姜黄素生物利用度研究进展

被引：8

作者：

张庆云

莫曾南

机构：

[1] 广西医科大学第一附属医院

来源：

中国药房 | 2009年 / 20卷 / 33期

关键词：

姜黄素类似物; 口服液; 灌胃; 大鼠; 混悬液; 混悬剂; 利用度; 姜黄素脂质体;

D O I：

暂无

中图分类号：

R285.5 [中药实验药理];

学科分类号：

1008 ;

摘要：

引用

页码：2631 / 2633

页数：3

共 9 条

[1] 姜黄素抑制人前列腺增生细胞BPH1增殖的研究 [J].

陈志强 ;

莫曾南 .

中国药房, 2008, (06) :404-406

[2] 姜黄素脂质体在大鼠体内药代动力学研究 [J].

许汉林 ;

孙芸 ;

邵继征 ;

熊利容 ;

张念 ;

黄成刚 .

湖北中医学院学报, 2007, (01) :42-43

[3] 姜黄素对肺癌A549细胞bcl-2、bax表达与生长的影响研究 [J].

田德增 ;

朱辉 ;

梁永杰 .

中国药房, 2007, (04) :263-264

[4]

EF24, a novel curcumin analog, disrupts the microtubule cytoskeleton and inhibits HIF-1[J] . Shala L. Thomas,Diansheng Zhong,Wei Zhou,Sanna Malik,Dennis Liotta,James P. Snyder,Ernest Hamel,Paraskevi Giannakakou.Cell Cycle . 2008 (15)

[5] Spicing up of the immune system by curcumin [J].

Jagetia, Ganesh Chandra ;

Aggarwal, Bharat B. .

JOURNAL OF CLINICAL IMMUNOLOGY, 2007, 27 (01) :19-35

[6] Comparison of systemic availability of curcumin with that of curcumin formulated with phosphatidylcholine [J].

Marczylo, Timothy H. ;

Verschoyle, Richard D. ;

Cooke, Darren N. ;

Morazzoni, Paolo ;

Steward, William P. ;

Gescher, Andreas J. .

CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2007, 60 (02) :171-177

[7]

Synthesis, characterization and antitumour activities of some synthetic curcuminoid analogues and their copper complexes[J] . Valapatukutikadan Davis John,Krishnannair Krishnankutty.Transition Metal Chemistry . 2005 (2)

[8] Influence of piperine on the pharmacokinetics of curcumin in animals and human volunteers [J].

Shoba, G ;

Joy, D ;

Joseph, T ;

Majeed, M ;

Rajendran, R ;

Srinivas, PSSR .

PLANTA MEDICA, 1998, 64 (04) :353-356

[9]

Chemopreventive anti-inflammatory activities of curcumin and other phytochemicalsmediated by MAP kinase phosphatase-5 in prostate cells. Nonn L,Duong D,Peehl DM. Carcinogenesis . 2007

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