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Particle Design for Recent Dosage Form Development

机译:用于最新剂型开发的颗粒设计

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摘要

Colloidal drug carriers, such as liposomes, lipid emulsions, and polymeric nanoparticles have great potential to provide effective drug delivery. A variety of investigations have been carried out for designing an optimal paniculate system for drug delivery in topical administration as well as in systemic administration. Liposome is one of most promising drug carriers, because its particle size and surface charge are easily controlled. We have also demonstrated feasibility of surface design of liposomes by coating its surface with functional polymers. The resultant polymer-coated liposomes showed higher stability in storage, prolonged blood circulation after intravenous injection, and mucoadhesive property. This presentation mainly demonstrates recent successful results with liposomal drug delivery systems in oral, pulmonary and ocular administration after showing the basic concept of polymer-coating liposomes and their behavior after administration. Recent trends in developing dosage forms will be also mentioned in the point of particle design.
机译:胶体药物载体,例如脂质体,脂质乳剂和聚合物纳米颗粒,具有提供有效药物递送的巨大潜力。已经进行了各种研究,以设计用于局部给药以及全身给药中的药物递送的最佳颗粒系统。脂质体是最有前途的药物载体之一,因为它的粒径和表面电荷易于控制。我们还证明了通过用功能性聚合物包被脂质体表面来设计脂质体表面的可行性。所得的聚合物包覆的脂质体显示出较高的储存稳定性,静脉内注射后血液循环延长和粘膜粘附特性​​。在展示了聚合物包衣脂质体的基本概念及其给药后的行为后,本演讲主要证明了脂质体药物递送系统在口服,肺部和眼部给药中的近期成功结果。在颗粒设计方面还将提到开发剂型的最新趋势。

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