推荐产品
形式
powder
质量水平
分子量
average Mn ~30,000
标记范围
12-15 wt. % Acetyl
36-40 wt. % Butyryl
折射率
n20/D 1.475 (lit.)
密度
1.25 g/mL at 25 °C (lit.)
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WGK
nwg
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Gheorghe Fundueanu et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 66(1), 11-20 (2006-11-07)
The aim of this work is to safely transport bioadhesive microspheres loaded with DNA to intestine and to test their bioadhesive properties. Poly(vinyl alcohol) (PVA) microspheres were prepared by dispersion reticulation with glutaraldehyde and further aminated. These microspheres were firstly
Soad A Yehia et al.
Drug delivery, 18(8), 620-630 (2011-11-25)
The purpose of this study is to increase the lag time and prevent release of budesonide, a corticosteroid drug used in Crohn's disease for the first 5 h and efficiently deliver it to the colon. Eudragit S100 spray-coated capsules and pulsatile
Mitra Jelvehgari et al.
Archives of pharmacal research, 32(7), 1019-1028 (2009-07-31)
The present research work compares the effect of microsphere preparation technique on micromeritics and release behaviors of theophylline microspheres. Microspheres were prepared by oil-in oil (O(1)/O(2)) emulsion solvent evaporation method (ESE) using different ratios of anhydrous theophylline to cellulose acetate
M Constantin et al.
International journal of pharmaceutics, 330(1-2), 129-137 (2006-10-10)
Poly(vinyl alcohol) (PVA) microspheres were prepared by dispersion reticulation with glutaraldehyde and further aminated. These microspheres were firstly loaded with diclofenac (DF) and then entrapped in cellulose acetate butyrate (CAB) microcapsules by an o/w solvent evaporation technique for intestinal delivery
Varaporn Buraphacheep Junyaprasert et al.
International journal of pharmaceutics, 352(1-2), 81-91 (2007-12-07)
A sustained release suspension of diltiazem, a short half-life calcium channel blocker, was developed to reduce frequency of drug administration, ease of dose adjustment and improve patient compliance. In this study, the sustained release of diltiazem was obtained by complexing
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