蛋白质纳米颗粒系统治疗肺部感染的研究进展

Praveen Tahilani, D P Chatterjee
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摘要

除了所谓的小分子药物外,蛋白质和多肽由于具有一些有利的特性而越来越受到药物治疗的关注。一般来说,这些化合物是通过肠道给药的。然而,非侵入性给药途径是研究的重要组成部分。其中包括在肺部疾病,如特发性肺纤维化,肺泡上皮受到影响的情况下,用于局部递送的蛋白质和肽的肺应用。为了确保细胞内递送,将通过电荷介导的凝聚制备尺寸在150纳米范围内的纳米颗粒,其物理化学性质具有特点,并装载了几种模型蛋白。纳米粒子制备的材料选择了以马铃薯淀粉为原料合成的带正电和负电的淀粉衍生物。虽然已知该尺寸范围内的纳米颗粒会增加细胞摄取,但它们在深肺中并未显示出高沉积。因此,一种由快速溶解的微颗粒基质和嵌入淀粉纳米颗粒组成的先进载体体系将被开发和表征。由于其空气动力学特性,该载体系统必须能够在肺深部沉积高剂量(~50%),同时(在体外模型中)显示在微颗粒基质快速溶解后,促进淀粉纳米颗粒进入肺泡上皮细胞的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advancements in Protein based Nano Particulate system for treatment of Pulmonary Infections- A Review
In addition to the so-called small molecule drugs, proteins and peptides are of increasing interest forpharmacotherapy, due to several advantageous properties. In general, those compounds are administered parenterally. However, non-invasive routes of administration represent a great part of research. Amongst others is the pulmonary application of proteins and peptides for local delivery in the case of pulmonary diseases, such as idiopathic pulmonary fibrosis, where the alveolar epithelium is affected. To ensure an intracellular delivery, nano particles in a size range of 150 nm will be prepared via charge-mediated coacervation, characterized for their physicochemical properties and loaded with several model-proteins. The material used for nano particle preparation was chosen to be positively and negatively charged starch derivatives, which were synthesized from potato starch. Although nano particles in that size range are known to show an increased cell uptake, they do not show a high deposition in the deep lung. Thus, an advanced carrier system consisting of a fast dissolving micro particle matrix with embedded starch nano particles will be developed and characterized. Due to its aerodynamic properties, that carrier system must be able to deposit a high fraction of the applied dose in the deep lung (~50%), while at the same time demonstrating (in in vitro models) the ability to facilitate uptake of starch nano particles into cells of the alveolar epithelium after fast dissolution of the micro particle matrix.
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