Advanced Functional Materials, ISSN 1616-301X, 09/2015, Volume 25, Issue 34, pp. 5479 - 5491
For mitochondria‐targeting delivery, a coupling reaction between poly(ε‐caprolactone) diol (PCL diol) and 4‐carboxybutyltriphenylphosphonium (4‐carboxybutyl...
self‐assembled nanomedicine | mitochondria‐targeting drug delivery | poly(ε‐caprolactone) | triphenylphosphonium | subcellular targeting | mitochondria-targeting drug delivery | self-assembled nanomedicine | poly(ε-caprolactone) | THERAPEUTICS | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | PROTEIN | MATERIALS SCIENCE, MULTIDISCIPLINARY | DOXORUBICIN | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | MICELLES | CHEMISTRY, MULTIDISCIPLINARY | PACLITAXEL | BREAST-CANCER CELLS | NANOPARTICLES | IN-VITRO | poly(epsilon-caprolactone) | CYTOTOXICITY | LIVING CELLS | Nanoparticles | Drugs | Uptakes | Drug delivery systems | Nanostructure | Nanofibers | Polymers | Diols | Anticancer properties
self‐assembled nanomedicine | mitochondria‐targeting drug delivery | poly(ε‐caprolactone) | triphenylphosphonium | subcellular targeting | mitochondria-targeting drug delivery | self-assembled nanomedicine | poly(ε-caprolactone) | THERAPEUTICS | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | PROTEIN | MATERIALS SCIENCE, MULTIDISCIPLINARY | DOXORUBICIN | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | MICELLES | CHEMISTRY, MULTIDISCIPLINARY | PACLITAXEL | BREAST-CANCER CELLS | NANOPARTICLES | IN-VITRO | poly(epsilon-caprolactone) | CYTOTOXICITY | LIVING CELLS | Nanoparticles | Drugs | Uptakes | Drug delivery systems | Nanostructure | Nanofibers | Polymers | Diols | Anticancer properties
Journal Article
International Journal of Biological Macromolecules, ISSN 0141-8130, 07/2019, Volume 132, pp. 451 - 460
Cancer cells divide uncontrollably due to their metabolic imbalance, resistance to mitochondria-mediated apoptosis, and ability to sustain telomere crisis by...
Mitochondria targeting | Glycol chitosan | Curcumin | Dequalinium | Cancer therapy | Drugs | Nanoparticles | Medical colleges | Telomeres | Drug delivery systems | Cell death | DNA polymerases | Glycols | Polymers | Vehicles
Mitochondria targeting | Glycol chitosan | Curcumin | Dequalinium | Cancer therapy | Drugs | Nanoparticles | Medical colleges | Telomeres | Drug delivery systems | Cell death | DNA polymerases | Glycols | Polymers | Vehicles
Journal Article
纳米研究:英文版, ISSN 1998-0124, 2018, Volume 11, Issue 2, pp. 1082 - 1098
Subcellular organelle-specific nanoparticles for simultaneous tumor targeting, imaging, and drug delivery are of enormous interest in cancer therapy. Herein,...
线粒体;装配;指向;交货;成像;地点;癌症治疗;肿瘤生长 | Condensed Matter Physics | Biomedicine, general | Biotechnology | Materials Science | Materials Science, general | fluorescence imaging | mitochondria-targeting | aggregation-induced emission | Atomic/Molecular Structure and Spectra | drug delivery | chemotherapy | Nanotechnology | Chemotherapy | Drug delivery | Fluorescence imaging | Aggregation-induced emission | Mitochondria-targeting | PHYSICS, APPLIED | BLOCK-COPOLYMERS | MATERIALS SCIENCE, MULTIDISCIPLINARY | DOXORUBICIN | CHITOSAN | CHEMISTRY, PHYSICAL | MESOPOROUS SILICA NANOPARTICLES | NANOSCIENCE & NANOTECHNOLOGY | POLYELECTROLYTE | PLATFORM | FLUORESCENT | THERAPY | AGGREGATION-INDUCED-EMISSION | HYPERSENSITIVITY | Drugs | Animal experimentation | Nanoparticles | Anthracyclines | Drug delivery systems | Fluorescence | Vehicles | Cancer | Self assembly | Therapy | Reactive oxygen species | Toxicity | Phosphine | Cytotoxicity | Event-related potentials | Agglomeration | Doxorubicin | Mitochondria | Biological effects | Animal tissues | Xenografts | Biocompatibility | Membrane potential | Nanorods
线粒体;装配;指向;交货;成像;地点;癌症治疗;肿瘤生长 | Condensed Matter Physics | Biomedicine, general | Biotechnology | Materials Science | Materials Science, general | fluorescence imaging | mitochondria-targeting | aggregation-induced emission | Atomic/Molecular Structure and Spectra | drug delivery | chemotherapy | Nanotechnology | Chemotherapy | Drug delivery | Fluorescence imaging | Aggregation-induced emission | Mitochondria-targeting | PHYSICS, APPLIED | BLOCK-COPOLYMERS | MATERIALS SCIENCE, MULTIDISCIPLINARY | DOXORUBICIN | CHITOSAN | CHEMISTRY, PHYSICAL | MESOPOROUS SILICA NANOPARTICLES | NANOSCIENCE & NANOTECHNOLOGY | POLYELECTROLYTE | PLATFORM | FLUORESCENT | THERAPY | AGGREGATION-INDUCED-EMISSION | HYPERSENSITIVITY | Drugs | Animal experimentation | Nanoparticles | Anthracyclines | Drug delivery systems | Fluorescence | Vehicles | Cancer | Self assembly | Therapy | Reactive oxygen species | Toxicity | Phosphine | Cytotoxicity | Event-related potentials | Agglomeration | Doxorubicin | Mitochondria | Biological effects | Animal tissues | Xenografts | Biocompatibility | Membrane potential | Nanorods
Journal Article
Journal of Drug Delivery Science and Technology, ISSN 1773-2247, 06/2017, Volume 39, pp. 501 - 507
Mitochondria, which play an essential effect in cell apoptosis, are targets for cancer treatment. Here, mitochondria targeted liposomes loaded with...
Mitochondria targeting | Liposomes | Hematoporphyrin monomethyl ether | TPP | Sonodynamic therapy | CELLS | MECHANISM | VESICLES | PHOTOSENSITIZER | CANCER-THERAPY | NANOPARTICLES | CARCINOGENESIS | IN-VIVO | PHARMACOLOGY & PHARMACY | PROGRESSION
Mitochondria targeting | Liposomes | Hematoporphyrin monomethyl ether | TPP | Sonodynamic therapy | CELLS | MECHANISM | VESICLES | PHOTOSENSITIZER | CANCER-THERAPY | NANOPARTICLES | CARCINOGENESIS | IN-VIVO | PHARMACOLOGY & PHARMACY | PROGRESSION
Journal Article
Asian Journal of Pharmaceutical Sciences, ISSN 1818-0876, 11/2017, Volume 12, Issue 6, pp. 498 - 508
The structure of mitochondria: outer mitochondrial membrane (OMM), inner mitochondrial membrane (IMM), the intermembrane space (IMS) and matrix. In this...
Nanoparticles | Liposomes | Diabetes | Mitochondria-targeting | DQAsomes | Cancer | GOLD NANOPARTICLES | OXIDATIVE STRESS | LIPOSOME-BASED CARRIER | DF-MITO-PORTER | ALZHEIMERS-DISEASE | HYDROXYAPATITE NANOPARTICLES | IN-VITRO | RESISTANT LUNG-CANCER | PLASMID DNA | PHARMACOLOGY & PHARMACY | MEMBRANE PERMEABILIZATION
Nanoparticles | Liposomes | Diabetes | Mitochondria-targeting | DQAsomes | Cancer | GOLD NANOPARTICLES | OXIDATIVE STRESS | LIPOSOME-BASED CARRIER | DF-MITO-PORTER | ALZHEIMERS-DISEASE | HYDROXYAPATITE NANOPARTICLES | IN-VITRO | RESISTANT LUNG-CANCER | PLASMID DNA | PHARMACOLOGY & PHARMACY | MEMBRANE PERMEABILIZATION
Journal Article
Biomaterials, ISSN 0142-9612, 2015, Volume 52, Issue 1, pp. 126 - 139
Abstract Mitochondrion-orientated transportation of smart liposomes has been developed as a promising strategy to deliver anticancer drugs directly to tumor...
Advanced Basic Science | Dentistry | Mitochondria targeting | pH response | Anticancer efficacy | Dual-functional liposome | Drug-resistant lung cancer | Paclitaxel | PH response | CELLS | MATERIALS SCIENCE, BIOMATERIALS | DELIVERY SYSTEMS | ENGINEERING, BIOMEDICAL | BREAST-CANCER | DNA DELIVERY | NANOPARTICLES | THERAPY | IN-VIVO | CONJUGATE | MULTIDRUG-RESISTANCE | TUMOR MICROENVIRONMENT | Protons | Lung Neoplasms - drug therapy | Caspase 9 - metabolism | Apoptosis - drug effects | Humans | Lung Neoplasms - metabolism | Molecular Sequence Data | Drug Resistance, Neoplasm | Lung Neoplasms - pathology | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - administration & dosage | Drug Delivery Systems | Peptides - metabolism | Female | Lung - metabolism | Paclitaxel - administration & dosage | Amino Acid Sequence | Lung - pathology | Peptides - chemistry | Cytochromes c - metabolism | Mitochondria - metabolism | Mitochondria - pathology | Paclitaxel - therapeutic use | Liposomes - chemistry | Animals | Mice, Nude | Lung - drug effects | Cell Line, Tumor | Liposomes - metabolism | Mice, Inbred BALB C | Phosphatidylethanolamines - metabolism | Phosphatidylethanolamines - chemistry | Antimitotic agents | Biological products | Lung cancer | Pharmacy | Drugstores | Lipids | Mitochondrial DNA | Drug resistance | Drug therapy | Antineoplastic agents | Hydrogen-ion concentration | Drugs | Mitochondria | Lungs | Peptides | Taxol | Liposomes | Tumors | Cancer
Advanced Basic Science | Dentistry | Mitochondria targeting | pH response | Anticancer efficacy | Dual-functional liposome | Drug-resistant lung cancer | Paclitaxel | PH response | CELLS | MATERIALS SCIENCE, BIOMATERIALS | DELIVERY SYSTEMS | ENGINEERING, BIOMEDICAL | BREAST-CANCER | DNA DELIVERY | NANOPARTICLES | THERAPY | IN-VIVO | CONJUGATE | MULTIDRUG-RESISTANCE | TUMOR MICROENVIRONMENT | Protons | Lung Neoplasms - drug therapy | Caspase 9 - metabolism | Apoptosis - drug effects | Humans | Lung Neoplasms - metabolism | Molecular Sequence Data | Drug Resistance, Neoplasm | Lung Neoplasms - pathology | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - administration & dosage | Drug Delivery Systems | Peptides - metabolism | Female | Lung - metabolism | Paclitaxel - administration & dosage | Amino Acid Sequence | Lung - pathology | Peptides - chemistry | Cytochromes c - metabolism | Mitochondria - metabolism | Mitochondria - pathology | Paclitaxel - therapeutic use | Liposomes - chemistry | Animals | Mice, Nude | Lung - drug effects | Cell Line, Tumor | Liposomes - metabolism | Mice, Inbred BALB C | Phosphatidylethanolamines - metabolism | Phosphatidylethanolamines - chemistry | Antimitotic agents | Biological products | Lung cancer | Pharmacy | Drugstores | Lipids | Mitochondrial DNA | Drug resistance | Drug therapy | Antineoplastic agents | Hydrogen-ion concentration | Drugs | Mitochondria | Lungs | Peptides | Taxol | Liposomes | Tumors | Cancer
Journal Article
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, ISSN 0031-6903, 11/2014, Volume 134, Issue 11, pp. 1143 - 1155
Many human diseases have been reported to be associated with mitochondrial dysfunction. Therefore, mitochondrial therapy would be expected to be useful and...
SYSTEM | CELLS | LIPOSOME-BASED CARRIER | PROTEIN | mitochondria | BONGKREKIC ACID | MACROMOLECULE | drug delivery system (DDS) | FUSOGENIC ENVELOPES | nano device | mitocondrial gene therapy | PLASMID DNA | DISEASE | PHARMACOLOGY & PHARMACY | TARGETING SIGNAL PEPTIDE | MITO-Porter | mitochondrial medicine | Biological Transport | Membrane Fusion | Nanostructures - administration & dosage | Humans | Mitochondria - metabolism | Liposomes | Drug Delivery Systems - methods
SYSTEM | CELLS | LIPOSOME-BASED CARRIER | PROTEIN | mitochondria | BONGKREKIC ACID | MACROMOLECULE | drug delivery system (DDS) | FUSOGENIC ENVELOPES | nano device | mitocondrial gene therapy | PLASMID DNA | DISEASE | PHARMACOLOGY & PHARMACY | TARGETING SIGNAL PEPTIDE | MITO-Porter | mitochondrial medicine | Biological Transport | Membrane Fusion | Nanostructures - administration & dosage | Humans | Mitochondria - metabolism | Liposomes | Drug Delivery Systems - methods
Journal Article
Biomedical Microdevices, ISSN 1387-2176, 8/2010, Volume 12, Issue 4, pp. 655 - 663
The use of ceramic nano-carriers containing anti-cancer drugs for targeted delivery that span both fundamental and applied research has attracted the interest...
Biomedical Engineering | Engineering | Amorphous silica-nanocage | Photodynamic | Engineering Fluid Dynamics | Biophysics and Biological Physics | Drug delivery | Time-dependent efficacy | Biodiagnose | Nanotechnology | Mitochondria-targeting | Amorphous silica-nanocage time-dependent efficacy | SYSTEM | CELLS | PHOTODYNAMIC THERAPY | INDUCED APOPTOSIS | ENGINEERING, BIOMEDICAL | MODIFIED SILICA NANOPARTICLES | NANOSCIENCE & NANOTECHNOLOGY | CANCER-THERAPY | CARRIER | HYPOCRELLIN | SINGLET OXYGEN | Photosensitizing Agents - chemistry | Photosensitizing Agents - therapeutic use | Humans | Molecular Conformation | Spectroscopy, Fourier Transform Infrared | Photochemotherapy | Drug Carriers - chemistry | Perylene - therapeutic use | Singlet Oxygen - metabolism | Photosensitizing Agents - pharmacology | Silicon Dioxide - metabolism | Biological Transport | Mitochondria - radiation effects | Indicators and Reagents - chemistry | Quinones - pharmacology | Photobleaching | Perylene - analogs & derivatives | Microscopy, Electron, Transmission | Drug Carriers - metabolism | Perylene - chemistry | Silanes - chemistry | Quinones - chemistry | Silicon Dioxide - chemistry | Quinones - therapeutic use | Models, Molecular | Mitochondria - metabolism | Mitochondria - drug effects | Perylene - pharmacology | Indicators and Reagents - metabolism | Hydrogen Bonding | Intracellular Space - metabolism | HeLa Cells | Nanomaterials | Mitochondria | Drug delivery systems | Photodynamic therapy
Biomedical Engineering | Engineering | Amorphous silica-nanocage | Photodynamic | Engineering Fluid Dynamics | Biophysics and Biological Physics | Drug delivery | Time-dependent efficacy | Biodiagnose | Nanotechnology | Mitochondria-targeting | Amorphous silica-nanocage time-dependent efficacy | SYSTEM | CELLS | PHOTODYNAMIC THERAPY | INDUCED APOPTOSIS | ENGINEERING, BIOMEDICAL | MODIFIED SILICA NANOPARTICLES | NANOSCIENCE & NANOTECHNOLOGY | CANCER-THERAPY | CARRIER | HYPOCRELLIN | SINGLET OXYGEN | Photosensitizing Agents - chemistry | Photosensitizing Agents - therapeutic use | Humans | Molecular Conformation | Spectroscopy, Fourier Transform Infrared | Photochemotherapy | Drug Carriers - chemistry | Perylene - therapeutic use | Singlet Oxygen - metabolism | Photosensitizing Agents - pharmacology | Silicon Dioxide - metabolism | Biological Transport | Mitochondria - radiation effects | Indicators and Reagents - chemistry | Quinones - pharmacology | Photobleaching | Perylene - analogs & derivatives | Microscopy, Electron, Transmission | Drug Carriers - metabolism | Perylene - chemistry | Silanes - chemistry | Quinones - chemistry | Silicon Dioxide - chemistry | Quinones - therapeutic use | Models, Molecular | Mitochondria - metabolism | Mitochondria - drug effects | Perylene - pharmacology | Indicators and Reagents - metabolism | Hydrogen Bonding | Intracellular Space - metabolism | HeLa Cells | Nanomaterials | Mitochondria | Drug delivery systems | Photodynamic therapy
Journal Article
Biomaterials, ISSN 0142-9612, 02/2018, Volume 154, pp. 169 - 181
Mitochondria, crucial regulators of inducing tumor cells apoptosis, can be treated as the prime target for tumor therapy. The selective and responsive release...
Intracellular transport and tracking | Mitochondria targeting | Breast cancer | Drug delivery system | Alkaline pH-responsive release | CARCINOMA-CELLS | ACTIVATION | MATERIALS SCIENCE, BIOMATERIALS | ENGINEERING, BIOMEDICAL | TUMOR-CELLS | TARGETING MITOCHONDRIA | LUNG-CANCER | INTRACELLULAR DELIVERY | POLY(L-LACTIC ACID) MATRIX | LIPOSOMES | TRIPHENYLPHOSPHONIUM | LIVING CELLS | Triterpenes - pharmacology | Apoptosis - drug effects | Triterpenes - therapeutic use | Mitochondria - ultrastructure | Drug Delivery Systems | Time Factors | Micelles | Cell Death | Glycolipids - chemistry | Onium Compounds - chemistry | Tissue Distribution - drug effects | Organophosphorus Compounds - chemistry | Mitochondria - metabolism | Mitochondria - drug effects | Static Electricity | Neoplasms - drug therapy | Particle Size | Xenograft Model Antitumor Assays | Animals | Signal Transduction - drug effects | Mice, Nude | Cell Line, Tumor | Drug Liberation | Neoplasms - pathology | Hydrogen-Ion Concentration | Cytochrome c | Drugs | Drug delivery systems | Therapeutics | Lipids | Hydrogen-ion concentration | Health aspects | Cancer | Homeopathy | Materia medica and therapeutics | Vehicles
Intracellular transport and tracking | Mitochondria targeting | Breast cancer | Drug delivery system | Alkaline pH-responsive release | CARCINOMA-CELLS | ACTIVATION | MATERIALS SCIENCE, BIOMATERIALS | ENGINEERING, BIOMEDICAL | TUMOR-CELLS | TARGETING MITOCHONDRIA | LUNG-CANCER | INTRACELLULAR DELIVERY | POLY(L-LACTIC ACID) MATRIX | LIPOSOMES | TRIPHENYLPHOSPHONIUM | LIVING CELLS | Triterpenes - pharmacology | Apoptosis - drug effects | Triterpenes - therapeutic use | Mitochondria - ultrastructure | Drug Delivery Systems | Time Factors | Micelles | Cell Death | Glycolipids - chemistry | Onium Compounds - chemistry | Tissue Distribution - drug effects | Organophosphorus Compounds - chemistry | Mitochondria - metabolism | Mitochondria - drug effects | Static Electricity | Neoplasms - drug therapy | Particle Size | Xenograft Model Antitumor Assays | Animals | Signal Transduction - drug effects | Mice, Nude | Cell Line, Tumor | Drug Liberation | Neoplasms - pathology | Hydrogen-Ion Concentration | Cytochrome c | Drugs | Drug delivery systems | Therapeutics | Lipids | Hydrogen-ion concentration | Health aspects | Cancer | Homeopathy | Materia medica and therapeutics | Vehicles
Journal Article
Colloids and Surfaces B: Biointerfaces, ISSN 0927-7765, 05/2018, Volume 165, pp. 56 - 66
The major goal of cancer chemotherapy is to maximize the therapeutic efficacy of anticancer drugs, while minimizing their associated side effects. Celastrol...
Mesoporous silica nanoparticles | HIF-1α inhibition | Mitochondria targeting | Celastrol | Cancer therapy | THERAPEUTICS | APOPTOSIS | MATERIALS SCIENCE, BIOMATERIALS | DRUG-DELIVERY | HIF-1 alpha inhibition | DOXORUBICIN | CONTROLLED-RELEASE | CHEMISTRY, PHYSICAL | ANTITUMOR-ACTIVITY | CANCER | CARRIERS | THERAPY | BIOPHYSICS | SEQUENTIAL DELIVERY | Medicinal plants | Proteins | Nanoparticles | Drugs | Drug delivery systems | Chemotherapy | Analysis | Medicine, Botanic | Medicine, Herbal | Silica | Cancer | Vehicles | Index Medicus
Mesoporous silica nanoparticles | HIF-1α inhibition | Mitochondria targeting | Celastrol | Cancer therapy | THERAPEUTICS | APOPTOSIS | MATERIALS SCIENCE, BIOMATERIALS | DRUG-DELIVERY | HIF-1 alpha inhibition | DOXORUBICIN | CONTROLLED-RELEASE | CHEMISTRY, PHYSICAL | ANTITUMOR-ACTIVITY | CANCER | CARRIERS | THERAPY | BIOPHYSICS | SEQUENTIAL DELIVERY | Medicinal plants | Proteins | Nanoparticles | Drugs | Drug delivery systems | Chemotherapy | Analysis | Medicine, Botanic | Medicine, Herbal | Silica | Cancer | Vehicles | Index Medicus
Journal Article
Nano Letters, ISSN 1530-6984, 04/2018, Volume 18, Issue 4, pp. 2475 - 2484
Photodynamic therapy (PDT) is an oxygen-dependent light-triggered noninvasive therapeutic method showing many promising aspects in cancer treatment. For...
NEAR-INFRARED LIGHT | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | Photodynamic therapy | DRUG-DELIVERY | COMBINATION THERAPY | PHOTOSENSITIZER | MATERIALS SCIENCE, MULTIDISCIPLINARY | nanoreactors | tumor hypoxia | CHEMISTRY, PHYSICAL | MESOPOROUS SILICA NANOPARTICLES | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | HIGHLY EFFICIENT | CHECKPOINT BLOCKADE | mitochondria targeting | IN-VIVO | UP-CONVERSION NANOPARTICLES | check-point-blockade therapy | SINGLET-OXYGEN | Tumor Microenvironment - drug effects | Immunotherapy - methods | Reactive Oxygen Species - metabolism | Nanoparticles - chemistry | Photosensitizing Agents - therapeutic use | Photochemotherapy - methods | Silicon Dioxide - chemistry | Tumor Hypoxia - drug effects | Delayed-Action Preparations - chemistry | Mitochondria - metabolism | Breast Neoplasms - drug therapy | Breast Neoplasms - metabolism | Drug Delivery Systems | Hydrogen Peroxide - metabolism | Breast Neoplasms - therapy | Photosensitizing Agents - administration & dosage | Animals | Cell Line, Tumor | Female | Mice | Hydrogen-Ion Concentration
NEAR-INFRARED LIGHT | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | Photodynamic therapy | DRUG-DELIVERY | COMBINATION THERAPY | PHOTOSENSITIZER | MATERIALS SCIENCE, MULTIDISCIPLINARY | nanoreactors | tumor hypoxia | CHEMISTRY, PHYSICAL | MESOPOROUS SILICA NANOPARTICLES | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | HIGHLY EFFICIENT | CHECKPOINT BLOCKADE | mitochondria targeting | IN-VIVO | UP-CONVERSION NANOPARTICLES | check-point-blockade therapy | SINGLET-OXYGEN | Tumor Microenvironment - drug effects | Immunotherapy - methods | Reactive Oxygen Species - metabolism | Nanoparticles - chemistry | Photosensitizing Agents - therapeutic use | Photochemotherapy - methods | Silicon Dioxide - chemistry | Tumor Hypoxia - drug effects | Delayed-Action Preparations - chemistry | Mitochondria - metabolism | Breast Neoplasms - drug therapy | Breast Neoplasms - metabolism | Drug Delivery Systems | Hydrogen Peroxide - metabolism | Breast Neoplasms - therapy | Photosensitizing Agents - administration & dosage | Animals | Cell Line, Tumor | Female | Mice | Hydrogen-Ion Concentration
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2016, Volume 55, Issue 44, pp. 13770 - 13774
Understanding the mechanism of action (MOA) of bioactive natural products will guide endeavor to improve their cellular activities. Artemisinin and its...
fluorescent probe | anticancer activity | drug delivery | triphenylphosphonium | mitochondria targeting | CELLS | OXIDATIVE STRESS | IRON CHELATORS | DESFERRIOXAMINE | CHEMISTRY, MULTIDISCIPLINARY | STRATEGIES | ANTIMALARIAL-DRUGS | HEME | PLASMODIUM-FALCIPARUM | TRADITIONAL CHINESE MEDICINE | MALARIA | Cell Survival - drug effects | Artemisinins - chemical synthesis | Antineoplastic Agents - chemical synthesis | HCT116 Cells | Humans | Structure-Activity Relationship | Mitochondria - drug effects | Antineoplastic Agents - chemistry | Dose-Response Relationship, Drug | Artemisinins - pharmacology | Drug Design | Antineoplastic Agents - pharmacology | Molecular Structure | Artemisinins - chemistry | Drug Screening Assays, Antitumor | Drugs | Proteins | Care and treatment | Drug delivery systems | Malaria | Heme | Cancer | Vehicles | Cell proliferation | Surgical implants | Transcription factors | Artemisinin | Attachment | Parasites | Drug development | Anticancer properties | Design optimization | Design | Mitochondria | Biomedical materials | Design improvements | Biocompatibility | Inhibition | Killing | Vector-borne diseases | Effectiveness | Analogue | Derivatives | Natural products | Proteomics | Antitumor activity
fluorescent probe | anticancer activity | drug delivery | triphenylphosphonium | mitochondria targeting | CELLS | OXIDATIVE STRESS | IRON CHELATORS | DESFERRIOXAMINE | CHEMISTRY, MULTIDISCIPLINARY | STRATEGIES | ANTIMALARIAL-DRUGS | HEME | PLASMODIUM-FALCIPARUM | TRADITIONAL CHINESE MEDICINE | MALARIA | Cell Survival - drug effects | Artemisinins - chemical synthesis | Antineoplastic Agents - chemical synthesis | HCT116 Cells | Humans | Structure-Activity Relationship | Mitochondria - drug effects | Antineoplastic Agents - chemistry | Dose-Response Relationship, Drug | Artemisinins - pharmacology | Drug Design | Antineoplastic Agents - pharmacology | Molecular Structure | Artemisinins - chemistry | Drug Screening Assays, Antitumor | Drugs | Proteins | Care and treatment | Drug delivery systems | Malaria | Heme | Cancer | Vehicles | Cell proliferation | Surgical implants | Transcription factors | Artemisinin | Attachment | Parasites | Drug development | Anticancer properties | Design optimization | Design | Mitochondria | Biomedical materials | Design improvements | Biocompatibility | Inhibition | Killing | Vector-borne diseases | Effectiveness | Analogue | Derivatives | Natural products | Proteomics | Antitumor activity
Journal Article
ACS Nano, ISSN 1936-0851, 09/2014, Volume 8, Issue 9, pp. 9379 - 9387
Mitochondria-targeting peptides have garnered immense interest as potential chemotherapeutics in recent years. However, there is a clear need to develop...
combined therapy | magnetic core-shell nanoparticle | magnetically facilitated delivery | mitochondria-targeting peptide | amphipathic tail-anchoring peptide | magnetic hyperthermia | GOLD NANOPARTICLES | PROTEIN | GENE DELIVERY | DRUG-DELIVERY | MATERIALS SCIENCE, MULTIDISCIPLINARY | MAGNETOFECTION | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | TARGETING MITOCHONDRIA | MAGNETIC NANOPARTICLES | CHEMISTRY, MULTIDISCIPLINARY | IN-VITRO | THERAPY | EXPRESSION | Amino Acid Sequence | Nanoparticles - chemistry | Apoptosis - drug effects | Humans | Molecular Sequence Data | Membrane Potential, Mitochondrial - drug effects | Integrins - metabolism | Drug Carriers - chemistry | Hyperthermia, Induced | Cell Line, Tumor | Hydrophobic and Hydrophilic Interactions | Oligopeptides - pharmacology | Oligopeptides - chemistry | magnetic core−shell nanoparticle
combined therapy | magnetic core-shell nanoparticle | magnetically facilitated delivery | mitochondria-targeting peptide | amphipathic tail-anchoring peptide | magnetic hyperthermia | GOLD NANOPARTICLES | PROTEIN | GENE DELIVERY | DRUG-DELIVERY | MATERIALS SCIENCE, MULTIDISCIPLINARY | MAGNETOFECTION | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | TARGETING MITOCHONDRIA | MAGNETIC NANOPARTICLES | CHEMISTRY, MULTIDISCIPLINARY | IN-VITRO | THERAPY | EXPRESSION | Amino Acid Sequence | Nanoparticles - chemistry | Apoptosis - drug effects | Humans | Molecular Sequence Data | Membrane Potential, Mitochondrial - drug effects | Integrins - metabolism | Drug Carriers - chemistry | Hyperthermia, Induced | Cell Line, Tumor | Hydrophobic and Hydrophilic Interactions | Oligopeptides - pharmacology | Oligopeptides - chemistry | magnetic core−shell nanoparticle
Journal Article
Theranostics, ISSN 1838-7640, 2016, Volume 6, Issue 13, pp. 2352 - 2366
Mitochondria in cancer cells maintain a more negative membrane potential than normal cells. Mitochondria are the primary source of cellular reactive oxygen...
Camptothecin | Photodynamic therapy | ROS-responsive | Mitochondria-targeting nanoparticles | Zinc phthalocyanine | CARCINOMA-CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | mitochondria-targeting nanoparticles | photodynamic therapy | COMBINATION THERAPY | NANOCARRIERS | MECHANISMS | DELIVERY | camptothecin | IN-VIVO | RESISTANCE | THERANOSTICS | EFFICIENT | LIPOSOMES | Cell Survival - drug effects | Reactive Oxygen Species - metabolism | Photochemotherapy - methods | Humans | Drug Liberation - radiation effects | Treatment Outcome | Lung Neoplasms - therapy | Mitochondria - metabolism | Mitochondria - drug effects | Cell Survival - radiation effects | Drug Delivery Systems | Animals | Heterografts | Drug Therapy - methods | Light | Cell Line, Tumor | Combined Modality Therapy - methods | Mice, Inbred BALB C | Nanoparticles - administration & dosage
Camptothecin | Photodynamic therapy | ROS-responsive | Mitochondria-targeting nanoparticles | Zinc phthalocyanine | CARCINOMA-CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | mitochondria-targeting nanoparticles | photodynamic therapy | COMBINATION THERAPY | NANOCARRIERS | MECHANISMS | DELIVERY | camptothecin | IN-VIVO | RESISTANCE | THERANOSTICS | EFFICIENT | LIPOSOMES | Cell Survival - drug effects | Reactive Oxygen Species - metabolism | Photochemotherapy - methods | Humans | Drug Liberation - radiation effects | Treatment Outcome | Lung Neoplasms - therapy | Mitochondria - metabolism | Mitochondria - drug effects | Cell Survival - radiation effects | Drug Delivery Systems | Animals | Heterografts | Drug Therapy - methods | Light | Cell Line, Tumor | Combined Modality Therapy - methods | Mice, Inbred BALB C | Nanoparticles - administration & dosage
Journal Article