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Evaluation of the Interplay Between the Complement Protein C1q and Hyaluronic Acid in Promoting Cell Adhesion
Published on: June 15, 2019
In vitro CT imaging and cellular evaluation of hyaluronic acid-functionalized Bi2S3@BSA nanoparticles
Farahnaz Seyedabutorabi1, Hamid Delavari2, Mohammad Hosntalab1
1Department of Medical Radiation Engineering, SR.C., Islamic Azad University, Tehran, Iran.
Abstract:
The development of high-atomic-number (high-Z) nanomaterials as computed tomography (CT) contrast agents has attracted considerable interest because of their strong X-ray attenuation. In this study, hyaluronic acid (HA)-functionalized bismuth sulfide nanoparticles (Bi2S3@BSA-HA) were synthesized and characterized, and their CT imaging performance was evaluated over a tube-voltage range of 80-130 kVp. CT attenuation was assessed as a function of Bi concentration and tube voltage and compared with non-functionalized Bi2S3@BSA nanoparticles and the clinical iodinated contrast agent Omnipaque. Contrast-to-noise ratio (CNR), cytocompatibility, and in vitro cellular CT imaging were also evaluated. Bi2S3@BSA-HA exhibited significantly higher CT attenuation than both Bi2S3@BSA and Omnipaque, reaching 146.8 ± 6.9 HU at 1.5 mg Bi mL-1 and 80 kVp. CT attenuation increased linearly with Bi concentration (R2 > 0.93) and decreased with increasing tube voltage. The HA-functionalized nanoparticles consistently exhibited higher CNR values across all investigated tube voltages. MTT assays demonstrated low cytotoxicity, with cell viability exceeding 90% after 24 h. In vitro cellular CT imaging showed higher CT numbers and CNR in HT-29 cells incubated with Bi2S3@BSA-HA than with Bi2S3@BSA. These findings demonstrate improved in vitro CT imaging performance with good cytocompatibility under the investigated conditions.

