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Gum Arabic is used in a variety of dosage forms, mainly as an oral binder. Gum Arabic has a low viscosity and high water solubility which results in rapid erosion, short disintegration time and fast drug dissolution. Beyond simple binding, GA functions as a release modifier or matrix former. For instance, Streubel et al. combined GA with HPMC to create floating tablets for verapamil and diltiazem. While the inclusion of GA increased porosity and maintained buoyancy for over 8 hours in 0.1M HCl, its rapid dissolution resulted in a complete drug release within 2 hours—a limitation for sustained-delivery needs. To overcome this, grafting acrylamide onto GA (5:1 ratio) has been shown to successfully extend the release of diltiazem and nifedipine to 6 and 14 hours, respectively.
References
Gum arabic (GA) served as a critical surface modifier in a cervical cancer drug delivery study. Researchers encapsulated the anticancer compound andrographolide (AND) within coconut-derived liposomes (CL) and modified their surface with GA. This GA modification enhanced encapsulation efficiency (93.5% vs. 87.7% in unmodified liposomes) by forming a protective coating that reduced drug leakage. GA-modified liposomes (CLANDGA) demonstrated improved stability (zeta potential −54.9 mV) and controlled drug release (38% at 48 hours vs. 37% in unmodified CLAND). In vitro tests on HeLa cells revealed GA’s synergistic effect, reducing IC50 to 47.82 mg/L compared to 59 mg/L for non-GA liposomes. FTIR analysis confirmed GA’s carboxyl groups formed non-covalent interactions with AND, while molecular docking indicated AND maintained binding affinity to HPV E6 proteins. These results demonstrate GA’s dual role in stabilizing nanocarriers and enhancing therapeutic efficacy against cervical cancer.
Fig. 2 Andrographolide-encapsulated nanoliposomes with gum Arabic surface modification. (Khairiah R, et al. 2025)
References
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