Background: Photodynamic therapy (PDT) is a common cancer treatment strategy that combines the use of light, a photosensitizer, and oxygen to precisely generate reactive oxygen species (ROS). However, the efficacy of this method is limited by the shallow tissue penetration of the short-wavelength lasers involved, and combination therapy with other treatments such as photothermal therapy (PTT) or radiation therapy requires additional lasers or instruments. A new dual therapy approach using a single laser could minimize the treatment procedure.
Methods: Chlorin e6 (Ce6) loaded-NaYF:Yb,Er@NaYF:Yb,Nd upconversion nanoparticles@mesoporous silica@mesoporous polydopamine nanoparticles (U@MSC@MP NPs) were fabricated to achieve PDT and PTT combination cancer therapy using a single 808 nm laser. The NaYF:Yb,Er@NaYF:Yb,Nd upconversion nanoparticles (UCNPs) were coated with mesoporous silica (MS) for Ce6-loading and coated with mesoporous polydopamine (MP) as a PTT photosensitizer. The PDT and PTT effects were measured using ROS generation detection and a thermal camera, respectively; in vitro cytotoxicity studies and in vivo antitumor efficacy analysis using tumor xenograft mouse models were performed to confirm the dual effects.
Results And Discussion: The PDT-PTT UCNPs were successfully synthesized and emit photoluminescence spectra that can be absorbed by Ce6 to induce the PDT effect. Significant ROS generation was observed from U@MSC@MP NPs following 808 nm laser irradiation for 5 min, which corresponded to intracellular ROS detection in human colorectal adenocarcinoma HT-29 cells. The NPs significantly reduced HT-29 cell viability compared with PDT or PTT alone, demonstrating the potential of the designed UCNPs. Moreover, the in vivo antitumor efficacy analysis confirmed the dual effect with no signs of toxicity, supporting the safety and biocompatibility of the synthesized NPs.
Conclusion: These findings suggest that the combination of PDT and PTT using a single laser can be achieved with UCNPs. This approach is a promising strategy for simplifying the cancer treatment procedures in clinical applications.
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http://dx.doi.org/10.2147/IJN.S503977 | DOI Listing |
J Colloid Interface Sci
March 2025
Department of Biomedical Engineering, The Hong Kong Polytechnic University, Kowloon 999077, Hong Kong, China; Joint Research Center in Biosensing and Precision Theranostics, The Hong Kong Polytechnic University, Kowloon 999077, Hong Kong, China; Hong Kong Polytechnic Shenzhen Research Institute, Shenzhen 518057, China. Electronic address:
The tumor microenvironment (TME) exhibits a specific feature of hypoxia, which poses significant challenges for oxygen (O)-dependent treatments. In this study, we developed an intelligent nanoplatform (PEGylated AIPH@MSN/CDs-MnO, denoted as A@M/C-Mn) by integrating a photosensitizer of red carbon dots (CDs) with a thermolabile initiator-loaded mesoporous silica nanoparticle (AIPH@MSN, denoted as A@M), and then growing manganese dioxide nanosheets (MnO NS) in situ and PEGylating the structure to achieve TME-responsive synergistic diagnosis and phototherapy against hypoxic tumors. The outer-layer MnO NS has the capability to decompose endogenous hydrogen peroxide (HO) in the acidic TME, thereby producing O to alleviate hypoxia while releasing Mn.
View Article and Find Full Text PDFBiomaterials
March 2025
Department of Chemistry, Korea University, Seoul 02841, Korea. Electronic address:
Small molecule-based multifunctional optical diagnostic materials have garnered considerable interest due to their highly customizable structures, tunable excited-state properties, and remarkable biocompatibility. We herein report the synthesis of a multifaceted photosensitizer, PPQ-CTPA, which exhibits exceptional efficacy in generating Type I reactive oxygen species (ROS) and thermal energy under near-infrared-II (NIR-II, >1000 nm) laser excitation at 1064 nm, thereby combining photodynamic therapy (PDT) and photothermal therapy (PTT) functionalities. To enhance therapeutic efficacy, we engineered lonidamine (LND) by conjugating it with triphenylphosphonium (TPP) cations, producing LND-TPP.
View Article and Find Full Text PDFInt J Nanomedicine
March 2025
College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, 08826, Republic of Korea.
Background: Photodynamic therapy (PDT) is a common cancer treatment strategy that combines the use of light, a photosensitizer, and oxygen to precisely generate reactive oxygen species (ROS). However, the efficacy of this method is limited by the shallow tissue penetration of the short-wavelength lasers involved, and combination therapy with other treatments such as photothermal therapy (PTT) or radiation therapy requires additional lasers or instruments. A new dual therapy approach using a single laser could minimize the treatment procedure.
View Article and Find Full Text PDFNoninvasive phototherapy with functional preservation is considered to be a promising cancer therapeutic method. However, the clinical application of tumor phototherapy is severely restrained by the lack of appropriate multimodal phototherapy agents exhibiting an ideal tissue penetration depth to maximize the antitumor efficiency as well as to maintain important tissue functions. Herein, an innovative near-infrared ray (NIR)-triggered photodynamic-photocatalytic-photothermal therapy (PDT-PCT-PTT) agent based on an atomically dispersed cobalt single-atom enzyme (Co-SAE) anchored on hollow N-doped carbon sphere (HNCS) has been strategically developed.
View Article and Find Full Text PDFNanoscale Adv
February 2025
School of Traditional Chinese Medicine, Bozhou University Anhui 236800 P. R. China
Cancer is a leading cause of death globally, and traditional treatment methods often come with non-negligible toxic side effects in its treatment, threatening patients' quality of life. Thus, developing novel, efficient, low-toxicity cancer treatment strategies is crucial. Nanozymes, as a class of powerful nanomaterials, can subtly mimic the catalytic activity of natural enzymes, making them a formidable alternative.
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