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Preparation of core-crosslinked linear-dendritic copolymer micelles with enhanced stability and their application for drug solubilisation

机译:具有增强的稳定性的核心交联的线性 - 树枝状共聚物胶束的制备及其在药物溶解中的应用

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摘要

In this study we explore the preparation of core-crosslinked micelles of linear-dendritic methoxy-poly(ethylene glycol) (MPEG)-copoly(ester-sulfide) (PES) polymers to improve the stability of such polymeric micelle systems against premature disintegration and drug release. A series of MPEG-PES copolymers were synthesised via stepwise reactions of acetylation and thiol-ene photoreaction. Surface tension measurement showed that the copolymers with ethenyl surface groups could\udself-associate in dilute aqueous solutions to form micelles. Crosslinking within the micelle cores in the presence of dithioerythritol (DTT) linker was initiated under UV radiation. The formation of core-crosslinked micelles was confirmed by HPLC in combination with charged aerosol detection (CAD). The copolymers were found to readily hydrolyse under\udacidic conditions due to the ester-containing dendrons. Drug solubilisation capacities of the micellar solutions were determined using griseofulvin as a poorly water-soluble model drug. The solubility of griseofulvin showed a 10-fold enhancement in 1% w/v micelle solution and increased with the concentration of the copolymers. Drug release studies indicated that a more sustained release of griseofulvin was achieved for the core-crosslinked micelles compared to the non-crosslinked micelles, attributable to greater stability of the crosslinked core structure. The findings of this study present a new pathway towards developing biodegradable polymeric nanocarriers.
机译:在这项研究中,我们探索了线性树突状甲氧基-聚(乙二醇)(MPEG)-共聚(酯-硫化物)(PES)聚合物的核交联胶束的制备,以提高此类聚合物胶束体系抵抗过早崩解和降解的稳定性。药物释放。通过乙酰化和硫醇-烯光反应的逐步反应,合成了一系列的MPEG-PES共聚物。表面张力测量表明,带有乙烯基表面基团的共聚物可以在稀水溶液中自行结合形成胶束。在二硫赤藓糖醇(DTT)接头存在下,胶束核心内的交联是在紫外线辐射下引发的。通过HPLC结合带电气溶胶检测(CAD)确认了核心交联的胶束的形成。由于含酯的树枝状结构,发现该共聚物在弱酸性条件下容易水解。使用灰黄霉素作为水溶性差的模型药物来确定胶束溶液的药物增溶能力。灰黄霉素的溶解度在1%w / v胶束溶液中显示出10倍的增加,并随共聚物浓度的增加而增加。药物释放研究表明,与未交联的胶束相比,核心交联的胶束实现了灰黄霉素的更持续释放,这归因于交联的核心结构的稳定性更高。这项研究的发现提出了开发可生物降解的聚合物纳米载体的新途径。

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