TY - JOUR
T1 - Dual-stimuli-responsive poly(vinyl alcohol) nanofibers for localized cancer treatment
T2 - Magnetic hyperthermia and drug release studies
AU - Gonçalves, Adriana
AU - Cabrita, Raquel
AU - Matos, Joana
AU - Rodrigues, Inês
AU - Vieira, Tânia
AU - Borges, João Paulo
AU - Soares, Paula I. P.
N1 - info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50025%2F2020/PT#
info:eu-repo/grantAgreement/FCT//2021.06558.BD/PT#
Funding Information:
DSC analysis was performed to study the effect of crosslinking degree on the crystallinity of PVA fibers. DSC recordings were taken between 25 and 250 °C since, at higher temperatures, PVA degrades, as seen in the results of the TG analysis. Fig. 7 (E) shows the DSC thermograms of non-crosslinked PVA, and PVA heat-treated for 10 min, 2 h, 8 h, and PVA crosslinked with GA 3 % for 20 min. It is possible to observe endothermic peaks in a range between 208 and 215 °C, corresponding to each sample's melting temperatures (Tm). The heat of melting (ΔH) and degree of crystallinity were calculated for each sample, where ΔH corresponds to the integration of the area under the melting peak. By dividing the heat of melting by the heat needed to melt a 100 % crystalline PVA sample (ΔHc = 138 J g−1) [42], the degree of crystallinity of each sample was calculated. Non-crosslinked PVA fibers have a crystallinity of 46 %. In general, a decrease in the degree of crystallinity was observed after heat treatment. Furthermore, it was found that increasing the heating time slightly increased the degree of crystallinity. The lowest degree of crystallinity (35 %) was observed for PVA fibers heated for 8 h. These results agree with FTIR results, where there was also lower crystallinity for the sample heated for 8 h. Furthermore, these results support the SEM images (Fig. 3), where there was higher water stability in fibers heat-treated for 8 h.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 Lisboa2020, under the projects PIDDAC (POCI-01-0145-FEDER-007688) and PTDC/CTMCTM/30623/2017 (DREaMM). P.S. and A.G. also acknowledge the individual contract CEECIND.03189.2020.
Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2024/4
Y1 - 2024/4
N2 - Smart materials are a promising option for a more personalized cancer treatment approach. In particular, materials that can respond to an external stimulus may be manipulated to provide a tailored response when and where it is needed. This work confined thermoresponsive poly (N-isopropyl acrylamide) microgels and superparamagnetic iron oxide nanoparticles into poly (vinyl alcohol) nanofibrous membranes. Physical and chemical crosslinking methods were tested to obtain membranes stable in physiological environments for long-term applications, and their effect on the membranes' morphology, swelling, and mechanical properties was evaluated. The results demonstrated that thermal crosslinking for 10 min is enough to obtain a robust membrane for biomedical applications that retain their components' magnetic and thermal responses. The swelling degree decreases with the increase of crosslinking time and is even smaller for chemically crosslinked membranes. Similarly, a high crosslinking degree is associated with more brittle membranes than ductile membranes with thermal crosslinking. Drug delivery assays using doxorubicin as a model drug demonstrated that only membranes with a smaller crosslinking degree are suitable for drug delivery purposes, with about 10 % of doxorubicin released for 15 days. Additionally, magnetic hyperthermia assays showed that composite membranes can increase the surrounding temperature by 10 °C in only 10 min of applying an alternating magnetic field. This work demonstrates the potential of combining stimuli-responsive materials using a simple, low-cost, and easily scalable technique (electrospinning) to produce smart materials for biomedical applications.
AB - Smart materials are a promising option for a more personalized cancer treatment approach. In particular, materials that can respond to an external stimulus may be manipulated to provide a tailored response when and where it is needed. This work confined thermoresponsive poly (N-isopropyl acrylamide) microgels and superparamagnetic iron oxide nanoparticles into poly (vinyl alcohol) nanofibrous membranes. Physical and chemical crosslinking methods were tested to obtain membranes stable in physiological environments for long-term applications, and their effect on the membranes' morphology, swelling, and mechanical properties was evaluated. The results demonstrated that thermal crosslinking for 10 min is enough to obtain a robust membrane for biomedical applications that retain their components' magnetic and thermal responses. The swelling degree decreases with the increase of crosslinking time and is even smaller for chemically crosslinked membranes. Similarly, a high crosslinking degree is associated with more brittle membranes than ductile membranes with thermal crosslinking. Drug delivery assays using doxorubicin as a model drug demonstrated that only membranes with a smaller crosslinking degree are suitable for drug delivery purposes, with about 10 % of doxorubicin released for 15 days. Additionally, magnetic hyperthermia assays showed that composite membranes can increase the surrounding temperature by 10 °C in only 10 min of applying an alternating magnetic field. This work demonstrates the potential of combining stimuli-responsive materials using a simple, low-cost, and easily scalable technique (electrospinning) to produce smart materials for biomedical applications.
KW - Drug delivery
KW - Magnetic hyperthermia
KW - Poly(vinyl alcohol) nanofibers
KW - Thermal crosslinking
UR - http://www.scopus.com/inward/record.url?scp=85185793438&partnerID=8YFLogxK
U2 - 10.1016/j.jddst.2024.105492
DO - 10.1016/j.jddst.2024.105492
M3 - Article
AN - SCOPUS:85185793438
SN - 1773-2247
VL - 94
JO - Journal of Drug Delivery Science and Technology
JF - Journal of Drug Delivery Science and Technology
M1 - 105492
ER -