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NanoCarrier Co solid lipid nanoparticles
Solid Lipid Nanoparticles, supplied by NanoCarrier Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/solid+lipid+nanoparticle/solid+lipid+nanoparticles/pmc12152548-19-0-7
Average 90 stars, based on 1 article reviews

solid lipid nanoparticles - by Bioz Stars, 2026-09

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Article Title: Stem Cells as a Target for the Delivery of Active Molecules to Skin by Topical Administration
Article Snippet: A solid lipid nanoparticle (SLN) is a sphere-shaped nanocarrier with an average diameter between 10 and 1000 nm.

Article Title: SLN enriched hydrogels for dermal application: Full factorial design study to estimate the relationship between composition and mechanical properties.
Article Snippet: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record.. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article.. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

Article Title: Nutlin3a-Loaded Nanoparticles Show Enhanced Apoptotic Activity on Prostate Cancer Cells.
Article Snippet: Escape from apoptosis, one of the characteristic features of cancer cells, is a case that reduces the therapeutic efficacy of apoptosis-inducing molecules used in the cancer treatment.. Stabilization of the P53 protein, which is responsible for the regulation of apoptosis mechanism in the cell, is therefore an important therapeutic goal.. Nutlin3a inhibits the degradation of the P53 protein, triggers P53-mediated apoptosis in cancer cells and enhances the effectiveness of chemotherapeutics.

Article Title: Unraveling Complex Hysteresis Phenomenon in 1,2-Dipalmitoyl-sn-Glycero-3-Phosphocholine Monolayer: Insight into Factors Influencing Surface Dynamics.
Article Snippet: An example of a nanocarrier that illustrates this concept is the solid lipid nanoparticle, which consists of a lipid core enveloped by a surfactant monolayer.

Article Title: Nanocarriers Used Most in Drug Delivery and Drug Release: Nanohydrogel, Chitosan, Graphene, and Solid Lipid
Article Snippet: Nanohydrogels, chitosan, graphene oxide, and solid lipid nanoparticle nanocarrier designs and applications are selectively given due to the great attention they have gained from being highly biocompatible and easy-to-manipulate nanocarrier options from organic and inorganic nanocarrier materials.

Image Search Results

( A ) I. Schematic illustration of the synthesis of SNP. II. Functionalization with aminopropyl groups. III. Functionalization with propyl methyl phosphonate groups. IV. Functionalization with octadecyl methyl groups. Reproduced from Ndayishimiye J, Cao Y, Kumeria T, Blaskovich MAT, Falconer JR, Popat A. Engineering mesoporous silica nanoparticles towards oral delivery of vancomycin. J Mater Chem B. 2021;9(35):7145–7166. © The Royal Society of Chemistry 2021. ( B ) I. Design and bio-functionalization of IME-responsive nanoparticles (NPs) for targeted drug delivery. II. Schematic of multifunctional NP design. III. Drug-loaded NPs-anti-ICAM-1 specifically target activated endothelial cells at infection sites after intravenous injection, binding to them, crossing blood vessels, and releasing drugs in response to local infection signals. IV. Structure and pH/enzyme-sensitive amphiphilic block copolymers. V. Coarse-grained simulation of CIP-PMs self-assembly using DPD methods. Reproduced from Zhang CY, Gao J, Wang Z. Bioresponsive nanoparticles targeted to infectious microenvironments for sepsis management. Adv Mater. 2018;30(43):e1803618. © 2018 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. ( C ) γ3 peptide grafted onto nanoparticle (NP) surfaces enhances uptake by activated endothelial cells (ECs) and specifically targets the lungs to alleviate inflammation. I. Schematic of the preparation of γ3 peptide-modified PLGA NPs loaded with SFX and TAC. II. Schematic of targeted therapy in mice with lung infection via intravenous injection of NPs. III. Digital images of lungs from mice with acute lung injury (ALI) infection treated with different formulations. IV. H&E sections of lungs from ALI mice receiving different treatments. V. Digital images of plated lungs from mice with acute lung infection caused by Pseudomonas aeruginosa receiving different treatments. VI. Colony-forming unit (CFU) counts. VII. Survival rate of different groups. I: PBS, II: free SFX, III: free TAC, IV: free S + T, V: PLGA/S + T, VI: γ3-PLGA/S + T. Data are shown as mean ± SD (n = 3). *p < 0.05, **p < 0.01, ***p < 0.001. Reproduced from Yang Y, Ding Y, Fan B, et al. Inflammation-targeting polymeric nanoparticles deliver sparfloxacin and tacrolimus for combating acute lung sepsis. J Control Release. 2020;321:463–474. Copyright © 2020 Elsevier B.V. All rights reserved.

Journal: International Journal of Nanomedicine

Article Title: Advancements, Challenges, and Future Prospects of Nanotechnology in Sepsis Therapy

doi: 10.2147/IJN.S488026

Figure Lengend Snippet: ( A ) I. Schematic illustration of the synthesis of SNP. II. Functionalization with aminopropyl groups. III. Functionalization with propyl methyl phosphonate groups. IV. Functionalization with octadecyl methyl groups. Reproduced from Ndayishimiye J, Cao Y, Kumeria T, Blaskovich MAT, Falconer JR, Popat A. Engineering mesoporous silica nanoparticles towards oral delivery of vancomycin. J Mater Chem B. 2021;9(35):7145–7166. © The Royal Society of Chemistry 2021. ( B ) I. Design and bio-functionalization of IME-responsive nanoparticles (NPs) for targeted drug delivery. II. Schematic of multifunctional NP design. III. Drug-loaded NPs-anti-ICAM-1 specifically target activated endothelial cells at infection sites after intravenous injection, binding to them, crossing blood vessels, and releasing drugs in response to local infection signals. IV. Structure and pH/enzyme-sensitive amphiphilic block copolymers. V. Coarse-grained simulation of CIP-PMs self-assembly using DPD methods. Reproduced from Zhang CY, Gao J, Wang Z. Bioresponsive nanoparticles targeted to infectious microenvironments for sepsis management. Adv Mater. 2018;30(43):e1803618. © 2018 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. ( C ) γ3 peptide grafted onto nanoparticle (NP) surfaces enhances uptake by activated endothelial cells (ECs) and specifically targets the lungs to alleviate inflammation. I. Schematic of the preparation of γ3 peptide-modified PLGA NPs loaded with SFX and TAC. II. Schematic of targeted therapy in mice with lung infection via intravenous injection of NPs. III. Digital images of lungs from mice with acute lung injury (ALI) infection treated with different formulations. IV. H&E sections of lungs from ALI mice receiving different treatments. V. Digital images of plated lungs from mice with acute lung infection caused by Pseudomonas aeruginosa receiving different treatments. VI. Colony-forming unit (CFU) counts. VII. Survival rate of different groups. I: PBS, II: free SFX, III: free TAC, IV: free S + T, V: PLGA/S + T, VI: γ3-PLGA/S + T. Data are shown as mean ± SD (n = 3). *p < 0.05, **p < 0.01, ***p < 0.001. Reproduced from Yang Y, Ding Y, Fan B, et al. Inflammation-targeting polymeric nanoparticles deliver sparfloxacin and tacrolimus for combating acute lung sepsis. J Control Release. 2020;321:463–474. Copyright © 2020 Elsevier B.V. All rights reserved.

Article Snippet: Vancomycin-loaded Solid Lipid Nanoparticles (VCM-AS-SLNs) , Ascorbic acid stearate (AS) used as a hyaluronidase inhibitor , Biomimetic and enzyme-responsive properties, binds vancomycin, reduces harmful effects at lower concentrations , [ ] .

Techniques: Infection, Injection, Binding Assay, Blocking Assay, Modification, Control

( A ) Summary of natural extracts from various natural sources, including plants, animals, or microbial species, for antibacterial applications. Reproduced from Chen C, Chen L, Mao C, et al. Natural extracts for antibacterial applications. Small. 2024;20(9):e2306553. © 2023 Wiley‐VCH GmbH. ( B ) Schematic of the synthesis of metal nanoparticles/nanocellulose composite materials. I. Simple mixing of cellulose source with prepared inorganic nanoparticles. II. Synthesis of nanoparticles using an external reducing agent. III. Synthesis of nanoparticles through surface modification of nanocellulose. IV. Synthesis of nanoparticles using nanocellulose itself without an external reducing agent. ( C ) Illustration of the synthesis of CNC/Ag composite nanoparticles. Reproduced from Oun AA, Shankar S, Rhim JW. Multifunctional nanocellulose/metal and metal oxide nanoparticle hybrid nanomaterials. Crit Rev Food Sci Nutr. 2020;60(3):435–460. Rights managed by Taylor & Francis. ( D ) I. Schematic of surface modification of Curcumin and SNP-immobilized Cu-MSN and their possible antibacterial mechanism. II. TEM images of Cur-Cu-MSN-SNP samples, scale bars: (a) 50 nm and (b) 200 nm. Reproduced from Kuthati Y, Kankala RK, Busa P, et al. Phototherapeutic spectrum expansion through synergistic effect of mesoporous silica trio-nanohybrids against antibiotic-resistant gram-negative bacterium. J Photochem Photobiol B. 2017;169:124–133. opyright © 2017 Elsevier B.V. All rights reserved.

Journal: International Journal of Nanomedicine

Article Title: Advancements, Challenges, and Future Prospects of Nanotechnology in Sepsis Therapy

doi: 10.2147/IJN.S488026

Figure Lengend Snippet: ( A ) Summary of natural extracts from various natural sources, including plants, animals, or microbial species, for antibacterial applications. Reproduced from Chen C, Chen L, Mao C, et al. Natural extracts for antibacterial applications. Small. 2024;20(9):e2306553. © 2023 Wiley‐VCH GmbH. ( B ) Schematic of the synthesis of metal nanoparticles/nanocellulose composite materials. I. Simple mixing of cellulose source with prepared inorganic nanoparticles. II. Synthesis of nanoparticles using an external reducing agent. III. Synthesis of nanoparticles through surface modification of nanocellulose. IV. Synthesis of nanoparticles using nanocellulose itself without an external reducing agent. ( C ) Illustration of the synthesis of CNC/Ag composite nanoparticles. Reproduced from Oun AA, Shankar S, Rhim JW. Multifunctional nanocellulose/metal and metal oxide nanoparticle hybrid nanomaterials. Crit Rev Food Sci Nutr. 2020;60(3):435–460. Rights managed by Taylor & Francis. ( D ) I. Schematic of surface modification of Curcumin and SNP-immobilized Cu-MSN and their possible antibacterial mechanism. II. TEM images of Cur-Cu-MSN-SNP samples, scale bars: (a) 50 nm and (b) 200 nm. Reproduced from Kuthati Y, Kankala RK, Busa P, et al. Phototherapeutic spectrum expansion through synergistic effect of mesoporous silica trio-nanohybrids against antibiotic-resistant gram-negative bacterium. J Photochem Photobiol B. 2017;169:124–133. opyright © 2017 Elsevier B.V. All rights reserved.

Techniques: Modification

( A ) I. Approaches for the design and fabrication of diverse stimuli-responsive biomaterials and their utilization in the formulation of stimuli-responsive nano-delivery systems. R, S, and COO- are ROS-responsive moieties. II. Strategies for designing and fabricating biomimetic nanoparticles targeting sepsis microenvironments. Ismail EA, Devnarain N, Govender T, Omolo CA. Stimuli-responsive and biomimetic delivery systems for sepsis and related complications. J Control Release. 2022;352:1048–1070. Copyright © 2022 Elsevier B.V. All rights reserved. ( B ) I. Nano-antibody production process using phage display technology. II. Effect of administration times on survival rate of rats. Reproduced from Liao S, Liu S, Zhang Y. Preparation of anti toll-like receptor-4 nano-antibody and its effect on gram negative sepsis. J Nanosci Nanotechnol. 2021;21(2):1048–1053. Copyright 2021, American Scientific Publishers.

Journal: International Journal of Nanomedicine

Article Title: Advancements, Challenges, and Future Prospects of Nanotechnology in Sepsis Therapy

doi: 10.2147/IJN.S488026

Figure Lengend Snippet: ( A ) I. Approaches for the design and fabrication of diverse stimuli-responsive biomaterials and their utilization in the formulation of stimuli-responsive nano-delivery systems. R, S, and COO- are ROS-responsive moieties. II. Strategies for designing and fabricating biomimetic nanoparticles targeting sepsis microenvironments. Ismail EA, Devnarain N, Govender T, Omolo CA. Stimuli-responsive and biomimetic delivery systems for sepsis and related complications. J Control Release. 2022;352:1048–1070. Copyright © 2022 Elsevier B.V. All rights reserved. ( B ) I. Nano-antibody production process using phage display technology. II. Effect of administration times on survival rate of rats. Reproduced from Liao S, Liu S, Zhang Y. Preparation of anti toll-like receptor-4 nano-antibody and its effect on gram negative sepsis. J Nanosci Nanotechnol. 2021;21(2):1048–1053. Copyright 2021, American Scientific Publishers.

Techniques: Formulation, Control

( A ) Synthesis and characterization of immunomodulatory particles. I. The particles are formulated from polymers with different molecular weights (low or high), compositions (glycolic acid (GA) and lactic acid (LA)), or surfactants (PVA or PEMA). II. Measurements of particle size and zeta potential. III. The interaction kinetics between particles and bone marrow-derived macrophages (BMMØs) depend on the emulsifying surfactant. ( B ) Particles regulate innate inflammatory responses. I. Schematic of cytokine inhibition assay. II. Inhibition of inflammatory cytokine production in BMMØs treated with particles (300 μg/mL) and stimulated with 100 ng/mL LPS. III. Particle-induced inhibition of BMMØ cytokine production is dependent on particle and LPS concentration. IV. Evaluation of live cell surface marker expression in BMMØs by flow cytometry. ( C ) Intravenous injection of PLA particles alters cytokine responses of splenocytes to LPS and CpG-ODN stimulation in mice. I. Evaluation of inflammatory cytokine secretion by splenocytes. II. Cytokine secretion after in vitro stimulation with LPS (100 ng/mL). III. Cytokine secretion after in vitro stimulation with CpG-ODN (100 ng/mL). Cytokines were measured by ELISA after 2 days of culture. Reproduced from Casey LM, Kakade S, Decker JT, et al. Cargo-less nanoparticles program innate immune cell responses to toll-like receptor activation. Biomaterials. 2019;218:119333. © 2019 Elsevier Ltd. All rights reserved.

Journal: International Journal of Nanomedicine

Article Title: Advancements, Challenges, and Future Prospects of Nanotechnology in Sepsis Therapy

doi: 10.2147/IJN.S488026

Figure Lengend Snippet: ( A ) Synthesis and characterization of immunomodulatory particles. I. The particles are formulated from polymers with different molecular weights (low or high), compositions (glycolic acid (GA) and lactic acid (LA)), or surfactants (PVA or PEMA). II. Measurements of particle size and zeta potential. III. The interaction kinetics between particles and bone marrow-derived macrophages (BMMØs) depend on the emulsifying surfactant. ( B ) Particles regulate innate inflammatory responses. I. Schematic of cytokine inhibition assay. II. Inhibition of inflammatory cytokine production in BMMØs treated with particles (300 μg/mL) and stimulated with 100 ng/mL LPS. III. Particle-induced inhibition of BMMØ cytokine production is dependent on particle and LPS concentration. IV. Evaluation of live cell surface marker expression in BMMØs by flow cytometry. ( C ) Intravenous injection of PLA particles alters cytokine responses of splenocytes to LPS and CpG-ODN stimulation in mice. I. Evaluation of inflammatory cytokine secretion by splenocytes. II. Cytokine secretion after in vitro stimulation with LPS (100 ng/mL). III. Cytokine secretion after in vitro stimulation with CpG-ODN (100 ng/mL). Cytokines were measured by ELISA after 2 days of culture. Reproduced from Casey LM, Kakade S, Decker JT, et al. Cargo-less nanoparticles program innate immune cell responses to toll-like receptor activation. Biomaterials. 2019;218:119333. © 2019 Elsevier Ltd. All rights reserved.

Techniques: Zeta Potential Analyzer, Derivative Assay, Inhibition, Concentration Assay, Marker, Expressing, Flow Cytometry, Injection, In Vitro, Enzyme-linked Immunosorbent Assay, Activation Assay

( A ) Interaction of nanoparticles (NPs) with macrophages and the regulation of macrophage pro/anti-inflammatory functions by NPs. (I) Upon entering the body, NPs bind to plasma proteins and are internalized by macrophages. NPs are endocytosed into endosomes, degraded, and then released extracellularly to exert their active effects; other endosomes fuse with lysosomes to form endolysosomes, exerting intracellular effects. (II) First, NPs can eliminate macrophage activation by phagocytosis and restriction of pathogen-associated molecular patterns (PAMPs); second, they inhibit the interaction between PAMPs and pattern recognition receptors (PRRs); third, NPs that enter the cytoplasm inhibit the transmission of inflammatory signaling pathways; finally, NPs inhibit the release of active products from inflammatory pathways, controlling cell and tissue damage caused by overactivated macrophages. (III) NPs modulate the pro-inflammatory activity of macrophages. NPs can enhance PRR activation to initiate macrophage inflammatory responses. Once in the cytoplasm, NPs activate downstream pathways and inflammasomes to induce the production of pro-inflammatory factors. NPs, nanoparticles; PAMPs, pathogen-associated molecular patterns; ROS, reactive oxygen species; ILs, interleukins; TNFs, tumor necrosis factors; MAPK, mitogen-activated protein kinase; NF-kB, nuclear factor-κB. ( B ) Regulation of macrophage polarization by nanoparticles (NPs). M1-type macrophages typically function during the cytokine storm phase of sepsis, releasing large amounts of pro-inflammatory mediators, including reactive oxygen species (ROS), interferons (IFNs), interleukins (ILs), and tumor necrosis factors (TNFs). In contrast, M2-type macrophages usually appear during the immune paralysis phase, secreting anti-inflammatory mediators, most notably IL-10. During excessive inflammatory stimulation, the continuous release of pro-inflammatory mediators by M1-type macrophages causes damage to the body, whereas, during immune paralysis, excessive activation of M2-type macrophages increases the risk of secondary infections. NPs can modulate macrophage polarization at different stages of sepsis to improve prognosis. NPs, nanoparticles; ROS, reactive oxygen species; ILs, interleukins; IFNs, interferons; TNFs, tumor necrosis factors. ( C ) Interference of macrophage pyroptosis by nanoparticles (NPs). NPs can block the activation of caspase-1 and caspase-4/5/11, reducing the release of DAMPs (damage-associated molecular patterns) and preventing unnecessary tissue and cell damage. NPs, nanoparticles; LPS, lipopolysaccharide; IL-1b, interleukin-1b; DAMPs, damage-associated molecular patterns; GSDMD, gasdermin D. Reproduced from Song C, Xu J, Gao C, Zhang W, Fang X, Shang Y. Nanomaterials targeting macrophages in sepsis: a promising approach for sepsis management. Front Immunol. 2022;13:1026173. Copyright © 2022 Song, Xu, Gao, Zhang, Fang and Shang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).

Journal: International Journal of Nanomedicine

Article Title: Advancements, Challenges, and Future Prospects of Nanotechnology in Sepsis Therapy

doi: 10.2147/IJN.S488026

Figure Lengend Snippet: ( A ) Interaction of nanoparticles (NPs) with macrophages and the regulation of macrophage pro/anti-inflammatory functions by NPs. (I) Upon entering the body, NPs bind to plasma proteins and are internalized by macrophages. NPs are endocytosed into endosomes, degraded, and then released extracellularly to exert their active effects; other endosomes fuse with lysosomes to form endolysosomes, exerting intracellular effects. (II) First, NPs can eliminate macrophage activation by phagocytosis and restriction of pathogen-associated molecular patterns (PAMPs); second, they inhibit the interaction between PAMPs and pattern recognition receptors (PRRs); third, NPs that enter the cytoplasm inhibit the transmission of inflammatory signaling pathways; finally, NPs inhibit the release of active products from inflammatory pathways, controlling cell and tissue damage caused by overactivated macrophages. (III) NPs modulate the pro-inflammatory activity of macrophages. NPs can enhance PRR activation to initiate macrophage inflammatory responses. Once in the cytoplasm, NPs activate downstream pathways and inflammasomes to induce the production of pro-inflammatory factors. NPs, nanoparticles; PAMPs, pathogen-associated molecular patterns; ROS, reactive oxygen species; ILs, interleukins; TNFs, tumor necrosis factors; MAPK, mitogen-activated protein kinase; NF-kB, nuclear factor-κB. ( B ) Regulation of macrophage polarization by nanoparticles (NPs). M1-type macrophages typically function during the cytokine storm phase of sepsis, releasing large amounts of pro-inflammatory mediators, including reactive oxygen species (ROS), interferons (IFNs), interleukins (ILs), and tumor necrosis factors (TNFs). In contrast, M2-type macrophages usually appear during the immune paralysis phase, secreting anti-inflammatory mediators, most notably IL-10. During excessive inflammatory stimulation, the continuous release of pro-inflammatory mediators by M1-type macrophages causes damage to the body, whereas, during immune paralysis, excessive activation of M2-type macrophages increases the risk of secondary infections. NPs can modulate macrophage polarization at different stages of sepsis to improve prognosis. NPs, nanoparticles; ROS, reactive oxygen species; ILs, interleukins; IFNs, interferons; TNFs, tumor necrosis factors. ( C ) Interference of macrophage pyroptosis by nanoparticles (NPs). NPs can block the activation of caspase-1 and caspase-4/5/11, reducing the release of DAMPs (damage-associated molecular patterns) and preventing unnecessary tissue and cell damage. NPs, nanoparticles; LPS, lipopolysaccharide; IL-1b, interleukin-1b; DAMPs, damage-associated molecular patterns; GSDMD, gasdermin D. Reproduced from Song C, Xu J, Gao C, Zhang W, Fang X, Shang Y. Nanomaterials targeting macrophages in sepsis: a promising approach for sepsis management. Front Immunol. 2022;13:1026173. Copyright © 2022 Song, Xu, Gao, Zhang, Fang and Shang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).

Techniques: Clinical Proteomics, Activation Assay, Transmission Assay, Protein-Protein interactions, Activity Assay, Blocking Assay

( A ) Design, synthesis, and hypothesized mechanism of macrophage membrane-coated MOFs (MMD-LL37) for delivering pLL37 in the treatment of sepsis. (I) MMD-LL37 inhibits potential inflammatory responses in sepsis by adsorbing pro-inflammatory cytokines. (II) Homologous targeting and intracellular delivery of antibacterial plasmids. (III) Transfection with the LL37 plasmid induces macrophages to act as “factories” for continuous LL37 production. (IV) Systematic elimination of bacteria hidden within macrophages and circulating in the bloodstream. ( B ) Representative images of blood plate colonies at 24 hours and 48 hours post-treatment. ( C ) Bacterial load in the blood at 24 hours and 48 hours post-administration. ( D ) Survival rate of septic mice under different treatment regimens. Reproduced from Cao H, Gao Y, Jia H, et al. Macrophage-membrane-camouflaged nonviral gene vectors for the treatment of multidrug-resistant bacterial sepsis. Nano Lett. 2022;22(19):7882–7891. Copyright © 2022 American Chemical Society. ( E ) (I) Design and schematic illustration elaborating the formulation of curcumin and CeO2-loaded nanoformulations for the treatment of lung infectious sepsis. (II) Histopathological observations of lung tissue with H&E and MTS staining 20 hours post-treatment following Pseudomonas aeruginosa infection. (III) Observations of the therapeutic potential of curcumin-loaded Ce/OCS nanoparticles in lung sections of induced bacterial sepsis; (a) Survival rate of mice in the peritonitis-induced sepsis model after treatment with different nanoformulations, (b) white blood cell count, (c) TNF-α, (d) IL-1β, (e) IL-6, and (f) protein content in peritoneal fluid after treatment with different formulations (including control (PBS), free curcumin, Ce/OCS, and Cur@Ce/OCS nanoparticles). Reproduced from Teng L, Zhang Y, Chen L, Shi G. Fabrication of a curcumin encapsulated bioengineered nano-cocktail formulation for stimuli-responsive targeted therapeutic delivery to enhance anti-inflammatory, anti-oxidant, and anti-bacterial properties in sepsis management. J Biomater Sci Polym Ed. 2023;34(12):1716–1740. Rights managed by Taylor & Francis.

Journal: International Journal of Nanomedicine

Article Title: Advancements, Challenges, and Future Prospects of Nanotechnology in Sepsis Therapy

doi: 10.2147/IJN.S488026

Figure Lengend Snippet: ( A ) Design, synthesis, and hypothesized mechanism of macrophage membrane-coated MOFs (MMD-LL37) for delivering pLL37 in the treatment of sepsis. (I) MMD-LL37 inhibits potential inflammatory responses in sepsis by adsorbing pro-inflammatory cytokines. (II) Homologous targeting and intracellular delivery of antibacterial plasmids. (III) Transfection with the LL37 plasmid induces macrophages to act as “factories” for continuous LL37 production. (IV) Systematic elimination of bacteria hidden within macrophages and circulating in the bloodstream. ( B ) Representative images of blood plate colonies at 24 hours and 48 hours post-treatment. ( C ) Bacterial load in the blood at 24 hours and 48 hours post-administration. ( D ) Survival rate of septic mice under different treatment regimens. Reproduced from Cao H, Gao Y, Jia H, et al. Macrophage-membrane-camouflaged nonviral gene vectors for the treatment of multidrug-resistant bacterial sepsis. Nano Lett. 2022;22(19):7882–7891. Copyright © 2022 American Chemical Society. ( E ) (I) Design and schematic illustration elaborating the formulation of curcumin and CeO2-loaded nanoformulations for the treatment of lung infectious sepsis. (II) Histopathological observations of lung tissue with H&E and MTS staining 20 hours post-treatment following Pseudomonas aeruginosa infection. (III) Observations of the therapeutic potential of curcumin-loaded Ce/OCS nanoparticles in lung sections of induced bacterial sepsis; (a) Survival rate of mice in the peritonitis-induced sepsis model after treatment with different nanoformulations, (b) white blood cell count, (c) TNF-α, (d) IL-1β, (e) IL-6, and (f) protein content in peritoneal fluid after treatment with different formulations (including control (PBS), free curcumin, Ce/OCS, and Cur@Ce/OCS nanoparticles). Reproduced from Teng L, Zhang Y, Chen L, Shi G. Fabrication of a curcumin encapsulated bioengineered nano-cocktail formulation for stimuli-responsive targeted therapeutic delivery to enhance anti-inflammatory, anti-oxidant, and anti-bacterial properties in sepsis management. J Biomater Sci Polym Ed. 2023;34(12):1716–1740. Rights managed by Taylor & Francis.

Techniques: Membrane, Transfection, Plasmid Preparation, Bacteria, Formulation, Staining, Infection, Cell Counting, Control

( A ) Schematic illustration of the synthesis, antibacterial mechanism, and regulation of macrophage polarization by CeO2@Ce6 nanocomposites for the treatment of periodontal disease. The enhanced antibacterial efficiency of CeO2@Ce6 may rely on ROS produced by aPDT and the inherent antibacterial activity of CeO2. Nanocomposites containing CeO2 exhibit SOD- and CAT-mimetic activities, capable of scavenging excess ROS by switching between Ce(III) and Ce(IV) states. CeO2@Ce6 nanocomposites can actively modulate macrophage polarization from the pro-inflammatory M1 phenotype to the anti-inflammatory (regenerative) M2 phenotype. Ce6: chlorin e6; aPDT: antimicrobial photodynamic therapy; ROS: reactive oxygen species; SOD: superoxide dismutase; CAT: catalase. ( B ) Schematic images illustrating the shift of macrophage polarization between the M1 phenotype and the M2 phenotype with the regulation of regenerative functions. Zhou X, Zhou Q, He Z, et al. ROS balance autoregulating core-shell CeO(2)@ZIF-8/Au nanoplatform for wound repair. Nanomicro Lett. 2024;16(1):156. Copyright © 2024, The Author(s). Creative Commons CC BY license. ( C ) Schematic diagram of Atv/PTP-TCeria NPs used for acute kidney injury (AKI). Atv/PTP-TCeria NPs can be passively targeted to the kidney and release the drug in response to high levels of ROS, while TCeria NPs target mitochondria to scavenge excess ROS, thereby improving AKI. Reproduced from Yu H, Jin F, Liu D, et al. ROS-responsive nano-drug delivery system combining mitochondria-targeting ceria nanoparticles with atorvastatin for acute kidney injury. Theranostics. 2020;10(5):2342–2357. Creative Commons Attribution License. ( D ) Schematic illustration depicting the on-demand delivery of melatonin to the liver during sepsis and its mechanism for reducing excess ROS and inflammation. Reproduced from Chen G, Deng H, Song X, et al. Reactive oxygen species-responsive polymeric nanoparticles for alleviating sepsis-induced acute liver injury in mice. Biomaterials. 2017;144:30–41. Copyright © 2017 Elsevier Ltd. All rights reserved.

Journal: International Journal of Nanomedicine

Article Title: Advancements, Challenges, and Future Prospects of Nanotechnology in Sepsis Therapy

doi: 10.2147/IJN.S488026

Figure Lengend Snippet: ( A ) Schematic illustration of the synthesis, antibacterial mechanism, and regulation of macrophage polarization by CeO2@Ce6 nanocomposites for the treatment of periodontal disease. The enhanced antibacterial efficiency of CeO2@Ce6 may rely on ROS produced by aPDT and the inherent antibacterial activity of CeO2. Nanocomposites containing CeO2 exhibit SOD- and CAT-mimetic activities, capable of scavenging excess ROS by switching between Ce(III) and Ce(IV) states. CeO2@Ce6 nanocomposites can actively modulate macrophage polarization from the pro-inflammatory M1 phenotype to the anti-inflammatory (regenerative) M2 phenotype. Ce6: chlorin e6; aPDT: antimicrobial photodynamic therapy; ROS: reactive oxygen species; SOD: superoxide dismutase; CAT: catalase. ( B ) Schematic images illustrating the shift of macrophage polarization between the M1 phenotype and the M2 phenotype with the regulation of regenerative functions. Zhou X, Zhou Q, He Z, et al. ROS balance autoregulating core-shell CeO(2)@ZIF-8/Au nanoplatform for wound repair. Nanomicro Lett. 2024;16(1):156. Copyright © 2024, The Author(s). Creative Commons CC BY license. ( C ) Schematic diagram of Atv/PTP-TCeria NPs used for acute kidney injury (AKI). Atv/PTP-TCeria NPs can be passively targeted to the kidney and release the drug in response to high levels of ROS, while TCeria NPs target mitochondria to scavenge excess ROS, thereby improving AKI. Reproduced from Yu H, Jin F, Liu D, et al. ROS-responsive nano-drug delivery system combining mitochondria-targeting ceria nanoparticles with atorvastatin for acute kidney injury. Theranostics. 2020;10(5):2342–2357. Creative Commons Attribution License. ( D ) Schematic illustration depicting the on-demand delivery of melatonin to the liver during sepsis and its mechanism for reducing excess ROS and inflammation. Reproduced from Chen G, Deng H, Song X, et al. Reactive oxygen species-responsive polymeric nanoparticles for alleviating sepsis-induced acute liver injury in mice. Biomaterials. 2017;144:30–41. Copyright © 2017 Elsevier Ltd. All rights reserved.

Techniques: Produced, Activity Assay

( A ) (I) Schematic and the actual structure of the system. Schematic representation of the structure of toxin nanosponges and their mechanism for neutralizing pore-forming toxins (PFTs). (II) TEM (transmission electron microscopy) images of nanosponges mixed with α-toxin (scale bar, 80 nm) and an enlarged view of a single toxin-adsorbed nanosponge (scale bar, 20 nm). Samples were negatively stained with uranyl acetate before TEM imaging. ( B ) In vivo toxin neutralization. (I–III) Skin lesions in mice three days after injection with α-toxin. (IV–VI) No skin lesions in mice injected with α-toxin/nanosponge mixture. Each group had n = 6 mice. Reproduced from Hu CM, Fang RH, Copp J, Luk BT, Zhang L. A biomimetic nanosponge that absorbs pore-forming toxins. Nat Nanotechnol. 2013;8(5):336–340. Copyright © 2013, Springer Nature Limited. ( C ) Antibacterial effect of AuNS100 on biofilms of V. cholerae adhering to epithelial surfaces. (I) Schematic illustration of V. cholerae interacting with villi in the inner mucus layer to form an intestinal biofilm. (II–IV) Microscopic images of small intestine sections from mice infected with V. cholerae before and after treatment. Reproduced from Chatterjee T, Saha T, Sarkar P, Hoque KM, Chatterjee BK, Chakrabarti P. The gold nanoparticle reduces Vibrio cholerae pathogenesis by inhibition of biofilm formation and disruption of the production and structure of cholera toxin. Colloids Surf B Biointerfaces. 2021;204:111811. Copyright © 2021. Published by Elsevier B.V.

Journal: International Journal of Nanomedicine

Article Title: Advancements, Challenges, and Future Prospects of Nanotechnology in Sepsis Therapy

doi: 10.2147/IJN.S488026

Figure Lengend Snippet: ( A ) (I) Schematic and the actual structure of the system. Schematic representation of the structure of toxin nanosponges and their mechanism for neutralizing pore-forming toxins (PFTs). (II) TEM (transmission electron microscopy) images of nanosponges mixed with α-toxin (scale bar, 80 nm) and an enlarged view of a single toxin-adsorbed nanosponge (scale bar, 20 nm). Samples were negatively stained with uranyl acetate before TEM imaging. ( B ) In vivo toxin neutralization. (I–III) Skin lesions in mice three days after injection with α-toxin. (IV–VI) No skin lesions in mice injected with α-toxin/nanosponge mixture. Each group had n = 6 mice. Reproduced from Hu CM, Fang RH, Copp J, Luk BT, Zhang L. A biomimetic nanosponge that absorbs pore-forming toxins. Nat Nanotechnol. 2013;8(5):336–340. Copyright © 2013, Springer Nature Limited. ( C ) Antibacterial effect of AuNS100 on biofilms of V. cholerae adhering to epithelial surfaces. (I) Schematic illustration of V. cholerae interacting with villi in the inner mucus layer to form an intestinal biofilm. (II–IV) Microscopic images of small intestine sections from mice infected with V. cholerae before and after treatment. Reproduced from Chatterjee T, Saha T, Sarkar P, Hoque KM, Chatterjee BK, Chakrabarti P. The gold nanoparticle reduces Vibrio cholerae pathogenesis by inhibition of biofilm formation and disruption of the production and structure of cholera toxin. Colloids Surf B Biointerfaces. 2021;204:111811. Copyright © 2021. Published by Elsevier B.V.

Techniques: Transmission Assay, Electron Microscopy, Staining, Imaging, In Vivo, Neutralization, Injection, Infection, Inhibition, Disruption

( A ) (I) Schematic illustration demonstrating the ability of human red blood cell-derived nanosponges (hRBC-NS) to capture β-H/C, thereby reducing cytotoxic damage to lung epithelial cells and mitigating macrophage inflammasome activation, leading to inhibited IL-1β production (II). Reproduced from Koo J, Escajadillo T, Zhang L, Nizet V, Lawrence SM. Erythrocyte-coated nanoparticles block cytotoxic effects of group B streptococcus beta-hemolysin/cytolysin. Front Pediatr. 2019;7:410. Copyright © 2019 Koo, Escajadillo, Zhang, Nizet and Lawrence. Creative Commons Attribution License (CC BY). ( B ) (I) Schematic diagram showing the preparation and characterization of red blood cell nanosponges (RBC-NS) and their use in treating mice subjected to MRSA toxin-induced toxic shock. (II) The schematic includes the survival rate of mice within 24 hours of treatment (n = 6 per cohort). Reproduced from Chen Y, Zhang Y, Chen M, et al. Biomimetic nanosponges suppress in vivo lethality induced by the whole secreted proteins of pathogenic bacteria. Small. 2019;15(6):e1804994. © 2019 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. ( C ) (I) Schematic illustration of using macrophage-derived nanoparticles (MΦ-NPs) to neutralize endotoxins and pro-inflammatory cytokines as a two-step process for sepsis management. (II) Levels of pro-inflammatory cytokines, including TNF-α and IL-6, in plasma (n = 6). (III) Survival rate (n = 10). Reproduced from Thamphiwatana S, Angsantikul P, Escajadillo T, et al. Macrophage-like nanoparticles concurrently absorbing endotoxins and proinflammatory cytokines for sepsis management. Proc Natl Acad Sci U S A. 2017;114(43):11488–11493. ( D ) (I) Schematic representation and detoxification process of Fe3O4@MMs. (II) Schematic structure of Fe3O4@MMs and the mechanism by which they neutralize LPS. (III) Transmission electron microscopy (TEM) image of PEI-modified Fe3O4 nanoparticles. (IV) TEM image of Fe3O4@MMs nanoparticles. (V) Enlarged view of a single Fe3O4@MMs nanoparticle. Reproduced from Shen S, Han F, Yuan A, et al. Engineered nanoparticles disguised as macrophages for trapping lipopolysaccharide and preventing endotoxemia. Biomaterials. 2019;189:60–68. Copyright © 2018 Elsevier Ltd. All rights reserved.

Journal: International Journal of Nanomedicine

Article Title: Advancements, Challenges, and Future Prospects of Nanotechnology in Sepsis Therapy

doi: 10.2147/IJN.S488026

Figure Lengend Snippet: ( A ) (I) Schematic illustration demonstrating the ability of human red blood cell-derived nanosponges (hRBC-NS) to capture β-H/C, thereby reducing cytotoxic damage to lung epithelial cells and mitigating macrophage inflammasome activation, leading to inhibited IL-1β production (II). Reproduced from Koo J, Escajadillo T, Zhang L, Nizet V, Lawrence SM. Erythrocyte-coated nanoparticles block cytotoxic effects of group B streptococcus beta-hemolysin/cytolysin. Front Pediatr. 2019;7:410. Copyright © 2019 Koo, Escajadillo, Zhang, Nizet and Lawrence. Creative Commons Attribution License (CC BY). ( B ) (I) Schematic diagram showing the preparation and characterization of red blood cell nanosponges (RBC-NS) and their use in treating mice subjected to MRSA toxin-induced toxic shock. (II) The schematic includes the survival rate of mice within 24 hours of treatment (n = 6 per cohort). Reproduced from Chen Y, Zhang Y, Chen M, et al. Biomimetic nanosponges suppress in vivo lethality induced by the whole secreted proteins of pathogenic bacteria. Small. 2019;15(6):e1804994. © 2019 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. ( C ) (I) Schematic illustration of using macrophage-derived nanoparticles (MΦ-NPs) to neutralize endotoxins and pro-inflammatory cytokines as a two-step process for sepsis management. (II) Levels of pro-inflammatory cytokines, including TNF-α and IL-6, in plasma (n = 6). (III) Survival rate (n = 10). Reproduced from Thamphiwatana S, Angsantikul P, Escajadillo T, et al. Macrophage-like nanoparticles concurrently absorbing endotoxins and proinflammatory cytokines for sepsis management. Proc Natl Acad Sci U S A. 2017;114(43):11488–11493. ( D ) (I) Schematic representation and detoxification process of Fe3O4@MMs. (II) Schematic structure of Fe3O4@MMs and the mechanism by which they neutralize LPS. (III) Transmission electron microscopy (TEM) image of PEI-modified Fe3O4 nanoparticles. (IV) TEM image of Fe3O4@MMs nanoparticles. (V) Enlarged view of a single Fe3O4@MMs nanoparticle. Reproduced from Shen S, Han F, Yuan A, et al. Engineered nanoparticles disguised as macrophages for trapping lipopolysaccharide and preventing endotoxemia. Biomaterials. 2019;189:60–68. Copyright © 2018 Elsevier Ltd. All rights reserved.

Techniques: Derivative Assay, Activation Assay, Blocking Assay, In Vivo, Bacteria, Clinical Proteomics, Transmission Assay, Electron Microscopy, Modification

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