Revolutionizing Nitrofurantoin Delivery: Unraveling Challenges and Pioneering Solutions for Enhanced Efficacy in UTI Treatment

Q2 Pharmacology, Toxicology and Pharmaceutics
Gouri Prasad Nanda, Mrunali Patel, Rashmin B. Patel
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引用次数: 0

Abstract

Nitrofurantoin is an antimicrobial drug, highly effective in the treatment of critical or chronic bacterial infections of the urinary tract, and hence, it is the first line choice of drug for the treatment of urinary tract infections (UTI). Although the molecule is legacy in nature, there are many challenges in terms of drug product formulation and efficacy thereof. The authors are mainly focused in this literature review on, but not limited to, understanding the molecule in terms of physico-chemical properties of the drug, pharmacokinetics and pharmacodynamics, approved and withdrawn formulations, challenges concerning drug formulation, the cause of drug shortage in the market, improvement areas in terms of formulation and its therapeutic effectiveness. The authors found during their widespread review that the major challenge in the existing conventional drug delivery system of nitrofurantoin is the fluctuation of plasma concentration owing to its variability in drug absorption. Further, they understood that the variability in absorption is due to inherent variability in particle size distribution. Based on the findings, authors also explored the possibilities to deliver the drug in novel drug delivery systems such as nano self-emulsifying emulsions, nanoemulsions and multiple emulsions where the drug can be presented in soluble form and hence the variability in absorption and fluctuation in plasma concentration of drug can be avoided and described briefly the salient features of each drug delivery in this review.
硝基呋喃妥因给药革命:破解挑战,开创解决方案,提高尿毒症治疗效果
硝基呋喃妥因是一种抗菌药物,对治疗泌尿道重症或慢性细菌感染非常有效,因此是治疗泌尿道感染(UTI)的一线药物。虽然该分子具有传承性,但在药物产品配方和疗效方面仍面临诸多挑战。作者在这篇文献综述中主要关注但不限于从药物的物理化学性质、药动学和药效学、已批准和已撤消的制剂、有关药物制剂的挑战、市场上药物短缺的原因、制剂方面的改进领域及其治疗效果等方面了解该分子。作者在广泛的研究中发现,硝基呋喃妥因现有常规给药系统面临的主要挑战是药物吸收的不稳定性导致的血浆浓度波动。此外,他们还了解到,吸收的可变性是由于粒度分布的固有可变性造成的。基于这些发现,作者还探索了在纳米自乳化乳剂、纳米乳剂和多重乳剂等新型给药系统中给药的可能性,在这些系统中,药物可以呈可溶状态,从而避免了药物吸收的可变性和血浆浓度的波动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Delivery Letters
Drug Delivery Letters Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
1.70
自引率
0.00%
发文量
30
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