Abstract

Objective: Evaluation Of Famotidine Loaded 3D-Nano-Cellulose Network three dimensional nano-cellulose network (3DNC) Used For Oral Administration. 3DNC is produced from bacteria living in fermented green tea and is the material containing nano-sized fibers, which is capable of loading Famotidine to form a prolonged release therapy to improve drug bioavailability.
 Methods: Used healthy white rabbits, weight approximately 2.5-2.7 kg, the same age, laboratory standard, is supplied from The National Institute of Drug Quality Control. The rabbits have adapted to laboratory conditions at least one week and have starveling in 12 h, supplied fully water during the preparation. Rabbits are divided into 4 groups (n=3 for each group). Every rabbit is given 1 capsule or 1 tablet with a single dose of 20 mg/rabbit: group 1 (commercial drugs), group 2 (3DNC-standard medium (SM) loaded drug), group 3 (3DNC-coconut medium (CM) loaded drug) Group 4 (3DNC-rice medium (RM) loaded drug).
 Results: The results have shown that 3DNC has the involvement of the nano-sized cellulose fibers with three-dimensional networks that are capable of loading Famotidine and prolonged drug release. The 3DNC cultured in the drug-loaded SM with slow-release and slow-release catalysts, the 3DNC was cultured in CMs and tablets with medium release rates, in comparison with the 3DNC was cultured in RM loaded at a rapid release rate in the same pH = 2.
 Conclusion: Experiment on rabbits showed that the drug-loaded 3DNCs could help to prolong the drug release, in which the extended-release time of the 3DNC cultured in SM and CM was higher than that of the 3DNC grown in RM. The 3DNC loaded drugs help improve Famotidine bioavailability compared to commercial tablets.

Highlights

  • The 3D-Nano-Cellulose Network three dimensional nano-cellulose network (3DNC) has the structure of super-thin nanofibers, great tensile, mechanical strength, and so on

  • The results of the drug release rate for the 3DNC types cultured in SM, CM, and RM loaded in the different pH media are shown in fig

  • The results indicated that the 3DNC cultured in SM loaded drug after 12 h had a higher drug release rate at pH = 2 (88.79%) and pH = 4.5 (86.47%), lower than at pH = 6.8 (74.36%)

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Summary

Introduction

The 3DNC has the structure of super-thin nanofibers, great tensile, mechanical strength, and so on. Some studies have proved that the 3DNC has the potential of being a delivery system with its properties. M et al [1] have indicated that the 3DNC membranes can increase the releasing time of the drug and improve the efficiency of drug use. Huang L. et al [2] have controlled the drug-releasing of the 3DNC in artificial models, including the stomach and intestine. Zhu X. et al [5] have studied the drug delivery system that increased the bioavailability of Famotidine in rats. M. et al [6] have evaluated the acid function of carboxymethyl-betacyclodextrin in improving the chemical stability, oral-route bioavailability, and bitter taste of Famotidine. The ọbjective of study is the evaluation Of Famotidine Loaded 3D-Nano-Cellulose Network three dimensional nano-cellulose network (3DNC) used for oral administration

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