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      Studies on jackfruit seed starch as a novel natural superdisintegrant for the design and evaluation of irbesartan fast dissolving tablets

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          Abstract

          Background

          In the present investigation, an attempt was made to isolate starch from jackfruit seed powder and utilize it as a superdisintegrant to design fast dissolving tablets of irbesartan.

          Methods

          Starch was isolated from jackfruit seeds via aqueous and alkali extraction processes and evaluated for its physicochemical properties, for phytochemical tests, and for acute toxicity studies. Irbesartan fast dissolving formulations were prepared using the wet granulation technique.

          Results

          Acute toxicity studies for the extract indicated that all rats were healthy with no physiological changes in their behavior. The prepared irbesartan tablet formulations were found to be stable according to the Indian Pharmacopoeia-specified limits for postcompression parameters. From in vitro dissolution studies, it was observed that formulations F5 and F8 containing 5% w/w of alkali extracted starch and 5% w/w of croscarmellose sodium showed faster disintegration and improved dissolution rate compared with the other formulations. Fourier transfer infrared spectroscopic and differential scanning colorimetric analysis performed on optimized formulations indicated that there were no major interactions between the drug and excipients. Accelerated stability studies carried out on optimized formulations showed all tablets to be stable.

          Conclusion

          The tablets prepared from jackfruit seed starch as superdisintegrant were found to be suitable for preparation of fast dissolving tablets.

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          Most cited references17

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          Preparation and evaluation of a compressed tablet rapidly disintegrating in the oral cavity.

          In order to make a compressed tablet which can rapidly disintegrate in the oral cavity, microcrystalline cellulose and low-substituted hydroxypropylcellulose were used as disintegrants, and ethenzamide and ascorbic acid were chosen as poorly and easily water soluble model drugs, respectively. The mixture of microcrystalline cellulose and low-substituted hydroxypropylcellulose was compressed at 100--500 kgf in the absence of an active ingredient. The properties of these tablets, such as hardness, porosity, the time required for complete wetting of a tested tablet (wetting time), water uptake and disintegration time determined by a new disintegration apparatus, were investigated to elucidate the wetting and disintegration characteristics of these tablets, When the MCC/L-HPC ratio was in the range of 8:2 to 9:1, the shortest disintegration time was observed. The disintegration of tablets containing ethenzamide or ascorbic acid was examined next. Tablet disintegration time in the oral cavity was also tested, and good correlation between the disintegration behaviors in vitro and in the oral cavity was recognized.
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            Development and evaluation of glyburide fast dissolving tablets using solid dispersion technique.

            Glyburide is a poorly water-soluble oral hypoglycemic agent, with problems of variable bioavailability and bio-inequivalence related to its poor water-solubility. This work investigated the possibility of developing glyburide tablets, allowing fast, reproducible, and complete drug dissolution, by using drug solid dispersion in polyethylene glycol. Phase-solubility studies were performed to investigate the drug-carrier interactions in solution, whereas differential scanning calorimetry, X-ray powder diffraction, and infrared spectroscopy were used to characterize the solid state of solid dispersions. The effects of several variables related to both solid dispersion preparation (cofusion or coevaporation technique, drug-to-carrier ratio, polyethylene glycol molecular weight) and tablet production (direct compression or previous wet-granulation, tablet hardness, drug, and solid dispersion particle size) on drug dissolution behavior were investigated. Tablets obtained by direct compression, with a hardness of 7-9 Kp, and containing larger sized solid dispersions (20-35 mesh, i.e., 850-500 microm) of micronized glyburide in polyethylene glycol 6000 prepared by the cofusion method gave the best results, with a 135% increase in drug dissolution efficiency at 60 min in comparison with a reference tablet formulation containing the pure micronized drug. Moreover, the glyburide dissolution profile from the newly developed tablets was clearly better than those from various commercial tablets at the same drug dosage.
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              Orodispersible tablets: An overview

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                Author and article information

                Contributors
                Journal
                Integr Med Res
                Integr Med Res
                Integrative Medicine Research
                Elsevier
                2213-4220
                2213-4239
                26 May 2017
                September 2017
                26 May 2017
                : 6
                : 3
                : 280-291
                Affiliations
                [0005]Department of Pharmaceutics, Chebrolu Hanumaiah Institute of Pharmaceutical Sciences, Guntur, India
                Author notes
                [* ] Corresponding author. Chebrolu Hanumaiah Institute of Pharmaceutical Sciences, Chowdavaram, Guntur 522 019, Andhra Pradesh, India. svidyadhara@ 123456gmail.com
                Article
                S2213-4220(16)30189-5
                10.1016/j.imr.2017.04.001
                5605381
                28951842
                863a1c6e-a0ab-4456-8202-3dcda9f46e81
                © 2017 Korea Institute of Oriental Medicine. Published by Elsevier.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 27 December 2016
                : 4 April 2017
                Categories
                Original Article

                fast dissolving tablets,irbesartan,jackfruit seeds,superdisintegrants

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