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1.
Int J Nanomedicine ; 17: 1139-1154, 2022.
Article in English | MEDLINE | ID: mdl-35321027

ABSTRACT

Background: The search for new formulations for photodynamic therapy is intended to improve the outcome of skin cancer treatment using significantly reduced doses of photosensitizer, thereby avoiding side effects. The incorporation of photosensitizers into nanoassemblies is a versatile way to increase the efficiency and specificity of drug delivery into target cells. Herein, we report the loading of rose bengal into vesicle-like constructs of amphiphilic triazine-carbosilane dendrons (dendrimersomes) as well as biophysical and in vitro characterization of this novel nanosystem. Methods: Using established protocol and analytical and spectroscopy techniques we were able to synthesized dendrons with strictly designed properties. Engaging biophysical methods (hydrodynamic diameter and zeta potential measurements, analysis of spectral properties, transmission electron microscopy) we confirmed assembling of our nanosystem. A set of in vitro techniques was used for determination ROS generation, (ABDA and H2DCFDA probes), cell viability (MTT assay) and cellular uptake (flow cytometry and confocal microscopy). Results: Encapsulation of rose bengal inside dendrimersomes enhances cellular uptake, intracellular ROS production and concequently, the phototoxicity of this photosensitizer. Conclusion: Triazine-carbosilane dendrimersomes show high capacity as drug carriers for anticancer photodynamic therapy.


Subject(s)
Carcinoma , Rose Bengal , Humans , Rose Bengal/chemistry , Rose Bengal/pharmacology , Silanes/pharmacology , Triazines/pharmacology
2.
Org Biomol Chem ; 18(47): 9639-9652, 2020 12 21.
Article in English | MEDLINE | ID: mdl-33206746

ABSTRACT

New amphiphilic carbosilane dendrons with pH-dependent behaviour based on the presence of carboxylate (propionate or succinate) groups at their peripheries and a fatty acid at the focal point were developed. In the presence of salts, they were able to form micelles with critical aggregation concentrations increasing with increasing dendron generation. Their thermodynamic parameters were calculated from surface tension measurements and their diameters at different pHs were measured by dynamic light scattering. These micelles were stable at basic pH but degraded under acidic conditions. No significant differences were found for the propionate and succinate based dendron micelles at basic or acidic pH, but the succinate dendron assemblies were more stable at neutral pH. The properties of these systems as drug nano-carriers were studied using both hydrophilic and hydrophobic molecules, and the drug loading varied with the structure and charge of the drug. In addition, due to the presence of multiple negative charges, the dendrons exhibited anti-HIV activity. Higher generation dendrons with more peripheral carboxylates that were not assembled into micelles were more active than micelles composed of lower generation dendrons having fewer peripheral carboxylates.


Subject(s)
Silanes
3.
Dalton Trans ; 44(44): 19294-304, 2015 Nov 28.
Article in English | MEDLINE | ID: mdl-26489707

ABSTRACT

A series of novel water-soluble ammonium-terminated carbosilane dendrons containing a ferrocene unit at the focal point were synthesized, in order to combine the unique redox activity of ferrocene and the precisely designed structure of the dendrons with the aim to evaluate them as a new class of potential organometallic-based antibacterial compounds. The synthetic route is based on the initial amination of ferrocenecarboxaldehyde with carbosilane dendrons that contain allyl groups on the surface followed by reduction of the in situ prepared imine product, and the subsequent functionalization of the periphery with terminal amine groups by hydrosilylation reactions. Systems quaternized with HCl are soluble and stable in water or other protic solvents. The obtained compounds were spectrally and electrochemically (cyclic voltammetry) characterized, and diffusion-ordered spectroscopy experiments were conducted to determine the size of the dendritic wedges in solution. The antibacterial activity of these compounds was evaluated using Gram-positive bacteria (Staphylococcus aureus) and Gram-negative bacteria (Escherichia coli), which shows that the first and second generations of cationic dendrons are broad spectrum antibacterial agents, i.e. selective and effective in both bacterial strains.


Subject(s)
Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/pharmacology , Ferrous Compounds/chemistry , Organometallic Compounds/chemical synthesis , Organometallic Compounds/pharmacology , Silanes/chemistry , Ammonium Compounds/chemistry , Electrochemical Techniques , Escherichia coli/drug effects , Metallocenes , Microbial Sensitivity Tests , Solubility , Staphylococcus aureus/drug effects
4.
Org Biomol Chem ; 9(14): 5238-48, 2011 Jul 21.
Article in English | MEDLINE | ID: mdl-21629893

ABSTRACT

A new family of amine- and ammonium-terminated hyperbranched polycarbosilanes (PCS) and dendrimers has been synthesized. The functionalization of a polycarbosilane matrix was carried out with peripheral allyl groups by two strategies in the case of PCS: 1) hydrosilylation of allyl amines with PCS containing terminal Si-H bonds, or 2) hydrosilylation of PCS-allyl with an aminosilane. Dendrimers with terminal amine groups were synthesized by hydrosilylation of allydimethylamine. Quaternized systems with MeI are soluble and stable in water or other protic solvent. The antibacterial properties of the ammonium-terminated hyperbranched polycarbosilanes and dendrimers have been evaluated showing that they act as potent biocides against Gram-positive and Gram-negative bacterial strains.


Subject(s)
Anti-Bacterial Agents/pharmacology , Escherichia coli/drug effects , Polymers/pharmacology , Quaternary Ammonium Compounds/pharmacology , Silanes/pharmacology , Staphylococcus aureus/drug effects , Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/chemistry , Dendrimers/chemical synthesis , Dendrimers/chemistry , Dendrimers/pharmacology , Microbial Sensitivity Tests , Molecular Structure , Polymers/chemical synthesis , Polymers/chemistry , Quaternary Ammonium Compounds/chemical synthesis , Quaternary Ammonium Compounds/chemistry , Silanes/chemical synthesis , Silanes/chemistry , Stereoisomerism
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