{"title":"杯[4]芳烃纳米纤维在MCF-7乳腺癌细胞治疗中的应用","authors":"Ş. Ertul, F. Ozcan","doi":"10.1109/NAP.2017.8190330","DOIUrl":null,"url":null,"abstract":"Synthesis of the p-tert-butylcalixarene compound with the amino group was carried out as given in Figure 1. The structure of the calixarene compound with the amino group was elucidated by 1H-NMR, FT-IR. After the synthesized compound was prepared in a suitable solvent medium, the nanofibers were withdrawn by electrospinning. The characterization of the nanofibers was performed by SEM.","PeriodicalId":6516,"journal":{"name":"2017 IEEE 7th International Conference Nanomaterials: Application & Properties (NAP)","volume":"35 1","pages":"04NB17-1-04NB17-3"},"PeriodicalIF":0.0000,"publicationDate":"2017-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Use of calix[4]arene nanofibers in the treatment of MCF-7 breast cancer cells\",\"authors\":\"Ş. Ertul, F. Ozcan\",\"doi\":\"10.1109/NAP.2017.8190330\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Synthesis of the p-tert-butylcalixarene compound with the amino group was carried out as given in Figure 1. The structure of the calixarene compound with the amino group was elucidated by 1H-NMR, FT-IR. After the synthesized compound was prepared in a suitable solvent medium, the nanofibers were withdrawn by electrospinning. The characterization of the nanofibers was performed by SEM.\",\"PeriodicalId\":6516,\"journal\":{\"name\":\"2017 IEEE 7th International Conference Nanomaterials: Application & Properties (NAP)\",\"volume\":\"35 1\",\"pages\":\"04NB17-1-04NB17-3\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2017 IEEE 7th International Conference Nanomaterials: Application & Properties (NAP)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/NAP.2017.8190330\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2017 IEEE 7th International Conference Nanomaterials: Application & Properties (NAP)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/NAP.2017.8190330","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Use of calix[4]arene nanofibers in the treatment of MCF-7 breast cancer cells
Synthesis of the p-tert-butylcalixarene compound with the amino group was carried out as given in Figure 1. The structure of the calixarene compound with the amino group was elucidated by 1H-NMR, FT-IR. After the synthesized compound was prepared in a suitable solvent medium, the nanofibers were withdrawn by electrospinning. The characterization of the nanofibers was performed by SEM.