Next Article in Journal
Oncogenomics as a Therapeutic Approach in Anaplastic Thyroid Carcinoma: A Literature Review
Previous Article in Journal
Prion Diseases and the Brain: A Narrative Review of Region-Specific Neurodegeneration in Transmissible Spongiform Encephalopathies
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Abstract

Innovative Biomaterial-Based Therapies Accelerate Wound Regeneration and Modulate Inflammation in Diabetic Mice †

by
Gildemar José Bezerra Crispim
1,2,*,
Gabriella de Oliveira Silva
1,2,
Graziela Anselmo Joanitti
2,
Cleia Abrantes da Silva
3,
Amilcar Sabino Damazo
3 and
Marcela Lemos Brettas Carneiro
1,2
1
Department of Nanoscience and Nanobiotechnology, Institute of Biology, University of Brasília, UnB, Brasília 70910-900, Brazil
2
Laboratory of Bioactive Compounds and Nanobiotechnology, University of Brasília, UnB, Brasília 70910-900, Brazil
3
Histology Laboratory, The School of Medicine, University of Brasília, UnB, Brasília 70910-900, Brazil
*
Author to whom correspondence should be addressed.
Presented at the 6th International Congress on Health Innovation—INOVATEC 2025, Hybrid, 21–23 November 2025.
Proceedings 2026, 137(1), 76; https://doi.org/10.3390/proceedings2026137076
Published: 2 March 2026
(This article belongs to the Proceedings of The 6th International Congress on Health Innovation—INOVATEC 2025)
Introduction: Diabetes is a major clinical challenge due to delayed tissue repair, persistent inflammation, and high risk of infection. Innovative strategies that integrate biomaterials, nanotechnology, and phototherapy have shown promise in accelerating healing and improving tissue organization. The local effects of natural latex biomembranes (NLB), enriched or not with curcumin and annatto nanoemulsions (CuraTex) and combined with blue LED phototherapy, on wound healing and tissue regeneration in diabetic mice was evaluated. Methodology: Male Balb/c mice with streptozotocin-induced diabetes were subjected to full-thickness wounds infected with Staphylococcus aureus and treated for 14 days with saline (negative control), antibacterial ointment (positive control), blue LED, NLB + LED, CuraTex, CuraTex + LED, or nanoemulgel + LED. Treatments were applied every 48 h with 5 min phototherapy sessions. Wound closure was analyzed digitally, and histological assessments evaluated tissue organization and inflammation. All procedures followed ethical guidelines and were approved by the Research Ethics Committee (protocol nº 23106.029983/2024-69). Results: Control groups showed incomplete healing and persistent inflammation. Blue LED alone improved contraction, while NLB + LED enhanced stability. CuraTex + LED promoted faster, more homogeneous closure, better histological organization, and greater modulation of inflammation. Conclusions: The combination of CuraTex and blue LED phototherapy accelerated regeneration and reduced inflammation in diabetic wounds, demonstrating a smart, biocompatible, and cost-effective approach for chronic wound management.

Author Contributions

G.J.B.C. contributed to conceptualization, methodology, investigation, data curation, formal analysis, visualization, and writing original draft. G.d.O.S. contributed to investigation, methodology, data curation, and writing review and editing. G.A.J. contributed to methodology, resources, supervision, and writing review and editing. M.L.B.C. contributed to conceptualization, supervision, funding acquisition, project administration, and writing review and editing. A.S.D. and C.A.d.S. contributed to histopathological analysis, validation, and writing review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Research Support Foundation of the Federal District (FAPDF), process n° 00193.00002360/2022-11, and by the Coordination for the Improvement of Higher Education Personnel (CAPES), Finance Code 001.

Institutional Review Board Statement

The animal study protocol was approved by the Ethics Committee on Animal Use (CEUA) of University of Brasília, under protocol number 23106.029983/2024-69, in accordance with national legislation and international guidelines for the care and use of laboratory animals.

Informed Consent Statement

Not applicable. This study did not involve human participants.

Data Availability Statement

The data presented in this study are available on request from the corresponding author. The data are not publicly available due to institutional restrictions.

Conflicts of Interest

The authors declare no conflict of interest.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Crispim, G.J.B.; Silva, G.d.O.; Joanitti, G.A.; Silva, C.A.d.; Damazo, A.S.; Carneiro, M.L.B. Innovative Biomaterial-Based Therapies Accelerate Wound Regeneration and Modulate Inflammation in Diabetic Mice. Proceedings 2026, 137, 76. https://doi.org/10.3390/proceedings2026137076

AMA Style

Crispim GJB, Silva GdO, Joanitti GA, Silva CAd, Damazo AS, Carneiro MLB. Innovative Biomaterial-Based Therapies Accelerate Wound Regeneration and Modulate Inflammation in Diabetic Mice. Proceedings. 2026; 137(1):76. https://doi.org/10.3390/proceedings2026137076

Chicago/Turabian Style

Crispim, Gildemar José Bezerra, Gabriella de Oliveira Silva, Graziela Anselmo Joanitti, Cleia Abrantes da Silva, Amilcar Sabino Damazo, and Marcela Lemos Brettas Carneiro. 2026. "Innovative Biomaterial-Based Therapies Accelerate Wound Regeneration and Modulate Inflammation in Diabetic Mice" Proceedings 137, no. 1: 76. https://doi.org/10.3390/proceedings2026137076

APA Style

Crispim, G. J. B., Silva, G. d. O., Joanitti, G. A., Silva, C. A. d., Damazo, A. S., & Carneiro, M. L. B. (2026). Innovative Biomaterial-Based Therapies Accelerate Wound Regeneration and Modulate Inflammation in Diabetic Mice. Proceedings, 137(1), 76. https://doi.org/10.3390/proceedings2026137076

Article Metrics

Back to TopTop