Encapsulating biopolymeric microparticles within floating capsules for oral delivery of drugs
Solid lipid microparticles (LMP) are alternatives to polymeric nanoparticles for the encapsulation of hydrophobic components that have poor bioavailability. However, the usual method of fabrication of solid LMP through high pressure homogenization had limitations that caused low encapsulation e...
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Format: | Final Year Project |
Language: | English |
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Nanyang Technological University
2022
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Online Access: | https://hdl.handle.net/10356/156249 |
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Institution: | Nanyang Technological University |
Language: | English |
Summary: | Solid lipid microparticles (LMP) are alternatives to polymeric nanoparticles for the
encapsulation of hydrophobic components that have poor bioavailability. However, the
usual method of fabrication of solid LMP through high pressure homogenization had
limitations that caused low encapsulation efficiency and potential damage to sensitive
molecules. Hence the electrospray technique was investigated as an alternative. In this
study, for the fabrication of solid LMP, the electrospray method was explored by varying
different parameters such as flow rate and voltage. Scanning Electron Microscopy (SEM)
was used to characterize the microparticles. Following the optimization of parameters,
curcumin was loaded into the microparticle. Release studies of the curcumin loaded
particles in simulated gastrointestinal fluids showed that the encapsulation was able to
retard the release of curcumin in simulated gastric fluid (SGF) and release it in the
simulated intestinal fluid (SIF). In order to prolong the release of curcumin, the curcumin
loaded LMP were further encapsulated into floating particles that can act as a reservoir
for LMP. Based on SEM images it was observed that the LMP were mainly localized on
the surface of the floating microparticles. Further in vitro release studies on the floating
particles need to be conducted to understand the behavior of LMP in the floating particles. |
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