Innovative Strategies and Advances in Drug Delivery Systems to Address Poor Solubility: A Comprehensive Review.

IF 2.5 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Hossamaldeen Bakrey, Abdulkadir Abdu, Riya Shivgotra, Bindu Soni, Manya Sharma, Alaa Bakrey, Subheet Kumar Jain
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引用次数: 0

Abstract

Poor solubility remains a significant obstacle in drug administration, adversely affecting the bioavailability and therapeutic efficacy of many drugs. It is also recognized as a primary factor contributing to issues with bioavailability, such as poor, inconsistent, limited, and highly variable bioavailability of marketed products. It is estimated that 40% of marketed drugs face bioavailability challenges primarily due to poor water solubility, and about 90% of pharmacological compounds exhibit poor water solubility in their early development stages. Addressing this issue is crucial for improving drug performance, efficacy, and patient outcomes. This review provides an overview of the challenges associated with poorly soluble drugs, including low bioavailability, limited dissolution rates, inconsistent absorption, decreased patient compliance, formulation difficulties, and associated costs and time constraints. Numerous strategies have been now investigated to tackle the issue of poor solubility. This review offers an updated overview of commonly used macro and nano drug delivery systems, including micelles, nanoemulsions, dendrimers, liposomes, lipid-based delivery systems, microemulsions, cosolvents, polymeric micelle preparation, drug nanocrystals, solid dispersion methods, crystal engineering techniques, and microneedle- based systems. Additionally, the review examines advanced techniques like cyclodextrin- based delivery systems, co-solvency and co-crystallization approaches, polymeric micelles, spray drying, co-precipitation, and amorphous solid dispersion. The role of computational modeling and formulation prediction is also addressed. Recent advancements in protein-based approaches, 3D printing, mesoporous silica nanoparticles, supramolecular delivery systems, magnetic nanoparticles, nanostructured lipid carriers, and lipid-based nanoparticles are highlighted as novel solutions for enhancing the solubility of poorly soluble drugs. The review concludes with predictions for the future, emphasizing the potential for further innovation in drug delivery methods to overcome the challenges associated with poorly soluble drugs.

解决溶解度差的药物输送系统的创新策略和进展:全面回顾。
溶解度差仍然是给药的一个重要障碍,对许多药物的生物利用度和治疗效果产生不利影响。它也被认为是导致生物利用度问题的主要因素,例如上市产品的生物利用度差、不一致、有限和高度可变。据估计,40%的上市药物主要由于水溶性差而面临生物利用度挑战,约90%的药理化合物在其早期开发阶段表现出水溶性差。解决这一问题对于改善药物性能、疗效和患者预后至关重要。这篇综述概述了与难溶性药物相关的挑战,包括低生物利用度、有限的溶出率、不一致的吸收、患者依从性降低、配方困难以及相关的成本和时间限制。现在已经研究了许多策略来解决溶解度差的问题。这篇综述提供了常用的宏观和纳米药物传递系统的最新概述,包括胶束、纳米乳液、树状大分子、脂质体、基于脂质的传递系统、微乳液、共溶剂、聚合物胶束制备、药物纳米晶体、固体分散方法、晶体工程技术和基于微针的系统。此外,回顾了先进的技术,如环糊精为基础的传递系统,共溶解和共结晶方法,聚合物胶束,喷雾干燥,共沉淀,和非晶固体分散。计算建模和配方预测的作用也得到了解决。基于蛋白质的方法、3D打印、介孔二氧化硅纳米颗粒、超分子递送系统、磁性纳米颗粒、纳米结构脂质载体和脂质纳米颗粒的最新进展被强调为提高难溶性药物的溶解度的新解决方案。该综述总结了对未来的预测,强调了进一步创新给药方法的潜力,以克服与难溶性药物相关的挑战。
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
Current drug targets
Current drug targets 医学-药学
CiteScore
6.20
自引率
0.00%
发文量
127
审稿时长
3-8 weeks
期刊介绍: Current Drug Targets aims to cover the latest and most outstanding developments on the medicinal chemistry and pharmacology of molecular drug targets e.g. disease specific proteins, receptors, enzymes, genes. Current Drug Targets publishes guest edited thematic issues written by leaders in the field covering a range of current topics of drug targets. The journal also accepts for publication mini- & full-length review articles and drug clinical trial studies. As the discovery, identification, characterization and validation of novel human drug targets for drug discovery continues to grow; this journal is essential reading for all pharmaceutical scientists involved in drug discovery and development.
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