Departments of Chemistry, Northwestern University, Evanston, IL 60208, USA.
Proc Natl Acad Sci U S A. 2010 Jan 26;107(4):1284-8. doi: 10.1073/pnas.0912811107. Epub 2009 Dec 23.
A chiral porphyrazine (pz), H(2)[pz(trans-A(2)B(2))] (247), has been prepared that exhibits preferential in vivo accumulation in the cells of tumors. Pz 247 exhibits near-infrared (NIR) emission with lambda > 700 nm in the required wavelength range for maximum tissue penetration. When MDA-MB-231 breast tumor cells are treated with 247, the agent shows strong intracellular fluorescence with an emission maximum, 704 nm, which indicates that it localizes within a hydrophobic microenvironment. Pz 247 is shown to associate with the lipophilic core of LDL and undergo cellular entry primarily through receptor-mediated endocytosis accumulating in lysosomes. Preliminary in vivo studies show that 247 exhibits preferential accumulation and retention in the cells of MDA-MB-231 tumors subcutaneously implanted in mice, thereby enabling NIR optical imaging with excellent contrast between tumor and surrounding tissue. The intensity of fluorescence from 247 within the tumor increases over time up to 48 h after injection presumably due to the sequestration of circulating 247/LDL complex by the tumor tissue. As the need for cholesterol, and thus LDL, is elevated in highly proliferative tumor cells over nontumorigenic cells, 247 has potential application for all such tumors.
一种手性卟啉(pz),H(2)[pz(trans-A(2)B(2))](247),已被制备,其在肿瘤细胞中表现出优先的体内积累。pz 247 在所需的最大组织穿透波长范围内表现出近红外(NIR)发射,lambda > 700nm。当 MDA-MB-231 乳腺癌细胞用 247 处理时,该试剂显示出强烈的细胞内荧光,发射最大值为 704nm,表明它定位于疏水性微环境中。pz 247 被证明与 LDL 的亲脂核心结合,并通过受体介导的内吞作用主要进入细胞,在溶酶体中积累。初步的体内研究表明,247 在皮下植入小鼠的 MDA-MB-231 肿瘤细胞中表现出优先积累和保留,从而能够进行具有出色肿瘤与周围组织对比度的近红外光学成像。注射后 48 小时内,肿瘤内 247 的荧光强度增加,这可能是由于肿瘤组织隔离了循环 247/LDL 复合物。由于在高度增殖的肿瘤细胞中对胆固醇(因此对 LDL)的需求增加,而在非肿瘤细胞中则没有,因此 247 具有适用于所有此类肿瘤的潜力。