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Abstract

A Thermoresponsive Injectable Microparticles/Hydrogel Drug Delivery System for Cancer Treatment †

by
Henrique Carrêlo
,
Paula I. P. Soares
,
João Paulo Borges
and
Maria Teresa Cidade
*
CENIMAT/i3N, Materials Science Department, Nova School of Sciences and Technology, New University of Lisbon, 2829-516 Caparica, Portugal
*
Author to whom correspondence should be addressed.
Presented at the Materials 2022, Polytechnic of Leiria, Marinha Grande, Portugal, 10–13 April 2022.
Mater. Proc. 2022, 8(1), 140; https://doi.org/10.3390/materproc2022008140
Published: 27 July 2022
(This article belongs to the Proceedings of MATERIAIS 2022)
Drug delivery systems (DDS) are systems that aim to deliver drugs/bioactive agents to the human body in a controllable and sustainable way. Microparticles are structures that have been intensively studied as DDS in several studies within the biomedical field. However, microparticles suffer from early burst release and a great amount of their cargo is released in a short period. The incorporation of the microparticles within a thermoresponsive hydrogel to form an injectable DDS is a viable way that can prolong the release of the particles’ content [1]. Since the hydrogel will form a barrier between the particles and the in vivo environment, the cargo will need to pass through these two barriers to be released. It is known that the particles will affect the transition temperature of thermoresponsive particles/hydrogel systems [1]. The transition temperature of the DDS should be between 24 °C (above the operating room temperature) and 36 °C (below body temperature of 37 °C) to assure that the system is in the sol state at the operating room temperature and in the gel state within the body. In this study, particles made with alginate and gellan gum were produced via co-axial air flow and then mixed with a Pluronic F127:F68 solution (20 wt%; 16:4). The effect of the particles content was analyzed. A rheological evaluation with oscillatory temperature ramps was carried out to determine the transition temperature of the DDS. The results showed that these systems are suitable for injectable thermoresponsive DDS for biomedical treatments.

Author Contributions

Conceptualization, H.C., P.I.P.S. and M.T.C.; methodology, H.C.; validation, P.I.P.S., J.P.B. and M.T.C.; writing—original draft preparation, H.C.; writing—review and editing, All.; supervision, P.I.P.S., J.P.B. and M.T.C.; funding acquisition, All. All authors have read and agreed to the published version of the manuscript.

Funding

This work is co-financed by FEDER, European funds, through the COMPETE 2020 POCI and PORL, National Funds through FCT—Portuguese Foundation for Science and Technology and POR Lisboa 2020, under the project POCI-01-0145-FEDER-007688, reference UIDB/50025/2020-2023, and project DREaMM, reference PTDC/CTM-CTM/30623/2017. H.C. and P.S. also acknowledge FCT for the PhD grant with reference SFRH-BD-144986-2019 and the individual contract CEECIND.03189.2020, respectively.

Conflicts of Interest

The authors declare no conflict of interest.

Reference

  1. Carrêlo, H.; Soares, P.I.P.; Borges, J.P.; Cidade, M.T. Injectable composite systems based on microparticles in hydrogels for bioactive cargo controlled delivery. Gels 2021, 7, 147. [Google Scholar] [CrossRef] [PubMed]
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MDPI and ACS Style

Carrêlo, H.; Soares, P.I.P.; Borges, J.P.; Cidade, M.T. A Thermoresponsive Injectable Microparticles/Hydrogel Drug Delivery System for Cancer Treatment. Mater. Proc. 2022, 8, 140. https://doi.org/10.3390/materproc2022008140

AMA Style

Carrêlo H, Soares PIP, Borges JP, Cidade MT. A Thermoresponsive Injectable Microparticles/Hydrogel Drug Delivery System for Cancer Treatment. Materials Proceedings. 2022; 8(1):140. https://doi.org/10.3390/materproc2022008140

Chicago/Turabian Style

Carrêlo, Henrique, Paula I. P. Soares, João Paulo Borges, and Maria Teresa Cidade. 2022. "A Thermoresponsive Injectable Microparticles/Hydrogel Drug Delivery System for Cancer Treatment" Materials Proceedings 8, no. 1: 140. https://doi.org/10.3390/materproc2022008140

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