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Abstracts Book - IMRC 2018

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• SB1-O022 Invited Talk<br />

CYCLODEXTRIN-BASED SUPRAMOLECULAR STRCUTURES AS<br />

DRUG DELIVERY NANOSYSTMES<br />

Yareli Rojas Aguirre 1 , Patricia Guadarrama 1 , Manuel Alexis Torres Mena 1<br />

1 Instituto de Investigaciones en Materiales, Polímeros, Mexico.<br />

For the last decade, research in the drug delivery field was focused in the design<br />

and development of nanosized drug delivery systems (nano-DDS). Advanced drug<br />

delivery nanoplatforms displaying sophisticated structures and multiple functions<br />

rapidly emerged. Despite the large number of publications, the translation of these<br />

works to clinical applications has been scarce. It is time then to understand where<br />

we are and what can we do to exploit the potential of nanosciences and transform<br />

it into drug delivery technologies with tangible results. Some of the key aspects that<br />

have to be address to overcome the drawbacks that the field is facing are: simple<br />

structures obtained through feasible and scalable synthetic methods; the<br />

“excipientability” (feasibility of a material to be proven as excipient) of the materials<br />

comprising the structures; and the understanding of the interaction of the materials<br />

with the biological barriers that the system will encounter until reaching the target.<br />

This, combined with suitable chemical approaches can result in important progress.<br />

For instance, DDS by supramolecular design is gaining great attention because,<br />

through the control of dynamic and tunable non-covalent interactions, suitable<br />

carriers can be engineered. Under this context, here we present the synthesis of<br />

simple βcyclodextrin (βCD)-based supramolecular structures and the evaluation of<br />

their potential as nano-DDS, which is done through the study of their<br />

nanoproperties: size, topology and surface charge. The study of nanoproperties is<br />

fundamental as they will determine the nano-DDS behavior in systemic circulation,<br />

the extravasation and the ability to be internalized by specific cells. Thus, in this<br />

work, the βCD derivatives are modified with materials that are currently used in the<br />

pharmaceutical industry (i.e. polyethylenglycol) and are synthesized by click<br />

chemistry (that has demonstrated to be highly quantitative for our systems). The<br />

size, shape and charge are studied in media emulating physiological conditions.<br />

Finally, all the information is integrated to determine the potential of the βCD<br />

structures as nano-DDS.<br />

Acknowledgment: Instituto de Investigaciones en Materiales, Proyecto 1306<br />

Keywords: Nanomedicine, Cyclodextrin, Drug Delivery<br />

Presenting authors email: yarelirojas@gmail.com

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