Objective: The short biological half-life (2-3 h) and low bioavailability (50 %) of ranitidine (RAN) following oral administration favor the development of a controlled release system. This study was aimed to develop and in vitro evaluate oral sustained-release RAN delivery system based on the bacterial nanocellulose material (BNM) produced by Komagataeibacter xylinus (K. xylinus) from selected culture media. Methods: BNMs are biosynthesized by K. xylinus in the standard medium (SM) and coconut water (CW). RAN was loaded in BNMs by the absorption method. The structural and physicochemical properties of BNMs and BNMs-RAN were evaluated via swelling behavior, FTIR, and FESEM techniques. Moreover, the effect of BNMs on RAN release profile and release kinetics was analyzed and evaluated. Results: The amount of loaded RAN or entrapment efficacy for BNM-CW is higher than for BNM-SM. The BNM-SM-RAN and BNM-CW-RAN exhibited a decreased initial burst release system followed by a prolonged RAN release up to 24 h in relation to the commercial tablets containing RAN. The RAN release from these formulations was found higher in the SGF medium than that of in SIF medium. RAN released from these formulations was found to follow the Korsmeyer-Peppas model and diffusion sustained drug release mechanism. The sustained release of RAN from BNM-SM-RAN was slower than for RAN from BNM-CW-RAN, but the mechanism of sustained RAN release was the same. Conclusion: Oral sustained-release RAN delivery system based on BNMs was successfully prepared and evaluated for various in vitro parameters. The biopolymers like BNM-SM and BNM-CW could be utilized to develop oral sustained RAN release dosage form.

Objective: The study aims for the fabrication, evaluation of drug loading capability and characterization of 3D-nano-cellulose network materials produced by bacteria of fermented aqueous green tea extract in selected culture media. Methods: 3D-nano-cellulose network (3DNC) materials can be produced by bacteria living in a fermented aqueous green tea extract. 3DNCs include nano-fibers forming networks, which are capable of drug loading to form a prolonged release therapy to improve drug bioavailability. In this study, 3DNC materials are biosynthesized by aerobic bacteria in the standard medium (SM), coconut water (CW) and rice water (RW). 3DNCs were prepared and evaluated for drug carrier using famotidine as a model drug. Famotidine was loaded in 3DNC by the absorption method. 3DNCs were characterized by using FE-SEM and FTIR spectroscopy. Results: The 3DNCs obtained from CW, and RW have the same characteristics as the 3DNC obtained from the SM, and 3DNCs can be fabricated with the desired thickness and diameter in all three types of culture media. 3DNCs absorbed famotidine in optimum condition without any difference in famotidine loading (28.2 mg) and famotidine entrapment efficiency (90 %). Investigation of the 3DNC structure using FE-SEM has shown that the cellulose fibers of 3DNC-SM and 3DNC-CW have a stable structure without structural change when loading drug under optimal condition. Conclusion: The results indicate the potential for using 3DNC-SM and 3DNC-CW to design the drug delivery system.