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Development of pH-Sensitive and Adjuvant-Based Polymer Lids for Microcontainers Leading to Targeted Delivery of Oral Vaccines

机译:基于pH敏感和辅助的聚合物盖的开发 微容器导致有针对性地口服疫苗

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摘要

Oral vaccination, one of the prominent ongoing research areas of drug delivery and immunology, requires effective targeted drug delivery method as well as triggered immune responses. In this thesis project, polymeric microcontainers (MCs) formed on silicon substrate were used as drug carriers. The focus of the thesis was on the development and optimization of pH-sensitive and adjuvant-based polymer lids on the drug-loaded MCs in order to facilitate the drug release at the desired area (small intestine) and to trigger immune response. In this study, the development of double-layered lids on top of the MCs was achieved by establishing a pH-sensitive outer lid made of Eudragit L100-55 polymer and an inner lid made of chitosan polymer incorporated with an adjuvant - MPLA (mono phosphoryl lipid A). The chitosan-MPLA lid is a novel polymeric lid which has not been in any literature yet for targeted oral drug delivery studies. The purpose of the outer lid was to protect the inner lid from dissolving in a gastric pH value (e.g. at pH 3.5); whereas, the adjuvant-based inner lid was needed to facilitate the drug release from the MCs in the small intestinal pH value (e.g. at pH 6.0) followed by triggering immune response. The model drug used in these studies was amorphous sodium salt of furosemide (ASSF), prepared in a spray dryer followed by loading the drug into the MCs using an embossing method. Next, different polymer solutions were spray-coated on the drug-loaded MCs to form single or double layer lids. To determine the most optimized lid formation, detailed lid morphology was analyzed using scanning electron microscope (SEM) and stylus profiler. The results show that both the inner and outer lids were homogenously formed where the inner lid had very smooth surface with an average thickness of 6.2 +/- 0.3 µm and the outer lid had porous texture with an average thickness of 31.4 +/- 2.8 µm. To investigate the pH-sensitivity of the lids, in vitro drug release experiments were performed in buffer media with different pH values (pH of rat’s gastric and intestinal media) using a micro dissolution apparatus. Finally, x-ray photoelectron spectroscopy (XPS) analysis was performed to detect the presence of MPLA in the inner lid. Both the release studies and lid morphology analysis exhibit that the optimized double-lids remains intact with a negligible drug release percentage at a pH value corresponding to the stomach, whereas it degrades and releases above 84% of the model drug in the medium corresponding to an intestinal pH value. Thus, the pH-sensitive and adjuvant-based double-lids development demonstrates the future potential to be used for different vaccine formulations in targeted oral drug delivery in in vivo and animal studies. Keywords: Oral Vaccination, Drug Delivery, Polymer Lid, Microcontainer, Spray Coating
机译:口服疫苗接种是药物输送和免疫学研究的重要领域之一,它需要有效的靶向药物输送方法以及触发的免疫反应。在本项目中,将在硅基板上形成的聚合物微容器(MC)用作药物载体。论文的重点是开发和优化载药MCs上的pH敏感和基于佐剂的聚合物盖,以促进药物在所需区域(小肠)的释放并触发免疫反应。在这项研究中,通过建立由Eudragit L100-55聚合物制成的pH敏感外盖和由壳聚糖聚合物制成并结合佐剂MPLA(单磷酰基)的内盖实现了MC顶部双层盖的开发。脂质A)。壳聚糖-MPLA盖是一种新颖的聚合物盖,尚未在任何文献中进行靶向口服药物递送研究。外盖的目的是保护内盖免于溶解在胃的pH值(例如在pH 3.5下)。然而,需要基于佐剂的内盖来促进药物在小肠pH值(例如pH 6.0)下从MC中释放出来,然后触发免疫反应。在这些研究中使用的模型药物是呋塞米的无定形钠盐(ASSF),在喷雾干燥器中制备,然后使用压印方法将其加载到MC中。接下来,将不同的聚合物溶液喷涂在载有药物的MC上,以形成单层或双层盖。为了确定最优化的盖子形成,使用扫描电子显微镜(SEM)和测针轮廓仪分析了详细的盖子形态。结果表明,内盖和外盖均均匀地形成,其中内盖的表面非常光滑,平均厚度为6.2 +/- 0.3 µm,外盖的多孔质地平均为31.4 +/- 2.8 µm 。为了研究盖子的pH敏感性,使用微溶出仪在具有不同pH值(大鼠的胃和肠介质的pH)的缓冲介质中进行了体外药物释放实验。最后,进行X射线光电子能谱(XPS)分析,以检测内盖中是否存在MPLA。释放研究和盖形态分析均显示,在与胃相对应的pH值下,优化的双盖仍保持完整,药物释放百分比可忽略不计,而在相当于200mg / ml的培养基中,其降解和释放的模型药物超过84%。肠道pH值。因此,pH敏感和基于佐剂的双盖剂的开发证明了在体内和动物研究中靶向疫苗口服给药中用于不同疫苗制剂的未来潜力。关键字:口服疫苗,药物输送,聚合物盖,微容器,喷涂

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    Nur-E-Habiba -;

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