PMID- 26589318 OWN - NLM STAT- MEDLINE DCOM- 20170414 LR - 20220310 IS - 1741-0444 (Electronic) IS - 0140-0118 (Linking) VI - 54 IP - 10 DP - 2016 Oct TI - A quantitative study of nanoparticle skin penetration with interactive segmentation. PG - 1469-79 LID - 10.1007/s11517-015-1405-5 [doi] AB - In the last decade, the application of nanotechnology techniques has expanded within diverse areas such as pharmacology, medicine, and optical science. Despite such wide-ranging possibilities for implementation into practice, the mechanisms behind nanoparticle skin absorption remain unknown. Moreover, the main mode of investigation has been qualitative analysis. Using interactive segmentation, this study suggests a method of objectively and quantitatively analyzing the mechanisms underlying the skin absorption of nanoparticles. Silica nanoparticles (SNPs) were assessed using transmission electron microscopy and applied to the human skin equivalent model. Captured fluorescence images of this model were used to evaluate degrees of skin penetration. These images underwent interactive segmentation and image processing in addition to statistical quantitative analyses of calculated image parameters including the mean, integrated density, skewness, kurtosis, and area fraction. In images from both groups, the distribution area and intensity of fluorescent silica gradually increased in proportion to time. Since statistical significance was achieved after 2 days in the negative charge group and after 4 days in the positive charge group, there is a periodic difference. Furthermore, the quantity of silica per unit area showed a dramatic change after 6 days in the negative charge group. Although this quantitative result is identical to results obtained by qualitative assessment, it is meaningful in that it was proven by statistical analysis with quantitation by using image processing. The present study suggests that the surface charge of SNPs could play an important role in the percutaneous absorption of NPs. These findings can help achieve a better understanding of the percutaneous transport of NPs. In addition, these results provide important guidance for the design of NPs for biomedical applications. FAU - Lee, Onseok AU - Lee O AD - Department of Medical IT Engineering, College of Medical Sciences, Soonchunhyang University, Asan City, Chungnam, Korea. FAU - Lee, See Hyun AU - Lee SH AD - Laboratory of Cell Signaling and Nanomedicine, Department of Dermatology, Korea University College of Medicine, Seoul, Korea. AD - Division of the Brain Korea 21 Project for Biomedical Science, Korea University College of Medicine, Seoul, Korea. FAU - Jeong, Sang Hoon AU - Jeong SH AD - Laboratory of Cell Signaling and Nanomedicine, Department of Dermatology, Korea University College of Medicine, Seoul, Korea. AD - Division of the Brain Korea 21 Project for Biomedical Science, Korea University College of Medicine, Seoul, Korea. FAU - Kim, Jaeyoung AU - Kim J AD - Research Institute for Skin Image, Korea University College of Medicine, Seoul, Korea. FAU - Ryu, Hwa Jung AU - Ryu HJ AD - Laboratory of Cell Signaling and Nanomedicine, Department of Dermatology, Korea University College of Medicine, Seoul, Korea. AD - Division of the Brain Korea 21 Project for Biomedical Science, Korea University College of Medicine, Seoul, Korea. FAU - Oh, Chilhwan AU - Oh C AD - Research Institute for Skin Image, Korea University College of Medicine, Seoul, Korea. FAU - Son, Sang Wook AU - Son SW AD - Laboratory of Cell Signaling and Nanomedicine, Department of Dermatology, Korea University College of Medicine, Seoul, Korea. skin4u@korea.ac.kr. AD - Division of the Brain Korea 21 Project for Biomedical Science, Korea University College of Medicine, Seoul, Korea. skin4u@korea.ac.kr. AD - Research Institute for Skin Image, Korea University College of Medicine, Seoul, Korea. skin4u@korea.ac.kr. AD - Department of Dermatology, Korea University Anam Hospital, Korea University College of Medicine, 126-1, Anam-dong 5-ga, Seongbuk-gu, Seoul, 136-705, Korea. skin4u@korea.ac.kr. LA - eng PT - Journal Article DEP - 20151120 PL - United States TA - Med Biol Eng Comput JT - Medical & biological engineering & computing JID - 7704869 RN - 7631-86-9 (Silicon Dioxide) SB - IM MH - Humans MH - Microscopy, Electron, Transmission MH - Microscopy, Fluorescence MH - *Nanoparticles MH - Silicon Dioxide MH - Skin/*metabolism OTO - NOTNLM OT - Human skin equivalent model OT - Nanoparticles OT - Segmentation OT - Skin penetration EDAT- 2015/11/22 06:00 MHDA- 2017/04/15 06:00 CRDT- 2015/11/22 06:00 PHST- 2015/02/21 00:00 [received] PHST- 2015/10/03 00:00 [accepted] PHST- 2015/11/22 06:00 [entrez] PHST- 2015/11/22 06:00 [pubmed] PHST- 2017/04/15 06:00 [medline] AID - 10.1007/s11517-015-1405-5 [pii] AID - 10.1007/s11517-015-1405-5 [doi] PST - ppublish SO - Med Biol Eng Comput. 2016 Oct;54(10):1469-79. doi: 10.1007/s11517-015-1405-5. Epub 2015 Nov 20.