Development and evaluation of novel herbal formulation for the treatment of peptic ulcer
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Abstract
Extract of Curcuma longa, Piper nigrum and Berberis aristata is reported to be useful in stomach
newlineailments and has been shown to possess antiulcer activity. Since, treatment for peptic ulceration
newlineincludes a consumption of multiple herbs displays synergistic impacts compare to single herb
newlineagainst peptic ulcer. This project work was defined to retain the herbal extracts based
newlinegastroretentive formulation in stomach for better antiulcer activity. Hence, formulation and
newlineevaluation floating tablet of spray dried extract of Curcuma longa, Piper nigrum and Berberis
newlinearistata was carried out. Prior to development of gastroretentive formulation, pharmacological
newlineactivity and simultaneous HPLC method were performed. From the pharmacological activity,
newlinecombined methanolic extracts of Curcuma longa (250mg/kg), Piper nigrum (125mg/kg) and
newlineBerberis aristata (125mg/kg) significantly diminished the ulcer index compared with Ranitidine
newlinein ethanol and pylorus model. HPLC method was carried out on Spectra system, P-400 HPLC
newlineusing CurosilPFP 5and#956; as stationary phase and mobile phase containing Methanol: 10mM
newlineAmmonium acetate with acetic acid (pH 3) (75:25%v/v) at flow rate of 1ml/min using UV
newlinedetection at 254nm. Hence, developed method was accurate, precise, simple, sensitive, selective,
newlinerobust and rapid. The floating tablets were formulated using hydrophilic polymers as Hydroxy
newlinepropyl methyl cellulose (HPMC K4M and HPMC E15), Sodium CMC and Sodium bicarbonate
newlineas a gas generating agent. The formulated tablets were evaluated for the quality control tests such
newlineas weight variation, hardness, friability, swelling index, floating lag time, total floating time and
newlinein vitro drug release study. The results of the present study clearly indicate the HPMC K4M and
newlineHPMC E15 (Batch F-11) in appropriate concentration shown buoyancy of tablet for 8 hours along
newlinewith the sustained drug release in 0.1N HCl as dissolution media.
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