Improving Riparin-A Dissolution through a Laponite Based Nanohybrid

Author:

Gomes Duanne Mendes1,Meirelles Lyghia Maria Araújo23,Araujo Paulo Monteiro1,de Sousa Rayran Walter Ramos4,Ferreira Paulo Michel Pinheiro4ORCID,Gutierrez Stanley Juan Chavez1,de Medeiros Maria das Graças Freire1,Raffin Fernanda Nervo5ORCID

Affiliation:

1. Post Program on Pharmaceutical Sciences, Federal University of Piauí—UFPI, Teresina 64049-550, Piauí, Brazil

2. Department of Pharmacy, Federal University of Piauí—UFPI, Teresina 64049-550, Piauí, Brazil

3. Health and Quality of Life Research Laboratory (LAPESQV), University Center Santo Agostinho—UNIFSA, Teresina 64049-550, Piauí, Brazil

4. Laboratory of Experimental Cancerology (LabCancer), Department of Biophysics and Physiology, Federal University of Piauí—UFPI, Teresina 64049-550, Piauí, Brazil

5. Post—Program on Development and Technological Innovation in Medications, Federal University of Rio Grande do Norte—UFRN, Natal 59012-570, Rio Grande do Norte, Brazil

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.

Publisher

MDPI AG

Subject

Pharmaceutical Science

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