KLUCEL LF PDF

Klucel™ LF Pharma, SDS · TDS*. Klucel™ M CS, Klucel™ M CS has excellent film-forming properties and thickens non-aqueous systems and provide lubricious. Klucel hydroxypropylcellulose (HPC) provides a remarkable set of physical properties for tablet binding, modified release, and film coating. This unique polymer. Klucel hydroxypropylcellulose (HPC) is a nonionic water-soluble cellulose ether with Klucel HPC is soluble in many polar organic solvents and in water below.

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In our experiments, HPC provided a matrix for the drug and aided formation of solid extrudate rods that could be pelletized. Compaction properties of l -lysine salts. In vitro release profiles tablets from extruded matrices. These observations correlated with the data generated from compaction profiles.

The thickness and diameter of the tablets was measured using a micrometer. ELF polymer, being more plastic, forms a denser compact on being compressed, thus slowing down the release due to decreased porosity This product is used in a variety of food applications, including whipped toppings, bakery cream fillings, edible nut and candy coatings and confectionery glazes.

Phase behavior of amorphous molecular dispersions II: T3 and T4 tablets were compressed from un-extruded mixtures with blend compositions similar to H3 and H4 tablets. Combined use of ordered mesoporous silica and precipitation inhibitors for improved oral absorption of the poorly soluble weak base itraconazole. Extruded systems were also studied similarly to evaluate crystallinity. Tablets compressed from milled extrudates exhibited rapid release owing to the increased surface area of the milled extrudate.

The hot-stage microscope confirmed the formation of a miscible amorphous system of KPR—EF mixtures Technologies such as solid dispersions have proven viable and been used extensively due to inherent advantages over other technologies 1.

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An immiscible amorphous system would exhibit two Tgs whereas a miscible system exhibits a single Tg on a DSC run. In vitro release of pellets—effect of drug load on release. Samples were collected at every 0. Published online Sep 8. The content of such third party sites is not within our control, and we cannot and will not take responsibility for the information or content.

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Pellets manufactured utilizing ELF polymer exhibited faster drug release in comparison to EF pellets. The dissolution profiles were compared utilizing model-independent, f 2 similarity factor values. Tablets were tested for hardness and the tensile strength calculated. Most of these techniques are multiple-batch processes that might also involve the use of organic solvents.

Klucel™ Hydroxypropylcellulose, Ashland – ChemPoint

Melt flow properties of hydroxypropyl cellulose for solubilization klcuel lipophilic actives. It combines organic solvent solubility, thermoplasticity, and surface activity with the thickening and stabilizing properties of other water-soluble cellulose polymers. F is the force measured at tablet failure, d and h are the diameter and thickness of the tablet, respectively.

Improved dissolution and pharmacokinetic behavior of cyclosporine A using high-energy amorphous solid dispersion approach. Endothermic onset and peak temperatures at melting were calculated from the software. Application of the solid dispersion method to the controlled release of medicine.

In vitro release studies were performed on tablets stored at different stability conditions. The soluble polymers formed channels allowing media to enter the matrix. A hot-stage microscope was used to replicate temperatures the material would be exposed to inside an extruder while polarized light microscope PLM was used to observe the changes in the material.

The studies were performed utilizing six replicates. The pellets were evaluated for post-extrusion content using HPLC method. Stabilization of hot-melt extrusion formulations containing solid solutions using polymer blends. Application of melt extrusion in the development of a physically and chemically stable high-energy amorphous solid dispersion of a poorly water-soluble drug.

Formulation of a fast-dissolving ketoprofen tablet using freeze-drying in blisters technique. This decrease in melting point temperature can also be attributed to drug—polymer interactions drop Earlier studies performed on HPC HF, a higher molecular weight grade of HPC, report the advantages of using plasticizers and plasticizing effect of drugs With a decrease in molecular weight of HPC, compactibility and plasticity increase with a consequential decrease in elasticity KPR on melting exhibits a tacky nature and cannot be extruded on its own without a matrix.

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Physical mechanical and tablet formation properties of hydroxypropylcellulose: Change in packaging or use of desiccant might help in overcoming these factors. Evaluation of the effects klucrl tableting speed on the relationships between compaction pressure, tablet tensile strength, and tablet solid fraction. Many polymers have been evaluated for use in HME including hydroxypropylcellulose Klucek 17polyvinyl pyrrolidone 18polyethylene oxide 19and sugars such as isomalt 20erythritol 21and mannitol However, such high energy kluvel tend to recrystallize or precipitate out from their supersaturated solutions.

In vitro and in vivo lkucel of fenofibrate solid dispersion prepared by hot-melt extrusion.

Stable nimodipine tablets with high bioavailability containing NM-SD prepared by hot-melt extrusion. Hot-melt extrusion HME is a versatile processing technology that can be used for solubility enhancement, granulation, and as a physico-chemical stability imparting technology In Vitro Randomized Controlled Trial.

Mannitol, a crystalline excipient, on compression, undergoes plastic deformation whereas HPC has a viscoelastic character that aids in holding the matrix together. Thus, a slower release, still in the domain of immediate release, might actually contribute towards increased bioavailability and better stability for SDs. HME was utilized to intimately mix the components into a homogenous matrix. It was also observed that during extrusion process these formulations exhibited decreased die swelling.

The extrudates can be further processed into pellets as multi-particulate systems, films, or into tablets by milling and addition of tabletting excipients The difference could be attributed to absorption of moisture onto tablets that affected the disintegration time and hence a slower release at high humidity conditions.