The acrylated palm oil (APO) nanoparticle is a potential product that can be used as carriers in
medical field. The main focus of the present study was to study the potential of the APO
nanoparticles for used in a controlled drug delivery system. The microemulsion system is used as a
medium to incorporate an active substance such as Thymoquinone (TQ) into the APO polymeric
micelle and then the radiation technique is used as a tool for the synthesis of TQ-loaded APO
nanoparticle. The nano-size TQ-loaded APO particles resulted the particle size of less than 150 nm
with spherical in shape. The TQ release profile was carried out in potassium buffer saline (PBS)
solutions (pH 7.4) at 37
oC. And, the zero-order model has been used to determine the mechanism
of the drug release from the corresponding nanoparticles, respectively. The TQ release was found
to be sustained and controlled in pH 7.4. At pH 7.4, the release of TQ followed the zero-order
model. The in-vitro drug release study showed a good prospect of the APO nanoparticle on being a
potential drug carrier as there are toxic against colon cancer cells and not toxic towards normal
cells. This suggested that the APO product produce using this radiation technique can be
developed into different type of carrier systems for controlled drug release applications.
The use of microemulsion in the development of nanoparticle based on acrylated palm oil product is demonstrated. Acr ylated palm oil microemulsions were prepared using ionic surfactant. Combination methods of emulsion polymerization and radiation crosslinking were applied to the microemulsion system for synthesizing nanoparticle. The ionizing radiat ion technique was introduced to generate a crosslinking reaction in the development of nanoparticle. The nanoparticle was evaluated in terms of particle diameter, surface charge, pH and conductance. Their image was captured using Tra nsmission electron microscopy (TEM). Results show that the size, charge and shape of the particles are influenced by c oncentration of surfactants, monomer concentration, radiation dose and time of storage. The study showed a promising method to produced nanoparticle. This nano-sized product has the potential to be utilized as controlled-drug-release-carrier.