Bovine serum albumin coated nanoparticles for in vitro activated fluorescence

被引:7
作者
Burdette, Mary K. [1 ]
Jenkins, Ragini [1 ]
Bandera, Yuriy [1 ,2 ]
Powell, Rhonda R. [3 ]
Bruce, Terri F. [3 ]
Yang, Xi [4 ]
Wei, Yanzhang [4 ]
Foulger, Stephen H. [1 ,2 ,5 ]
机构
[1] Clemson Univ, Dept Mat Sci & Engn, Adv Mat Res Lab 226, Anderson, SC 29625 USA
[2] COMSET, Adv Mat Res Lab 226, Anderson, SC USA
[3] Clemson Univ, Clemson Light Imaging Facil, Clemson, SC 29634 USA
[4] Clemson Univ, Dept Biol Sci, Clemson, SC 29634 USA
[5] Clemson Univ, Dept Bioengn, Clemson, SC 29634 USA
基金
美国国家科学基金会;
关键词
SULFONATED ALUMINUM PHTHALOCYANINES; SILICON(IV) PHTHALOCYANINES; PHOTODYNAMIC THERAPY; LIMITED PROTEOLYSIS; CANCER-CELLS; THERANOSTICS; PORPHYRIN; FRAGMENTS; DELIVERY;
D O I
10.1039/c6nr05883c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A fluorophore modified nanoparticle was developed that can only fluoresce when a specific environmental parameter interacts with the system. The model system consisted of an azide modified bovine serum albumin (azBSA) that had been covalently attached to an alkyne modified silicon phthalocyanine (alSiPc) derivative through a copper catalyzed azide/alkyne Huisgen cycloaddition (click reaction). The azBSA/alSiPc assembly was then clicked to a ca. 67 nm poly(propargyl acrylate) (PA) nanoparticle (PA/azBSA/alSiPc). The resulting particles did not exhibit any florescence when the alSiPc was excited. Incubating the particles at 37 degrees C for 30 min with a proteolytic enzyme (trypsin) degraded the linking BSA and resulted in the appearance of florescence that was attributed to a "free" silicon phthalocyanine. The PA/azBSA/alSiPc particles were incubated with human non-small cell lung cancer cells (A549) and the florescence of the initially quenched particles was achieved with cellular uptake.
引用
收藏
页码:20066 / 20073
页数:8
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