Yurt, F.Saka, E.T.Biyiklioglu, Z.Tunçel, A.Ozel, D.Ocakoglu, K.2020-12-012020-12-0120201088-42461088-4246https://doi.org/10.1142/S1088424620500455https://hdl.handle.net/11454/61714In this study, two SiPcs have been selected and the photodynamic therapy potentials were evaluated of the Pcs. Synthesis of Axially 2-decyn-1-oxy disubstituted Es-SiPc-2 was newly synthesized by the reaction of SiPcCl2 with 2-decyn-1-ol in the presence of NaH in toluene. Furthermore, their nuclear imaging potentials were evaluated in human colon adenocarcinoma (HT-29) and human lung fibroblast cell (WI-38) cell lines. The uptake results have indicated that Es-SiPc labeled with 131I radionuclide (131I-Es-SiPc) was approximately 2-fold higher in the HT-29 cell line than the WI-38 cell line. In other words, the target/non-target tissue ratio is defined as two in the HT-29/WI-38 cell lines. Besides, the uptake values of 131I-Es-SiPc were found to be higher than 131I-Es-SiPc-2. 131I-Es-SiPc and 131I-Es-SiPc-2 are promising for imaging or treating colon adenocarcinoma. In vitro photodynamic therapy (PDT) studies have shown that both compounds are suitable and can be used in this field. Also, Es-SiPc has been shown to have higher phototoxicity than Es-SiPc-2. © 2020 World Scientific Publishing Company.en10.1142/S1088424620500455info:eu-repo/semantics/closedAccess1 3 1 Icolon adenocarcinomaphotodynamic therapysilicon phthalocyanineSynthesis of axially disubstituted silicon phthalocyanines and investigation of their in vitro cytotoxic/phototoxic anticancer activitiesArticle2-s2.0-85093503758Q3