RESUMO
The assessment of ricinoleic acid (RA) incorporated into polymeric nanoparticles is a challenge that has not yet been explored. This bioactive compound, the main component of castor oil, has attracted attention in the pharmaceutical field for its valuable anti-inflammatory, antifungal, and antimicrobial properties. This work aims to develop a new and simple analytical method using high-performance liquid chromatography with diode-array detection (HPLC-DAD) for the identification and quantification of ricinoleic acid, with potential applicability in several other complex systems. The method was validated through analytical parameters, such as linearity, limit of detection and quantification, accuracy, precision, selectivity, and robustness. The physicochemical properties of the nanocapsules were characterized by dynamic light scattering (DLS) to determine their hydrodynamic mean diameter, polydispersity index (PDI), and zeta potential (ZP), via transmission electron microscopy (TEM) and quantifying the encapsulation efficiency. The proposed analytical method utilized a mobile phase consisting of a 65:35 ratio of acetonitrile to water, acidified with 1.5% phosphoric acid. It successfully depicted a symmetric peak of ricinoleic acid (retention time of 7.5 min) for both the standard and the RA present in the polymeric nanoparticles, enabling the quantification of the drug loaded into the nanocapsules. The nanocapsules containing ricinoleic acid (RA) exhibited an approximate size ranging from 309 nm to 441 nm, a PDI lower than 0.2, ζ values of approximately -30 mV, and high encapsulation efficiency (~99%). Overall, the developed HPLC-DAD procedure provides adequate confidence for the identification and quantification of ricinoleic acid in PLGA nanocapsules and other complex matrices.
RESUMO
This paper reports on a preliminary evaluation of the grain size distribution of cadmium, lead and copper in sediment from Catarina Beach, Ilha Solteira, in the state of São Paulo, Brazil. Surface sediments were fractionated with <63 microm nylon sieves and subjected to three digestion procedures: the proposed open digestion, the standard USEPA-3050B and closed digestion in a Teflon tube. The metals were determined by atomic absorption spectrometry. The results of the three procedures showed no significant differences. The 309 mg Kg1 concentration of copper found at the P3 sampling point exceeded the PEL (probable effect level) value of 197 mg Kg1, which represents an environmental hazard to aquatic organisms. The sediments organic matter content determined by the loss on ignition was 6.8, 1.7 and 0.6% in the P3, P1 and P2 samples, respectively. The distribution of metal concentrations in sieved sediment followed the order P3 < P2 < P1 thereby suggesting an interaction with organic matter.