推荐产品
等级
pharmaceutical primary standard
API类
starch
制造商/商品名称
USP
应用
pharmaceutical (small molecule)
格式
neat
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一般描述
本品按现行药典规定交付。所有为支持本产品而提供的信息，包括SDS和任何产品信息单均由药典颁发机构制定并发布。如需进一步信息和支持，请访问现行药典网站。
应用
羧甲淀粉钠A类USP 参考标准，用于指定的质量测试和分析。
分析说明
这些产品仅供测试和化验使用。它们不适用于人类或动物，也不能用于诊断、治疗或治愈任何类型的疾病。
其他说明
可能适用相应的销售限制。
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Samata Mehta et al.
International journal of pharmaceutics, 422(1-2), 310-317 (2011-11-22)
A design of experiments (DOE) approach (2-level full factorial design) was used to investigate the effect of several formulation and process variables on the properties of fast disintegrating tablets comprising starch-based pellets and excipient granules and to optimize and validate
G Szakonyi et al.
Journal of pharmaceutical and biomedical analysis, 63, 106-111 (2012-03-01)
Water contents of superdisintegrant pharmaceutical excipients were determined by attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy using simple linear regression. Water contents of the investigated three common superdisintegrants (crospovidone, croscarmellose sodium, sodium starch glycolate) varied over a wide range
R C A Schellekens et al.
Journal of controlled release : official journal of the Controlled Release Society, 132(2), 91-98 (2008-09-09)
Conventional pH-responsive coatings used for oral drug delivery to the lower parts of the gastro-intestinal tract often show a poor performance. A new system for site-specific pulsatile delivery in the ileo-colonic regions is described. The system is based on the
Solventless visible light-curable coating: II. Drug release, mechanical strength and photostability.
Sagarika Bose et al.
International journal of pharmaceutics, 393(1-2), 41-47 (2010-04-08)
Solventless photocurable film coating was used to obtain modified release coatings. Different pore-forming agents were used to achieve immediate and sustained release of a blue dye contained in the coated pellets (non-pareil beads). A super-disintegrant, sodium starch glycolate, was used
Randa Latif
Pharmaceutical development and technology, 18(6), 1372-1378 (2012-09-12)
This report describes zero-order approximation for metoclopramide hydrochloride sublingual tablet formulation. Effects of type and concentration of excipients on release were investigated. Study revealed that highest rate of dissolution was attained with crosspovidone and decreased in the order crosspovidone >
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