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Amphiphilic Block Copolymer Microspheres Derived from Castor Oil Poly(ε-carpolactone) and Poly(ethylene glycol): Preparation Characterization and Application in Naltrexone Drug Delivery

机译:蓖麻油聚ε-己内酯和聚乙二醇衍生的两亲嵌段共聚物微球:纳曲酮药物的制备表征及应用

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摘要

In the present study, the newly synthesized castor oil-derived thioether-containing ω-hydroxyacid (TEHA) block copolymers with polycaprolactone (TEHA-b-PCL), with methoxypoly(ethylene glycol) (mPEG), (TEHA-b-mPEG) and with poly(ethylene glycol) (PEG) (TEHA-b-PEG-b-TEHA), were investigated as polymeric carriers for fabrication of naltrexone (NLX)-loaded microspheres by the single emulsion solvent evaporation technique. These microspheres are appropriate for the long-term treatment of opioid/alcohol dependence. Physical properties of the obtained microspheres were characterized in terms of size, morphology, drug loading capacity, and drug release. A scanning electron microscopy study revealed that the desired NLX-loaded uniform microspheres with a mean particle size of 5–10 µm were obtained in all cases. The maximum percentage encapsulation efficiency was found to be about 25.9% for the microspheres obtained from the TEHA-b-PEG-b-TEHA copolymer. Differential scanning calorimetry and X-ray diffractometry analysis confirmed the drug entrapment within microspheres in the amorphous state. In vitro dissolution studies revealed that all NLX-loaded formulations had a similar drug release profile: An initial burst release after 24 h, followed by a sustained and slower drug release for up to 50 days. The analysis of the release kinetic data, which were fitted into the Korsmeyer–Peppas release model, indicated that diffusion is the main release mechanism of NLX from TEHA-b-PCL and TEHA-b-mPEG microspheres, while microspheres obtained from TEHA-b-PEG-b-TEHA exhibited a drug release closer to an erosion process.
机译:在本研究中,新合成的蓖麻油衍生的含硫醚的ω-羟基酸(TEHA)嵌段共聚物与聚己内酯(TEHA-b-PCL),甲氧基聚乙二醇(mPEG),(TEHA-b-mPEG)以及与聚乙二醇(PEG)(TEHA-b-PEG-b-TEHA)一起被研究为通过单乳液溶剂蒸发技术制造载有纳曲酮(NLX)的微球的聚合物载体。这些微球适用于阿片类/酒精依赖的长期治疗。根据尺寸,形态,载药量和药物释放来表征获得的微球的物理性质。扫描电子显微镜研究表明,在所有情况下均获得了所需的,平均粒径为5-10μm的NLX负载的均匀微球。对于从TEHA-b-PEG-b-TEHA共聚物获得的微球,发现最大百分比包封效率为约25.9%。差示扫描量热法和X射线衍射分析法证实了药物以无定形状态滞留在微球内。体外溶出度研究表明,所有NLX加载制剂均具有相似的药物释放曲线:24小时后首次爆发释放,随后持续且缓慢的药物释放长达50天。拟合到Korsmeyer-Peppas释放模型中的释放动力学数据分析表明,扩散是NLX从TEHA-b-PCL和TEHA-b-mPEG微球中释放的主要机理,而从TEHA-b中获得的微球-PEG-b-TEHA在更接近侵蚀过程时显示出药物释放。

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