PREPARATION OF PVA NANOFIBER FOR PROTEIN DELIVERY BY ELECTROSPINNING METHOD AND ITS MODIFICATION FOR pH RESPONSIVE RELEASE
Electrospinning is a process to form fibers by utilizing electrostatic forces. Recently, nanofibers have been applied in wide variety fields including filtration, protective clothing, scaffold for tissue engineering, and drug delivery e.g therapeutic protein. Protein delivery by oral route has ma...
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Format: | Theses |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/45788 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Electrospinning is a process to form fibers by utilizing electrostatic forces.
Recently, nanofibers have been applied in wide variety fields including filtration,
protective clothing, scaffold for tissue engineering, and drug delivery e.g
therapeutic protein. Protein delivery by oral route has many obstacles such as low
permeability, lack of lipophilicity, rapid inactivation and enzymatic degradation in
the gastrointestinal tract. The aim of this study was to prepare PVA nanofiber for
protein delivery system by electrospinning method and its modification with pH
responsive polymer for enteric relesae. Bovine serum albumin (BSA) was used as
a model of protein, while Eudragit L-100 was used as a pH responsive polymer.
PVA nanofiber was prepared by electrospinning method. PVA nanofiber was
prepared with various polymer concentrations, voltages, flow rates, needlecollector lengths and addition of surfactant (Triton X-100). PVA/BSA (20:1)
nanofiber was produced with various voltages only. Characterization of nanofiber
was evaluated by optical microscopy, SEM, EDS, FTIR, DSC, and XRD.
Modification of PVA/BSA nanofiber with Eudragit L-100 was conducted by dip
coating method. Smooth and uniform PVA nanofiber was produced with
concentration of PVA 10% (w/v), voltage 15 kV, flow rate 3 µL/minute, needlecollector length of 12 cm, and addition of Triton X-100 (0,05% w/v). Smooth and
uniform PVA/BSA (20:1) nanofiber was obtained by voltage 12 kV, flow rate 3
µL/minute, needle-collector length of 12 cm, and 0,05% Triton X-100 (w/v).
Diameter size of PVA nanofiber was 294 ± 45 nm while diameter size of
PVA/BSA (20:1) nanofiber was 319 ± 50 nm. An in vitro evaluation for protein
relase was studied using HCl buffer pH 1.2 and phosphate buffer pH 6.8.
Modification of PVA/BSA nanofiber with Eudragit L-100 delayed the release of
BSA in HCl pH 1.2 for 2 hours. In contrast, BSA from PVA/BSA nanofiber
coated with Eudragit L-100 was released in phosphate buffer pH 6.8 for 22 hours.
This result suggests that Eudragit L-100-coated PVA nanofiber containing BSA
shows enteric release of BSA.
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