Laboratory of Pharmaceutical Technology and Biopharmacy, CIRM, University of Liege, 4000, Belgium.
Laboratory of General Biochemistry and Physical Pharmacy, Ghent Research Group on Nanomedicines, Ghent University, 9000, Belgium.
J Control Release. 2016 Aug 28;236:68-78. doi: 10.1016/j.jconrel.2016.06.028. Epub 2016 Jun 18.
Topical vaginal sustained delivery of siRNA presents a significant challenge due to the short residence time of formulations. Therefore, a drug delivery system capable to adhere to the vaginal mucosa is desirable, as it could allow a prolonged delivery and increase the effectiveness of the therapy. The aim of this project is to develop a polymeric solid mucoadhesive system, loaded with lipoplexes, able to be progressively rehydrated by the vaginal fluids to form a hydrogel and to deliver siRNA to vaginal tissues. To minimize adhesive interactions with vaginal mucus components, lipoplexes were coated with different derivatives of polyethylene glycol: DPSE-PEG2000, DPSE-PEG750 and ceramide-PEG2000. Based on stability and diffusion properties in simulated vaginal fluids, lipoplexes containing DSPE-PEG2000 were selected and incorporated in hydroxyethyl cellulose (HEC) hydrogels. Solid systems, called sponges, were then obtained by freeze-drying. Sponges meet acceptable mechanical characteristics and their hardness, deformability and mucoadhesive properties are not influenced by the presence of lipoplexes. Finally, mobility and stability of lipoplexes inside sponges rehydrated with vaginal mucus, mimicking in situ conditions, were evaluated by advanced fluorescence microscopy. The release rate was found to be influenced by the HEC concentration and consequently by the viscosity after rehydration. This study demonstrates the feasibility of entrapping pegylated lipoplexes into a solid matrix system for a prolonged delivery of siRNA into the vagina.
由于制剂在阴道内的停留时间短,因此,局部阴道持续递送 siRNA 具有很大的挑战性。因此,需要一种能够黏附在阴道黏膜上的药物递送系统,因为它可以延长药物的释放时间并提高治疗效果。本项目的目的是开发一种聚合物固体制剂黏附系统,负载脂质体,能够通过阴道分泌物逐渐水合形成水凝胶,并将 siRNA 递送到阴道组织。为了最大限度地减少与阴道黏液成分的黏附相互作用,用不同的聚乙二醇衍生物对脂质体进行了包被:DPSE-PEG2000、DPSE-PEG750 和神经酰胺-PEG2000。基于在模拟阴道液中的稳定性和扩散特性,选择了含有 DPSE-PEG2000 的脂质体,并将其掺入羟乙基纤维素 (HEC) 水凝胶中。然后通过冷冻干燥获得称为海绵的固体系统。海绵具有可接受的机械特性,其硬度、可变形性和黏膜黏附特性不受脂质体的影响。最后,通过高级荧光显微镜评估了在模拟原位条件下用阴道黏液重新水化的海绵中脂质体的迁移和稳定性。结果发现,释放率受到 HEC 浓度的影响,进而受到重新水化后的黏度的影响。本研究证明了将聚乙二醇化脂质体包埋在固体基质系统中用于延长 siRNA 向阴道内递药的可行性。