发光学报
髮光學報
발광학보
CHINESE JOURNAL OF LUMINESCENCE
2015年
9期
989-995
,共7页
卜承飞%刘丽炜%王倩%张卜天%胡思怡%任玉%朱泠西
蔔承飛%劉麗煒%王倩%張蔔天%鬍思怡%任玉%硃泠西
복승비%류려위%왕천%장복천%호사이%임옥%주령서
AgInS2%量子点%荧光%体外%细胞成像
AgInS2%量子點%熒光%體外%細胞成像
AgInS2%양자점%형광%체외%세포성상
AgInS2%quantum dots%fluorescence%in vitro%cell imaging
成功制备出高品质的三元AgInS2量子点。通过配体交换法将油溶性AgInS2量子点转为水溶性量子点,通过dBSA修饰水溶性量子点形成配位体壳,使量子点具有更好的稳定性(4周)。从透射电子显微镜( TEM)观察到dBSA修饰后的量子点的粒径增加,分散性较好,并且在可见光区域有明显的光致发光。用叶酸对dBSA-MPA量子点进行修饰,并通过傅立叶变换红外光谱进行了验证。将得到的FA-dBSA-MPA纳米复合材料应用于能与叶酸受体特异性结合的乳腺癌细胞中,并在荧光倒置显微镜中检测到量子点成功对乳腺癌细胞进行了标记。与dBSA-MPA量子点相比,表面被叶酸修饰后的量子点与癌细胞的结合效率显著提高。
成功製備齣高品質的三元AgInS2量子點。通過配體交換法將油溶性AgInS2量子點轉為水溶性量子點,通過dBSA脩飾水溶性量子點形成配位體殼,使量子點具有更好的穩定性(4週)。從透射電子顯微鏡( TEM)觀察到dBSA脩飾後的量子點的粒徑增加,分散性較好,併且在可見光區域有明顯的光緻髮光。用葉痠對dBSA-MPA量子點進行脩飾,併通過傅立葉變換紅外光譜進行瞭驗證。將得到的FA-dBSA-MPA納米複閤材料應用于能與葉痠受體特異性結閤的乳腺癌細胞中,併在熒光倒置顯微鏡中檢測到量子點成功對乳腺癌細胞進行瞭標記。與dBSA-MPA量子點相比,錶麵被葉痠脩飾後的量子點與癌細胞的結閤效率顯著提高。
성공제비출고품질적삼원AgInS2양자점。통과배체교환법장유용성AgInS2양자점전위수용성양자점,통과dBSA수식수용성양자점형성배위체각,사양자점구유경호적은정성(4주)。종투사전자현미경( TEM)관찰도dBSA수식후적양자점적립경증가,분산성교호,병차재가견광구역유명현적광치발광。용협산대dBSA-MPA양자점진행수식,병통과부립협변환홍외광보진행료험증。장득도적FA-dBSA-MPA납미복합재료응용우능여협산수체특이성결합적유선암세포중,병재형광도치현미경중검측도양자점성공대유선암세포진행료표기。여dBSA-MPA양자점상비,표면피협산수식후적양자점여암세포적결합효솔현저제고。
AgInS2 quantum dots ( QDs) were synthesized using hot colloidal method and transferred into water via a ligand exchange route. To enhance the stability of these QDs, dBSA was coated on the aqueous QDs as a ligand shell. After dBSA modification, a size increase was observed from the transmission electron microscopy ( TEM) re-sults. The prepared dBSA-MPA QDs exhibited good monodispersity, enhanced stability ( stable for 4 weeks) and bright photoluminescence. Then the QDs were functionalized with folic acid ( FA) and the successful conjugation was confirmed by the Fourier transform infrared ( FT-IR) spectroscopy. The resulting FA-dBSA-MPA QDs nanocomposites were tested in breast cancer cells ( MCF-7 cells) with elevated folate receptor expression. Compared to the unconju-gated dBSA-MPA QDs, the presence of FA on the surface of QDs significantly improved the uptake rate of the nanop-articles by the cancer cells.