Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 8 of 8 entries
Sorted by: Best Match Show Resources per page
Physico-chemical aspects of the interaction between DNA and oppositely charged mixed liposomes.

Biophysical chemistry

Mel'nikova YS, Mel'nikov SM, Löfroth JE.
PMID: 17030332
Biophys Chem. 1999 Oct 04;81(2):125-41. doi: 10.1016/s0301-4622(99)00088-5.

The mechanism of complex formation between DNA and oppositely charged dioctadecyldimethylammonium bromide/dioleoyl phosphatidylethanolamine (DODAB/DOPE) and 1,2-dioleoyl-3-trimethylammonium propane (DOTAP)/DOPE mixed liposomes, as well as the physico-chemical properties of DNA-mixed liposome complexes, were examined. Fluorescence microscopy showed that the interaction between...

Cite
Mel'nikova YS, Mel'nikov SM, Löfroth JE. Physico-chemical aspects of the interaction between DNA and oppositely charged mixed liposomes. Biophys Chem. 1999;81(2):125-41doi: 10.1016/s0301-4622(99)00088-5.
Mel'nikova, Y. S., Mel'nikov, S. M., & Löfroth, J. E. (1999). Physico-chemical aspects of the interaction between DNA and oppositely charged mixed liposomes. Biophysical chemistry, 81(2), 125-41. https://doi.org/10.1016/s0301-4622(99)00088-5
Mel'nikova, Y S, et al. "Physico-chemical aspects of the interaction between DNA and oppositely charged mixed liposomes." Biophysical chemistry vol. 81,2 (1999): 125-41. doi: https://doi.org/10.1016/s0301-4622(99)00088-5
Mel'nikova YS, Mel'nikov SM, Löfroth JE. Physico-chemical aspects of the interaction between DNA and oppositely charged mixed liposomes. Biophys Chem. 1999 Oct 04;81(2):125-41. doi: 10.1016/s0301-4622(99)00088-5. PMID: 17030332.
Copy Download .nbib Format: NLM
Synchrotron Characterization of Hexagonal and Cubic Lipidic Phases Loaded with Azolate/Phosphane Gold(I) Compounds: A New Approach to the Uploading of Gold(I)-Based Drugs.

Nanomaterials (Basel, Switzerland)

Astolfi P, Pisani M, Giorgini E, Rossi B, Damin A, Vita F, Francescangeli O, Luciani L, Galassi R.
PMID: 32947840
Nanomaterials (Basel). 2020 Sep 16;10(9). doi: 10.3390/nano10091851.

Gold(I) phosphane compounds have recently attracted a renewed interest as potential new protagonists in cancer therapy. A class of phosphane gold(I) complexes containing azolate ligands has been successfully tested against several cancer cell lines and, in particular, against basal-like...

Cite
Astolfi P, Pisani M, Giorgini E, et al. Synchrotron Characterization of Hexagonal and Cubic Lipidic Phases Loaded with Azolate/Phosphane Gold(I) Compounds: A New Approach to the Uploading of Gold(I)-Based Drugs. Nanomaterials (Basel). 2020;10(9)doi: 10.3390/nano10091851.
Astolfi, P., Pisani, M., Giorgini, E., Rossi, B., Damin, A., Vita, F., Francescangeli, O., Luciani, L., & Galassi, R. (2020). Synchrotron Characterization of Hexagonal and Cubic Lipidic Phases Loaded with Azolate/Phosphane Gold(I) Compounds: A New Approach to the Uploading of Gold(I)-Based Drugs. Nanomaterials (Basel, Switzerland), 10(9), . https://doi.org/10.3390/nano10091851
Astolfi, Paola, et al. "Synchrotron Characterization of Hexagonal and Cubic Lipidic Phases Loaded with Azolate/Phosphane Gold(I) Compounds: A New Approach to the Uploading of Gold(I)-Based Drugs." Nanomaterials (Basel, Switzerland) vol. 10,9 (2020). doi: https://doi.org/10.3390/nano10091851
Astolfi P, Pisani M, Giorgini E, Rossi B, Damin A, Vita F, Francescangeli O, Luciani L, Galassi R. Synchrotron Characterization of Hexagonal and Cubic Lipidic Phases Loaded with Azolate/Phosphane Gold(I) Compounds: A New Approach to the Uploading of Gold(I)-Based Drugs. Nanomaterials (Basel). 2020 Sep 16;10(9). doi: 10.3390/nano10091851. PMID: 32947840; PMCID: PMC7558674.
Copy Download .nbib Format: NLM
Liposome-based Formulation for Intracellular Delivery of Functional Proteins.

Molecular therapy. Nucleic acids

Chatin B, Mével M, Devallière J, Dallet L, Haudebourg T, Peuziat P, Colombani T, Berchel M, Lambert O, Edelman A, Pitard B.
PMID: 26102064
Mol Ther Nucleic Acids. 2015 Jun 23;4:e244. doi: 10.1038/mtna.2015.17.

The intracellular delivery of biologically active protein represents an important emerging strategy for both fundamental and therapeutic applications. Here, we optimized in vitro delivery of two functional proteins, the β-galactosidase (β-gal) enzyme and the anti-cytokeratin8 (K8) antibody, using liposome-based...

Cite
Chatin B, Mével M, Devallière J, et al. Liposome-based Formulation for Intracellular Delivery of Functional Proteins. Mol Ther Nucleic Acids. 2015;4:e244doi: 10.1038/mtna.2015.17.
Chatin, B., Mével, M., Devallière, J., Dallet, L., Haudebourg, T., Peuziat, P., Colombani, T., Berchel, M., Lambert, O., Edelman, A., & Pitard, B. (2015). Liposome-based Formulation for Intracellular Delivery of Functional Proteins. Molecular therapy. Nucleic acids, 4e244. https://doi.org/10.1038/mtna.2015.17
Chatin, Benoît, et al. "Liposome-based Formulation for Intracellular Delivery of Functional Proteins." Molecular therapy. Nucleic acids vol. 4 (2015): e244. doi: https://doi.org/10.1038/mtna.2015.17
Chatin B, Mével M, Devallière J, Dallet L, Haudebourg T, Peuziat P, Colombani T, Berchel M, Lambert O, Edelman A, Pitard B. Liposome-based Formulation for Intracellular Delivery of Functional Proteins. Mol Ther Nucleic Acids. 2015 Jun 23;4:e244. doi: 10.1038/mtna.2015.17. PMID: 26102064.
Copy Download .nbib Format: NLM
Improvement of Peptide-Based Tumor Immunotherapy Using pH-Sensitive Fusogenic Polymer-Modified Liposomes.

Molecules (Basel, Switzerland)

Yoshizaki Y, Yuba E, Komatsu T, Udaka K, Harada A, Kono K.
PMID: 27681717
Molecules. 2016 Sep 26;21(10). doi: 10.3390/molecules21101284.

To establish peptide vaccine-based cancer immunotherapy, we investigated the improvement of antigenic peptides by encapsulation with pH-sensitive fusogenic polymer-modified liposomes for induction of antigen-specific immunity. The liposomes were prepared by modification of egg yolk phosphatidylcholine and l-dioleoyl phosphatidylethanolamine with...

Cite
Yoshizaki Y, Yuba E, Komatsu T, et al. Improvement of Peptide-Based Tumor Immunotherapy Using pH-Sensitive Fusogenic Polymer-Modified Liposomes. Molecules. 2016;21(10)doi: 10.3390/molecules21101284.
Yoshizaki, Y., Yuba, E., Komatsu, T., Udaka, K., Harada, A., & Kono, K. (2016). Improvement of Peptide-Based Tumor Immunotherapy Using pH-Sensitive Fusogenic Polymer-Modified Liposomes. Molecules (Basel, Switzerland), 21(10), . https://doi.org/10.3390/molecules21101284
Yoshizaki, Yuta, et al. "Improvement of Peptide-Based Tumor Immunotherapy Using pH-Sensitive Fusogenic Polymer-Modified Liposomes." Molecules (Basel, Switzerland) vol. 21,10 (2016). doi: https://doi.org/10.3390/molecules21101284
Yoshizaki Y, Yuba E, Komatsu T, Udaka K, Harada A, Kono K. Improvement of Peptide-Based Tumor Immunotherapy Using pH-Sensitive Fusogenic Polymer-Modified Liposomes. Molecules. 2016 Sep 26;21(10). doi: 10.3390/molecules21101284. PMID: 27681717; PMCID: PMC6274290.
Copy Download .nbib Format: NLM
Hydrophobic nanoparticles promote lamellar to inverted hexagonal transition in phospholipid mesophases.

Soft matter

Bulpett JM, Snow T, Quignon B, Beddoes CM, Tang TY, Mann S, Shebanova O, Pizzey CL, Terrill NJ, Davis SA, Briscoe WH.
PMID: 26391613
Soft Matter. 2015 Dec 07;11(45):8789-800. doi: 10.1039/c5sm01705j.

This study focuses on how the mesophase transition behaviour of the phospholipid dioleoyl phosphatidylethanolamine (DOPE) is altered by the presence of 10 nm hydrophobic and 14 nm hydrophilic silica nanoparticles (NPs) at different concentrations. The lamellar to inverted hexagonal...

Cite
Bulpett JM, Snow T, Quignon B, et al. Hydrophobic nanoparticles promote lamellar to inverted hexagonal transition in phospholipid mesophases. Soft Matter. 2015;11(45):8789-800doi: 10.1039/c5sm01705j.
Bulpett, J. M., Snow, T., Quignon, B., Beddoes, C. M., Tang, T. Y., Mann, S., Shebanova, O., Pizzey, C. L., Terrill, N. J., Davis, S. A., & Briscoe, W. H. (2015). Hydrophobic nanoparticles promote lamellar to inverted hexagonal transition in phospholipid mesophases. Soft matter, 11(45), 8789-800. https://doi.org/10.1039/c5sm01705j
Bulpett, Jennifer M, et al. "Hydrophobic nanoparticles promote lamellar to inverted hexagonal transition in phospholipid mesophases." Soft matter vol. 11,45 (2015): 8789-800. doi: https://doi.org/10.1039/c5sm01705j
Bulpett JM, Snow T, Quignon B, Beddoes CM, Tang TY, Mann S, Shebanova O, Pizzey CL, Terrill NJ, Davis SA, Briscoe WH. Hydrophobic nanoparticles promote lamellar to inverted hexagonal transition in phospholipid mesophases. Soft Matter. 2015 Dec 07;11(45):8789-800. doi: 10.1039/c5sm01705j. PMID: 26391613.
Copy Download .nbib Format: NLM
Cationic liposome-mediated gene transfer to tumor cells in vitro and in vivo.

Methods in molecular medicine

Son K, Sorgi F, Gao X, Huang L.
PMID: 24493437
Methods Mol Med. 1997;7:329-37. doi: 10.1385/0-89603-484-4:329.

Development of safe and effective technology for delivering functional DNA into cells in an intact organism is crucial to broad applications of gene therapy to human disease. Both viral and nonviral vectors have been developed. Of the technologies currently...

Cite
Son K, Sorgi F, Gao X, et al. Cationic liposome-mediated gene transfer to tumor cells in vitro and in vivo. Methods Mol Med. 1997;7:329-37doi: 10.1385/0-89603-484-4:329.
Son, K., Sorgi, F., Gao, X., & Huang, L. (1997). Cationic liposome-mediated gene transfer to tumor cells in vitro and in vivo. Methods in molecular medicine, 7329-37. https://doi.org/10.1385/0-89603-484-4:329
Son, K, et al. "Cationic liposome-mediated gene transfer to tumor cells in vitro and in vivo." Methods in molecular medicine vol. 7 (1997): 329-37. doi: https://doi.org/10.1385/0-89603-484-4:329
Son K, Sorgi F, Gao X, Huang L. Cationic liposome-mediated gene transfer to tumor cells in vitro and in vivo. Methods Mol Med. 1997;7:329-37. doi: 10.1385/0-89603-484-4:329. PMID: 24493437.
Copy Download .nbib Format: NLM
Frequency-resolved intramolecular excimer fluorescence study of lipid bilayer and nonbilayer phases.

Biophysical journal

Liu LI, Cheng KH, Somerharju P.
PMID: 19431901
Biophys J. 1993 Jun;64(6):1869-77. doi: 10.1016/S0006-3495(93)81558-3.

Frequency-domain fluorescence intensity decays of the intramolecular excimer forming (DipyPE) in a fully hydrated dioleoyl-phosphatidylethanolamine (DOPE) suspension have been measured at the monomer (395 nm) and excimer (475 nm) emissions and at different temperatures (0-30 degrees C). A classical...

Cite
Liu LI, Cheng KH, Somerharju P. Frequency-resolved intramolecular excimer fluorescence study of lipid bilayer and nonbilayer phases. Biophys J. 1993;64(6):1869-77doi: 10.1016/S0006-3495(93)81558-3.
Liu, L. I., Cheng, K. H., & Somerharju, P. (1993). Frequency-resolved intramolecular excimer fluorescence study of lipid bilayer and nonbilayer phases. Biophysical journal, 64(6), 1869-77. https://doi.org/10.1016/S0006-3495(93)81558-3
Liu, L I, et al. "Frequency-resolved intramolecular excimer fluorescence study of lipid bilayer and nonbilayer phases." Biophysical journal vol. 64,6 (1993): 1869-77. doi: https://doi.org/10.1016/S0006-3495(93)81558-3
Liu LI, Cheng KH, Somerharju P. Frequency-resolved intramolecular excimer fluorescence study of lipid bilayer and nonbilayer phases. Biophys J. 1993 Jun;64(6):1869-77. doi: 10.1016/S0006-3495(93)81558-3. PMID: 19431901; PMCID: PMC1262521.
Copy Download .nbib Format: NLM
Study of Resveratrol's Interaction with Planar Lipid Models: Insights into Its Location in Lipid Bilayers.

Membranes

Meleleo D.
PMID: 33672841
Membranes (Basel). 2021 Feb 14;11(2). doi: 10.3390/membranes11020132.

Resveratrol, a polyphenolic molecule found in edible fruits and vegetables, shows a wide range of beneficial effects on human health, including anti-microbial, anti-inflammatory, anti-cancer, and anti-aging properties. Due to its poor water solubility and high liposome-water partition coefficient, the...

Cite
Meleleo D. Study of Resveratrol's Interaction with Planar Lipid Models: Insights into Its Location in Lipid Bilayers. Membranes (Basel). 2021;11(2)doi: 10.3390/membranes11020132.
Meleleo, D. (2021). Study of Resveratrol's Interaction with Planar Lipid Models: Insights into Its Location in Lipid Bilayers. Membranes, 11(2), . https://doi.org/10.3390/membranes11020132
Meleleo, Daniela. "Study of Resveratrol's Interaction with Planar Lipid Models: Insights into Its Location in Lipid Bilayers." Membranes vol. 11,2 (2021). doi: https://doi.org/10.3390/membranes11020132
Meleleo D. Study of Resveratrol's Interaction with Planar Lipid Models: Insights into Its Location in Lipid Bilayers. Membranes (Basel). 2021 Feb 14;11(2). doi: 10.3390/membranes11020132. PMID: 33672841; PMCID: PMC7918209.
Copy Download .nbib Format: NLM
Showing 1 to 8 of 8 entries