Development and Characterization of Oil Entrapped Stomach Site Specific 5-Fluorouracil Loaded Microcapsules

Anjan De, S. Chakraborty, A. Mukherjee, J. Chattopadhyay
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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.
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5-氟尿嘧啶微胶囊的研制与表征
目的:5-氟尿嘧啶(5-FU),一种嘧啶抗代谢物,具有渗透性,但溶解度低。已知常规静脉注射5-FU会引起严重的全身毒性作用,因此限制了其在肿瘤疾病中的广泛应用。因此,本研究旨在开发胃部位特异性负载5-氟尿嘧啶(5-FU)微胶囊,以评估加入矿物油对海藻酸盐和果胶微胶囊理化性质的影响。设计/方法:采用离子化凝胶法制备矿物油包埋的5-FU浮珠。在不同批次微球的制备过程中,矿物油与水的比(v/v)、药物与聚合物的比(w/w)在两个水平上作为变量;要么高,要么低。结果:获得了光滑的球形珠子,其标称重量变化。各批微球悬浮24小时,延迟时间为41-84秒,药物释放时间为9小时。Higuchi等阶动力学模型表明药物从微球中扩散控制释放。研究还证实了矿物油对药物包埋(64.3 ~ 80.15%)和体外释放的影响。与低含油微球相比,高含油微球提高了药物的包封效率,但减慢了药物的释放速度。配方D为最佳配方。实际意义:人们认为,饱和供应可以在局部和所需的组织部位提供恒定的池,以便在癌症条件下获得治疗效果。社会意义:5-FU的口服生物利用度仅为28%,这限制了其依从性和口服使用。这种5-FU递送策略是药物饱和供应的保留配方。论文价值:优化后的配方5-FU在9 h内释放率为99.987%,药物包封率为82.51%。结果发现具有统计学意义,因此开发的配方具有增强的治疗价值和商业潜力。
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