Anjan De, S. Chakraborty, A. Mukherjee, J. Chattopadhyay
{"title":"Development and Characterization of Oil Entrapped Stomach Site Specific 5-Fluorouracil Loaded Microcapsules","authors":"Anjan De, S. Chakraborty, A. Mukherjee, J. Chattopadhyay","doi":"10.5530/RJPS.2014.3.5","DOIUrl":null,"url":null,"abstract":"Purpose: 5-Fluorouracil (5-FU), a pyrimidine antimetabolite attains permeability but is low in solubility. Conventional intravenous administration of 5-FU is known to cause severe systemic toxic effects and thus restricts its versatile use in neoplastic diseases. Therefore, the present study was undertaken to develop stomach site specific 5-Fluorouracil (5-FU) loaded microcapsules in order to evaluate the effect of incorporated mineral oil on physiochemical properties of alginate and pectin microcapsules. Design/methodology: Mineral oil entrapped buoyant beads of 5-FU was prepared by the ionotropic gelation technique. During the preparation of various batches of beads, the ratio of mineral oil to water (v/v), the ratio of drug to polymer (w/w), were kept as variables at two levels; either high or low. Findings: Smooth, spherical beads with nominal weight variation were obtained. All batches of beads floated for 24 hours with a lag time of 41-84 sec. The release of drug followed for 9 h. Higuchi and other order kinetic modeling indicated a diffusion-controlled release of drug from the beads. The study also demonstrated the influence of mineral oil on drug entrapment (64.3 to 80.15%) and in vitro release. Higher level of oil increased drug entrapment efficiency but retarded drug release rate as compared to lower level of oil containing beads. Formulation D was found to be the optimized formulation. Practical implications: It is perceived that a saturation supply can provide a constant pool locally and up to the desired tissue sites such that the therapeutic effects can be attained in cancerous conditions. Social Implications: Oral bioavailability of 5-FU is only 28% and that limits its compliance and oral usage. This strategy for 5-FU delivery is a retentive formulation for a saturation supply of the drug. Value of paper: The optimized formulation showed 99.987% release of 5-FU in 9 h with 82.51% drug entrapment. The results were found statistically significant hence the developed formulation has enhanced therapeutic value and commercial potential.","PeriodicalId":21459,"journal":{"name":"RGUHS Journal of Pharmaceutical Sciences","volume":"25 1","pages":"110-119"},"PeriodicalIF":0.0000,"publicationDate":"2014-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RGUHS Journal of Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5530/RJPS.2014.3.5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: 5-Fluorouracil (5-FU), a pyrimidine antimetabolite attains permeability but is low in solubility. Conventional intravenous administration of 5-FU is known to cause severe systemic toxic effects and thus restricts its versatile use in neoplastic diseases. Therefore, the present study was undertaken to develop stomach site specific 5-Fluorouracil (5-FU) loaded microcapsules in order to evaluate the effect of incorporated mineral oil on physiochemical properties of alginate and pectin microcapsules. Design/methodology: Mineral oil entrapped buoyant beads of 5-FU was prepared by the ionotropic gelation technique. During the preparation of various batches of beads, the ratio of mineral oil to water (v/v), the ratio of drug to polymer (w/w), were kept as variables at two levels; either high or low. Findings: Smooth, spherical beads with nominal weight variation were obtained. All batches of beads floated for 24 hours with a lag time of 41-84 sec. The release of drug followed for 9 h. Higuchi and other order kinetic modeling indicated a diffusion-controlled release of drug from the beads. The study also demonstrated the influence of mineral oil on drug entrapment (64.3 to 80.15%) and in vitro release. Higher level of oil increased drug entrapment efficiency but retarded drug release rate as compared to lower level of oil containing beads. Formulation D was found to be the optimized formulation. Practical implications: It is perceived that a saturation supply can provide a constant pool locally and up to the desired tissue sites such that the therapeutic effects can be attained in cancerous conditions. Social Implications: Oral bioavailability of 5-FU is only 28% and that limits its compliance and oral usage. This strategy for 5-FU delivery is a retentive formulation for a saturation supply of the drug. Value of paper: The optimized formulation showed 99.987% release of 5-FU in 9 h with 82.51% drug entrapment. The results were found statistically significant hence the developed formulation has enhanced therapeutic value and commercial potential.