پديد آورندگان :
Choopani ، Rasool Shahid Beheshti University of Medical Sciences - School of Traditional Medicine, Traditional Medicine and Materia Medica Research Center - Department of Traditional Medicine , Hajimehdipoor ، Homa Shahid Beheshti University of Medical Sciences - School of Traditional Medicine, Traditional Medicine and Materia Medica Research Center - Department of Traditional Pharmacy , Molaei ، Karam Shahid Beheshti University of Medical Sciences - Traditional Medicine and Materia Medica Research Center , Kashafroodi ، Haniye Shahid Beheshti University of Medical Sciences - Traditional Medicine and Materia Medica Research Center , Tavakolifar ، Fatemeh Shahid Beheshti University of Medical Sciences - Traditional Medicine and Materia Medica Research Center , Ara ، Leila Shahid Beheshti University of Medical Sciences - Traditional Medicine and Materia Medica Research Center
كليدواژه :
Coriander Triphala , Tablet , Formulation , Iranian traditional medicine , Quality control ,
چكيده فارسي :
Background: Coriander Triphala is one of the famous drugs in traditional medicine which is consisted of Terminalia chebula, T. bellirica, Phyllanthus emblica, Coriandrum sativum, almond oil and honey. Traditional dosage forms should be converted to modern forms for better acceptance and suitable characteristics and stability. Objective: In the present investigation, the traditional form of Coriander Triphala was converted to film coated tablet and quality control of the tablet was performed. Methods: The fruits of T. chebula, T. bellirica, Ph. emblica, C. sativum in equal proportions along with almond oil and honey in different proportions were used for tablet formulation with other excipients. Sixteen formulations were made and after preformulation studies, twelve of them were selected for making tablet. Prepared tablets went through primary quality control tests such as weight variation, friability, hardness and disintegration time. Finally, the best formulation was coated by green colored water soluble material and its physicochemical characteristics were determined. Results: Among different formulations, the tablet consisted of 98 mg of each species, 14 mg almond oil, 148 mg honey along with lactose, Avicel PH102, croscarmellose sodium, PVP K30, magnesium stearate and silicone dioxide was the best one. Weight variation, hardness, disintegration time, total tannins content as pyrogallol were found 1192 mg ± 5 %, 20 kp, 25 min and 64.19 mg/tablet, respectively. Over 90 % of tannins were released after 60 min during dissolution test. Conclusion: The formulated tablet with suitable characteristics is a good substitution for traditional form and could be produced in industrial scale after complementary clinical trial studies.
