Modified Cellulose, HPMC

Powders intended for nasal administration have to be optimized in terms of particle size and morphology as these properties are related to potential irritation in the nasal cavity [23], Certain procedures (e.g., spray drying process) can modify the particle size of the drug powder raw material, but in order to optimize the morphology and flowability properties of some pure drug powders, excipients need to be used. Sacchetti et al. [28] reported that the use of mannitol as a filler and hydroxy-propylmethyl cellulose (HPMC) as a shaper of spray-dried caffeine microparticles modified the typical needle shape of spray-dried caffeine to a more convenient roundish shape. Further addition of polyethylene glycol (PEG) resulted in increased... 

Cellulosic membranes are developed as a novel dmg delivery system, which is expressed to use on the skin and used as a mucus membrane of stomach, ear, nose, eye, rectum, and vagina. The goal excipients of these preparations are adhesive and film-former polymers. Modified cellulose, especially cellulose ethers, are extensively applied in bio-adhesives such as nasal, vaginal, ocular, buccal, and transdermal inventions only or by blend with additional polymers. Further newly applied ethers of cellulose in bio-adhesives contain anionic ether derivatives such as sodium carboxy-methyl cellulose (NaCMC) and non-ionic cellulose ethers such as hydoxypropyl cellulose (HPC), carboxymethyl cellulose (CMC), hydroxyethyl cellulose, ethyl cellulose (EC), hydroxylpropylmethyl cellulose (HPMC), or methyl cellulose (MC). Capability of polymer to absorb water from mucus and pH of objective area are main features defining the adhesive power of polymers. One benefit of cellulose ethers, such as HPC and NaCMC, is smaller dependence of adhesion period and their adhesion strength to pH of medium than thiolated bio-adhesive polymers and polyacrylate... 

These stabilizers are added to the formulation in order to stabilize the emulsion formed during particle preparation. These stabilizers, however, can also influence the properties of the particles formed. The type and concentration of the stabilizer selected may affect the particle size. Being present at the boundary layer between the water phase and the organic phase during particle formation, the stabilizer can also be incorporated on the particle surface, modifying particle properties such as particle zeta potential and mucoadhesion (203). Other polymers have also been evaluated as stabilizers in earlier studies such as cellulosic derivatives methylcellu-lose (MC), hydroxyethylcellulose ( ), hydroxypropylcellulose (HPC), and hydroxypropylmethylcellulose (HPMC), as well as gelatin type A and B, carbomer and poloxamer (203). 

Buccoadhesive-controlled release tablets for delivery of nifedipine were prepared by direct compression of carboxymethyl cellulose (CMC) with carbomer (CP) and compared to those prepared with PVP, PVA, HPMC, and acacia by a modified tensiometry method in vitro. It was found that the adhesion force was significantly affected by the mixing ratio of CP CMC in the tablets. CMC is necessary for controlling the release rate, whereas CP is important in providing bioadhesion. The tablets containing 15% CMC and 35% CP were found to have optimum drug release rate and bioadhesion [81]. 

Cellulose ethers have also been used in the ceramic industry (7). Since their appearance in 1959, water-based cellulose ethers have replaced solvent-based adhesives. The adhesives used for ceramic tile are ready-mixed products based on natural or synthetic rubber, polyvinyl acetate, and other resins, and they all contain cellulose ethers of one kind or another (e.g. MC, EC, HPMC, HEMC, HEC). These cellulose ethers reduce water loss, modify the viscosity of the mix, and can provide excellent adhesion for dry, very porous tiles. 

For all cIEF methods, polymer solutions are added into the samples, including methyl cellulose (MC) and (hydroxypropyl)methylcellulose (HPMC). These polymers modify the capillary surface [10-12] and enhance separation resolution. The existence of the polymer in the sample solution reduces diffusion coefficients of the proteins, thus, as described in Section 19.3.3, enhancing the separation resolution. In all cIEF applications described in this chapter, 0.35-0.5% of MC are added to the samples. 

Another advantage is that natural polymers can be modified using suitable reagents to obtain semisynthetic polymers. Modified starch/dextran, cyclodextrins, cellulose, alginate, scleroglucan and chitosan derivatives are the most important semisynthetic polymers for the drug industry [17-19]. In this respect, starting from the natural cellulose, at least 10 semisynthetic derivatives are widely used for the optimization of pharmaceutical formulations cellulose acetate (CA), cellulose acetate butyrate (CAB), cellulose acetate phthalate (CAP), methylcellulose (MC), ethylcellulose (EC), hydroxy-ethyl cellulose (HEC), hydroxypropyl cellulose (HPC), hydroxypropyl methylcellulose (HPMC), carboxymethylcellulose (CMC), nitrocellulose [16,20,21]. 

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