Preparation, Characterization and Evaluation of Flavonolignan Silymarin Effervescent Floating Matrix Tablets for Enhanced Oral Bioavailability

Author:

Ahmad Sher1ORCID,Khan Jamshaid Ali1,Kausar Tabassum Naheed2,Mahnashi Mater H.3ORCID,Alasiri Ali4,Alqahtani Abdulsalam A.4ORCID,Alqahtani Thamer S.4,Walbi Ismail A.5ORCID,Alshehri Osama M.5ORCID,Elnoubi Osman A.6,Mahmood Fawad1,Sadiq Abdul7ORCID

Affiliation:

1. Department of Pharmacy, University of Peshawar, Peshawar 25120, KP, Pakistan

2. Mumtaz Maternity Hospital, Hashtnagri, Peshawar 25220, KP, Pakistan

3. Department of Pharmaceutical Chemistry, College of Pharmacy, Najran University, Najran 55461, Saudi Arabia

4. Department of Pharmaceutics, College of Pharmacy, Najran University, Najran 55461, Saudi Arabia

5. Department of Clinical Pharmacy, College of Pharmacy, Najran University, Najran 55461, Saudi Arabia

6. College of Applied Medical Sciences, Najran University, Najran 55461, Saudi Arabia

7. Department of Pharmacy, University of Malakand, Chakdara 18000, KP, Pakistan

Abstract

The convenient and highly compliant route for the delivery of active pharmaceutical ingredients is the tablet. A versatile platform of tablets is available for the delivery of therapeutic agents to the gastrointestinal tract. This study aimed to prepare gastro retentive drug delivery floating tablets of silymarin to improve its oral bioavailability and solubility. Hydroxypropyl methylcellulose (HPMCK4M and HPMCK15), Carbopol 934p and sodium bicarbonate were used as a matrix, floating enhancer and gas generating agent, respectively. The prepared tablets were evaluated for physicochemical parameters such as hardness, weight variation, friability, floating properties (floating lag time, total floating time), drug content, stability study, in vitro drug release, in vivo floating behavior and in vivo pharmacokinetics. The drug–polymer interaction was studied by Differential Scanning Calorimetry (DSC) thermal analysis and Fourier transform infrared (FTIR). The floating lag time of the formulation was within the prescribed limit (<2 min). The formulation showed good matrix integrity and retarded the release of drug for >12 h. The dissolution can be described by zero-order kinetics (r2 = 0.979), with anomalous diffusion as the release mechanism (n = 0.65). An in vivo pharmacokinetic study showed that Cmax and AUC were increased by up to two times in comparison with the conventional dosage form. An in vivo imaging study showed that the tablet was present in the stomach for 12 h. It can be concluded from this study that the combined matrix system containing hydrophobic and hydrophilic polymers min imized the burst release of the drug from the tablet and achieved a drug release by zero-order kinetics, which is practically difficult with only a hydrophilic matrix. An in vivo pharmacokinetic study elaborated that the bioavailability and solubility of silymarin were improved with an increased mean residence time.

Funder

Deputy for Research and Innovation, Ministry of Education, Kingdom of Saudi Arabia

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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