Abstract:Given their superior penetration depths, photosensitizers with longer absorption wavelengths present broader application prospects in photodynamic therapy (PDT). Herein, Ag2S quantum dots were discovered, for the first time, to be capable of killing tumor cells through the photodynamic route by near‐infrared light irradiation, which means relatively less excitation of the probe compared with traditional photosensitizers absorbing short wavelengths. On modification with polydopamine (PDA), PDA‐Ag2S was obtained… Show more
“…8,9 Secondly, their high intensity and resistance towards photobleaching permit the longterm tracking of live, single-molecules, which offers detailed information on intracellular trafficking and processing. 10,11 QDs are also being extensively used in the development of anticancer interventions either directly for photodynamic [12][13][14][15] or photothermal [16][17][18] therapy applications, or in combination with existing drug formulations, 5,19,20 rendering them as promising theranostic agents.…”
Despite the progress in nanotechnology for biomedical applications, great efforts are still employed in optimizing nanoparticle (NP) design parameters to improve functionality and minimize bio-nanotoxicity. In this study, we developed CdSe/CdS/ZnS core/shell/shell quantum dots (QDs) that are compact ligandcoated and surface-functionalized with an HIV-1-derived TAT cell-penetrating peptide (CPP) analog to improve both biocompatibility and cellular uptake. Multiparametric studies were performed in different mammalian and murine cell lines to compare the effects of varying QD size and number of surface CPPs on cellular uptake, viability, generation of reactive oxygen species, mitochondrial health, cell area, and autophagy. Our results showed that the number of cell-associated NPs and their respective toxicity is higher for the larger QDs. Meanwhile, increasing the number of surface CPPs also enhanced cellular uptake and induced cytotoxicity through the generation of mitoROS and autophagy. Thus, here we report the optimal size and surface CPP combinations for improved QD cellular uptake.
“…8,9 Secondly, their high intensity and resistance towards photobleaching permit the longterm tracking of live, single-molecules, which offers detailed information on intracellular trafficking and processing. 10,11 QDs are also being extensively used in the development of anticancer interventions either directly for photodynamic [12][13][14][15] or photothermal [16][17][18] therapy applications, or in combination with existing drug formulations, 5,19,20 rendering them as promising theranostic agents.…”
Despite the progress in nanotechnology for biomedical applications, great efforts are still employed in optimizing nanoparticle (NP) design parameters to improve functionality and minimize bio-nanotoxicity. In this study, we developed CdSe/CdS/ZnS core/shell/shell quantum dots (QDs) that are compact ligandcoated and surface-functionalized with an HIV-1-derived TAT cell-penetrating peptide (CPP) analog to improve both biocompatibility and cellular uptake. Multiparametric studies were performed in different mammalian and murine cell lines to compare the effects of varying QD size and number of surface CPPs on cellular uptake, viability, generation of reactive oxygen species, mitochondrial health, cell area, and autophagy. Our results showed that the number of cell-associated NPs and their respective toxicity is higher for the larger QDs. Meanwhile, increasing the number of surface CPPs also enhanced cellular uptake and induced cytotoxicity through the generation of mitoROS and autophagy. Thus, here we report the optimal size and surface CPP combinations for improved QD cellular uptake.
“…synthesized polydopamine (PDA)‐functionalized Ag 2 S QDs for fluorescence imaging‐guided PDT of tumors ( Figure a). [ 77 ] As shown in Figure 16b, PDT with the designed nanotheranostic was more effective than unfunctionalized nanoparticles. Li et al.…”
Section: Bioapplications Of Nir Ag2s Qdsmentioning
confidence: 99%
“…Reproduced with permission. [ 77 ] Copyright 2019, Wiley‐VCH. c) Schematic illustration and d) SDT efficacy of (QD@P)Rs.…”
Section: Bioapplications Of Nir Ag2s Qdsmentioning
Quantum dots (QDs) with near‐infrared fluorescence (NIR) are an emerging class of QDs with unique capabilities owing to the deeper tissue penetrability of NIR light compared with visible light. NIR light also effectively overcomes organism autofluorescence, making NIR QDs particularly attractive in biological imaging applications for disease diagnosis. Considering latest developments, Ag2S QDs are a rising star among NIR QDs due to their excellent NIR fluorescence properties and biocompatibility. This review presents the various methods to synthesize NIR Ag2S QDs, and systematically discusses their applications in biosensing, bioimaging, and theranostics. Major challenges and future perspectives concerning the synthesis and bioapplications of NIR Ag2S QDs are discussed.
“…The chemical structures of organic sensitizers and schematic illustration of inorganic and hybrid sensitizers used in cancer therapy are shown in Figure 2 , Figure 3 . The characteristic parameters of the sensitizers used in different tumor cells or animal models are summarized in Table 1 28 , 29 , 30 , 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 , 54 , 55 , 56 , 57 , 58 , 59 , 60 , 61 , 62 , 63 , 64 , 65 , 66 , 67 . …”
Section: Sensitizers For Cancer Therapymentioning
confidence: 99%
“…Semiconductor QDs have attracted increasing attention due to tunable band gaps, high molar extinction coefficients, sufficient photostability, and the ability to generate multiple electron–hole pairs 129 . Ag 2 S QDs could be used as either sonosensitizer or photosensitizer to generate ROS for PDT and SDT 61 , 62 . Biocompatible Ag 2 S QDs prepared using high-temperature pyrolysis method were modified with PEGylated phospholipids to form nanoparticles, which had photodynamic behavior under 808 nm NIR irradiation.…”
Many sensitizers have not only photodynamic effects, but also sonodynamic effects. Therefore, the combination of sonodynamic therapy (SDT) and photodynamic therapy (PDT) using sensitizers for sono-photodynamic therapy (SPDT) provides alternative opportunities for clinical cancer therapy. Although significant advances have been made in synthesizing new sensitizers for SPDT, few of them are successfully applied in clinical settings. The anti-tumor effects of the sensitizers are restricted by the lack of tumor-targeting specificity, incapability in deep intratumoral delivery, and the deteriorating tumor microenvironment. The application of nanotechnology-based drug delivery systems (NDDSs) can solve the above shortcomings, thereby improving the SPDT efficacy. This review summarizes various sensitizers as sono/photosensitizers that can be further used in SPDT, and describes different strategies for enhancing tumor treatment by NDDSs, such as overcoming biological barriers, improving tumor-targeted delivery and intratumoral delivery, providing stimuli-responsive controlled-release characteristics, stimulating anti-tumor immunity, increasing oxygen supply, employing different therapeutic modalities, and combining diagnosis and treatment. The challenges and prospects for further development of intelligent sensitizers and translational NDDSs for SPDT are also discussed.
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