Dahoumane Si Amar, Nguyen Minh Ngoc, Thorel Alain, Boudou Jean-Paul, Chehimi Mohamed M, Mangeney Claire
ITODYS, Universite Paris Diderot and CNRS (UMR 7086), 15 rue Jean de Baif, 75013 Paris, France.
Langmuir. 2009 Sep 1;25(17):9633-8. doi: 10.1021/la9009509.
Diazonium salt chemistry and atom transfer radical polymerization (ATRP) were combined in view of preparing new bioactive hairy diamond nanoparticles containing, or potentially containing, nitrogen-vacancy (NV) fluorescent centers (fluorescent nanodiamonds, or fNDs). fNDs were modified by ATRP initiators using the electroless reduction of the diazonium salt BF(4)(-),(+)N(2)-C(6)H(4)-CH(CH(3))-Br. The strongly bound aryl groups -C(6)H(4)-CH(CH(3))-Br efficiently initiated the ATRP of tert-butyl methacrylate (tBMA) at the surface of the nanodiamonds, which resulted in obtaining ND-PtBMA hybrids. The grafted chain thickness, estimated from X-ray photoelectron spectroscopy (XPS), was found to increase linearly with respect to time before reaching a plateau value of ca. 2 nm. These nanoobjects were further hydrolyzed into ND-PMAA (where PMAA is the poly(methacrylic acid) graft) and further decorated by bovine serum albumin through the 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide (EDC/NHS) coupling procedure.
鉴于制备含有或可能含有氮空位(NV)荧光中心的新型生物活性毛发状金刚石纳米颗粒(荧光纳米金刚石,或fNDs),重氮盐化学与原子转移自由基聚合(ATRP)相结合。使用重氮盐BF(4)(-)、(+)N(2)-C(6)H(4)-CH(CH(3))-Br的化学还原法,通过ATRP引发剂对fNDs进行修饰。强结合的芳基-C(6)H(4)-CH(CH(3))-Br在纳米金刚石表面有效地引发了甲基丙烯酸叔丁酯(tBMA)的ATRP,从而得到ND-PtBMA杂化物。通过X射线光电子能谱(XPS)估计,接枝链厚度在达到约2nm的平台值之前随时间呈线性增加。这些纳米物体进一步水解为ND-PMAA(其中PMAA是聚(甲基丙烯酸)接枝物),并通过1-乙基-3-(3-二甲基氨基丙基)碳二亚胺/N-羟基琥珀酰亚胺(EDC/NHS)偶联程序进一步用牛血清白蛋白修饰。