TY - JOUR
T1 - Nano-in-microparticles approach
T2 - targeted gastric ulcer therapy using trans-resveratrol nanoparticles encapsulated in hyaluronic acid and alginate microparticles
AU - Spósito, Larissa
AU - Morais-Silva, Gessynger
AU - Fonseca, Diana
AU - Neves, Matheus Morais
AU - Vieira Silva, Murilo
AU - Bauab, Taís Maria
AU - Parreira, Paula
AU - Martins, M. Cristina L.
AU - Meneguin, Andréia Bagliotti
AU - Chorilli, Marlus
N1 - Publisher Copyright:
© 2025
PY - 2025/5/1
Y1 - 2025/5/1
N2 - Gastric ulcers affect 4 million people worldwide and occur when the stomach's defenses are compromised, allowing harmful agents, such as nonsteroidal anti-inflammatory drugs and Helicobacter pylori, to damage the tissue. The naturally occurring polyphenol, trans-resveratrol (RESV), demonstrates promising potential for treating gastric diseases. However, its therapeutic application is limited by its photosensitivity and solubility. To overcome these challenges, RESV was encapsulated in a new nano-in-microparticle system comprised of chitosan nanoparticles incorporated into hyaluronic acid and alginate microparticles (RESV-MNP). RESV-MNP exhibited spherical morphology (~2 μm) and encapsulation efficiency of 79 %, releasing about 41 % of RESV within 24 h, showing a prolonged release profile compared to the free drug. Additionally, RESV-MNP interacted with porcine mucin in an acid environment. RESV-MNP showed no toxicity against AGS/MKN-74 cell lines in vitro and in acute toxicity tests using Galleria mellonella and hemolysis. RESV-MNP presented a minimum inhibitory and bactericidal concentration (MIC/MBC) of 3.9 μg/mL, eradicating H. pylori after 24 h. At 2×MIC, RESV-MNP completely eradicated H. pylori biofilm. In an in vitro infection assay, RESV-MNP reduced H. pylori load. The formulation effectively reduced the mortality rate of H. pylori-infected larvae in the G. mellonella model. Furthermore, RESV-MNP demonstrated gastroprotective effects, reducing the extent and severity of indomethacin-gastric lesions in rats.
AB - Gastric ulcers affect 4 million people worldwide and occur when the stomach's defenses are compromised, allowing harmful agents, such as nonsteroidal anti-inflammatory drugs and Helicobacter pylori, to damage the tissue. The naturally occurring polyphenol, trans-resveratrol (RESV), demonstrates promising potential for treating gastric diseases. However, its therapeutic application is limited by its photosensitivity and solubility. To overcome these challenges, RESV was encapsulated in a new nano-in-microparticle system comprised of chitosan nanoparticles incorporated into hyaluronic acid and alginate microparticles (RESV-MNP). RESV-MNP exhibited spherical morphology (~2 μm) and encapsulation efficiency of 79 %, releasing about 41 % of RESV within 24 h, showing a prolonged release profile compared to the free drug. Additionally, RESV-MNP interacted with porcine mucin in an acid environment. RESV-MNP showed no toxicity against AGS/MKN-74 cell lines in vitro and in acute toxicity tests using Galleria mellonella and hemolysis. RESV-MNP presented a minimum inhibitory and bactericidal concentration (MIC/MBC) of 3.9 μg/mL, eradicating H. pylori after 24 h. At 2×MIC, RESV-MNP completely eradicated H. pylori biofilm. In an in vitro infection assay, RESV-MNP reduced H. pylori load. The formulation effectively reduced the mortality rate of H. pylori-infected larvae in the G. mellonella model. Furthermore, RESV-MNP demonstrated gastroprotective effects, reducing the extent and severity of indomethacin-gastric lesions in rats.
KW - Helicobacter pylori
KW - Gastric disease
KW - Drug delivery system
UR - http://www.scopus.com/inward/record.url?scp=85218116389&partnerID=8YFLogxK
U2 - 10.1016/j.ijbiomac.2025.141010
DO - 10.1016/j.ijbiomac.2025.141010
M3 - Article
C2 - 39954886
AN - SCOPUS:85218116389
SN - 0141-8130
VL - 305
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
IS - part 2
M1 - 141010
ER -