Physicochemical characterization of a lycopene-loaded mesoporous silica nanoparticle formulation

Author:

Carvalho Gabriela Corrêa1,Marena Gabriel Davi2,Nascimento André Luiz Carneiro Soares do2,Camargo Bruna Almeida Furquim2,Sábio Rafael Miguel2,Lourenço Felipe Rebello3,Santos Hélder A.4,Chorilli Marlus2

Affiliation:

1. School of Pharmaceutical Sciences, São Paulo State University (UNESP), 14800-903 Araraquara, Brazil; Department of Biomedical Engineering, University Medical Center Groningen, University of Groningen Ant. Deusinglaan 1, Groningen 9713 AV, The Netherlands; W.J. Kolff Institute for Biomedical Engineering and Materials Science, University Medical Center Groningen, University of Groningen Ant. Deusinglaan 1, Groningen 9713 AV, The Netherlands

2. School of Pharmaceutical Sciences, São Paulo State University (UNESP), 14800-903 Araraquara, Brazil

3. Faculty of Pharmaceutical Sciences, University of São Paulo (USP), 05508-000 São Paulo, Brazil

4. Department of Biomedical Engineering, University Medical Center Groningen, University of Groningen Ant. Deusinglaan 1, Groningen 9713 AV, The Netherlands; W.J. Kolff Institute for Biomedical Engineering and Materials Science, University Medical Center Groningen, University of Groningen Ant. Deusinglaan 1, Groningen 9713 AV, The Netherlands; Drug Research Program, Division of Pharmaceutical Chemistry and Technology, Faculty of Pharmacy, University of Helsinki, FI-00014 Helsinki, Finland

Abstract

Abstract Lycopene (LYC), a carotenoid extracted mainly from tomatoes, has several biological properties, making its use desirable as a nutraceutical and pharmaceutical active ingredient. However, the use of LYC in therapy has limitations related to its solubility and stability. In this study, mesoporous silica nanoparticles (MSNs) are used to load and protect LYC from degradation. The exact amount of drug incorporated was determined by analytical techniques, such as high performance liquid chromatography (HPLC) and thermal analysis. For this we developed and validated an HPLC method for LYC quantification and evaluated the LYC impregnated in MSNs, followed by thermogravimetry analysis (TGA) technique analysis. Differential scanning calorimetry (DSC) was also used in order to confirm drug incorporation. Additionally, an in vitrorelease study was also carried out. The HPLC method was duly validated for the range of 26–125 µg/mL and proved to be suitable for LYC quantification. DSC measurements suggest an improvement in the stability of the impregnated drug, which was reinforced by the release assay. Overall, the developed method is suitable to test LYC-loaded porous materials to enable the use in therapeutic applications.

Publisher

Research Square Platform LLC

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