IIUM Repository

Lyophilized amorphous dispersion of telmisartan in a combined carrier–alkalizer system: formulation development and in vivo study

Aljapairai, Khater Ahmed Saeed and Alkhalidi, Hala M. and Mahmood, Syed and Almurisi, Samah Hamed and Doolaanea, Abd Almonem and Al-Sindi, Taha A. and Chatterjee, Bappaditya (2020) Lyophilized amorphous dispersion of telmisartan in a combined carrier–alkalizer system: formulation development and in vivo study. ACS Omega, 5 (50). pp. 32466-32480. ISSN 2470-1343

[img] PDF (Full text) - Published Version
Restricted to Registered users only

Download (5MB) | Request a copy
[img] PDF (SCOPUS) - Supplemental Material
Restricted to Repository staff only

Download (372kB) | Request a copy

Abstract

Telmisartan suffers from low oral bioavailability due to its poor water solubility. The research work presents a formulation of solid dispersed (SD) telmisartan formulation as a ternary mixture of a drug, a polymeric carrier (poly(vinylpyrrolidone) (PVP) K30), and an alkalizer (Na2CO3). The preparation method, which was lyophilization of an aqueous solution containing the ingredients, was free from any organic solvent. The developed SD formulations resulted in a significant improvement in in vitro dissolution (>90% drug dissolution in 15 min) compared to pure telmisartan. Solid-state characterization by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and X-ray diffraction (XRD) studies indicated the conversion of crystalline telmisartan into an amorphous form. Fourier transform infrared (FTIR) spectroscopy revealed the drug–polymer interaction that was responsible for reducing the chances of recrystallization. A short-term stability study showed that selected SD formulations were stable in terms of in vitro dissolution and retained their amorphous structure in ambient and accelerated conditions over 2 months. Selected formulations (drug/PVP K30/Na2CO3 as 1:1:2 or 1:2:2 weight ratio) resulted in >2.48 times relative oral bioavailability compared to marketed formulations. It was considered that the incorporation of an alkalizer and a hydrophilic polymer, and amorphization of telmisartan by lyophilization, could enhance in vitro dissolution and improve oral bioavailability.

Item Type: Article (Journal)
Additional Information: 6923/88239
Subjects: R Medicine > RS Pharmacy and materia medica
Kulliyyahs/Centres/Divisions/Institutes (Can select more than one option. Press CONTROL button): Kulliyyah of Medicine
Kulliyyah of Medicine > Department of Basic Medical
Kulliyyah of Pharmacy
Kulliyyah of Pharmacy > Department of Basic Medical Sciences
Kulliyyah of Pharmacy > Department of Pharmaceutical Technology
Depositing User: Dr. Abd Almonem Doolaanea
Date Deposited: 04 Feb 2021 15:17
Last Modified: 04 Feb 2021 15:17
URI: http://irep.iium.edu.my/id/eprint/88239

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year