首页> 外文期刊>Drug delivery. >Formulation and In Vivo Evaluation of Membrane-Moderated Transdermal Therapeutic Systems of Nicardipine Hydrochloride using Carvone as a Penetration Enhancer.
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Formulation and In Vivo Evaluation of Membrane-Moderated Transdermal Therapeutic Systems of Nicardipine Hydrochloride using Carvone as a Penetration Enhancer.

机译:使用香芹酮作为渗透促进剂的盐酸尼卡地平的膜调节透皮治疗系统的配制和体内评估。

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摘要

A membrane-moderated transdermal therapeutic system (TTS) of nicardipine hydrochloride was developed using 2%w/w hydroxy propyl cellulose (HPC) gel as a reservoir system containing 8%w/w of carvone as a penetration enhancer. The permeability flux of nicardipine hydrochloride through ethylene vinyl acetate (EVA) copolymer membrane was found to increase with an increase in vinyl acetate content in the copolymer. The effect of various pressure-sensitive adhesives (MA-31, MA-38, or TACKWHITE A 4MED) on the permeability of nicardipine hydrochloride through EVA 2825 membrane (28%w/w vinyl acetate) or EVA 2825 membrane/skin composite also was studied. The results showed that nicardipine hydrochloride permeability through EVA 2825 membrane coated with TACKWHITE A 4MED/skin composite was higher than that coated with MA-31 or MA-38. Thus, a new TTS for nicardipine hydrochloride was formulated using EVA 2825 membrane coated with a pressure-sensitive adhesive TACKWHITE A 4MED and 2%w/w HPC gel as reservoir containing 8%w/w of carvone as a penetration enhancer. The bioavailability studies in healthy human volunteers indicated that the TTS of nicardipine hydrochloride, designed in the present study, provided steady-state plasma concentration of the drug with minimal fluctuations for 23 hr with improved bioavailability in comparison with the immediate-release capsule dosage form.
机译:使用2%w / w羟丙基纤维素(HPC)凝胶作为储库系统开发了盐酸尼卡地平的膜调节透皮治疗系统(TTS),该系统包含8%w / w的香芹酮作为渗透促进剂。发现盐酸尼卡地平通过乙烯乙酸乙烯酯(EVA)共聚物膜的渗透通量随共聚物中乙酸乙烯酯含量的增加而增加。各种压敏粘合剂(MA-31,MA-38或TACKWHITE A 4MED)对盐酸尼卡地平通过EVA 2825膜(28%w / w醋酸乙烯酯)或EVA 2825膜/皮肤复合材料的渗透性的影响也很明显。研究。结果表明,盐酸尼卡地平通过TACKWHITE A 4MED /皮肤复合材料涂层的EVA 2825膜的渗透性高于MA-31或MA-38涂层。因此,使用涂有压敏胶TACKWHITE A 4MED和2%w / w HPC凝胶的EVA 2825膜作为储库,其中包含8%w / w的香芹酮作为渗透促进剂,配制了盐酸尼卡地平的新TTS。在健康人类志愿者中进行的生物利用度研究表明,在本研究中设计的盐酸尼卡地平TTS与速释胶囊剂型相比,能够在23小时内将药物的稳态血浆浓度波动最小化,并改善了生物利用度。

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