Sol-gel synthesis is commonly used to modify the surface of mesoporous silica nanoparticles (MSN) with organic groups through the co-condensation method. The template removal, and the site-controlled addition of organic groups and their partial occlusion inside the framework walls are still a challenge in the one-pot synthesis. Here, we optimize the synthesis of amino-modified MSN by the combination of efficient template removal methodology with the precise time of the amino precursor addition to achieve superb mesoporous material. The addition after the growth process produces a sample with a significantly higher amount of NH2 on the external surface when compared to the standard procedure. The template removal by reflux with isopropanol/H+ eliminated ca. 90% of cetyltrimethylammonium bromide (CTAB), and preserved the mechanical and thermal properties, even with thin walls (2.1 nm). The synthesized nanoparticles possess stability, appropriate size, and a positive surface. This makes them excellent nanocarriers, especially in the biomedical field.

Ftalocianinas (Pc) são compostos sintéticos de interesse em diversas áreas. Contudo, sua elevada hidrofobicidade favorece o indesejável processo de agregação em meio aquoso. Estudos realizados com a Pc de hidroxi-alumínio (AlPcOH) em diferentes misturas água/etanol (v/v) mostraram que esta encontra-se na forma monomérica em proporções de água inferiores a 30%. Em 40 e 50% água/etanol tem-se a formação de dímeros unidos por ligação hidrogênio ou em ponte Al-O-Al, enquanto que em porcentagens de água superiores a 60% o processo de agregação é complexo, envolvendo múltiplos equilíbrios e agregados de tamanhos grandes (tipo J).

Phthalocyanines (Pc) are synthetic compounds of interest in various fields. However, their high hydrophobicity promotes the undesirable aggregation process in aqueous media. Studies carried out with aluminum phthalocyanine hydroxide (AlPcOH) in different water/ethanol mixtures (v/v) have shown that in proportions of water lower than 30% the Pc is in the monomeric form. At 40 and 50% water/ethanol there was formation of dimers linked by hydrogen bonding or Al-O-Al bridged, while in percentages of water higher than 60% the aggregation process is complex, with multiple equilibria and higher-order aggregates (J-type).

In this work, the spectroscopic properties of 5,10,15,20-tetrakis(4-methoxyphenyl)porphyrin (TMPP) in solvents of different polarities and water/ethanol mixtures were studied by electronic absorption spectroscopy and resonance light scattering associated with statistical analysis. The molar absorption coefficient and emission maximum of TMPP were dependent on solvent polarity. In the water/ethanol mixture, TMPP remained monomeric up to 25% of water, when it reaches its critical aggregation percentage. Oblique head-to-tail aggregate was found at intermediate water content (35 - 55%), while formation of a J-type aggregate was observed at higher water content (> 60%).

The physicochemical properties (solubilization, structural organization and stability) of meso-tetrakis(p-methoxyphenyl)porphyrin (TMPP), a promising photosensitizer for photodynamic therapy, solubilized in polymeric micelles of tri-block copolymers PluronicTM P-123 and F-127, were studied. The formulations obtained by the solid dispersion method led to monomerization of TMPP in these copolymers. Solubility studies showed that P-123 solubilizes double the photosensitizer than F-127. The self-aggregation phenomenon was affected by the [TMPP]/[poloxamer] ratio and medium temperature. The decrease in the temperature of these systems promoted the formation of different kinds of TMPP aggregates intrinsically connected with the structural changes occurring in the micelles.