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具有改善可压缩性和协同作用的快速溶解药物共晶。

Fast dissolving drug-drug eutectics with improved compressibility and synergistic effects.

机构信息

Solid State Pharmaceutical Research Group (SSPRG), , Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, India.

Department of Pharmacology, National Institute of Pharmaceutical Education and Research, Hyderabad, India.

出版信息

Eur J Pharm Sci. 2017 Jun 15;104:82-89. doi: 10.1016/j.ejps.2017.03.042. Epub 2017 Mar 31.

Abstract

Combinational therapy has become increasingly popular in recent times due to various advantages like greater therapeutic effect, reduced number of prescriptions, lower administrative costs, and an increase in patient compliance. Drug-drug multicomponent adducts could help in combination of drugs at supramolecular level. Two drug-drug eutectics of etodolac with paracetamol (EP) and etodolac with propranolol hydrochloride (EPHC) were successfully designed and synthesized for the first time. These eutectics significantly improved dissolution and material properties. A 6 to 9 fold enhancement in % dissolution efficiency was found at 1min suggesting the fast dissolving capabilities of the eutectic mixtures when compared to plain drug. In addition, eutectic mixtures have shown improved hardness compared to plain drugs. EP and EPHC have shown around 5 fold and 3 fold improvements in hardness respectively at 10MPa when compared to plain etodolac. Cell culture studies have shown improved effects of EP. Western blotting analysis revealed that the said combination successfully reduced various inflammatory mediators like TNF-α, COX-2 and IL-6. Whereas, the eutectic combination EPHC has shown enhanced cytotoxic effects with synergistic combination index and favorable dose reduction index. The generated multi-component systems EP and EPHC with fast dissolving capabilities, improved hardness at lower pressures and synergistic effects represent prospective combinations for effective treatment of osteoarthritis and cancer chemotherapy respectively.

摘要

联合治疗由于具有更大的治疗效果、减少处方数量、降低行政成本以及提高患者依从性等优点,近年来越来越受到关注。药物-药物多组分加合物可以帮助在超分子水平上组合药物。本文首次成功设计和合成了依托考昔与对乙酰氨基酚(EP)和依托考昔与盐酸普萘洛尔(EPHC)的两种药物-药物共晶。这些共晶显著改善了溶解性能和材料性能。在 1min 时,发现 %溶解效率提高了 6 到 9 倍,这表明共晶混合物的快速溶解能力优于普通药物。此外,与普通药物相比,共晶混合物的硬度也有所提高。与普通依托考昔相比,EP 和 EPHC 在 10MPa 时的硬度分别提高了 5 倍和 3 倍。细胞培养研究表明 EP 具有更好的效果。Western 印迹分析显示,该组合成功降低了各种炎症介质,如 TNF-α、COX-2 和 IL-6。而共晶组合 EPHC 则表现出协同组合指数和有利的剂量减少指数的增强细胞毒性作用。具有快速溶解能力、在较低压力下提高硬度和协同作用的多组分体系 EP 和 EPHC 分别代表了治疗骨关节炎和癌症化疗的有效联合治疗的前景。

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