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Original Research

Development of enteric submicron particle formulation of papain for oral delivery

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Pages 2097-2111 | Published online: 23 Sep 2011

Figures & data

Table 1 Different batches of SPs prepared with HPMCP, Eudragit L 100 and Eudragit S 100 polymer

Table 2 Effect of formulation variables on yield, encapsulation efficiency and particle size of HPMCP, Eudragit L 100 and Eudragit S 100 SPs prepared by double emulsion solvent evaporation technique

Figure 1 Effect of pH 1.2 on the aggregation of optimized papain loaded enteric SPs of HPMCP (A), Eudragit L 100 (B) and Eudragit S 100 (C).

Figure 1 Effect of pH 1.2 on the aggregation of optimized papain loaded enteric SPs of HPMCP (A), Eudragit L 100 (B) and Eudragit S 100 (C).

Figure 2 Effect of pH on the release of enzyme from the optimized formulation of papain loaded SPs of HPMCP (HS4), Eudragit L 100 (LS4) and Eudragit S 100 (SS4) at pH 6, 6.8 and 7.4 respectively.

Figure 2 Effect of pH on the release of enzyme from the optimized formulation of papain loaded SPs of HPMCP (HS4), Eudragit L 100 (LS4) and Eudragit S 100 (SS4) at pH 6, 6.8 and 7.4 respectively.

Figure 3 SDS-PEGE analysis of papain samples. Lane 1: molecular weight markers (14–94kDa); lane 2: papain (reference standard); lane 3, 4 and 5: papain released from optimized formulations of papain loaded HPMCP, Eudragit L 100 and Eudragit S 100 SPs respectively.

Figure 3 SDS-PEGE analysis of papain samples. Lane 1: molecular weight markers (14–94kDa); lane 2: papain (reference standard); lane 3, 4 and 5: papain released from optimized formulations of papain loaded HPMCP, Eudragit L 100 and Eudragit S 100 SPs respectively.

Figure 4 Intrinsic fluorescence spectra of papain (reference standard) and papain released from optimized formulations of papain loaded HPMCP, Eudragit L 100 and Eudragit S 100 SPs respectively.

Figure 4 Intrinsic fluorescence spectra of papain (reference standard) and papain released from optimized formulations of papain loaded HPMCP, Eudragit L 100 and Eudragit S 100 SPs respectively.

Figure 5 The FTIR spectra Eudragit L 100, Eudragit S 100, HPMCP, papain powder and optimized formulation of papain loaded HPMCP, Eudragit L 100 and Eudragit S 100 SPs.

Figure 5 The FTIR spectra Eudragit L 100, Eudragit S 100, HPMCP, papain powder and optimized formulation of papain loaded HPMCP, Eudragit L 100 and Eudragit S 100 SPs.

Figure 6 XRD pattern of Eudragit S 100, Eudragit L 100, HPMCP, papain powder and optimized formulation of papain loaded HPMCP, Eudragit L 100 and Eudragit S 100 SPs.

Figure 6 XRD pattern of Eudragit S 100, Eudragit L 100, HPMCP, papain powder and optimized formulation of papain loaded HPMCP, Eudragit L 100 and Eudragit S 100 SPs.

Figure 7 The DSC thermograms of Eudragit S 100, Eudragit L 100, HPMCP, papain powder and optimized formulations of papain loaded Eudragit S 100, Eudragit L 100 and HPMCP SPs.

Figure 7 The DSC thermograms of Eudragit S 100, Eudragit L 100, HPMCP, papain powder and optimized formulations of papain loaded Eudragit S 100, Eudragit L 100 and HPMCP SPs.

Figure 8 SEM micrographs of optimised formulations of papain loaded HPMCP (A), Eudragit L 100 (B) and Eudragit S 100 SPs (C).

Figure 8 SEM micrographs of optimised formulations of papain loaded HPMCP (A), Eudragit L 100 (B) and Eudragit S 100 SPs (C).

Table 3 Stability of free papain and optimised formulations of papain (HS4, LS4 and SS4) under accelerated storage conditions (40°C ± 2°C/75% ± 5% RH)

Table 4 Stability of free papain and optimised formulations of papain (HS4, LS4 and SS4) under room temperature storage (30°C ± 2°C/65% ± 5% RH)