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Littérature scientifique sur le sujet « Pro-liposome »

Auteur : Grafiati

Publié le 7 juin 2025

Mis à jour le 2 août 2025

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Articles de revues sur le sujet "Pro-liposome"

Yadav, Chandan, Md Asif, Juber Akhtar, et al. "An outline on curcumin: Its pro-liposome and liposome formulations." RESEARCH JOURNAL OF PHARMACY AND TECHNOLOGY 13, no. 12 (2020): 6276–83. http://dx.doi.org/10.5958/0974-360x.2020.01092.6.

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Hirose, Masanori, Shigenori Sugisaki, Keishi Suga, and Hiroshi Umakoshi. "Detection of L-Proline-Catalyzed Michael Addition Reaction in Model Biomembrane." Journal of Chemistry 2019 (February 26, 2019): 1–8. http://dx.doi.org/10.1155/2019/4926435.

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A method to detect the L-proline- (L-Pro-) catalyzed Michael addition reaction in model biomembranes has been established, using N-[p(2-benzimidazolyl)phenyl]maleimide and acetone as reactants. The effect of liposome membranes on this reaction was kinetically analyzed using fluorescence spectroscopy. The kinetics of the reaction were different from those of the constituent lipids of the liposomes. Zwitterionic 1,2-dipalmitoyl-sn-glycero-3-phosphocholine liposome, which is in the solid-ordered phase, had a better value of reaction rate, suggesting that the reaction rate constants of this reacti

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Prajakta, Kangutkar* Samruddhi More Shital Kambale Dr. D. R. Jadage. "A Review: Proliposomes As Effective and Stable Drug Delivery System." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 1021–30. https://doi.org/10.5281/zenodo.15352388.

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A new medication delivery method called proliposomes uses dry, granular materials that, when hydrated, produce liposomal solutions. Enhanced stability, prolonged drug release, and better bioavailability are all provided by them. Size, in vitro drug release, and trapping effectiveness are characteristics of proliposomes, which can be made in a variety of ways. They may find use in pulmonary, topical, and oral administration, especially for medications that are poorly soluble. By offering targeted distribution, proliposomes can increase treatment efficacy and lessen adverse effects. They are a d

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Sanchez-Aranguren, Lissette, Milda Grubliauskiene, Hala Shokr, et al. "Sodium Thiosulphate-Loaded Liposomes Control Hydrogen Sulphide Release and Retain Its Biological Properties in Hypoxia-like Environment." Antioxidants 11, no. 11 (2022): 2092. http://dx.doi.org/10.3390/antiox11112092.

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Hypoxia, or insufficient oxygen availability is a common feature in the development of a myriad of cardiovascular-related conditions including ischemic disease. Hydrogen sulphide (H2S) donors, such as sodium thiosulphate (STS), are known for their cardioprotective properties. However, H2S due to its gaseous nature, is released and cleared rapidly, limiting its potential translation to clinical settings. For the first time, we developed and characterised liposome formulations encapsulating STS and explored their potential for modulating STS uptake, H2S release and the ability to retain pro-angi

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Zhang, Ying, Haijing Qu, and Xiangdong Xue. "Blood–brain barrier penetrating liposomes with synergistic chemotherapy for glioblastoma treatment." Biomaterials Science 10, no. 2 (2022): 423–34. http://dx.doi.org/10.1039/d1bm01506k.

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A temozolomide and pro-apoptotic peptide co-loading liposome with blood–brain barrier penetrating capability exhibits highly synergistic and effective anti-tumor effect on both subcutaneous and intracranial glioblastoma mouse models.

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Lu, Yuan, Dankui Liao, Xuezhen Feng, et al. "Development and Adsorption Characterization of Metal Affinity-Immobilized Magnetic Liposome." Journal of Nanomaterials 2020 (February 11, 2020): 1–8. http://dx.doi.org/10.1155/2020/8731360.

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A metal affinity-immobilized magnetic liposome (MA-IML) was prepared in this research, which was with lipid and Ni2+ content of 143.25 μg/mg and 32 μmol/mg, respectively. The antihypertensive peptides Ile-Pro-Pro (IPP) and Val-Pro-Pro (VPP) could be adsorbed onto MA-IML under specific conditions, and the adsorption kinetics was explored. The pseudo-second-order kinetics (R2 value>0.98) was more suitable to describe the adsorption process of IPP and VPP than the intraparticle diffusion model and pseudo-first-order kinetic model. The results indicated that MA-IML could be used as an adsorbent

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An, Duopeng, Xiaochen Yu, Lijing Jiang, et al. "Reversal of Multidrug Resistance by Apolipoprotein A1-Modified Doxorubicin Liposome for Breast Cancer Treatment." Molecules 26, no. 5 (2021): 1280. http://dx.doi.org/10.3390/molecules26051280.

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Multidrug resistance (MDR) remains a major problem in cancer therapy and is characterized by the overexpression of p-glycoprotein (P-gp) efflux pump, upregulation of anti-apoptotic proteins or downregulation of pro-apoptotic proteins. In this study, an Apolipoprotein A1 (ApoA1)-modified cationic liposome containing a synthetic cationic lipid and cholesterol was developed for the delivery of a small-molecule chemotherapeutic drug, doxorubicin (Dox) to treat MDR tumor. The liposome-modified by ApoA1 was found to promote drug uptake and elicit better therapeutic effects than free Dox and liposome

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Kundawala, Aliasgar J., Khushbu S. Chauhan, Harsha V. Patel, and Swati K. Kurtkoti. "Inhalable Spray Dried Pro-Liposome Powder Containing Budesonide for Pulmonary Delivery." International Journal of Pharmaceutical Sciences and Nanotechnology 14, no. 4 (2021): 5538–48. http://dx.doi.org/10.37285/ijpsn.2021.14.4.3.

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Budesonide is an anti-asthmatic agent which is used to control the symptoms of asthma like bronchospasm, oedema. Drug delivered to lung through inhalation will provide systemic and local drug delivery at lower dose in chronic and acute diseases. Dry powder inhalers are the best choice for targeting the anti-asthmatic drugs through pulmonary route. The objective of the present study is to prepare inhalable lipid coated budesonide microparticles by spray drying method so effective delivery of budesonide to the lungs can be achieved. The microparticles in the form of dry powder were obtained by e

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Gaspar, Maria Manuela, Oliviero Gobbo, and Carsten Ehrhardt. "Generation of liposome aerosols with the Aeroneb Pro and the AeroProbe nebulizers." Journal of Liposome Research 20, no. 1 (2010): 55–61. http://dx.doi.org/10.3109/08982100903085150.

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Gaspar, Maria Manuela, Oliviero Gobbo, and Carsten Ehrhardt. "Generation of liposome aerosols with the Aeroneb Pro and the AeroProbe nebulizers." Journal of Liposome Research 00, no. 00 (2009): 090706063146008–7. http://dx.doi.org/10.1080/08982100903085150.

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Thèses sur le sujet "Pro-liposome"

Tshanga, Siphokazi Sisanda. "Antibacterial activity of liposome encapsulated cyclo(TYR-PRO)." Thesis, Nelson Mandela Metropolitan University, 2011. http://hdl.handle.net/10948/1450.

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Cyclic dipeptides (CDPs) are amino acid-based compounds, some of which possess antibacterial activity. The encapsulation of certain drugs into liposomes has been found to improve their activity in terms of bioavailability and duration of action. Liposomes are small vesicles that are under investigation as drug carriers for the delivery of therapeutic agents. A number of liposome formulations are currently under clinical trial review, whilst some have already been approved for clinical use. The aim of this study was to optimize a liposomal cyclo(Tyr-Pro) formulation and to assess its antibacter

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Moon, Taylor J. "Development of a Dual-Agonist Immunostimulatory Nanoparticle to Trigger Interferon β-Driven Anti-Tumor Immunity". Case Western Reserve University School of Graduate Studies / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1607349015331713.

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Actes de conférences sur le sujet "Pro-liposome"

Takahashi, Atsushi, Kousuke Hiromori, Naomi Shibasaki-Kitakawa, and Ryota Takahashi. "Quantitative Evaluation of Oxidative Stability of Biomembrane Lipids in the Presence of Vitamin E." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/zlem3137.

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In this report, the oxidation of biomembranelipids, phospholipid (LH) and cholesterol (ChH), was examined experimentally in the presence of vitamin E (VEH) by using a liposome system, which is widely used as a biomembrane model. A kinetic model was constructed by taking into account mechanisms of antioxidation and pro-oxidation by VEH and the co-oxidation mechanisms of biomembrane lipids reported previously (Takahashi et al., 2016). The model constants for VEH-related reactions were estimated based on the experimental results. The model quantitatively described the concentration profiles of LH

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