<abstract xml:lang="en" xmlns="http://www.w3.org/1999/xhtml"><p><italic>In situ</italic> forming intragastric controlled-release formulation is a new technology in the field of oral controlled-release delivery systems. The objective of this study was to develop formulations that can control drug release up to 24 hours. In addition, a combination of appropriate polymers and solvents was selected that could form a drug loaded gel at the process temperature of 60-70 °C, which gel could turn into a rigid mass upon exposure to dissolution fluid at body temperature. The drug release mechanism from this rigid mass was controlled by different formulation factors such as different polymer grades, polymer concentrations, hydrophobicity or hydrophilicity of solvents, different drug loadings, and physicochemical properties of additional excipients. After evaluating different formulation factors, Ethocel 10 FP and triethyl citrate were selected for further studies using hydrochlorothiazide as a model drug. Polynomial correlation between viscosity of the blank gel and drug release profile was also obtained.</p></abstract>

In situ forming intragastric controlled-release formulation is a new technology in the field of oral controlled-release delivery systems. The objective of this study was to develop formulations that can control drug release up to 24 hours. In addition, a combination of appropriate polymers and solvents was selected that could form a drug loaded gel at the process temperature of 60-70 °C, which gel could turn into a rigid mass upon exposure to dissolution fluid at body temperature. The drug release mechanism from this rigid mass was controlled by different formulation factors such as different polymer grades, polymer concentrations, hydrophobicity or hydrophilicity of solvents, different drug loadings, and physicochemical properties of additional excipients. After evaluating different formulation factors, Ethocel 10 FP and triethyl citrate were selected for further studies using hydrochlorothiazide as a model drug. Polynomial correlation between viscosity of the blank gel and drug release profile was also obtained.

Development and evaluation of <italic>in situ</italic> novel intragastric controlled-release formulation of hydrochlorothiazide

Jodhpur National University, Jodhpur, Rajshathan, India

Department of Pharmaceutical Technology, Nootan Pharmacy College, Visnagar-384315 (GUJ) India

Acta Pharmaceutica

Development and evaluation of  novel intragastric controlled-release formulation of hydrochlorothiazide

In situ forming intragastric controlled-release formulation is a new technology in the field of oral controlled-release delivery systems. The objective of this...

Development and evaluation of in situ novel intragastric controlled-release formulation of hydrochlorothiazide

Publié en ligne: 15 mars 2011

Pages: 73 - 82

DOI: https://doi.org/10.2478/v10007-011-003-9

Mots clés
fizikalna kompatibilnost, hidroklortiazid, stupanj polimerizacije, gel s uklopljenim lijekom, koncentracija polimera, viskoznost

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