Análise comparativa de contagens de plaquetas entre metodologias de impedância e óptica em amostras de sangue de indivíduos hospitalizados / Comparative analysis of platelet count between electrical impedance and optical platelet count methods in blood samples from hospitalized individuals

Objetivo: Comparar resultados de contagens plaquetárias de indivíduos hospitalizados realizadas por impedância (PLT-I) e metodologia óptica fluorescente (PLT-O). Métodos: Em estudo retrospectivo, foram avaliados dados sequenciais arquivados de contagens plaquetárias de trezentos indivíduos adultos hospitalizados, incluindo casos de anemias microcíticas e hemolíticas, neoplasias hematológicas, entre outras doenças. Todos os casos continham contagens de plaquetas PLT-I e PLT-O realizadas no equipamento Sysmex XE-5000. Resultados: Não houve diferença significativa entre os valores de contagens plaquetárias entre a PLT-I e PLT-O (p=0,614). Quando avaliamos os valores de plaquetas entre diferentes grupos em relação às metodologias, não houve diferença entre as contagens plaquetárias naqueles com VCM abaixo de 80 fL (p=0,936), VCM abaixo de 70 (p=0,821), plaquetas abaixo de 100×109/L (p=0,369) e plaquetas abaixo de 50×109/L (p=0,314). Além disso, a correlação entre PLT-I e PLT-O foi forte. Conclusão: Os valores de contagens plaquetárias, provenientes de pacientes não saudáveis, realizadas no analisador XE-5000 pelos métodos óptico e impedância, mostraram forte correlação e boa concordância.

A simple HPLC method for the determination of halcinonide in lipid nanoparticles: development, validation, encapsulation efficiency, and in vitro drug permeation

ABSTRACT Halcinonide is a high-potency topical glucocorticoid used for skin inflammation treatments that presents toxic systemic effects. A simple and quick analytical method to quantify the amount of halcinonide encapsulated into lipid nanoparticles, such as polymeric lipid-core nanoparticles and solid lipid nanoparticles, was developed and validated regarding the drug's encapsulation efficiency and in vitro permeation. The development and validation of the analytical method were carried out using the high performance liquid chromatography with the UV detection at 239 nm. The validation parameters were specificity, linearity, precision and accuracy, limits of detection and quantitation, and robustness. The method presented an isocratic flow rate of 1.0 mL.min-1, a mobile phase methanol:water (85:15 v/v), and a retention time of 4.21 min. The method was validated according to international and national regulations. The halcinonide encapsulation efficiency in nanoparticles was greater than 99% and the in vitro drug permeation study showed that less than 9% of the drug permeated through the membrane, indicating a nanoparticle reservoir effect, which can reduce the halcinonide's toxic systemic effects. These studies demonstrated the applicability of the developed and validated analytical method to quantify halcinonide in lipid nanoparticles.