# Dual Potential of Cetuximab Conjugated Hydroxyapatite Zirconium Nanoparticle as Nanocarrier for Radioenhancer in X-Ray Dynamic Therapy and 177Lu-based Radioimmunotherapy of Lung Cancer

**Authors:** Ahmad Kurniawan, Isa Mahendra, Asep Rizaludin, Marhendra Satria Utama, Ronny Lesmana, Fitria Dwi Ayuningtyas, Maria Rosa Dewanti, Dani Gustaman Syarif, Muhamad Basit Febrian

PMC · DOI: 10.7150/ntno.101699 · 2025-03-03

## TL;DR

Researchers developed a nanoparticle that can deliver radiation therapy to lung cancer cells using X-rays and a radioactive isotope, improving treatment effectiveness.

## Contribution

A novel CTX-conjugated HApZr nanoparticle was created for dual use in X-ray dynamic therapy and radioimmunotherapy.

## Key findings

- HApZr-CTX nanoparticles showed enhanced ROS generation in A549 cells under X-ray irradiation.
- The nanocarrier successfully loaded 177Lu and was internalized by lung cancer cells.
- In mice, [177Lu]Lu-HApZr-CTX accumulated primarily in the lungs after injection.

## Abstract

This study aimed to synthesize cetuximab (CTX) conjugated hydroxyapatite zirconium (HApZr-CTX) as a nanocarrier for active delivery of photosensitizer and therapeutic radionuclide. The system enabled targeted radioenhancer in X-ray dynamic therapy and radioimmunotherapy for lung cancer. The results showed that HApZr-CTX had the main characteristics of hydroxyapatite crystal in X-ray powder diffraction (XRD), with particle size twice bigger, according to DLS-PSA and TEM measurements. Cellular ROS generation was elevated almost three times in A549 cells after being treated using 125 µg/mL HApZr-CTX and irradiated with 5 Gy of X-ray photon compared to untreated cells. The viability of the treated lung cancer cell line decreased after exposure to external radiation. Moreover, as a radioimmunotherapy candidate, 177Lu was successfully loaded into HApZr-CTX nanocarrier and internalized in A549 more than half of the given dose after 0.5 h incubation. [177Lu]Lu-HApZr-CTX was primarily accumulated in the lung organs of healthy mice one-hour post-injection. In conclusion, HApZr-CTX nanoparticles have the potential to be used as a radioenhancer in X-ray dynamic therapy and radioimmunotherapy for lung cancer therapy.

## Linked entities

- **Chemicals:** hydroxyapatite (PubChem CID 14781), zirconium (PubChem CID 23995), 177Lu (PubChem CID 161046)
- **Diseases:** lung cancer (MONDO:0005138)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** Lung Cancer (MESH:D008175)
- **Chemicals:** 177Lu (MESH:C000615061), CTX (MESH:D000068818), 177Lu]Lu-HApZr-CTX (-), hydroxyapatite (MESH:D017886)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11898717/full.md

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Source: https://tomesphere.com/paper/PMC11898717