Bakrey Hossamaldeen, Abdu Abdulkadir, Shivgotra Riya, Soni Bindu, Sharma Manya, Bakrey Alaa, Jain Subheet Kumar
Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
Department of Clinical Pharmacy, University of Khartoum, Khartoum, 11111, Sudan.
Curr Drug Targets. 2025 Jul 21. doi: 10.2174/0113894501375776250713110838.
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.
药物溶解度差仍然是药物给药过程中的一个重大障碍,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,例如市售产品生物利用度差、不一致、有限以及高度可变。据估计,40%的市售药物面临生物利用度挑战主要是由于水溶性差,并且约90%的药理化合物在其早期开发阶段表现出水溶性差。解决这个问题对于提高药物性能、疗效和患者治疗效果至关重要。本综述概述了与难溶性药物相关的挑战,包括低生物利用度、有限的溶解速率、不一致的吸收、患者依从性降低、制剂困难以及相关成本和时间限制。目前已经研究了许多策略来解决溶解度差的问题。本综述提供了常用的宏观和纳米药物递送系统的最新概述,包括胶束、纳米乳剂、树枝状大分子、脂质体、基于脂质的递送系统、微乳剂、助溶剂、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,该综述还研究了先进技术,如基于环糊精的递送系统、共溶剂化和共结晶方法、聚合物胶束、喷雾干燥、共沉淀和无定形固体分散。还讨论了计算建模和制剂预测的作用。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基于脂质纳米颗粒的最新进展被强调为提高难溶性药物溶解度的新解决方案。综述最后对未来进行了预测,强调了药物递送方法进一步创新以克服与难溶性药物相关挑战的潜力。