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聚(乳酸-共-乙醇酸)纳米粒子对荧光材料局部保留的影响:小鼠的实验研究。

Effect of Poly(Lactide-Co-Glycolide) Nanoparticles on Local Retention of Fluorescent Material: An Experimental Study in Mice.

机构信息

Department of Radiology, Seoul Metropolitan Government-Seoul National University Boramae Hospital, Seoul 07061, Korea.

Department of Radiology, Seoul National University Bundang Hospital, Seongnam 13620, Korea.

出版信息

Korean J Radiol. 2018 Sep-Oct;19(5):950-956. doi: 10.3348/kjr.2018.19.5.950. Epub 2018 Aug 6.

Abstract

OBJECTIVE

Poly(lactide-co-glycolide) (PLGA) nanoparticles are promising materials for the development of new drug-releasing systems. The purpose of this study was to evaluate the retention time of materials loaded in nanoparticles as compared with that of the material alone by imaging in nude mice.

MATERIALS AND METHODS

Mice (n = 20) were injected with 0.1 mL fluorescent material 1,1'-dioctadecyl-3,3,3',3' tetramethylindotricarbocyanine iodide (DiR)-loaded PLGA nanoparticles (200 nm) into the right paraspinal muscle, and the same volume of pure DiR solution was injected into the left paraspinal muscle. Fluorescence images were obtained using an optical imaging system. Fluorescent images were taken 1 day after the injection, and seven more images were taken at 1-week intervals. Image analysis was done with ImageJ program, and one region of interest was chosen manually, which corresponded to the highest signal-intensity area of fluorescence signal intensity.

RESULTS

After 7 weeks, 12 mice showed a right-sided dominant signal, representing the DiR loaded PLGA nanoparticles; 5 mice showed a left-side dominant signal, representing the free DiR solution; and 3 mice showed no signal at all beginning 1 day after the injection. During the 7-week period, the mean signal intensities of the free DiR solution and DiR-loaded PLGA nanoparticles diverged gradually. On day 1, the mean signal intensity of free DiR solution was significantly higher than that of DiR-loaded PLGA ( < 0.001). Finally, by week 7, DiR-loaded PLGA express significantly high signal intensity compared with free DiR solution ( = 0.031).

CONCLUSION

The results of the current study suggested that therapeutic agents bound to PLGA nanoparticles may exhibit prolonged retention times.

摘要

目的

聚(乳酸-共-乙醇酸)(PLGA)纳米粒是开发新型药物释放系统的有前途的材料。本研究的目的是通过在裸鼠成像来评估与单独材料相比,负载在纳米粒中的材料的保留时间。

材料和方法

将 0.1mL 荧光材料 1,1'-二辛基-3,3,3',3'四甲基吲哚碳酰亚胺碘化物(DiR)负载的 PLGA 纳米粒(200nm)注入右侧脊柱旁肌,将相同体积的纯 DiR 溶液注入左侧脊柱旁肌。使用光学成像系统获得荧光图像。注射后 1 天获取荧光图像,之后每隔 1 周获取 7 张图像。使用 ImageJ 程序进行图像分析,手动选择一个感兴趣区域,该区域对应于荧光信号强度的最高信号强度区域。

结果

7 周后,12 只小鼠表现出右侧主导信号,代表 DiR 负载的 PLGA 纳米粒;5 只小鼠表现出左侧主导信号,代表游离 DiR 溶液;3 只小鼠从注射后 1 天开始根本没有信号。在 7 周期间,游离 DiR 溶液和 DiR 负载的 PLGA 纳米粒的平均信号强度逐渐发散。在第 1 天,游离 DiR 溶液的平均信号强度明显高于 DiR 负载的 PLGA(<0.001)。最后,到第 7 周时,DiR 负载的 PLGA 表达的信号强度明显高于游离 DiR 溶液(=0.031)。

结论

本研究结果表明,与 PLGA 纳米粒结合的治疗剂可能表现出延长的保留时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed11/6082767/b4e89a11f36a/kjr-19-950-g001.jpg

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