi: 10.1023/b:pham.0000036914.22132.cc.

引用本文的文献

1
Prediction of aqueous intrinsic solubility of druglike molecules using Random Forest regression trained with Wiki-pS0 database.使用基于Wiki-pS0数据库训练的随机森林回归预测类药物分子的水相固有溶解度。
ADMET DMPK. 2020 Mar 4;8(1):29-77. doi: 10.5599/admet.766. eCollection 2020.
2
Challenges of Dissolution Methods Development for Soft Gelatin Capsules.软胶囊溶出方法开发的挑战
Pharmaceutics. 2021 Feb 4;13(2):214. doi: 10.3390/pharmaceutics13020214.
3
Cocrystal Solubility Product Prediction Using an in combo Model and Simulations to Improve Design of Experiments.
使用组合模型和模拟进行共晶溶解度乘积预测,以改进实验设计。
Pharm Res. 2018 Feb 2;35(2):40. doi: 10.1007/s11095-018-2343-3.
4
Characterization of Supersaturated Danazol Solutions - Impact of Polymers on Solution Properties and Phase Transitions.超饱和达那唑溶液的特性——聚合物对溶液性质和相变的影响
Pharm Res. 2016 May;33(5):1276-88. doi: 10.1007/s11095-016-1871-y. Epub 2016 Feb 18.
5
Non-linear increases in danazol exposure with dose in older vs. younger beagle dogs: the potential role of differences in bile salt concentration, thermodynamic activity, and formulation digestion.在老年比格犬与年轻比格犬中,达那唑暴露量随剂量呈非线性增加:胆汁盐浓度、热力学活性和制剂消化差异的潜在作用。
Pharm Res. 2014 Jun;31(6):1536-52. doi: 10.1007/s11095-013-1260-8. Epub 2014 Jan 30.
6
Glyceride lipid formulations: molecular dynamics modeling of phase behavior during dispersion and molecular interactions between drugs and excipients.甘油酯类脂质体制剂:分散过程中相行为的分子动力学模拟及药物与赋形剂间的分子相互作用。
Pharm Res. 2013 Dec;30(12):3238-53. doi: 10.1007/s11095-013-1206-1. Epub 2013 Oct 3.
7
Evaluation of a nanoemulsion formulation strategy for oral bioavailability enhancement of danazol in rats and dogs.评价一种纳米乳制剂策略对达那唑在大鼠和犬体内口服生物利用度的增强作用。
J Pharm Sci. 2013 Oct;102(10):3808-15. doi: 10.1002/jps.23667. Epub 2013 Jul 22.
8
Increasing the proportional content of surfactant (Cremophor EL) relative to lipid in self-emulsifying lipid-based formulations of danazol reduces oral bioavailability in beagle dogs.在达那唑的自乳化脂质基制剂中,相对于脂质增加表面活性剂(聚氧乙烯蓖麻油)的比例会降低比格犬的口服生物利用度。
Pharm Res. 2007 Apr;24(4):748-57. doi: 10.1007/s11095-006-9194-z. Epub 2007 Feb 15.
9
Susceptibility to lipase-mediated digestion reduces the oral bioavailability of danazol after administration as a medium-chain lipid-based microemulsion formulation.作为中链脂质基微乳制剂给药后,对脂肪酶介导消化的敏感性降低了达那唑的口服生物利用度。
Pharm Res. 2004 Aug;21(8):1405-12. doi: 10.1023/b:pham.0000036914.22132.cc.
10
Pharmacological effects of formulation vehicles : implications for cancer chemotherapy.制剂载体的药理作用:对癌症化疗的影响
Clin Pharmacokinet. 2003;42(7):665-85. doi: 10.2165/00003088-200342070-00005.