Sholto Alan, Lee Sangwan, Hoffman Brian M, Barrett Anthony G M, Ehrenberg Benjamin
Department of Physics and Nano Medicine Research Center, Institute of Nanotechnology and Advanced Materials, Bar Ilan University, Ramat Gan, Israel.
Photochem Photobiol. 2008 May-Jun;84(3):764-73. doi: 10.1111/j.1751-1097.2007.00268.x. Epub 2008 Jan 14.
Three novel classes of porphyrazine-like structures were synthesized to form modular structures in which lipophilicity and water solubility can be tuned. Subtle modification of solubility is an important criterion in selecting a compound for biological photosensitization. The general structure takes the form H2[pz(AnB4-n)], where the core is a porphyrazine (pz) group, A is a pyrrole ring with two sulfide linkages (SR moieties) and B is a pyrrole fused with a 4,7-bis(isopropyloxy)benzo group, with n=4, 3 and 2. These molecules possess their longest wavelength absorption band between 700 and 810 nm, hence laser beams of higher tissue penetration depth could be used to illuminate them in photodynamic therapy (PDT). Armed with absorption bands in the far-red and near-infrared (near-IR), and a capability to tune the solubility, these molecules could make for better sensitizers because of optimized uptake by lipidic membranes and better optical properties. We tested several derivatives of the A4, A3B and A2B2 structures for their singlet oxygen quantum yields in methanol and in liposomes, using 9,10-dimethyl anthracene (DMA) as a singlet oxygen target. Singlet oxygen quantum yields in liposomes ranged from 0.01 to 0.44, with the A2B2 group showing the most promise. In the binding assay to find the equilibrium binding constant, Kb, we detected fluorescence changes due to a change in environment. Peripheral long-chain moieties (the R group in the SR moieties) dominate lipid binding. These moieties range in the hydrophobicity that they induce from C8H17 and benzene, which rendered the molecule totally insoluble in water, to polyethylene glycol (PEG) and carboxylate groups, which imparted water solubility. Each molecule had between 4 and 8 such identical chains. Chains bearing an ether or ester link resulted in measurable equilibrium constants, with a higher Kb for ether substituents. Results for Kb ranged from 0.23 to 26.52 (mg mL(-1))(-1). A delicate balance exists between water solubility and good partitioning to membranes. In general, a higher oxygen-to-carbon ratio in the chains improves binding. Fewer chains and a centrally coordinated zinc ion further improve binding and singlet oxygen production.
合成了三类新型的类卟啉结构以形成模块化结构,其中亲脂性和水溶性可以调节。溶解度的细微改变是选择用于生物光致敏的化合物的重要标准。一般结构为H2[pz(AnB4-n)],其中核心是卟啉(pz)基团,A是带有两个硫醚键(SR部分)的吡咯环,B是与4,7-双(异丙氧基)苯并基团稠合的吡咯,n = 4、3和2。这些分子在700至810nm之间具有其最长波长吸收带,因此在光动力疗法(PDT)中可以使用具有更高组织穿透深度的激光束来照射它们。由于在远红和近红外(近红外)区域具有吸收带,并且具有调节溶解度的能力,这些分子由于脂质膜的优化摄取和更好的光学性质而可以成为更好的敏化剂。我们使用9,10-二甲基蒽(DMA)作为单线态氧靶标,测试了A4、A3B和A2B2结构的几种衍生物在甲醇和脂质体中的单线态氧量子产率。脂质体中的单线态氧量子产率范围为0.01至0.44,其中A2B2基团显示出最大的潜力。在用于测定平衡结合常数Kb的结合试验中,我们检测到由于环境变化引起的荧光变化。外围长链部分(SR部分中的R基团)主导脂质结合。这些部分的疏水性范围从导致分子完全不溶于水的C8H17和苯,到赋予水溶性的聚乙二醇(PEG)和羧酸盐基团。每个分子具有4至8个这样的相同链。带有醚或酯键的链导致可测量的平衡常数,醚取代基的Kb更高。Kb的结果范围为0.23至26.52(mg mL(-1))(-1)。水溶性和对膜的良好分配之间存在微妙的平衡。一般来说,链中较高的氧碳比可改善结合。较少的链和中心配位的锌离子进一步改善结合和单线态氧的产生。