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Hydroxypropyl methylcellulose processability

Iyer et al. [50] investigated the effects of roto-granulation on the performance of hydroxypropyl methylcellulose (HPMC), gelatin, and poly(-vinylpyrrolidone) (Povidone, PVP). In this process, all three binders produced similar results. However, HPMC was preferred due to prolonged drug release profiles, smaller particle size, and better content uniformity. [Pg.301]

For hydroxypropyl methylcellulose acetate succinate, a novel enteric dry coating method has been developed [31]. The unique feature of this method is that the enteric polymer is added in powder form (e.g., mixed with talcum directly to tablets or pellets) whereas a plasticizer diluted with paraffin is sprayed separately. The tablet core temperature is around 40°C, and the film is cured for a short time. To achieve a homogenous film, the rates of powder feeding and plasticizer spray have to be adjusted such that the two processes start and end simultaneously. [Pg.21]

Shah N, Railkar AS, Phuapradit W, Zeng FW, Malick AW. Effect of processing techniques in controlling the relca.se rate and mechanical strength of hydroxypropyl methylcellulose based hydrogel matrices. Eur J Pharm Biopharm 1996 42(3) 183-7. [Pg.303]

Huang Y, Khanvilkar KH, Moure AD, Hilliard-Lott M. Effects of manufacturing process variables on in vitro dissolution characteristics of extended-relca.se tablets formulated with hydroxypropyl methylcellulose. Drug Dev Ind Pharm 2003 29(l) 79-88. [Pg.308]

Mitchell A, Reynolds TD, Dasbach TP. A cpoorly water-soluble drugs using hydroxypropyl methylcellulose, Int J Pharm 2003 250 3-11. Rambali B, Bacrt L. Jans E. Masscart DL. Influence of the roll compactor parameter settings and the compression pressure on the buccal bio-adhesive properties. Int J Pharm 2001 220 129. ... [Pg.333]

To illustrate the method we examine the data of Wehrle, Palmieri, and Stamm (6), who report the optimized production of theophylline pellets by a simple one-step process in a high speed Stephan granulator. The formulation consisted of 20% theophylline drug substance, 30% lactose, and 50% microcrystalline cellulose. It was granulated with a 15% hydroalcoholic solution of hydroxypropyl-methylcellulose. [Pg.316]

Mitchell SA, Reynolds TD, Dasbach TP. A compaction process to enhance dissolution of poorly water-soluble drugs using hydroxypropyl methylcellulose. Int J Pharm 2003 250 3-11. [Pg.425]

Vojdani, E., Torres, J.A., 1989. Potassium sorbate permeability of methylcellulose and hydroxypropyl methylcellulose multi-layer films. Journal of Food Processing and Preservation 13, 417—430. [Pg.231]


See other pages where Hydroxypropyl methylcellulose processability is mentioned: [Pg.171]    [Pg.453]    [Pg.352]    [Pg.354]    [Pg.117]    [Pg.284]    [Pg.2571]    [Pg.353]    [Pg.192]    [Pg.99]    [Pg.66]    [Pg.171]    [Pg.126]    [Pg.397]    [Pg.404]    [Pg.231]    [Pg.102]    [Pg.238]    [Pg.100]    [Pg.326]    [Pg.880]    [Pg.1085]   
See also in sourсe #XX -- [ Pg.3206 ]




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