Enhancement efficacy of omeprazole by conjugation with silver nanoparticles as a urease inhibitor

Omeprazole, a proton pump inhibitor, is used for gastric and duodenal ulcers, gastroesophageal reflux disease, infection, etc. Current research is based on the loading of omeprazole on surface silver nanoparticles by chemical method. The appearance of an absorption peak at 421 nm confirmed the synth...

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Veröffentlicht in:Green processing and synthesis 2024-04, Vol.13 (1), p.110294-31
Hauptverfasser: Zia, Aneesa, Shahzad, Ayesha, Riaz, Nadia, Khan, Sara, Farooq, Umar, Bukhari, Syed Majid, Sarwar, Rizwana, Khalid, Asaad, Kashtoh, Hamdy, Khan, Ajmal, Al-Harrasi, Ahmed
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Sprache:eng
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Zusammenfassung:Omeprazole, a proton pump inhibitor, is used for gastric and duodenal ulcers, gastroesophageal reflux disease, infection, etc. Current research is based on the loading of omeprazole on surface silver nanoparticles by chemical method. The appearance of an absorption peak at 421 nm confirmed the synthesis of nanoparticles. The FT-IR further confirmed the conjugation of functional groups present in omeprazole moiety with silver. The size and morphology were elucidated by transmission electron microscopy and X-ray diffraction which revealed a spherical shape with an average particle size of 16–20 nm. To know enhancement in their efficacy, the omeprazole-loaded nanoparticles were evaluated against antibacterial, urease inhibition, and antioxidant activities. Nanoparticles showed significant antibacterial potential against and with 12 ± 0.41 and 13.6 ± 1.02 mm zones of inhibition, respectively. Almost 2.43 times enhanced urease inhibitory activity was found for nanoparticles (IC = 2.17 ± 0.10 µg·mL ) as compared to omeprazole (IC = 5.28 ± 0.14 µg·mL ). The radical scavenging activity of nanoparticles also increased significantly. The synthesized nanoparticles were docked in the active site of urease to investigate their binding mode. Due to excellent urease and bacterial inhibition, these nanoparticles can be used for ulcers.
ISSN:2191-9550
2191-9542
2191-9550
DOI:10.1515/gps-2023-0229