Investigation of CT imaging-based BiS drug-loaded nanoparticles for the diagnosis and therapy of colorectal cancer.
Colorectal cancer ranks as the third most prevalent cancer globally, with its incidence increasing in many developed countries.
APA
Lu Q, Zhang B, et al. (2026). Investigation of CT imaging-based BiS drug-loaded nanoparticles for the diagnosis and therapy of colorectal cancer.. Journal of pharmaceutical sciences, 115(1), 104033. https://doi.org/10.1016/j.xphs.2025.104033
MLA
Lu Q, et al.. "Investigation of CT imaging-based BiS drug-loaded nanoparticles for the diagnosis and therapy of colorectal cancer.." Journal of pharmaceutical sciences, vol. 115, no. 1, 2026, pp. 104033.
PMID
41109525
Abstract
Colorectal cancer ranks as the third most prevalent cancer globally, with its incidence increasing in many developed countries. While chemotherapy demonstrates efficacy for certain patients, it is associated with significant side effects, and prolonged treatment may result in drug resistance. Consequently, this study synthesized BiS nanosheets via the solution-based method and integrated them with mesoporous silica exhibiting excellent pore channel properties to develop the BiS@mSiO-PEG/5-FU nanomaterials. Photothermal testing revealed that BiS@mSiO-PEG/5-FU exhibited superior photothermal heating performance, remarkable photothermal stability, and a photothermal conversion efficiency of 28.3 %, enabling effective photothermal therapy. The drug loading capacity of BiS@mSiO-PEG/5-FU was determined to be 24.8 %, with enhanced drug release under acidic conditions and laser irradiation, thereby improving chemotherapeutic efficacy and achieving synergistic effects between chemotherapy and photothermal therapy. Furthermore, BiS@mSiO-PEG demonstrated robust CT imaging capabilities (14.95 HU mg/mL), establishing the BiS@mSiO-PEG/5-FU nanomaterials as a platform with integrated diagnostic and therapeutic functionalities.
MeSH Terms
Colorectal Neoplasms; Bismuth; Humans; Nanoparticles; Fluorouracil; Tomography, X-Ray Computed; Animals; Sulfides; Drug Liberation; Silicon Dioxide; Mice; Polyethylene Glycols; Cell Line, Tumor; Drug Carriers; Antineoplastic Agents; Photothermal Therapy
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