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Acacia gum is a natural heteropolysaccharide derived from Acacia senegal and Acacia seyal. It has gained significant attention due to its unique macromolecular structure and functional biopolymer properties. This review critically evaluates its role in biomedical, pharmaceutical, and industrial applications, with emphasis on the molecular mechanisms that influence its interactions with biological and synthetic systems, especially the arabinogalactan polysaccharide complex of Acacia gum, which facilitates the electrostatic and hydrogen bonding interactions, influencing nanoparticle stability, drug delivery, and hydrogel formation. Similarly, comparative analysis with synthetic polymers such as polyethylene glycol, polyvinyl pyrrolidone, and polyacrylic acid displays its superior colloidal stability, biodegradability, and emulsifying properties, presenting it as a promising alternative for biomedical applications. However, its potential as a nanocarrier in nucleic acid delivery remains unexplored, which requires further research to fully understand the molecular-level interactions. By integrating recent molecular insights with practical considerations, this review establishes a critical foundation for advancing Acacia gum from a largely descriptive biopolymer to a strategically engineered material with significant translational applications in medicine and industry.
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http://dx.doi.org/10.1016/j.ijbiomac.2025.145412 | DOI Listing |
Carbohydr Polym
November 2025
Department of Pharmaceutical Analysis, SVKM's Dr. Bhanuben Nanavati College of Pharmacy, Mumbai, Maharashtra 400056, India. Electronic address:
Gum Arabic (GA), a naturally occurring polysaccharide, has emerged as a promising biomaterial for drug delivery systems (DDS) due to its high water solubility, emulsifying capacity, biocompatibility, and biodegradability. Its structural richness in arabinogalactan facilitates strong interactions with biomolecules, enabling the development of various drug formulations including hydrogels, nanoparticles, liposomes, and emulsions. GA-based DDS have demonstrated significant potential in enhancing the solubility of poorly water-soluble drugs, protecting bioactive compounds from degradation, and enabling sustained and controlled drug release.
View Article and Find Full Text PDFJ Agric Food Chem
September 2025
School of Food Science and Engineering, South China University of Technology, Guangzhou 510640, P.R. China.
Salt reduction remains a critical challenge in oil-containing systems. We examined the influence of gum arabic (GA)-stabilized emulsions with varying oil contents (0.5, 1, and 2%) on saltiness perception.
View Article and Find Full Text PDFPlant-based milks are increasingly popular in producing ice cream and frozen desserts as dairy alternatives. Their distinct nutritional and physicochemical characteristics affect the final product. This study aimed to incorporate soursop fruit puree and gum arabic from var.
View Article and Find Full Text PDFBiopolymers
September 2025
Centro Conjunto de Investigación en Química Sustentable, Universidad Autónoma del Estado de México, Universidad Nacional Autónoma de México, Estado de México, Mexico.
A plastic film made from Gum Arabic and sorbitol (BioFilm-EAp) was developed to enhance the stability of bioactive compounds from Argemone platyceras (EAp) and preserve their antimicrobial properties. The EAp compounds identified through spectrophotometric methods in ethanolic extracts of leaves and stems included alkaloids (3320 and 1260 cm), flavonoids (1739 cm), and phenols (1260 cm). Additionally, the extracts demonstrated the ability to inhibit the growth of Escherichia coli and Staphylococcus aureus.
View Article and Find Full Text PDFPharmaceuticals (Basel)
August 2025
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Mansoura University, Mansoura 35516, Egypt.
Sepsis-associated acute kidney injury (SA-AKI) is a substantial contributor to mortality in critically ill patients. This study aimed to investigate the impact of gum acacia (GA) and dexamethasone (DEX) combination on lipopolysaccharide (LPS)-induced SA-AKI in rats. : Thirty-six male Sprague Dawley rats were separated into six groups, including the control, GA group, LPS-induced AKI group, DEX + LPS group, GA + LPS group, and GA + DEX + LPS group.
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