推荐产品
等級
pharmaceutical primary standard
API 家族
starch
製造商／商標名
USP
應用
pharmaceutical (small molecule)
格式
neat
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一般說明
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。
應用
Sodium Starch Glycolate Type A USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia. Also, for use with USP monograph such as Sodium Starch Glycolate
分析報告
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。
其他說明
可能适用相应的销售限制。
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 1
閃點（°F）
Not applicable
閃點（°C）
Not applicable
其他客户在看
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
Aiman A Obaidat et al.
Acta pharmaceutica (Zagreb, Croatia), 61(1), 83-91 (2011-03-17)
The aim of this study was to prepare fast-dissolving tablets of meloxicam after its complexation with β-cyclodextrin (β-CD) and to investigate the effect of using different superdisintegrants on the disintegration and release of meloxicam from the tablets. A complex of
Sagarika Bose et al.
International journal of pharmaceutics, 393(1-2), 32-40 (2010-02-09)
Film coating is generally accomplished by spraying polymers dissolved in solvents onto a cascading bed of tablets. The limitations associated with the use of solvents (both aqueous and organic) can be overcome by the use of solventless coating technologies. In
Balasubramaniam Jagadish et al.
Chemical & pharmaceutical bulletin, 58(3), 293-300 (2010-03-02)
The present study investigated the effect of co-grinding raloxifene HCL (RHCL) with different superdisintegrants, namely crospovidone (CP), croscarmellose sodium (CCS) and sodium starch glycolate (SSG), using a ball mill, in order to determine the potential effect on dissolution rate and
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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