Abstract:Multi-structure assemblies consisting of gold nanoparticles and porphyrin were fabricated by using diblock copolymer, poly(ethylene glycol)-block-poly(4-vinylpyridine) (PEG-b-P4VP). The copolymer of PEG-b-P4VP was used in the formation of core-shell micelles in water, in which the P4VP block serves as the core, while the PEG block forms the shell. In the micellar core, gold nanoparticle and metalloporphyrin were dispersed through the axial coordination. Structural and morphological characterizations of the com… Show more
“…Porphyrins generally cause severe phototoxicity in the skin when exposed to light, which hinders their clinical application. − Au NPs are superior electron/energy receivers, which could convert the excited singlet state of porphyrins through electron/energy transfer, thereby reducing the formation of the triplet state of porphyrins. − Energy/electron transfer may occur from CuPpIX to Au NPs under light conditions, which could reduce the ROS production excited by light to prevent porphyrins from damaging the skin. Therefore, engineered Au@BSA-CuPpIX may weaken and even eliminate the phototoxicity of porphyrins to protect skin from damage.…”
Intratumoral pathogens can contribute to cancer progression
and
affect therapeutic response. Fusobacterium nucleatum, a core pathogen of colorectal cancer (CRC), is an important cause
of low therapeutic efficacy and metastasis. Thus, the modulation of
intratumoral pathogens may provide a target for cancer therapy and
metastasis inhibition. Herein, we propose an intratumoral F. nucleatum-modulating strategy for enhancing the therapeutic
efficacy of CRC and inhibiting lung metastasis by designing an antibacterial
nanoplatform (Au@BSA-CuPpIX), which produced reactive oxygen species
(ROS) under ultrasound and exhibited strong antibacterial activity.
Importantly, Au@BSA-CuPpIX reduced the levels of apoptosis-inhibiting
proteins by inhibiting intratumoral F. nucleatum,
thereby enhancing ROS-induced apoptosis. In vivo results
demonstrated that Au@BSA-CuPpIX effectively eliminated F.
nucleatum to enhance the therapeutic efficacy of sonodynamic
therapy (SDT) for orthotopic CRC and inhibit lung metastasis. Notably,
entrapped gold nanoparticles reduced the phototoxicity of metalloporphyrin
accumulated in the skin during tumor treatment, preventing severe
inflammation and damage to the skin. Therefore, this study proposes
a strategy for the elimination of F. nucleatum in
CRC to enhance the therapeutic effect of SDT, thus providing a promising
paradigm for improving cancer treatment with fewer toxic side effects
and promoting the clinical translational potential of SDT.
“…Porphyrins generally cause severe phototoxicity in the skin when exposed to light, which hinders their clinical application. − Au NPs are superior electron/energy receivers, which could convert the excited singlet state of porphyrins through electron/energy transfer, thereby reducing the formation of the triplet state of porphyrins. − Energy/electron transfer may occur from CuPpIX to Au NPs under light conditions, which could reduce the ROS production excited by light to prevent porphyrins from damaging the skin. Therefore, engineered Au@BSA-CuPpIX may weaken and even eliminate the phototoxicity of porphyrins to protect skin from damage.…”
Intratumoral pathogens can contribute to cancer progression
and
affect therapeutic response. Fusobacterium nucleatum, a core pathogen of colorectal cancer (CRC), is an important cause
of low therapeutic efficacy and metastasis. Thus, the modulation of
intratumoral pathogens may provide a target for cancer therapy and
metastasis inhibition. Herein, we propose an intratumoral F. nucleatum-modulating strategy for enhancing the therapeutic
efficacy of CRC and inhibiting lung metastasis by designing an antibacterial
nanoplatform (Au@BSA-CuPpIX), which produced reactive oxygen species
(ROS) under ultrasound and exhibited strong antibacterial activity.
Importantly, Au@BSA-CuPpIX reduced the levels of apoptosis-inhibiting
proteins by inhibiting intratumoral F. nucleatum,
thereby enhancing ROS-induced apoptosis. In vivo results
demonstrated that Au@BSA-CuPpIX effectively eliminated F.
nucleatum to enhance the therapeutic efficacy of sonodynamic
therapy (SDT) for orthotopic CRC and inhibit lung metastasis. Notably,
entrapped gold nanoparticles reduced the phototoxicity of metalloporphyrin
accumulated in the skin during tumor treatment, preventing severe
inflammation and damage to the skin. Therefore, this study proposes
a strategy for the elimination of F. nucleatum in
CRC to enhance the therapeutic effect of SDT, thus providing a promising
paradigm for improving cancer treatment with fewer toxic side effects
and promoting the clinical translational potential of SDT.
“…Thanks to these features, the complex showed excellent photocatalytic activity in reducing methyl viologen (MV 2+ ). [ 114 ] When Pd QDs were incorporated into PDI/TiO 2 NPs via hydrothermal reduction, in addition to electron transfer from PDI to Pd QDs, Pd QDs resembled Au NPs in the SPR enhanced absorption or the back‐electron transfer from plasmonic Pd QDs to PDI. [ 115 ] The back‐electron transfer was revealed by the enhanced photoelectrical conversion efficiency and the back‐electron reduction of PDI into PDI radical anions.…”
Photocatalysis offers a practical solution to the ever increasing energy and environmental issues by using a semiconductor to harvest freely available sunlight. Photoactive organic semiconductor nanocrystals (OSNs) are promising photocatalysts due to their structure and function which are easily tunable by molecular design. Extensive studies have yielded significant progress on OSNs in terms of photoresponse, charge carrier mobility, as well as photoconversion efficiency. This review provides a comprehensive discussion of the emerging crystal and interface engineering strategies used in optimizing structure/property of OSNs. The basic mechanisms involved in organic photocatalysis are discussed, for a better understanding of its dependence on the molecular and supramolecular structures. Then, the intermolecular interactions in molecular packing and the kinetic and thermodynamic control over the crystal growth process are summarized, with the aim of tuning the optical and electrical properties. Band energy alignment, charge carrier dynamics, and charge transfer are discussed in different heterostructures. In each case, structure/property relationships and how to tune them are emphasized. Finally, challenges and opportunities for the practical use of the organic photocatalysts are discussed.
“…28,29 The switching of the conformations of these micellar nano-architectures can therefore be used to tune the conductance, capacitance, energy and power densities of supercapacitor electrodes for the storage of electrical charges. [28][29][30] For example, this method is applied in conductive electrophoretic image displays, electrorheological uids, and ink jet imprintings. [29][30][31][32] Therefore, the aim of this particular work is to primarily use a green method to specically design different sustainable micellar nano-architectures based on poly(1,4-butylene succinate) cores, and uncarbonized starch heads with impregnated nano-magnetite.…”
Section: Introductionmentioning
confidence: 99%
“…[28][29][30] For example, this method is applied in conductive electrophoretic image displays, electrorheological uids, and ink jet imprintings. [29][30][31][32] Therefore, the aim of this particular work is to primarily use a green method to specically design different sustainable micellar nano-architectures based on poly(1,4-butylene succinate) cores, and uncarbonized starch heads with impregnated nano-magnetite. The effect of each micellar design on the overall electrochemical conductivity and capacitive performance of starch-PBS nanohybrids will be studied.…”
In this work, we report on a reverse micellization approach to prepare uncarbonized starch and poly(1,4-butylene succinate) hybrids with exceptional charge storage performance.
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