达那唑在人体及模拟胃肠液中的溶解度比较。 - Suppr | 超能文献

相似文献

1

A comparison of the solubility of danazol in human and simulated gastrointestinal fluids.达那唑在人体及模拟胃肠液中的溶解度比较。

Pharm Res. 2000 Jul;17(7):891-4. doi: 10.1023/a:1007576713216.

2

Solubility and stability of dalcetrapib in vehicles and biological media.达塞曲匹在溶媒和生物介质中的溶解度和稳定性。

Int J Pharm. 2012 Nov 1;437(1-2):103-9. doi: 10.1016/j.ijpharm.2012.07.071. Epub 2012 Aug 4.

3

Investigating the effects of amphipathic gastrointestinal compounds on the solution behaviour of salt and free base forms of clofazimine: An in vitro evaluation.研究两亲性胃肠化合物对氯法齐明盐和游离碱形式在溶液中行为的影响：体外评价。

Int J Pharm. 2018 Dec 1;552(1-2):180-192. doi: 10.1016/j.ijpharm.2018.09.012. Epub 2018 Sep 17.

4

A mechanistic study of danazol dissolution in ionic surfactant solutions.达那唑在离子表面活性剂溶液中溶解的机理研究。

J Pharm Sci. 2003 Feb;92(2):424-35. doi: 10.1002/jps.10309.

5

Use of conventional surfactant media as surrogates for FaSSIF in simulating in vivo dissolution of BCS class II drugs.在模拟体内溶解 BCS 类 II 药物时，使用传统表面活性剂作为 FaSSIF 的替代物。

Eur J Pharm Biopharm. 2011 Aug;78(3):531-8. doi: 10.1016/j.ejpb.2011.02.007. Epub 2011 Feb 15.

6

Selection of In Vivo Predictive Dissolution Media Using Drug Substance and Physiological Properties.使用药物物质和生理特性选择体内预测性溶出介质。

AAPS J. 2020 Jan 27;22(2):34. doi: 10.1208/s12248-020-0417-8.

7

Exploring the Impact of Intestinal Fluid Components on the Solubility and Supersaturation of Danazol.探讨肠液成分对丹那唑溶解度和过饱和度的影响。

J Pharm Sci. 2021 Jun;110(6):2479-2488. doi: 10.1016/j.xphs.2020.12.039. Epub 2021 Jan 9.

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

Effects of alkali and simulated gastric and intestinal fluids on danazol stability.

J Pharm Biomed Anal. 2003 Mar 26;31(4):743-51. doi: 10.1016/s0731-7085(02)00660-x.

10

Bile salt composition is secondary to bile salt concentration in determining hydrocortisone and progesterone solubility in intestinal mimetic fluids.在确定肠模拟液中氢化可的松和孕酮的溶解度时，胆汁盐组成次于胆汁盐浓度。

Int J Pharm. 2012 Jan 17;422(1-2):295-301. doi: 10.1016/j.ijpharm.2011.11.012. Epub 2011 Nov 15.

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

Fasted intestinal solubility limits and distributions applied to the biopharmaceutics and developability classification systems.禁食状态下肠道溶解度限值及其分布在生物药剂学和开发性分类系统中的应用。

Eur J Pharm Biopharm. 2022 Jan;170:160-169. doi: 10.1016/j.ejpb.2021.12.006. Epub 2021 Dec 16.

3

Small scale in vitro method to determine a bioequivalent equilibrium solubility range for fasted human intestinal fluid.

本文引用的文献

1

Lysolecithin.溶血卵磷脂

J Pharm Pharmacol. 1961 Jun;13:321-54. doi: 10.1111/j.2042-7158.1961.tb11831.x.

2

Dissolution of hydrocortisone in human and simulated intestinal fluids.氢化可的松在人体和模拟肠液中的溶解情况。

Pharm Res. 2000 Feb;17(2):183-9. doi: 10.1023/a:1007517414200.

3

Gastric juice as a dissolution medium: surface tension and pH.胃液作为一种溶解介质：表面张力和pH值。