Radiolabeling and preclinical animal model evaluation of DTPA coupled 99mTc-labelled flutamide complex ([99mTc]DTPA-FLUT) as a potential radiotracer for cancer imaging

Author:

Naqvi Syed Ali Raza1ORCID,Hassan Ahmad Junaid1,Janjua Muhammad Ramzan Saeed Ashraf1,Abbas Naseem2,Zahoor Ameer Fawad1,Hassan Sadaf Ul3,Hussain Amjad4

Affiliation:

1. Department of Chemistry, Government College University Faisalabad, Faisalabad, Punjab, Pakistan

2. Institute of Chemical Sciences, Bahauddin Zakariya University, Multan, Pakistan

3. Department of Chemistry, COMSATS University Islamabad, Lahore Campus, Lahore, Pakistan

4. Institute of Chemistry, University of Okara, Okara, Punjab, Pakistan

Abstract

Background Advances in molecular imaging strategies have had an effect on precise diagnosis and treatment. Research has been intensified to develop more effective and versatile radiopharmaceuticals to uplift diagnostic efficiency and, consequently, the treatment. Purpose To label the flutamide (FLUT) coupled with diethylenetriamine pentaacetate (DTPA) with technetium-99 m (99mTc) and to evaluate its binding efficiency with rhabdomyosarcoma (RMS) cancer cells. Material and methods Radiolabeling of FLUT with 185 MBq freshly eluted 99mTcO4−1 was carried out via DTPA bifunctional chelating agent using stannous chloride reducing agent at pH 5. The labeled compound was assessed for its purity using chromatography analysis, stability in saline and blood serum, AND charge using paper electrophoresis. Normal biodistribution was studied using a mouse model, while binding affinity with RMS cancer cells was studied using an internalization assay. The in vivo accumulation of RMS cancer cells in a rabbit model was monitored using a SPECT gamma camera. Results Radiolabeling reaction displayed a pharmaceutical yield of 97% and a stability assay showed >95% intact radiopharmaceutical up to 6 h in saline and blood serum. In vitro internalization studies showed the potential of [99mTc]DTPA-FLUT to enter into cancer cells. This biodistribution study showed rapid blood clearance and minimum uptake by body organs, and scintigraphy displayed the [99mTc]DTPA-FLUT uptake by lesion, induced by RMS cancer cell lines in rabbit. Conclusion Stable, newly developed [99mTc]DTPA-FLUT seeks its way to internalize into RMS cancer cells, indicating it could be a potential candidate for the diagnosis of RMS cancer.

Publisher

SAGE Publications

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