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Surface Modification of Microcporous of Polycaprolactone (PCL) Microcarrier to Improve Microcarrier Biocompatibility

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@article{IJASEIT7060,
   author = {Nurhusna Samsudin and Yumi Z. H Y. Hashim and Mohd A. Arifin and Hamzah M. Salleh},
   title = {Surface Modification of Microcporous of Polycaprolactone (PCL) Microcarrier to Improve Microcarrier Biocompatibility},
   journal = {International Journal on Advanced Science, Engineering and Information Technology},
   volume = {8},
   number = {4-2},
   year = {2018},
   pages = {1642--1647},
   keywords = {Halal; porous microcarrier; UV/O3 treatment; microcarrier cell culture.},
   abstract = {

Oil/water emulsion solvent evaporation method was employed to fabricate polycaprolactone (PCL) microcarriers. In order to produce porous microcarrier, the method was slightly modified. The porous network channels were generated inside the microcarrier by introducing camphene that was dissolved in the same solvent used to dissolve raw PCL. The evaporation of solvent and sublimination of camphene during the process of emulsion solvent evaporation method, produce solidified porous microcarrier beads. The surface porous microcarriers beads were further modified to make it competent for cell attachment and proliferation. The surface of these microcarriers were modified with UV/O3 system to introduce functional group and charge on the surface. The treatment followed with the immobilization of halal gelatin on the surface to imorove the biocompatibility of the microcarrier. Porous microcarrier with optimal size distribution was successfully fabricated. The average pore size of 11.74±8.32 µm was obtained with the concentration of 20% (w/v) of camphene. The porous PCL microcarrier was further tailored with gelatin through surface treatment with UV/O3 system and gelatin immobilization and validation of its compatibility towards mammalian cell was tested with cultivation of green monkyer kidney cell (Vero) in the suspension culture. Vero cells attach and proliferatie well on the gelatin coated porous PCL microcarrier with maximum cell number  of 3.90 × 105 cells/ml as compared to cell proliferation on UV/O3 treated porous PCL microcarrier (1.83 × 105 cells/ml). The developed microcarrier may be potentially applicable as a cell delivery scaffold for cell tissue culture and tissue engineering application.

},    issn = {2088-5334},    publisher = {INSIGHT - Indonesian Society for Knowledge and Human Development},    url = {http://ijaseit.insightsociety.org/index.php?option=com_content&view=article&id=9&Itemid=1&article_id=7060},    doi = {10.18517/ijaseit.8.4-2.7060} }

EndNote

%A Samsudin, Nurhusna
%A Hashim, Yumi Z. H Y.
%A Arifin, Mohd A.
%A Salleh, Hamzah M.
%D 2018
%T Surface Modification of Microcporous of Polycaprolactone (PCL) Microcarrier to Improve Microcarrier Biocompatibility
%B 2018
%9 Halal; porous microcarrier; UV/O3 treatment; microcarrier cell culture.
%! Surface Modification of Microcporous of Polycaprolactone (PCL) Microcarrier to Improve Microcarrier Biocompatibility
%K Halal; porous microcarrier; UV/O3 treatment; microcarrier cell culture.
%X 

Oil/water emulsion solvent evaporation method was employed to fabricate polycaprolactone (PCL) microcarriers. In order to produce porous microcarrier, the method was slightly modified. The porous network channels were generated inside the microcarrier by introducing camphene that was dissolved in the same solvent used to dissolve raw PCL. The evaporation of solvent and sublimination of camphene during the process of emulsion solvent evaporation method, produce solidified porous microcarrier beads. The surface porous microcarriers beads were further modified to make it competent for cell attachment and proliferation. The surface of these microcarriers were modified with UV/O3 system to introduce functional group and charge on the surface. The treatment followed with the immobilization of halal gelatin on the surface to imorove the biocompatibility of the microcarrier. Porous microcarrier with optimal size distribution was successfully fabricated. The average pore size of 11.74±8.32 µm was obtained with the concentration of 20% (w/v) of camphene. The porous PCL microcarrier was further tailored with gelatin through surface treatment with UV/O3 system and gelatin immobilization and validation of its compatibility towards mammalian cell was tested with cultivation of green monkyer kidney cell (Vero) in the suspension culture. Vero cells attach and proliferatie well on the gelatin coated porous PCL microcarrier with maximum cell number  of 3.90 × 105 cells/ml as compared to cell proliferation on UV/O3 treated porous PCL microcarrier (1.83 × 105 cells/ml). The developed microcarrier may be potentially applicable as a cell delivery scaffold for cell tissue culture and tissue engineering application.

%U http://ijaseit.insightsociety.org/index.php?option=com_content&view=article&id=9&Itemid=1&article_id=7060 %R doi:10.18517/ijaseit.8.4-2.7060 %J International Journal on Advanced Science, Engineering and Information Technology %V 8 %N 4-2 %@ 2088-5334

IEEE

Nurhusna Samsudin,Yumi Z. H Y. Hashim,Mohd A. Arifin and Hamzah M. Salleh,"Surface Modification of Microcporous of Polycaprolactone (PCL) Microcarrier to Improve Microcarrier Biocompatibility," International Journal on Advanced Science, Engineering and Information Technology, vol. 8, no. 4-2, pp. 1642-1647, 2018. [Online]. Available: http://dx.doi.org/10.18517/ijaseit.8.4-2.7060.

RefMan/ProCite (RIS)

TY  - JOUR
AU  - Samsudin, Nurhusna
AU  - Hashim, Yumi Z. H Y.
AU  - Arifin, Mohd A.
AU  - Salleh, Hamzah M.
PY  - 2018
TI  - Surface Modification of Microcporous of Polycaprolactone (PCL) Microcarrier to Improve Microcarrier Biocompatibility
JF  - International Journal on Advanced Science, Engineering and Information Technology; Vol. 8 (2018) No. 4-2
Y2  - 2018
SP  - 1642
EP  - 1647
SN  - 2088-5334
PB  - INSIGHT - Indonesian Society for Knowledge and Human Development
KW  - Halal; porous microcarrier; UV/O3 treatment; microcarrier cell culture.
N2  - 

Oil/water emulsion solvent evaporation method was employed to fabricate polycaprolactone (PCL) microcarriers. In order to produce porous microcarrier, the method was slightly modified. The porous network channels were generated inside the microcarrier by introducing camphene that was dissolved in the same solvent used to dissolve raw PCL. The evaporation of solvent and sublimination of camphene during the process of emulsion solvent evaporation method, produce solidified porous microcarrier beads. The surface porous microcarriers beads were further modified to make it competent for cell attachment and proliferation. The surface of these microcarriers were modified with UV/O3 system to introduce functional group and charge on the surface. The treatment followed with the immobilization of halal gelatin on the surface to imorove the biocompatibility of the microcarrier. Porous microcarrier with optimal size distribution was successfully fabricated. The average pore size of 11.74±8.32 µm was obtained with the concentration of 20% (w/v) of camphene. The porous PCL microcarrier was further tailored with gelatin through surface treatment with UV/O3 system and gelatin immobilization and validation of its compatibility towards mammalian cell was tested with cultivation of green monkyer kidney cell (Vero) in the suspension culture. Vero cells attach and proliferatie well on the gelatin coated porous PCL microcarrier with maximum cell number  of 3.90 × 105 cells/ml as compared to cell proliferation on UV/O3 treated porous PCL microcarrier (1.83 × 105 cells/ml). The developed microcarrier may be potentially applicable as a cell delivery scaffold for cell tissue culture and tissue engineering application.

UR - http://ijaseit.insightsociety.org/index.php?option=com_content&view=article&id=9&Itemid=1&article_id=7060 DO - 10.18517/ijaseit.8.4-2.7060

RefWorks

RT Journal Article
ID 7060
A1 Samsudin, Nurhusna
A1 Hashim, Yumi Z. H Y.
A1 Arifin, Mohd A.
A1 Salleh, Hamzah M.
T1 Surface Modification of Microcporous of Polycaprolactone (PCL) Microcarrier to Improve Microcarrier Biocompatibility
JF International Journal on Advanced Science, Engineering and Information Technology
VO 8
IS 4-2
YR 2018
SP 1642
OP 1647
SN 2088-5334
PB INSIGHT - Indonesian Society for Knowledge and Human Development
K1 Halal; porous microcarrier; UV/O3 treatment; microcarrier cell culture.
AB 

Oil/water emulsion solvent evaporation method was employed to fabricate polycaprolactone (PCL) microcarriers. In order to produce porous microcarrier, the method was slightly modified. The porous network channels were generated inside the microcarrier by introducing camphene that was dissolved in the same solvent used to dissolve raw PCL. The evaporation of solvent and sublimination of camphene during the process of emulsion solvent evaporation method, produce solidified porous microcarrier beads. The surface porous microcarriers beads were further modified to make it competent for cell attachment and proliferation. The surface of these microcarriers were modified with UV/O3 system to introduce functional group and charge on the surface. The treatment followed with the immobilization of halal gelatin on the surface to imorove the biocompatibility of the microcarrier. Porous microcarrier with optimal size distribution was successfully fabricated. The average pore size of 11.74±8.32 µm was obtained with the concentration of 20% (w/v) of camphene. The porous PCL microcarrier was further tailored with gelatin through surface treatment with UV/O3 system and gelatin immobilization and validation of its compatibility towards mammalian cell was tested with cultivation of green monkyer kidney cell (Vero) in the suspension culture. Vero cells attach and proliferatie well on the gelatin coated porous PCL microcarrier with maximum cell number  of 3.90 × 105 cells/ml as compared to cell proliferation on UV/O3 treated porous PCL microcarrier (1.83 × 105 cells/ml). The developed microcarrier may be potentially applicable as a cell delivery scaffold for cell tissue culture and tissue engineering application.

LK http://ijaseit.insightsociety.org/index.php?option=com_content&view=article&id=9&Itemid=1&article_id=7060 DO - 10.18517/ijaseit.8.4-2.7060