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核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

Development and Evaluation of the Biological Activities of a Plain Mucoadhesive Hydrogel as a Potential Vehicle for Oral Mucosal Drug Delivery.

作者信息

Pardo-Rendón Ana G, Mejía-Méndez Jorge L, López-Mena Edgar R, Bernal-Chávez Sergio A

机构信息

Departamento de Ciencias Químico Biológicas, Universidad de las Américas Puebla, San Andrés Cholula 72810, Puebla, Mexico.

Programa de Edafología, Colegio de Postgraduados, Campus Montecillo, Carr. México Texcoco km 36.4, Montecillo 56230, Mexico.

出版信息

Gels. 2024 Sep 3;10(9):574. doi: 10.3390/gels10090574.


DOI:10.3390/gels10090574
PMID:39330176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11431386/
Abstract

This study aimed to develop HGs based on cationic guar gum (CGG), polyethylene glycol (PEG), propylene glycol (PG), and citric acid (CA) using a 2 factorial experimental design to optimize their properties. HGs were characterized through FTIR and Raman spectroscopy, scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). The biological activities of HGs were determined by evaluating their mucoadhesive capacity and antibacterial activity in vitro, whereas their toxicity was analyzed using nauplii as an in vivo model. Results revealed that HGs were successfully optimized for their viscosity, pH, and sensory properties, and it was observed that varying concentrations of PEG-75 did not influence them. Through SEM analyses, it was noted that increased levels of PEG-75 resulted in HGs with distinct porosity and textures, whereas FTIR and Raman spectroscopy exhibited representative peaks of the raw materials used during the synthesis process. TGA studies indicated the thermal stability of HGs, as they presented degradation patterns at 100 and 300 °C. The synthesized HGs exhibited similar mucoadhesion kinetic profiles, demonstrating a displacement factor at an equilibrium of 0.57 mm/mg at 5 min. The antibacterial activity of HGs was appraised as poor against Gram-positive and Gram-negative bacteria due to their MIC values (>500 μg/mL). Regarding , treatment with HGs neither decreased their viability nor induced morphological changes. The obtained results suggest the suitability of CGG/PEG HGs for oral mucosa drug delivery and expand the knowledge about their mucoadhesive capacity, antibacterial potential, and in vivo biocompatibility.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/c73365c950ad/gels-10-00574-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/4ca5c23a2191/gels-10-00574-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/6e27cbd04467/gels-10-00574-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/ba2480414cf3/gels-10-00574-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/4da9158bcdaf/gels-10-00574-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/048ffe4c8bfe/gels-10-00574-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/20c3ba281763/gels-10-00574-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/7b1867f63900/gels-10-00574-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/c73365c950ad/gels-10-00574-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/4ca5c23a2191/gels-10-00574-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/6e27cbd04467/gels-10-00574-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/ba2480414cf3/gels-10-00574-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/4da9158bcdaf/gels-10-00574-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/048ffe4c8bfe/gels-10-00574-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/20c3ba281763/gels-10-00574-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/7b1867f63900/gels-10-00574-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5100/11431386/c73365c950ad/gels-10-00574-g007.jpg

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[2]
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本文引用的文献

[1]
Transepithelial transport of nanoparticles in oral drug delivery: From the perspective of surface and holistic property modulation.

Acta Pharm Sin B. 2024-9

[2]
Novel Thermosensitive and Mucoadhesive Nasal Hydrogel Containing 5-MeO-DMT Optimized Using Box-Behnken Experimental Design.

Polymers (Basel). 2024-7-29

[3]
Inhalable mucin-permeable nanomicelles deliver antibiotics for effective treatment of chronic pneumonia.

J Mater Chem B. 2024-8-28

[4]
Nanoporous, Ultrastiff, and Transparent Plastic-like Polymer Hydrogels Enabled by Hydrogen Bonding-Induced Self-Assembly.

ACS Appl Mater Interfaces. 2024-8-14

[5]
Fabrication and Characterization of Porous PEGDA Hydrogels for Articular Cartilage Regeneration.

Gels. 2024-6-26

[6]
Effects of a semi-interpenetrating network hydrogel loaded with oridonin and DNase-I on the healing of chemoradiotherapy-induced oral mucositis.

Biomater Sci. 2024-8-20

[7]
Influence of algal-extracellular polymeric substances (EPS) on the pristine and combined toxicity of TiO NPs and PSNPs in Artemia salina: Eco-corona enhances the toxic effects.

Ecotoxicol Environ Saf. 2024-9-1

[8]
Clinical features and risk factors for Sjogren's syndrome patients suffering from oral candidiasis in Shanxi, China.

BMC Oral Health. 2024-7-17

[9]
β-Cyclodextrin/dialdehyde glucan-coated keratin nanoparticles for oral delivery of insulin.

Int J Biol Macromol. 2024-9

[10]
Application of Mucoadhesive Hydrogel with Anti-Inflammatory and Pro-Repairing Dual Properties for the Treatment of Chemotherapy-Induced Oral Mucositis.

ACS Appl Mater Interfaces. 2024-7-17

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