Preparation and Evaluation for Pulstile Release Capsules of Phenytoin
DOI:
https://doi.org/10.22270/ijmspr.v10i4.129Keywords:
Phenytoin, polyethylene glycol 4000, sodium chloride, purified talc,, magnesium stearate, microcrystalline celluloseAbstract
The core Eighty tablets were evaluated for their drug concentration, hardness weight fluctuation thickness, friability, and disintegration speed. Identify the tablet actual thickness, followed by its diameter, was determined by calipers like vernier calipers, where a sample of 5 to 6 tablets was randomly selected and the average values of thickness and diameter were determined. The standard USP method was used to test the pills' different weights. From the batch, 20 pills were arbitrarily selected, and each one was weighed to ensure for weight. variance. A percentage deviation from the average weight was calculated.
Keywords: Phenytoin, polyethylene glycol 4000, sodium chloride, purified talc, magnesium stearate, microcrystalline cellulose
References
Chien Yie W Novel drug delivery systems. 2nd ed. Marcel Dekker.Drugs and pharm Sci. 2021; 50: 139-140.
Swamivelmanickam M, Manavalan R, Valliappan K. Mouth Dissolving Tablets: An Overview. Int. J. of Pharm. Sci. and Res. 2020; 1(12): 43-55.
Jain CP, Naruk PS. Formulation and evaluation of fast dissolving tablets of valsartan. Int J. of Pharm. & pharm Sci. 2019; 1(1): 219-226.
Jeevan JB, Suneela G. Development of Fast Dissolving Tablets of Glibenclamide Using Crospovidone and its Kneading Mixture. Ind J. of Pharm Edu. Res. 2020; 44(4): 334-340.
Anjan KM, Murthy PN, Jagannath S, Sudarsan B, Sahoo SK. Formulation Design and Optimization of Mouth Dissolving Tablets of Levocetrizine Hydrochloride Using Sublimation Technique. Ind J. of Pharm.Edu.Res. 2019; 43(1): 39-45.
Seager H. Drug-delivery Products and the Zydis Fast-dissolving Dosage Form. J. Pharm. Pharmacol. 1997; 50: 375-382. https://doi.org/10.1111/j.2042-7158.1998.tb06876.x PMid:9625481
Kumar GA, Wadood SA, Maurya SD, Ramchand D, Interpenetrating polymeric network hydrogel for stomach-specific drug delivery of clarithromycin: Preparation and evaluation, Asian Journal of Pharmaceutics-October-December 2010; 179-184. https://doi.org/10.4103/0973-8398.76738
Bradoo R. Fast Dissolving Drug Delivery Systems, JAMA India. 2001; 4(10): 27-31.
Kuchekar BS, Atul, Badhan, C. Mahajan HS. Mouth dissolving tablets: A novel drug delivery system. Pharm Tim. 2003; 35: 7-9.
Behnke K, Sogaard J, Martin S, Bauml J, Ravindran AV, Agren H, et al. Mirtazapine orally disintegrating tablet versus sertraline: A prospective onset of action study. J Cli Psy pharmacol. 2003; 23: 358-64. https://doi.org/10.1097/01.jcp.0000085408.08426.05 PMid:12920411
Fu Y, Yang S, Jeong SH, Kimura S, Park K. Orally fast disintegrating tablets: Developments, technologies, taste-masking and clinical studies. Cri Rev The Dru Car Sys. 2004; 21: 433-76. https://doi.org/10.1615/CritRevTherDrugCarrierSyst.v21.i6.10 PMid:15658933
Dollo G, Chevanne F, Le CP, Chemtob C, Le VR. Bioavailability of phloroglucinol in man. J Pharm Bel. 1999; 54: 75-82.
Maurya SD, Prajapati S, Gupta A, Saxena G, Dhakar RC, Formulation Development and Evaluation of Ethosome of Stavudine, Indian J.Pharm. Educ. Res. 2010;44(1)
Maurya SD, Aggarwal S, Tilak VK, Dhakar RC, Singh A, Maurya G, Enhanced Transdermal Delivery of Indinavir Sulfate via Transfersomes, Pharmacie Globale (IJCP) 2010;1(06):1-7
Allen LV, Wang B. Process for making a particulate support matrix for making a rapidly dissolving dosage form. US Patent.2001; 6,207,199.
Allen LV, Wang B. Process for making a particulate support matrix for making a rapidly dissolving tablet. US Patent. 1996; 5,587,180.
Fitri K, Khairani TN, Sianturi KT, Leny L, Hafiz I, Anti-inflammatory Activity of Ethanol Extract of Lotus (Nelumbo nucifera G.) Seed Against White Male Rats Using Paw Edema Method, Journal of Drug Delivery and Therapeutics,2021;11(4):1-4 https://doi.org/10.22270/jddt.v11i2-S.4622
Bhaskaran S, Narmada GV. Rapid dissolving tablet A Novel dosage form Ind Pharm. 2002; 1: 9-12.
Koizumi K, Watanabe Y, Morita K, Utoguchi N, Matsumoto M. New method of preparing high-porosity rapidly saliva soluble compressed tablets using mannitol with camphor: A subliming material. Int J Pharm 1997; 152: 127-31. https://doi.org/10.1016/S0378-5173(97)04924-7
Meyers GL, Battist GE, Fuisz RC. Process and apparatus for making rapidly dissolving dosage units and product there form. PCT Patent WC 95/34293-A1; 1995.
Published
How to Cite
Issue
Section
Copyright (c) 2024 Kalidas Mandal, Rakesh Kumar Jat

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

.