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抗坏血酸亚铁非泡腾漂浮型迷你胶囊,作为口服铁补充剂。

Ferrous ascorbate non-effervescent floating mini-caplets as an oral iron supplement.

作者信息

Trivedi Shital, Kevlani Vijay, Shah Shreeraj

机构信息

Research Scholar, Gujarat Technological University, Ahmedabad, 382424, Gujarat, India.

Department of Pharmaceutical Technology, L. J. Institute of Pharmacy, L J University, Ahmedabad, Gujarat, India.

出版信息

Drug Deliv Transl Res. 2025 May;15(5):1554-1566. doi: 10.1007/s13346-024-01691-x. Epub 2024 Aug 12.

Abstract

This research aimed to develop non-effervescent floating mini-caplets of Ferrous Ascorbate (FA) using low-density polymers to overcome the problems of poor bioavailability associated with immediate-release iron products. Methods: The excipients and method (melt granulation) were selected based on pre-and post-compression parameters in trial batches. The formulation was optimized by a full factorial 3 experimental design. An optimized formulation was evaluated for drug release kinetic, accelerated stability study, and in vivo study in healthy adult New Zealand female rabbits. Results: The optimized formulation F6 mini-caplets (42.5% FA, 45% Glyceryl palmitostearate as Precirol, 10% polyvinyl pyrrolidone K-30, and 2.5% lactose) were found to have instant floating and 12 h floating duration in 0.1N Hydrochloric acid (HCl) dissolution medium. In vitro drug release (diffusion mechanism) at 1 h and 5 h was 30-35% and 65-70%, respectively. It was found stable for three months under an accelerated stability study. In vivo study showed significantly increased serum iron levels and decreased unsaturated iron binding capacity (UIBC) in the test group (optimized formulation) compared to control and standard (immediate-release iron). Conclusion: Based on the in vitro and in vivo results, we conclude that non-effervescent floating FA mini-caplets have higher bioavailability compared to immediate release FA, which may be attributed to prolonged iron release at its absorption site due to their retention in the gastric region. Hence, non-effervescent floating FA mini-caplets may act as a potential approach for iron deficiency.

摘要

本研究旨在使用低密度聚合物开发抗坏血酸亚铁(FA)的非泡腾漂浮型迷你胶囊,以克服速释铁产品生物利用度差的问题。方法:根据试验批次的压前和压后参数选择辅料和方法(熔融制粒)。通过全因子3实验设计对配方进行优化。对优化后的配方进行药物释放动力学、加速稳定性研究以及在健康成年新西兰雌性兔体内的研究。结果:发现优化后的配方F6迷你胶囊(42.5% FA、45% 甘油棕榈硬脂酸酯作为Precirol、10% 聚乙烯吡咯烷酮K-30和2.5% 乳糖)在0.1N盐酸(HCl)溶解介质中具有即时漂浮性和12小时的漂浮持续时间。在1小时和5小时时的体外药物释放(扩散机制)分别为30 - 35%和65 - 70%。在加速稳定性研究中发现其在三个月内稳定。体内研究表明,与对照组和标准组(速释铁)相比,试验组(优化后的配方)的血清铁水平显著升高,不饱和铁结合能力(UIBC)降低。结论:基于体外和体内结果,我们得出结论,非泡腾漂浮型FA迷你胶囊与速释FA相比具有更高的生物利用度,这可能归因于它们在胃区域的滞留,使其在吸收部位的铁释放延长。因此,非泡腾漂浮型FA迷你胶囊可能是治疗缺铁的一种潜在方法。

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