Matrix tablets containing paracetamol and hydroxypropyl methylcellulose (HPMC 2906) of different viscosity grades (50, 400, 1500, and 4000 mPa·s) were evaluated for drug release and change in matrix tablet mass [Δ M (%)] after exposure to 0.09, 0.15, 0.31, and 0.52 M ionic strengths of dissolution media. At 0.09 and 0.15 M ionic strength, drug‐release profiles reflected the extended release characteristic; in addition the increase in Δ M was slow and continuous within first few hours. At 0.31 M the higher viscosity grade matrices showed extensive initial swelling and the loss of extended release whereas at 0.52 M a similar tablet performance is observed for the matrices of all viscosity grades. Notably, when extensive increase in Δ M occurs in the very beginning of exposure to medium the loss of extended release from the matrix is expected.
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Krese et al. (2016) studied this question.
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