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用于定量壳聚糖纳米粒中与蜂胶共包封的氟康唑的高效液相色谱法验证

HPLC Method Validated for Quantification of Fluconazole Co-Encapsulated with Propolis Within Chitosan Nanoparticles.

作者信息

da Silva Jacqueline Teixeira, de Oliveira Matheus Gabriel, de Paula José Realino, Alves Suzana Ferreira, Pellegrini Flavio, Amaral Andre Correa

机构信息

Laboratory of Nano & Biotechnology, Instituto de Patologia Tropical E Saúde Pública, Universidade Federal de Goiás, Rua 235, s/ n, Setor Universitário, Goiânia, GO Brazil.

Faculty of Pharmacy, Universidade Federal de Goiás, Goiânia, GO Brazil.

出版信息

Indian J Microbiol. 2021 Sep;61(3):364-369. doi: 10.1007/s12088-021-00954-2. Epub 2021 Jun 16.

Abstract

UNLABELLED

Considering the cases of fungal resistance to classic antifungals, it is necessary to develop more efficient and innovative therapies capable of reversing this situation. Fluconazole is an antifungal frequently used in the treatment of mycosis and some fungi developed resistance to its mechanism of action. In this work, fluconazole and green propolis were co-encapsulated in chitosan nanoparticles to be explored in order to promote a synergistic effect to enhance its therapeutic efficacy. However, because of the complexity of the chemical composition of green propolis, it was necessary to develop a simple and precise methodology to quantify fluconazole in the formulation. High Efficiency Liquid Chromatography methodology was developed and validated following the Brazilian regulatory guidelines (ANVISA, RDC 166/2017) for the separation of co-eluted peaks of fluconazole and green propolis in the nanoparticle supernatant. Applying the method developed, it was possible to quantify fluconazole in the same sample containing propolis. Thus, the results allow to affirm that it is a specific test, effective, precise and robust, which helped to determine the efficiency of association of the compounds within the nanoparticle. The method can be applied to quantify compounds that have similar chromatographic retention times.

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1007/s12088-021-00954-2.

摘要

未标注

考虑到真菌对传统抗真菌药物产生耐药性的情况,有必要开发更有效、更具创新性的疗法来扭转这种局面。氟康唑是一种常用于治疗真菌病的抗真菌药物,一些真菌对其作用机制产生了耐药性。在这项研究中,氟康唑和绿蜂胶被共包封在壳聚糖纳米颗粒中进行探索,以促进协同效应,提高其治疗效果。然而,由于绿蜂胶化学成分的复杂性,有必要开发一种简单而精确的方法来定量制剂中的氟康唑。按照巴西监管指南(巴西国家卫生监督局,RDC 166/2017)开发并验证了高效液相色谱法,用于分离纳米颗粒上清液中氟康唑和绿蜂胶的共洗脱峰。应用所开发的方法,可以在含有蜂胶的同一样品中定量氟康唑。因此,结果表明这是一种特异性、有效、精确且稳健的测试,有助于确定纳米颗粒内化合物的结合效率。该方法可用于定量具有相似色谱保留时间的化合物。

补充信息

在线版本包含可在10.1007/s12088-021-00954-2获取的补充材料。

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