Deep eutectic solvents as emerging carriers for antihyperlipidemic drugs: current trends and future perspectives.

IF 2.9 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Sushant Gaikwad, Ambar Marne, Ashwini Gawade, Ashwin Kuchekar
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引用次数: 0

Abstract

The therapeutic effectiveness of the most antihyperlipidemic drugs, particularly Biopharmaceutics Classification system Class II drugs like statins, is severely limited by their low aqueous solubility and resulting low and variable oral bioavailability (e.g. ∼5% for simvastatin). Deep Eutectic solvents and Therapeutic Deep Eutectic System are explored in this review as an environmentally friendly and innovative next-generation platform designed to overcome these fundamental biopharmaceutical limitations. These systems function as good solubilizers, improving the dissolution rate and the thermodynamic stability of antihyperlipidemic drugs significantly. This directly enhances the drug absorption kinetics, resulting in more predictable and enhanced oral bioavailability. Commercialization of DESs still faces major challenges. Large-scale-up is difficult because their high viscosity reduces mixing and mass transfer efficiency. Also, a complete evaluation of their cytotoxicity, biodegradability, and long-term thermal stability is still needed to ensure their safe and sustainable use as effective pharmaceutical excipients.

深共晶溶剂作为新型抗高血脂药物载体:当前趋势和未来展望。
大多数抗高脂血症药物的治疗效果,特别是生物制药分类系统II类药物,如他汀类药物,严重受到其低水溶性和导致低和可变的口服生物利用度(例如辛伐他汀约为5%)的限制。本文探讨了深共晶溶剂和治疗性深共晶系统作为一种环境友好和创新的下一代平台,旨在克服这些基本的生物制药限制。这些体系是良好的增溶剂,显著提高了抗高脂血症药物的溶解速度和热力学稳定性。这直接提高了药物吸收动力学,导致更可预测和提高口服生物利用度。DESs的商业化仍面临重大挑战。由于它们的高粘度降低了混合和传质效率,因此很难进行大规模放大。此外,还需要对它们的细胞毒性、生物降解性和长期热稳定性进行完整的评估,以确保它们作为有效的药物辅料的安全和可持续使用。
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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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