用于生物医学应用的简单和可定制的明胶纳米颗粒封装系统

J. Cary, F. Pierson, A. Whittington
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引用次数: 0

摘要

目的:多年来,双脱溶技术一直被用于将具有蛋白质亲和力的小亲水性药物包封在明胶纳米颗粒中。扩大可封装材料的类型将使双重脱溶方法可用于更广泛的生物医学应用,包括生物输送。方法:在这里,我们使用双重脱溶技术来封装两种不同尺寸的聚苯乙烯珠,作为在新的递送系统中封装类似大小,形状,zeta电位和官能团的生物制剂如病毒和核酸的第一步。人们需要易于生产和可针对不同生物医学应用进行定制的药物输送系统。考虑到这些参数,我们创建了一个简单的明胶纳米颗粒封装系统,该系统具有化学修饰的潜力,可用于靶向目的和封装不同的材料。结果:将包封材料与空纳米颗粒的尺寸和形状相匹配,得到了理想的窄尺寸分布的包封纳米颗粒,在蒸馏水中室温保存1个多月,参数稳定。此外,与其他生理pH范围相比,包封系统在pH 3-4时最稳定。透射电子显微镜验证了动态光散射发现的尺寸范围,并显示惰性材料在每种配方中被封装,部分封装和未封装的纳米颗粒。结论:该包封材料制备方法可减少生物制剂添加后的额外过滤,包封范围具有理想的长效生物缓释效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Simple and Customizable Gelatin Nanoparticle Encapsulation System for Biomedical Applications
Objective: The double desolvation technique has been used to encapsulate small, hydrophilic drugs with protein affinity in gelatin nanoparticles for many years. Expanding the types of materials that can be encapsulated would allow the double desolvation method to be used for a wider range of biomedical applications, including biological delivery. Methods: Here, we use the double desolvation technique to encapsulate two different sizes of polystyrene beads as a first step toward encapsulating biologics like viruses and nucleic acids of similar size, shape, zeta potential, and functional groups in a new delivery system. Drug delivery systems that are easy to produce and customizable to different biomedical applications are in demand. With these parameters in mind, we created a simple gelatin nanoparticle encapsulation system with the potential for chemical modification for targeting purposes and encapsulation of different materials. Results: Matching the encapsulation material to the size and shape of the empty nanoparticles resulted in encapsulated nanoparticles of ideal narrow size distribution with stable storage parameters at room temperature over a 1-month period in distilled water. Additionally, the encapsulation system was shown to be most stable at pH 3-4 compared to other physiological pH ranges. Transmission electron microscopy verified the size ranges found using dynamic light scattering and revealed the inert material was encapsulated, partially encapsulated, and non-encapsulated nanoparticles in each formulation. Conclusion: This matched encapsulation material fabrication method may decrease the need for additional filtration after biologics are added and the encapsulation range would be ideal for sustained biologic release over time.
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