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Necrotic tissue of wound can be removed by debridement using proteolytic enzymes. This study <br /> <br /> aims to develop an in situ hydrogel preparation to create a controlled papain release. Papain was <br /> <br /> encapsulated in sodium alginate microparticles (MP). MP w...
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Main Author: | |
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Format: | Final Project |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/25216 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Necrotic tissue of wound can be removed by debridement using proteolytic enzymes. This study <br />
<br />
aims to develop an in situ hydrogel preparation to create a controlled papain release. Papain was <br />
<br />
encapsulated in sodium alginate microparticles (MP). MP was prepared by mixing the sodium <br />
<br />
alginate solution and papain solution with stirring at 9000 rpm for 4 min and continued with <br />
<br />
sonication. MP formulation was optimized statistically using Box-Behnken design with factors <br />
<br />
consisting of alginate, CaCl2, and duration of sonication. The parameters used to determine the <br />
<br />
optimal MP formulas are particle size in the range 1-5 μm, the maximum of entrappment efficiency <br />
<br />
(EE) and the loading of papain (LP). The optimum MP formula consisted of 0,084% alginate; 0,02% <br />
<br />
CaCl2; and 58,2 seconds of sonication with a homogenizer ultrasonic. This MP formula showed the <br />
<br />
particle size of 3,9 μm; EE 82,1%; and LP 65,82%. Further, the MP was dispersed into an in situ <br />
<br />
forming hydrogel (HMP) prepared with components of alginate as the base, polyvinylohol (PVA) as <br />
<br />
humectant, and CaCl2 as crosslinking agents. The optimum HMP formula consisted of 1% alginate, <br />
<br />
5% PVA, and 0,4% CaCl2. The HMP preparation showed a viscosity before crosslinking of 60,05+0,14 <br />
<br />
mPa and an water absorption capacity of 125+3%. Papain release of HMP was 8,62% for three days. <br />
<br />
The HMP preparation showed controlled release profile, in vitro debridement process, and in situ <br />
<br />
performance at body temperature. <br />
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