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Rational Designing of Hypocrellin B-Loaded Mesoporous Silicia-NaYF4@NaSmF4 Core@Shell Upconversion Nanoparticles for
Selvamuthu Preethi1, Ponnusamy Chandrasekar1, Darson Jaison2
1Department of Pharmaceutical Technology, Bharathidasan Institute of Technology, University College of Engineering, Anna University, Tiruchirappalli 620 024, Tamil Nadu, India.
Researchers developed novel upconversion nanoparticles (UCNPs) loaded with Hypocrellin B (HB) for photodynamic therapy (PDT) against breast cancer. This innovative approach enhances PDT efficacy, offering a promising minimally invasive treatment option.
Area of Science:
- Nanotechnology and Materials Science
- Biomedical Engineering
- Oncology
Background:
- Breast cancer remains a leading cause of death globally, necessitating advanced therapeutic strategies.
- Conventional treatments face limitations, driving interest in minimally invasive alternatives like photodynamic therapy (PDT).
- Upconversion nanoparticles (UCNPs) show potential for enhancing PDT efficacy in biological applications.
Purpose of the Study:
- To synthesize and characterize mesoporous silica core-shell UCNPs loaded with Hypocrellin B (HB).
- To evaluate the efficacy of HB-loaded UCNPs as a photodynamic therapeutic agent for breast cancer.
- To investigate the mechanism of cancer cell death induced by UCNP-mediated PDT.
Main Methods:
- Layer-by-layer synthesis (hydrothermal and coprecipitation) of mesoporous silica core-shell UCNPs loaded with HB.
- Structural and morphological characterization using XRD, FESEM, and HRTEM.
- In vitro drug release studies, cell viability assays (IC50 determination), reactive oxygen species (ROS) detection, apoptosis assays, and mitochondrial membrane potential (ΔΨm) measurements.
Main Results:
- Successfully synthesized HB-loaded mSi-CS-UCNPs with distinct structural and morphological properties.
- Demonstrated controlled in vitro release of HB from the UCNP carriers.
- Under 980 nm near-infrared (NIR) light irradiation, HB-loaded UCNPs significantly reduced cancer cell viability (IC50 = 29 μg/mL) via enhanced ROS production, apoptosis induction, and mitochondrial dysfunction.
Conclusions:
- HB-loaded mSi-CS-UCNPs effectively activate photosensitizers under NIR light, generating singlet oxygen (¹O₂) for cancer cell death.
- This UCNP-based PDT modality offers a promising approach for treating breast cancer through apoptosis or necrosis induction.
- The developed nanoplatform holds potential as a minimally invasive therapeutic strategy for breast cancer treatment.
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