Development of N-alkylated benzimidazole based cubosome hydrogel for topical treatment of burns

The current study focuses on assessing the activity of the N-alkylated benzimidazole based cubosomal hydrogel (cubogel) for the topical treatment of burn wounds. The study involves the synthesis of six benzimidazole derivatives (1-6) and their characterization by FT-IR and 1H and 13C NMR spectroscop...

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Published in:RSC Advances
Main Author: Nawaz M.; Hayat S.; Farooq U.; Iqbal M.A.; Khalid S.H.; Nee T.W.; Khaw K.Y.; Munir R.; Ijaz M.U.
Format: Article
Language:English
Published: Royal Society of Chemistry 2024
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85207660913&doi=10.1039%2fd4ra04816d&partnerID=40&md5=0d911ff82bf144cfe3d1d11c0122c70e
id 2-s2.0-85207660913
spelling 2-s2.0-85207660913
Nawaz M.; Hayat S.; Farooq U.; Iqbal M.A.; Khalid S.H.; Nee T.W.; Khaw K.Y.; Munir R.; Ijaz M.U.
Development of N-alkylated benzimidazole based cubosome hydrogel for topical treatment of burns
2024
RSC Advances
14
44
10.1039/d4ra04816d
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85207660913&doi=10.1039%2fd4ra04816d&partnerID=40&md5=0d911ff82bf144cfe3d1d11c0122c70e
The current study focuses on assessing the activity of the N-alkylated benzimidazole based cubosomal hydrogel (cubogel) for the topical treatment of burn wounds. The study involves the synthesis of six benzimidazole derivatives (1-6) and their characterization by FT-IR and 1H and 13C NMR spectroscopy. The further study involves the design and formation of nanoparticles known as cubosomes loaded with selected 1-benzyl-1-benzimidazole (API 6) and the development of a cubogel for the topical treatment of burn wounds. Cubosomes were prepared by the homogenization method, using glyceryl monooleate (GMO) as a lipid polymer and poloxamer 407 (P407) as a surfactant. Cubosomes undergo in vitro characterizations (measurement of particle size, zeta potential, polydispersity index (PDI), % entrapment efficiency, drug release in phosphate buffer saline of pH 6.8, and surface morphology by utilizing TEM (transmission electron microscopy). Formulation D3 (2.5% of GMO, 1% of P407, and 2.5% of PVA) emerged as the optimized formulation, displaying a minimum particle size (PS) of 129.9 ± 1 nm, entrapment efficiency (%EE) of 96.67 ± 0.89%, and a drug release of 86 ± 2.7% at 24 h. Carbopol 940 hydrogel was prepared and incorporated with the optimized formulation to prepare cubogel. This optimized cubogel provided 92.56 ± 0.014% in vitro drug release within 24 h. An in vivo histopathological study was conducted on an animal model (rabbit) to assess the efficacy of cubogel in wound healing and wound contraction. Then cubogel was compared with the commercially available creams Clotrimazole® and Polyfax®. The wound treated with newly developed cubogel has maximum wound contraction (96.70%) as compared to the standard creams. The findings revealed that the newly formulated cubogel was highly effective in treating burns, showing superior performance to commercial products without inducing side effects. Additionally, benzimidazole derivative loaded cubogel caused a sustained release for treating burn wounds without any bacterial infections. The current results further suggested phase 0 clinical trials. © 2024 The Royal Society of Chemistry.
Royal Society of Chemistry
20462069
English
Article
All Open Access; Gold Open Access
author Nawaz M.; Hayat S.; Farooq U.; Iqbal M.A.; Khalid S.H.; Nee T.W.; Khaw K.Y.; Munir R.; Ijaz M.U.
spellingShingle Nawaz M.; Hayat S.; Farooq U.; Iqbal M.A.; Khalid S.H.; Nee T.W.; Khaw K.Y.; Munir R.; Ijaz M.U.
Development of N-alkylated benzimidazole based cubosome hydrogel for topical treatment of burns
author_facet Nawaz M.; Hayat S.; Farooq U.; Iqbal M.A.; Khalid S.H.; Nee T.W.; Khaw K.Y.; Munir R.; Ijaz M.U.
author_sort Nawaz M.; Hayat S.; Farooq U.; Iqbal M.A.; Khalid S.H.; Nee T.W.; Khaw K.Y.; Munir R.; Ijaz M.U.
title Development of N-alkylated benzimidazole based cubosome hydrogel for topical treatment of burns
title_short Development of N-alkylated benzimidazole based cubosome hydrogel for topical treatment of burns
title_full Development of N-alkylated benzimidazole based cubosome hydrogel for topical treatment of burns
title_fullStr Development of N-alkylated benzimidazole based cubosome hydrogel for topical treatment of burns
title_full_unstemmed Development of N-alkylated benzimidazole based cubosome hydrogel for topical treatment of burns
title_sort Development of N-alkylated benzimidazole based cubosome hydrogel for topical treatment of burns
publishDate 2024
container_title RSC Advances
container_volume 14
container_issue 44
doi_str_mv 10.1039/d4ra04816d
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85207660913&doi=10.1039%2fd4ra04816d&partnerID=40&md5=0d911ff82bf144cfe3d1d11c0122c70e
description The current study focuses on assessing the activity of the N-alkylated benzimidazole based cubosomal hydrogel (cubogel) for the topical treatment of burn wounds. The study involves the synthesis of six benzimidazole derivatives (1-6) and their characterization by FT-IR and 1H and 13C NMR spectroscopy. The further study involves the design and formation of nanoparticles known as cubosomes loaded with selected 1-benzyl-1-benzimidazole (API 6) and the development of a cubogel for the topical treatment of burn wounds. Cubosomes were prepared by the homogenization method, using glyceryl monooleate (GMO) as a lipid polymer and poloxamer 407 (P407) as a surfactant. Cubosomes undergo in vitro characterizations (measurement of particle size, zeta potential, polydispersity index (PDI), % entrapment efficiency, drug release in phosphate buffer saline of pH 6.8, and surface morphology by utilizing TEM (transmission electron microscopy). Formulation D3 (2.5% of GMO, 1% of P407, and 2.5% of PVA) emerged as the optimized formulation, displaying a minimum particle size (PS) of 129.9 ± 1 nm, entrapment efficiency (%EE) of 96.67 ± 0.89%, and a drug release of 86 ± 2.7% at 24 h. Carbopol 940 hydrogel was prepared and incorporated with the optimized formulation to prepare cubogel. This optimized cubogel provided 92.56 ± 0.014% in vitro drug release within 24 h. An in vivo histopathological study was conducted on an animal model (rabbit) to assess the efficacy of cubogel in wound healing and wound contraction. Then cubogel was compared with the commercially available creams Clotrimazole® and Polyfax®. The wound treated with newly developed cubogel has maximum wound contraction (96.70%) as compared to the standard creams. The findings revealed that the newly formulated cubogel was highly effective in treating burns, showing superior performance to commercial products without inducing side effects. Additionally, benzimidazole derivative loaded cubogel caused a sustained release for treating burn wounds without any bacterial infections. The current results further suggested phase 0 clinical trials. © 2024 The Royal Society of Chemistry.
publisher Royal Society of Chemistry
issn 20462069
language English
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