用于转移和递送治疗药物的皮内注射中的分子分布

E. Lallow, Kishankumar J. Busha, Sarah H. Park, Maria Atzampou, N. C. Jhumur, Yasir Demiryurek, C. Roberts, J. Shan, J. Zahn, D. Shreiber, Young K Park, J. Singer, J. Maslow, Hao Lin
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引用次数: 1

摘要

皮内注射是一种广泛应用于实验室和临床的技术。假设在注射过程中形成的圆顶状气泡的边界代表注射材料的横向范围。这项工作系统地表征了大鼠皮肤注射后的货物分子分布(水坑)作为注射量和分子/颗粒大小的函数。总的来说,结果表明,水坑形成一个横向包含在气泡内的子域,其面积与注入材料的分子大小成反比。注射50 μL和100 μL时,无论分子/颗粒大小如何,气泡的平均面积分别为40.97±6.30 mm2和55.64±8.20 mm2。另一方面,水坑面积与分子大小有关,50µL注射时,水坑面积在45.38±8.29 mm2 ~ 6.14±4.50 mm2之间,100µL注射时,水坑面积在66.64±11.22 mm2 ~ 11.50±9.67 mm2之间。注射后10分钟内的横向分布似乎没有时间依赖性。货物渗透深度的趋势也相似,较小的颗粒深入真皮层和皮下脂肪层。由于水坑的面积可能明显小于气泡的面积,因此建立碱基表征对于了解细胞与注射生物物质的相互作用至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular distribution in intradermal injection for transfer and delivery of therapeutics
Intradermal (ID) injection is a technique widely used in laboratorial and clinical applications. The boundary of the dome-like bleb formed during injection is assumed to represent the lateral extent of the injected material. This work systematically characterizes cargo molecule distribution (puddle) as a function of injection volume and molecular/particle size in rat skin post ID injection. In general, results indicate that the puddle forms a subdomain laterally contained within the bleb, with an area inversely correlating to the molecular size of the injected material. For 50 μL and 100 µL injections, the average area of the bleb was 40.97 ± 6.30 mm2 and 55.64 ± 8.20 mm2, respectively, regardless of the molecular/particle size. On the other hand, the area of the puddle was dependent on the molecular size and ranged between 45.38 ± 8.29 mm2 and 6.14 ± 4.50 mm2 for 50 µL injections, and 66.64 ± 11.22 mm2 and 11.50 ± 9.67 mm2 for 100 µL injections. The lateral distribution appears to have no time-dependency up to 10 min post injection. The trend in the depth of cargo penetration is also similar, with smaller particles extending deeper into the dermis and subcutaneous fat layers. Because the area of puddle can be significantly less than that of the bleb, establishing base characterization is essential to understand cellular interactions with the injected biological substances.
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