grade
pharmaceutical primary standard
API family
starch
manufacturer/tradename
USP
application(s)
pharmaceutical (small molecule)
format
neat
General description
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。
Application
A 型淀粉甘醇酸钠USP参考标准品，预期用途是美国药典规定的指定质量测试和检测。也用于USP各论，例如：粉甘醇酸钠
Analysis Note
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。
Other Notes
可能适用相应的销售限制。
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
M Maghsoodi et al.
Pharmaceutical development and technology, 16(3), 243-249 (2010-02-24)
Spherical crystallization (SC) of carbamazepine (CBZ) was carried out for preparation of the agglomerates using the solvent change method. The potential of the intraagglomerate addition of sodium starch glycolate (SSG) as a disintegrant agent and povidone (PVP) as a hydrophilic
John Rojas et al.
AAPS PharmSciTech, 13(4), 1054-1062 (2012-08-18)
Spironolactone is a drug derived from sterols that exhibits an incomplete oral absorption due to its low water solubility and slow dissolution rate. In this study, formulations of spironolactone with four disintegrants named as croscarmellose sodium, crospovidone, sodium starch glycolate
Alvaro Goyanes et al.
Drug development and industrial pharmacy, 37(7), 825-831 (2011-03-17)
Chitosan-silica coprecipitate (C-S) has recently been proposed as a tablet disintegrant. In this study we compared it with a 1:1 physical mixture of chitosan and silica (C/S) at the same composition as the coprecipitate, and with the widely used commercial
Ritesh M Pabari et al.
International journal of pharmaceutics, 430(1-2), 18-25 (2012-04-03)
A two factor, three level (3(2)) face centred, central composite design (CCD) was applied to investigate the main and interaction effects of tablet diameter and compression force (CF) on hardness, disintegration time (DT) and porosity of mannitol based orodispersible tablets
Ramji Anil Kumar Arza et al.
AAPS PharmSciTech, 10(1), 220-226 (2009-03-12)
Drugs that have narrow absorption window in the gastrointestinal tract (GIT) will have poor absorption. For these drugs, gastroretentive drug delivery systems offer the advantage in prolonging the gastric emptying time. Swellable, floating, and sustained release tablets are developed by
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