Oday Sajjad Alsawad1,2
,
Ahmed Abduljabbar1
For correspondence:- Oday Alsawad Email: Oday.azeez@uobasrah.edu.iq
Received: 18 February 2026 Accepted: 20 May 2026 Published: 31 May 2026
Citation: Alsawad OS, Abduljabbar A. Evaluation of sustained-release metformin hydrochloride matrix tablets using blends of chitosan and xanthan. Trop J Pharm Res 2026; 25(5):607-617 doi: https://dx.doi.org/10.4314/tjpr.v25i5.2
© 2026 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Purpose: To develop sustained-release metformin matrix tablets using chitosan and xanthan, and to compare their performance with hydroxypropyl methylcellulose (HPMC; K100M) matrix and a commercial sustained-release (SR) product. Method: Metformin matrix tablet formulations were prepared by direct compression of chitosan-xanthan blends at ratios of 1:0 to 0:1, developed based on a 3x2-factorial design (polymer levels 25 – 35 % w/w). A formulation based on HPMC K100M (30 % w/w) and a commercial product were used as controls. Formulated tablets were tested for pre- and post-compression characteristics, swelling/erosion, in vitro dissolution, release kinetics and accelerated stability. Results: All blends showed fair to good flow (angle of repose 27.9 – 33.8°, Hausner ratio ≤ 1.24), friability (< 0.6 %) and content uniformity (98.1 – 101.3 %). Increasing polymer level and xanthan proportion slowed metformin release. Optimised 30 % chitosan: xanthan (1:1) matrix released 95.2 % metformin content after 12 h, closely matching HPMC formulation (96.0 %), and commercial SR product (f? = 67). The optimized product (F5) release fitted Higuchi/Korsmeyer-Peppas models (R² ≥ 0.99; n = 0.63), indicating anomalous diffusion. Stability testing showed no significant changes in all parameters tested (p > 0.05). Conclusion: Chitosan-xanthan matrices, especially the 1:1 mixture at 30 % w/w, produce stable metformin SR tablets with dissolution behaviour equal to those of HPMC and a commercially available SR metformin product, suggesting their use as alternatives to synthetic/semi-synthetic polymers in once-daily metformin dosage forms.