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为控制大分子的释放而定制液晶脂纳米材料。

Tailoring liquid crystalline lipid nanomaterials for controlled release of macromolecules.

机构信息

Drug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, 381 Royal Parade, Parkville, VIC, Australia.

Drug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, 381 Royal Parade, Parkville, VIC, Australia; ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, Monash University, 381 Royal Parade, Parkville, VIC, Australia.

出版信息

Int J Pharm. 2015 Nov 10;495(1):241-248. doi: 10.1016/j.ijpharm.2015.08.072. Epub 2015 Aug 28.

Abstract

Lipid-based liquid crystalline materials are being developed as drug delivery systems. However, the use of these materials for delivery of large macromolecules is currently hindered by the small size of the water channels in these structures limiting control over diffusion behaviour. The addition of the hydration-modulating agent, sucrose stearate, to phytantriol cubic phase under excess water conditions incrementally increased the size of these water channels. Inclusion of oleic acid enabled further control of swelling and de-swelling of the matrix via a pH triggerable system where at low pH the hexagonal phase is present and at higher pH the cubic phase is present. Fine control over the release of various sized model macromolecules is demonstrated, indicating future application to controlled loading and release of large macromolecules such as antibodies.

摘要

脂质基液晶材料正被开发为药物传递系统。然而,这些材料在用于传递大分子时,目前受到这些结构中水通道尺寸较小的限制,限制了对扩散行为的控制。在过量水条件下,向植烷三醇立方相中添加水合调节剂硬脂蔗糖酯,逐渐增大了这些水通道的尺寸。油酸的加入通过 pH 触发系统进一步控制基质的溶胀和去溶胀,其中在低 pH 值下存在六方相,在较高 pH 值下存在立方相。对各种大小的模型大分子的释放进行了精细控制,表明未来可应用于对大分子如抗体的控释和加载。

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