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Improving Riparin-A Dissolution through a Laponite Based Nanohybrid.
Gomes, Duanne Mendes; Meirelles, Lyghia Maria Araújo; Araujo, Paulo Monteiro; de Sousa, Rayran Walter Ramos; Ferreira, Paulo Michel Pinheiro; Gutierrez, Stanley Juan Chavez; de Medeiros, Maria das Graças Freire; Raffin, Fernanda Nervo.
Afiliação
  • Gomes DM; Post Program on Pharmaceutical Sciences, Federal University of Piauí-UFPI, Teresina 64049-550, Piauí, Brazil.
  • Meirelles LMA; Department of Pharmacy, Federal University of Piauí-UFPI, Teresina 64049-550, Piauí, Brazil.
  • Araujo PM; Health and Quality of Life Research Laboratory (LAPESQV), University Center Santo Agostinho-UNIFSA, Teresina 64049-550, Piauí, Brazil.
  • de Sousa RWR; Post Program on Pharmaceutical Sciences, Federal University of Piauí-UFPI, Teresina 64049-550, Piauí, Brazil.
  • Ferreira PMP; Laboratory of Experimental Cancerology (LabCancer), Department of Biophysics and Physiology, Federal University of Piauí-UFPI, Teresina 64049-550, Piauí, Brazil.
  • Gutierrez SJC; Laboratory of Experimental Cancerology (LabCancer), Department of Biophysics and Physiology, Federal University of Piauí-UFPI, Teresina 64049-550, Piauí, Brazil.
  • de Medeiros MDGF; Post Program on Pharmaceutical Sciences, Federal University of Piauí-UFPI, Teresina 64049-550, Piauí, Brazil.
  • Raffin FN; Post Program on Pharmaceutical Sciences, Federal University of Piauí-UFPI, Teresina 64049-550, Piauí, Brazil.
Pharmaceutics ; 15(8)2023 Aug 14.
Article em En | MEDLINE | ID: mdl-37631350
ABSTRACT
(1)

Background:

Riparin-A presents several pharmacological activities already elucidated, such as antimicrobial modulator, antileishmania, anxiolytic, anti-inflammatory, antinociceptive, and antioxidant. Even with important bioactive effects, the applicability of Riparin-A is limited due to its low solubility in water, impairing its dissolution in biological fluids. Thus, the objective of this study was to develop a nanohybrid based on Riparin-A and Laponite to obtain a better dissolution profile and evaluate its cytotoxic potential. (2)

Methods:

The formation of a hybrid system was highlighted by X-ray powder diffraction, infrared spectroscopy, and thermal analysis. Solubility, dissolution, and cytotoxicity studies were performed; (3)

Results:

An increase in the solubility and aqueous dissolution rate of Riparin-A was observed in the presence of clay. Diffractometric analysis of the hybrid system suggests the amorphization of Riparin-A, and thermal analyses indicated attenuation of decomposition and melting of the Riparin-A after interaction with clay. Furthermore, the nanosystem did not exhibit cytotoxic activity on normal and tumorigenic lines. (4)

Conclusions:

These results are promising for the development of the Riparin-A/Laponite nanosystem for therapeutic purposes, suggesting an increase in the range of possible routes of administration and bioavailability of this bioactive compound.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Pharmaceutics Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Pharmaceutics Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil