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Integrin $\alpha$(2)$\beta$(1)-Targeted Self-Assembled Nanocarriers for Tumor Bioimaging. | School of Pharmacy

Integrin $\alpha$(2)$\beta$(1)-Targeted Self-Assembled Nanocarriers for Tumor Bioimaging.

Citation:

Arnon Fluksman, Steinberg, Eliana , Orehov, Natalie , Shai, Ela , Lahiani, Adi , Katzhendler, Jehoshua , Marcinkiewicz, Cezary , Lazarovici, Philip , and Benny, Ofra . 2020. “Integrin $\Alpha$(2)$\Beta$(1)-Targeted Self-Assembled Nanocarriers For Tumor Bioimaging.”. Acs Applied Bio Materials, 3, 9, Pp. 6059–6070. doi:10.1021/acsabm.0c00662.

Abstract:

Recent developments in near-infrared (NIR) dyes and imaging modalities enable tumor fluorescent images in preclinical and clinical settings. However, NIR dyes have several drawbacks, and therefore, there is an unmet diagnostic need for NIR dye encapsulation in appropriate pharmaceutical nanocarriers with targeting abilities for the purpose of achieving effective diagnosis and image-guided surgeries. Because integrin receptors are established diagnostic targets, the cyclic Arg-Gly-Asp (RGD) peptides, recognizing the $\alpha$(V)$\beta$(3) integrin, have been extensively investigated for radiology and bioimaging of tumors. However, the Lys(Arg)-Thr-Ser [K(R)TS] cyclic peptides, selective for collagen receptors $\alpha$(1)$\beta$(1)/$\alpha$(2)$\beta$(1) integrins, which are overexpressed in many tumors, were not yet investigated and therefore used here for tumor bioimaging with a unique $\alpha$(2)$\beta$(1)-integrin-targeted nanocarrier, encapsulating the indocyanine green NIR dye. We synthesized three kinds of peptides: two cyclic RTS peptides functional only in the cyclic conformation and a linear peptide lacking the cyclic cysteine constrained RTS loop. We used them for the preparation of integrin-targeted self-assembled nanocarriers (ITNCs), referred to as OF5 and OF27, and a nontargeted control nanocarrier, referred to as OF70. Their selective association was demonstrated with $\alpha$(2)$\beta$(1) integrin expressing cell cultures and three-dimensional tumor spheroids and by competition with a $\alpha$(2)$\beta$(1) selective disintegrin. Cytotoxicity experiments in vitro demonstrated the safety of the ITNCs. The targeting potential and the biodistribution of the ITNCs, applied intravenously in A431 tumor-bearing nude mice, were evaluated in vivo using NIR bioimaging. Time-dependent biodistributions indicated that the ITNC OF27 showed higher fluorescent signals in main tissues, with no cytotoxic effects to major organs, and presented higher accumulation in tumors. Cumulatively, these results highlight the potential of the ITNC OF27 as an optical and innovative pharmaceutical bioimaging system, suitable for integrin $\alpha$(2)$\beta$(1) receptor in vivo tumor targeting and visualization in the NIR region.