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Abstracts Book - IMRC 2018

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• SB2-P005<br />

EFFECT OF MODIFICATION OF THE SURFACE OF MESOPOROUS<br />

SILICA IN THE ADSORTION-DESORTION OF GRISEOFULVINE<br />

Arlet Ariadne Rodriguez Castañeda 1 , Ma. del Carmen Salazar Hernández 1,2 , Mercedes Salazar<br />

Hernández 3 , Raul Miranda Avilés 3 , Agustín Hilario Rocha Ramírez 4<br />

1<br />

Instituto Politécnico Nacional - IPN, Materiales y Termofluidos, Mexico. 2 Universidad de<br />

Guanajuato, Minas, metalúrgica y geología, Mexico. 3 Universidad de Guanajuato, Minas,<br />

Metalurgia y Geologia, Mexico. 4 Instituto Politécnico Nacional - IPN, Biología, Mexico.<br />

Mesoporous silica (SM) is a material that has been used for the adsorption of<br />

different materials since it has a hollow matrix that is capable of retaining all<br />

types of molecules. This derives an interest in the pharmaceutical industry to<br />

use mesoporous silica as an excipient of drugs, since it has been shown that it<br />

is able to control the desorption of drugs, unlike traditional tablets. The control<br />

in the desorption of the drugs adsorbed in the MS is due to the interactions that<br />

the organic molecule has with the surface of the silica. In this work we study the<br />

modification of the surface of silica with different functional groups that can<br />

change the physicochemical properties regarding the adsorption and<br />

desorption of a model drug that is Griseofulvin. The MS synthesis is performed<br />

using the molecular sieve methodology. The obtained MS is modified with thiol<br />

(-S) and octyl (-R) groups by post-synthesis; the of the functional groups to the<br />

surface of the silica is observed by infrared spectroscopy and the percentage of<br />

modification is quantified by gravimetry. Griseofulvin is adsorbed on silica and<br />

the amount of drug adsorbed by gravimetry is quantified; the desorption<br />

kinetics is studied at 37 o C at a pH of 7, which simulates the physiological<br />

conditions of adsorption in the duodenum. As results, the effect of the<br />

functional group on the pharmacokinetics of SiO2/Griseofulvin is demonstrated.<br />

Acknowledgment:<br />

The authors wish to acknowledge the financial support of the Instituto<br />

Politécnico Nacional through grants SIP-<strong>2018</strong>1395.<br />

Keywords: Mesoporous silica, Drug deliver, Griseofulvin<br />

Presenting authors email: arletrdz@hotmail.com

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