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. 2019 Apr 20;11(4):193. doi: 10.3390/pharmaceutics11040193

Table 6.

In vitro evaluation parameters of various GRDDS.

GRDDS Evaluation Comment References
Low-density system, raft-forming system Floating Lag Time (FLT), total floating time (TFT), floating strength The test is carried out in a simulated gastric fluid (SGF) at 37 °C. The time between introduction of dosage form and its buoyancy on the SGF (FLT) and the time during which the dosage form remains buoyant (TFT) were measured. The floating strength is measured using specifically designed basket holder connected with analytical balance. The reduction of weight on the analytical balance over time determines the floating strength. [9,17,19,31,97,98]
Superporous hydrogel system, expandable system Swelling studies The test is carried out by placing the weighed amount of dosage form into the swelling medium (0.01 N HCl) and weight, diameter, and length of swollen samples are measured at predetermined time point. [61,99]
Raft-forming and Mucoadhesion systems Viscosity and Rheology Viscosity of polymer affects the consistency of the dosage form upon contact with the gastric fluid. Brookfield/Ostwald’s viscometer and texture analyzer are commonly used. [100]
Expandable system In vitro unfolding study The test is carried out by placing the folded dosage form into the dissolution medium and examining its unfolding behavior in different time interval. [101]
Ion-exchange resin system Particle size, ion exchange capacity, moisture content Particle size analysis is carried out using a sieve shaker, laser diffraction, and coulter counter analyzer. The ion exchange capacity depends upon the functional group available for crosslinking. Moisture content can be measured with Karl Fischer. [96,102,103,104]
Applicable for all GRDDS In vitro drug release The test is carried out in SGF at a predefined time interval (generally 0 to 12 h) using USP type-II apparatus at 50 rpm and maintained at 37 °C. [9,27,72,80]
Gel strength The high gel strength is desirable for better mechanical integrity. [9,105]
Drug-excipient interaction study It can be studied by using FT-IR spectroscopy, Differential scanning calorimetry, and High Performance Liquid Chromatography. [17,106]