Precision phototherapy requires tight control over several therapeutic steps, which traditional methods often struggle to achieve. Here, this study reports an orthogonal trichromatic upconversion nanoparticle with a rather simple nanoarchitecture, NaErF@NaYbF@NaYbF:Nd@NaYF:Yb,Tm. Unlike conventional designs that rely on multiple activators and complicated multi-shelled structures (up to six nanoshells), the reported triple-shelled UCNPs utilize only two activator ions (Er⁺ and Tm⁺) but still enables to release red, green, and blue colors in response to three different NIR light excitations, thus significantly reducing structural complexity and synthetic workload. Integrating these UCNPs with photosensitizers and nitric oxide (NO) donors further achieve to a precision photodynamic therapy, which allows for step-wise control throughout the entire PDT process by independent activation of bioimaging, photochemical internalization, respiration prohibition via NO release, and ROS generation via specific light illuminations. Both in vitro and in vivo results demonstrate high efficiency of presented methodology, highlighting its great potential for NIR light-activated precision phototherapy.
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http://dx.doi.org/10.1002/smtd.202401742 | DOI Listing |
J Nanobiotechnology
March 2025
Cancer Center, Dongguan Key Laboratory of Precision Diagnosis and Treatment for Tumors, The 10th Affiliated Hospital of Southern Medical University, Southern Medical University, Guangzhou, 510280, China.
Radiotherapy (RT) effectiveness is limited by low DNA damage in tumor cells, surrounding tissue harm, and tumor radioresistance with active DNA repair. Herein, we have engineered a two-dimensional nanomaterial consisting of MXene nanosheets at its core, coated with gold nanorods and a cisplatin shell, and further modified with polyvinyl alcohol, referred to as APMP. The APMP exploits its distinctive electronic properties and photothermal effects to augment radiosensitivity and impede DNA damage repair mechanisms.
View Article and Find Full Text PDFJ Comput Chem
March 2025
Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas, USA.
In photopharmacology, molecular photoswitches enable light-controlled drug activities, offering precision in targeting biomolecular functions while minimizing side effects. Photostatins (PSTs) are photoswitchable analogs of combretastatin A-4 (CA4), designed to inhibit tubulin polymerization for cancer treatment. However, the influence of substituents and molecular environments on their photochemistry remains unclear.
View Article and Find Full Text PDFDalton Trans
March 2025
Key Laboratory for Biobased Materials and Energy of Ministry of Education, College of Materials and Energy, South China Agricultural University, Guangzhou 510642, China.
In recent years, photodynamic therapy (PDT) and gas therapy (GT) have emerged as research hotspots due to their excellent cancer treatment efficacy. By combining the advantages of both, the simultaneous and controllable release of reactive oxygen species (ROS) and nitric oxide (NO) has become a possibility. This paper describes the design of two Ru(II) complexes, [Ru(bpy)(NFIP)](PF) (Ru1, bpy = 2,2'-bipyridine, NFIP = 4-nitro-3-trifluoromethylaniline-1-imidazo[4,5-][1,10]phenanthroline) and [Ru(phen)(NFIP)](PF) (Ru2, phen = 1,10-phenanthroline), through the integration of the polypyridyl ruthenium structure and a photoresponsive NO donor.
View Article and Find Full Text PDFUnderstanding laser interactions with subcellular compartments is crucial for advancing optical microscopy, phototherapy, and optogenetics. While continuous-wave (CW) lasers rely on linear absorption, femtosecond (fs) lasers enable nonlinear multiphoton absorption confined to the laser focus, offering high axial precision. However, current fs laser delivery methods lack the ability to target dynamic molecular entities and automate target selection, limiting real-time perturbation of biomolecules with mobility or complex distribution.
View Article and Find Full Text PDFJ 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.
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