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Mesoporous silica formulation strategies for drug dissolution enhancement: a review

机译:介孔二氧化硅制剂提高药物溶出度的策略:综述

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摘要

Introduction: Silica materials, in particular mesoporous silicas, have demonstrated excellent properties to enhance the oral bioavailability of poorly water-soluble drugs. Current research in this area is focused on investigating the kinetic profile of drug release from these carriers and manufacturing approaches to scale-up production for commercial manufacture.Areas covered: This review provides an overview of different methods utilized to load drugs onto mesoporous silica carriers. The influence of silica properties and silica pore architecture on drug loading and release are discussed. The kinetics of drug release from mesoporous silica systems is examined and the manufacturability and stability of these formulations are reviewed. Finally, the future prospects of mesoporous silica drug delivery systems are considered.Expert opinion: Substantial progress has been made in the characterization and development of mesoporous drug delivery systems for drug dissolution enhancement. However, more research is required to fully understand the drug release kinetic profile from mesoporous silica materials. Incomplete drug release from the carrier and the possibility of drug re-adsorption onto the silica surface need to be investigated. Issues to be addressed include the manufacturability and regulation status of formulation approaches employing mesoporous silica to enhance drug dissolution. While more research is needed to support the move of this technology from the bench to a commercial medicinal product, it is a realistic prospect for the near future.
机译:简介:二氧化硅材料,特别是中孔二氧化硅,具有出色的性能,可增强水溶性差的药物的口服生物利用度。目前该领域的研究重点是研究从这些载体释放药物的动力学特性以及用于商业化生产的大规模生产的制造方法。涵盖的领域:本综述概述了将药物加载到介孔二氧化硅载体上的不同方法。讨论了二氧化硅性质和二氧化硅孔结构对药物负载和释放的影响。检查了介孔二氧化硅体系中药物释放的动力学,并综述了这些制剂的可制造性和稳定性。最后,对介孔二氧化硅药物传递系统的未来前景进行了展望。专家意见:在介孔药物传递系统的表征和开发方面已经取得了实质性进展,以增强药物的溶出度。然而,需要更多的研究来充分了解中孔二氧化硅材料的药物释放动力学特性。需要研究药物从载体中释放不完全以及药物重新吸附到二氧化硅表面的可能性。要解决的问题包括采用中孔二氧化硅增强药物溶解的制剂方法的可制造性和监管状况。尽管需要更多的研究来支持这项技术从实验台向商业医用产品的转移,但这是不远的将来的现实前景。

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