Nicardipine hydrochloride
- 网络盐酸尼卡地平
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Study on drug release of nicardipine hydrochloride controlled release tablets
盐酸尼卡地平控释片的释放度研究
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Conclusion : PLA can be used to prepare oral nicardipine hydrochloride sustained-release .
结论:聚乳酸可用于制备口服盐酸尼卡地平缓释制剂。
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Study on preparation and stability of nicardipine hydrochloride sustained release pellets
盐酸尼卡地平缓释微丸的制备及其稳定性研究
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Study on Percutaneous Absorption of Nicardipine Hydrochloride Gel through Rabbit Skin in vivo
盐酸尼卡地平凝胶家兔在体透皮吸收研究
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Studies on preparation of monolithic osmotic pump tablet of nicardipine hydrochloride
难溶性药物盐酸尼卡地平单室单层渗透泵片的制备
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We perfused the lung of the second group with Nicardipine Hydrochloride .
Ⅱ组体外循环方法同Ⅰ组,在肺低温保护液中加入尼卡地平。
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Nicardipine hydrochloride transdermal controlled release patches with gel matrix were prepared .
制备盐酸尼卡地平的凝胶骨架控释贴剂。
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Study on Nicardipine Hydrochloride Intestinal dissolved Sustained-release Solid Dispersion
盐酸尼卡地平缓释固体分散体的研究
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Objective : To prepare nicardipine hydrochloride sustained-release pellets , and to research factors affecting the release rate in vitro .
前言:目的:制备盐酸尼卡地平缓释微丸,并考察影响其溶出度的因素。
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Conclusion : nicardipine hydrochloride bi-layer osmotic pump tablets had obvious in vitro-in vivo controlled release effect .
本文的研究结果表明:以聚氧乙烯为主要辅料,用醋酸纤维素包衣制成的盐酸尼卡地平双层渗透泵控释片具有明显的控释作用。
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RESULTS In the presence of laurocapram , the permeation flux of nicardipine hydrochloride was increased by 20 times .
结果:在月桂氮芯卓酮存在下,尼卡地平的透皮流量增加20.8倍。
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Preparation of Nicardipine Hydrochloride Transdermal Controlled-Release Patches with Gel-matrix and the Study on Penetration Enhancers
凝胶骨架控释型盐酸尼卡地平贴剂的制备及透皮促渗剂研究
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Preparation and Study of m-Nisoldipine Intragastric Floating Sustained-release Tablet ; Prescription screening of Nicardipine hydrochloride sustained-release tablet and determination of release rate
间尼索地平胃内漂浮型缓释片的研制盐酸尼卡地平缓释片的制备及释放度测定
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Nicardipine hydrochloride ( 1 ) intestinal dissolved sustained release solid dispersion was developed using PEG 6000 ( 2 ) and acrylic resin ⅱ( 3 ) as mixed carrier by the solvent evaporating method .
应用聚乙二醇(PEG)6000(2)和号丙烯酸树脂(3)为混和载体,用溶剂法制备了盐酸尼卡地平(1)肠溶缓释固体分散体。
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The in vitro permeation kinetics of nicardipine hydrochloride ( 1 ) through the depilatory rat skin and the effect of laurocapram ( 2 ) using a modified diffusion cell were evaluated .
用改良的扩散装置评价了盐酸尼卡地平(1)通过脱毛大鼠皮肤的渗透动力学以及促渗剂月桂氮酮(2)的作用。
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Conclusion Nicardipine hydrochloride is not only of confirmative effect in the treatment and prevention of CVS after SAH but also promotes speedy rehabilitation of nerve functions and adds no risks of re-hemorrhage .
结论丹颐防治SAH后CVS疗效确切,并能促进神经功能的尽快恢复,且无增加再出血的危险。
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The controls were treated with dehydration and routine hemostasis and in the Nicardipine hydrochloride group with the same treatment , plus utilization of intravenous dripping of 100 ml Nicardipine hydrochloride 1 / d for 10 days .
SAH对照组用脱水,止血等常规疗法,丹颐组在常规疗法基础上加用丹颐100ml,静脉滴注,1/d,共10d。