LIQUISOLID COMPACTS PDF

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Liquisolid Compacts: An Approach to Enhance the. Dissolution Rate of Nimesulide. Srinivas Vaskula, Sateesh Kumar Vemula, Vijaya Kumar. PDF | ABSTACT Liquisolid compacts were used to formulate water insoluble drugs in non volatile solvents and convert into acceptable flowing. PDF | The aim of this study was to investigate the use of liquisolid technique in improving the dissolution of Glimepiride in a solid dosage form. This study was.

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The flowable liquid retention potential was calculated using the following equation: A lesser amount of Neusilin was required to adsorb the same amount of liquid vehicle than Avicel and Fujicalin, which lowered the weight of tablet. To calculate the required amounts of powder excipients including both carrier and coating materials a mathematical approach for the formulation of A powder may be able to retain only limited amounts of liquid while maintaining acceptable flow and compression properties.

Six tablets from each formulation were tested for hardness. The less drug concentration in the vehicle means more fraction of the drug is liable to be in the liquid solution form i.

Indexed in Web of Science. Fujicalin, also to some extent, proved to be a better carrier than Avicel. This question is for testing whether you are a human visitor and to prevent automated spam submissions.

Liquisolid Compact Technique: A Novel Approach to Solubility Enhancement | OMICS International

The solubility of CBZ in polyethylene glycol was found to be greater co,pacts the other solvents. The and for liquid vehicles were used to calculate. Spireas S, Sadu S Enhancement of prednisolone dissolution properties using liquisolid compacts.

Fujicalin Dibasic calcium phosphate anhydrous and Neusilin Magnesium aluminometasilicate were obtained as gift sample from Fuji Chemical Industry Co. The tensile strength of the tablet was also sufficient.

Liquisolid Compact Technique: A Novel Approach to Solubility Enhancement

The lowest liquid factor was obtained for Avicel PHand accordingly, the amount of carrier was higher than other formulations. The three principal suggested mechanisms include an increased surface area of drug particles, an increased aqueous solubility, and an improved wettability of the drug particles.

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From the results of different batches prepared by three different carriers shown in Table 6compacfs was found that Neusilin proved to be the superior carrier than others. New chemical entities are often macromolecules with high lipophillicity show poor solubility and high permeability and present a technological challenge mainly due to their poor bioavailabilitywhich leads to poor absorption. The liquisolid approach is a potential technology due to its simplified manufacturing comapcts, cheaper production costs and the prospect of industrial scale up due to the good flow and compaction properties.

Authors and affiliation s: Results of hardness, friability, and disintegration time are represented in Table 4. Ann Jose ankara escort. The appropriate amounts of carrier and coating materials used for each formulation depend upon of that formulation. The solubility is an important factor in liquisolid systems, as higher solubility of drug in liquid vehicle can lead to higher dissolution rates since the compacfs will be more molecularly dispersed and more surface of drug will be exposed to the dissolution media.

Formulation and Evaluation of Liquisolid Compacts for Olmesartan Medoxomil

Supernatant was filtered through membrane filter using 0. Visit for more related articles at Journal of Pharmacovigilance. International Journal of ChemTech Research compactz Composition of liquids solid compacts batches is shown in Table 1. The hardness of the tablets was determined using Monsanto hardness tester.

Guidelines Upcoming Special Issues. Over past few decades, many techniques have been developed, to improve the solubility and dissolution of poorly soluble substances, with different degrees of success which includes micronization, lyohilization, solid dispersion, etc. The poor dissolution rate of water-insoluble drugs is still a major problem confronting the pharmaceutical industry.

Withdrawn samples were filtered through a 0. It liquksolid highly lipophilic log P 5.

Olmesartan cokpacts to be more soluble in Acrysol EL than other vehicles. The powder characteristics were evaluated by different flow parameters to comply with pharmacopoeial limits.

Another measure of tablets strength is friability. Abstract Olmesartan medoxomil is an angiotensin type II receptor blocker, antihypertensive agent, administered orally.

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Journal of Drug Delivery. This is an open access article distributed under the Creative Commons Attribution Licensewhich permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Agri and Aquaculture Journals Dr. Several techniques have been reported to improve drug solubility, among which the liquisolid technology is one of the most promising approaches.

Moreover, the inclusion of disintegrating agents may further enhance the drug release from this system. Solubility and dissolution are the core cmopacts of any physical or chemical science including biopharmaceutical and pharmacokinetic considerations in therapy of any medicine. The maximum liquid load on the carrier material is termed as the liquid load factor Lf. Formulation containing Neusilin-Neusilin and Neusilin- Aerosil showed no disintegration while all other formulations showed disintegration up to seconds.

Moreover, the more vehicle available means an even distribution of the vehicle over the remaining undissolved drug particles that will help in good wetting compacte the drug during the dissolution step. lqiuisolid

The pronounced effect of the different carriers was not observed on dissolution profile liquioslid the flow properties and tensile strength were considered for optimizing the carrier. As shown in Table 5LSA 15 showed prompt drug release with value of Formulated liquisolid compacts showed all physical parameters within prescribed limit.

These peaks can be considered as characteristic peaks of olmesartan medoxomil and were not affected and prominently observed in IR spectra of olmesartan medoxomil along with oil and carrier liqquisolid shown in Figure 4 b. Out of which the recent research focus on liquisolid compact technique or powdered solution technique as one of the successful ljquisolid to achieve the goal. The was then used to decide the optimum amount of carrier and coating materials required to ensure dry-looking, free-flowing and compactible powdered systems.