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This study explored the potential of β-cyclodextrin to improve the aqueous solubility and dissolution of danazol, investigated a simple and less expensive method for preparation of a danazol-β-cyclodextrin binary system, and explored the potential application of a danazol-β-cyclodextrin binary system as a single-dose emergency contraceptive. Phase solubility analysis indicated formation of a first-order soluble complex with stability constant 972.03 M−1, while Job's plot affirmed 1∶1 stoichiometry. The hyperchromic shift in the UV-Vis spectrum of danazol in the presence of β-cyclodextrin indicated solubilization capability of β-cyclodextrin for danazol. The extrinsic Cotton effect with a negative peak at 280.7 nm confirmed the inclusion of danazol in the asymmetric locus of β-cyclodextrin.1H-nuclear magnetic resonance analysis suggested that the protons of the steroidal skeleton of danazol display favorable interactions with the β-cyclodextrin cavity. The danazol-β-cyclodextrin binary system was prepared by kneading, solution, freeze-drying, and milling methods. The extent of the enhancement of dissolution rate was found to be dependent on the preparation method. Dissolution studies showed a similar relative dissolution rate (2.85) of the danazol-β-cyclodextrin binary system prepared by the freeze-drying and milling (in the presence of 13% moisture) methods. In a mouse model, the danazol-β-cyclodextrin binary system at 51.2 mg/kg (equivalent to a 400-mg human dose) showed 100% inhibition of implantation when given postcoitally. Moreover, the danazol-β-cyclodextrin binary system is safe up to 2000 mg/kg in the mouse (15.52 g/70 kg human) as a single oral dose. Thus, the danazol-β-cyclodextrin binary system could serve as a new therapeutic application: an oral emergency contraceptive at a physiologically acceptable single dose. Published: May 11, 2007  相似文献   
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蓖麻提取物对鼠抗生育作用的实验研究   总被引:11,自引:2,他引:9  
秦晓娜  甘明哲  高平 《四川动物》2006,25(1):176-179
利用蓖麻提取物对昆明种小鼠进行了短期与长期的抗生育实验,研究发现蓖麻提取物(蓖麻油和蓖麻蛋白)对小鼠有明显的抗生育作用。蓖麻蚩白及其与蓖麻油的混合物在抗早孕方面的效果均可达到100%,蓖麻油抗着床的效果也可达到100%。蓖麻油长期抗鼠生育效果明显,在210d(正常小鼠的妊娠期是21~23d)内有效降低小鼠生育代数与产仔数,生育抑制率达80%以上。蓖麻提取物对离体小鼠子宫的影响也非常显著,通过增强小鼠子宫内部收缩有效减少着床机率。在中止妊娠的实验中发现,服用了蓖麻蛋白及其与蓖麻油的混合物的小鼠子宫内没有着床位点。  相似文献   
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Experiments were conducted to study the functional implication of a mannose-binding glycoprotein found in the day 4 post coital (p.c.) rat uterus, using a mono-specific polyclonal antibody raised against the glycoprotein. Western Blot and immunohistochemical techniques were employed to study the distribution of the glycoprotein, and the results suggest that this glycoprotein is present only in the day 4 p.c. uterus and is specifically localized in the stromal cells. Administration of anti-UA (Uterine Agglutinin) antiserum against the glycoprotein into the day 4 p.c. uterine lumen inhibits carrying of embryo to term. The antiserum is not embryo toxic. After in vivo in utero intra-luminal administration of anti-UA antiserum in day 4 p.c. rat the antiserum has been specifically localized in the uterine stroma by immunohistochemistry. After intravenous injection, the glycoprotein is cleared mainly through the kidney and liver. The possible role of this glycoprotein in the implantation process in rats has been discussed. From the data it is evident that UA may not be directly involved in sugar-sugar interactions with embryo since it is not present in any significant amount in pregnant uterus from day 5 onwards. Since other experiments show that UA does have some role to play in early pregnancy, UA probably acts through some other factor, and preliminary studies suggest that this factor maybe TGF-3.  相似文献   
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家兔配后1天灌服抗孕-53(10.5mg/kg),第11天剖腹检查,对照组着床数为9.7±1.6(平均值±SEM),实验组为0.4±0.4;兔妊娠第7—9天连续灌服抗孕-53(每天5mg/kg),17天剖检,对照组活胎数为7.5±1.1,实验组活胎数为0.3±0.3,死胎数为7.0±0.5;兔妊娠第22天肌肉注射抗孕-53(1.25mg/kg)一针,30天剖检,对照组活胎数为12.2±0.2,实验组均为死胎11.9±0.5。说明抗孕-53有明显抗着床、抗早孕和终止中期妊娠的作用。抗孕-53对家兔抗着床时,血浆孕酮和雌激素变化不显著;抗孕-53对早孕家兔血浆孕酮水平明显下降,但对血浆雌激素水平无影响。  相似文献   
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