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Cancer remains one of the leading causes of death worldwide, prompting extensive research into novel theranostic (combined word of diagnostic and therapeutic) strategies. Nanomedicine has emerged as a potential breakthrough in cancer theranosis, overcoming limitations of conventional approaches. Among such approaches, carbon dots (CDs) with a size smaller than 10 nm have garnered significant attention for their potential use in cancer theranosis, owing to their low toxicity, good water solubility, easy synthesis, facile surface modification, and unique optical and photothermal and photodynamic properties. Researchers have demonstrated that surface functionalization of CDs with diverse hydrophilic groups can be easily achieved by choosing proper carbon precursors in synthesis, and further surface modification of CDs with cancer-targeting ligands, photosensitizers, anticancer drugs, and genes can also be easily achieved using various methods, thereby establishing a versatile approach for cancer theranosis. This review described the various surface modification methods of CDs, in vitro and in vivo toxicity of CDs, and various cancer theranostic methods such as drug delivery, photodynamic therapy, photothermal therapy, gene therapy, sonodynamic therapy, and gas therapy. Therefore, CDs can serve as various mono and combined theranostic modalities, offering us new methods for cancer theranosis.
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http://dx.doi.org/10.3390/nano15110781 | DOI Listing |
Colloids Surf B Biointerfaces
December 2025
Department of Energy and Materials Engineering, Dongguk University-Seoul, Seoul 04620, Republic of Korea. Electronic address:
A theranostic hybrid nanomaterial was synthesized by incorporating functional moieties such as anticancer drug methotrexate (MTX), cancer targeting ligand folic acid (FA) and a radioisotope, Co-57, into topological sites of layered double hydroxide (LDH). The surface of the drug intercalated LDH (MTX-LDH) was successfully modified with FA utilizing hexamethylene diamine (HDA) as a spacer. The radioisotope, Co-57, was then incorporated into the frameworks of the surface-modified LDH (Co@FHML) via a hydrothermal method in order to preserve the crystalline phase and particle size of the LDH during the incorporation.
View Article and Find Full Text PDFDrug Dev Res
August 2025
Institute of Nuclear Medicine and Allied Sciences, Defence Research and Development Organization, Delhi, India.
Mesoporous silica nanoparticles have been extensively utilized for targeted drug delivery; the drugs are encapsulated in the pores, while the surface can be modified to make the nanoparticles target-specific. The work presented here focuses on the development of multifunctional theranostic mesoporous silica nanoparticles with estrogen receptor-positive [ER(+)] breast cancer as the target. The surface of the nanoparticles was dually functionalized to make the nanoparticles target-specific using an estradiol derivative via a facile click reaction and to attach a Tc complexing agent (DTPA) for SPECT imaging.
View Article and Find Full Text PDFEur J Pharm Sci
July 2025
Nanobiotechnology for Life Sciences Group, Department of Chemistry in Pharmaceutical Sciences, Faculty of Pharmacy, Universidad Complutense de Madrid (UCM), Plaza Ramón y Cajal s/n, Madrid E-28040, Spain; Microscopy and Dynamic Imaging Unit, Fundación Centro Nacional de Investigaciones Cardiovascu
Triple negative breast cancer (TNBC) represents one of the most aggressive types of cancer, with a difficult treatment leading to poor prognosis of the disease. Herein we report the synthesis of a custom-made cyclic RGD peptide (cRGD), and its use in decorating liposomes for targeted drug delivery of doxorubicin to TNBC cells overexpressing integrin receptor αβ. Liposomes carrying dibenzocyclooctine groups on their surface were produced using an optimized large scale microfluidic-assisted approach and subsequently conjugated with cRGD bearing an acyl azide group by means of a click chemistry reaction.
View Article and Find Full Text PDFNanomaterials (Basel)
May 2025
Department of Chemistry, College of Natural Sciences, Kyungpook National University, Taegu 41566, Republic of Korea.
Cancer remains one of the leading causes of death worldwide, prompting extensive research into novel theranostic (combined word of diagnostic and therapeutic) strategies. Nanomedicine has emerged as a potential breakthrough in cancer theranosis, overcoming limitations of conventional approaches. Among such approaches, carbon dots (CDs) with a size smaller than 10 nm have garnered significant attention for their potential use in cancer theranosis, owing to their low toxicity, good water solubility, easy synthesis, facile surface modification, and unique optical and photothermal and photodynamic properties.
View Article and Find Full Text PDFArch Pharm (Weinheim)
March 2025
Department of Labeled Compounds, Hot Laboratories Centre, Egyptian Atomic Energy Authority (EAEA), Cairo, Egypt.
Biocompatible silver nanoparticles (AgNPs) are employed with an active ingredient of milk thistle extract, silybin (SIB), to treat cancers. Strong cytotoxic effects of SIB-AgNPs against two distinct cell lines (MCF-7 and HepG2) are observed on a stable nano-platform that contains spherical nanoparticles within a limited size range. With a high radiochemical purity, radioiodination of SIB-AgNPs was accomplished.
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