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Bioavailability and stability of nifedipine-enteric coating agent solid dispersion.

作者信息

Hasegawa A, Nakagawa H, Sugimoto I

出版信息

Chem Pharm Bull (Tokyo). 1985 Jan;33(1):388-91. doi: 10.1248/cpb.33.388.

DOI:10.1248/cpb.33.388
PMID:4006028
Abstract
摘要

相似文献

1
Bioavailability and stability of nifedipine-enteric coating agent solid dispersion.
Chem Pharm Bull (Tokyo). 1985 Jan;33(1):388-91. doi: 10.1248/cpb.33.388.
2
Application of solid dispersions of nifedipine with enteric coating agent to prepare a sustained-release dosage form.
Chem Pharm Bull (Tokyo). 1985 Apr;33(4):1615-9. doi: 10.1248/cpb.33.1615.
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Stability and bioavailability of nifedipine in fine granules.硝苯地平细颗粒剂的稳定性和生物利用度
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Reproducibility of nifedipine absorption from GITS tablets: comparison of single-dose pharmacokinetics using 10, 20, 40 and 60 mg nifedipine.硝苯地平胃肠道治疗系统(GITS)片剂吸收的重现性:使用10毫克、20毫克、40毫克和60毫克硝苯地平的单剂量药代动力学比较
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Enteric solid dispersion of ciclosporin A (CiA) having potential to deliver CiA into lymphatics.具有将环孢素A(CiA)输送至淋巴管潜力的环孢素A肠溶固体分散体。
Chem Pharm Bull (Tokyo). 1989 Feb;37(2):471-4. doi: 10.1248/cpb.37.471.
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Development of novel sustained-release system, disintegration-controlled matrix tablet (DCMT) with solid dispersion granules of nilvadipine (II): in vivo evaluation.新型缓释系统——尼伐地平固体分散颗粒崩解控制型骨架片(DCMT)的研制(II):体内评价
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[Solid dispersion obtained from nifedipine and enteric coating agents. I. Dissolution behavior].
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[Properties of tetracycline hydrochloride tablets and their bioavailability].[盐酸四环素片的性质及其生物利用度]
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Drug input rate from the GI-tract. Michaelis-Menten kinetics and the bioavailability of slow release verapamil and nifedipine.来自胃肠道的药物输入速率。米氏动力学以及缓释维拉帕米和硝苯地平的生物利用度。
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Design and optimization of diclofenac sodium controlled release solid dispersions by response surface methodology.采用响应面法设计与优化双氯芬酸钠控释固体分散体
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Development of extended-release solid dispersions of nonsteroidal antiinflammatory drugs with aqueous polymeric dispersions: optimization of drug release via a curve-fitting technique.非甾体抗炎药与水性聚合物分散体的缓释固体分散体的研制:通过曲线拟合技术优化药物释放
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