In vitro CT imaging and cellular evaluation of hyaluronic acid-functionalized Bi 2 S 3 @BSA nanoparticles
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 (Bi 2 S 3 @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 Bi 2 S 3 @BSA nanoparticles and the clinical iodinated contrast agent Omnipaque. Contrast-to-noise ratio (CNR), cytocompatibility, and in vitro cellular CT imaging were also evaluated. Bi 2 S 3 @BSA-HA exhibited significantly higher CT attenuation than both Bi 2 S 3 @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 (R 2 > 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 Bi 2 S 3 @BSA-HA than with Bi 2 S 3 @BSA. These findings demonstrate improved in vitro CT imaging performance with good cytocompatibility under the investigated conditions.
Authors
- Farshid Babapour Mofrad (ORCID: https://orcid.org/0000-0002-5892-7971)
- Hamid Delavari (ORCID: https://orcid.org/0000-0003-0570-9767)
- Farahnaz Seyedabutorabi
- Mohammad Hosntalab
Institutions
- Islamic Azad University, Tehran (IR)
- Tarbiat Modares University (IR)
Publication Details
- Journal
- Journal of X-Ray Science and Technology
- Published
- 2026-09-11
- DOI
- https://doi.org/10.1177/08953996261486734
- Primary Topic
- Advanced X-ray and CT Imaging
- Type
- article
- Field-Weighted Citation Impact
- 0.00