Browsing by Author "Wijayawardana, S"

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Open Access
Fe3O4 Chitosan Nanocomposite as a pH-Responsive Delivery System for Enhanced Delivery of Punica Granatum L. Polyphenols
(American Chemical Society, 2025-10-17) Rukshan, R; Rajapaksha, N; Wijayawardana, S; Thambiliyagodage, C; Senevirathne, U; Jayanetti, M; Samarakoon, U
Punica granatum extract (PG), consisting of punicalagin, ellagic acid, and gallic acid, was loaded onto an Fe3O4/Chitosan (Fe3O4@Chi) nanocomposite (Fe3O4@Chi-PG) to enhance pharmacokinetic properties. Fe3O4was synthesized via the coprecipitation method and coupled with chitosan in 2% acetic acid solution via glutaraldehyde cross-linking. The presence of interested polyphenols in the pomegranate extract was confirmed by HPLC analysis, and the extract was post-loaded to the nanocarrier. XRD confirmed the crystallographic orientation of the nanocarrier, and SEM analysis confirmed the successful coupling of Fe3O4onto the chitosan surface during the fabrication of Fe3O4@Chi. BET surface area analysis revealed the presence of micro- and mesopores in the synthesized materials. Significant reduction of the BET surface area and the pore volume of Fe3O4@Chi-PG compared to Fe3O4@Chi suggested the loading of the porous network and surface by PG. The presence of vibrational bands corresponding to the functional groups of the relevant bioactive compounds was confirmed via FT-IR analysis. The IC50values of the nanocomposite for DPPH and egg albumin denaturation assays were 18.69 and 257.69 μg/mL, respectively. The PG encapsulation efficiency of Fe3O4@Chi-PG was reported to be 86.44%. The pH-responsive release of the polyphenols was studied by fitting the release data into five kinetic models, including Korsemeyer–Peppas (KP) and Peppas–Sahlin (PS). The KP and PS models were selected to interpret the release mechanism based on the R2≥ 0.95 value. A combination of Fickian diffusion, relaxation, and swelling dominates the polyphenol release. Quasi-Fickian diffusion is responsible for the release in media with pH 1–6.7, whereas anomalous transport occurs at pH 7.4 (n = 0.46) according to the KP model. Polymer relaxation is the dominant mechanism for the release of bioactive compounds at pH 7.4, as exhibited by R/F > 1. However, the contribution of relaxation to the release of polyphenols at pH 2.5, 4, and 5.5 was negligible according to the parameters (kR= 0). Characteristics of chitosan, including protonation and deprotonation of NH2groups, surface charge of Fe3O4, ionization of COOH and OH groups of the polyphenols, and molecular weight of the active compounds, contributed to the differences in the release behavior.
Open Access
In vitro release kinetics of bioactive compounds (gallic acid, ellagic acid, and eugenol) from chitosan polymer and the bioactivity of herb-loaded chitosan–CuO nanocomposites
(Nature Research, 2025-10-13) Ekanayake, G; Wijayawardana, S; Jayanetti, M; Thambiliyagodage, C; Liyanaarachchi, H; Mendis, A
The biological efficacy of nanocomposites comprised of chitosan, CuO nanoparticles, and extracts of Phyllanthus emblica, and Syzygium aromaticum was studied. The study assessed the pH– and ionic strength-responsive controlled release of the bioactive compounds, gallic acid, ellagic acid and eugenol, from the chitosan biopolymer. Release data were fitted into zero-order, first-order, Korsmeyer–Peppas (KP), Peppas–Sahlin (PS), Higuchi, and Hixson–Crowell kinetic models to evaluate the release mechanism. According to KP and PS models (R2 ≥ 0.96), release was governed by quasi-Fickian diffusion (n < 0.43), where the diffusion occurs along with the polymer relaxation and swelling. P.emblica-coated chitosan (PeC) composite exhibited a burst release at acidic media conditions, and a quasi-Fickian diffusion at pH 5.5–7.4. Higher ionic strength caused salting-in effects for PeC in 0.4 M media, resulting in a transiently increased release. In acidic conditions, diffusion-controlled release was observed for S.aromaticum-coated chitosan (SaC) composite, with the optimal release at pH 4 media. Release was facilitated by hydrophobic nanochannels at elevated pH (8.5–10) and ionic strength of 0.5 M NaCl. The PS model’s relaxation contributions were significant at 0.4 M NaCl and 5 mg drug loading. Both composites demonstrated enhanced release at physiological conditions (0.1–0.2 M NaCl, pH 7.4). Sustained release of SaC was achieved in near-neutral/moderate ionic strength media, whereas PeC exhibited sustained release in acid/low ionic strength media. The PeC and SaC composites showed IC50 values of 10.78 µg/mL and 19.27 µg/mL for the DPPH radical scavenging ability, respectively. Recorded IC50 values for the egg albumin denaturation assay were 467 µg/mL and 390.44 µg/mL, respectively. The antibacterial activity against Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, and Staphylococcus aureus showed maximum inhibition zones of 11.83 ± 0.06 mm (Chitosan: CuO 1:2), 12.67 ± 0.20 mm (1:4), 16.50 ± 0.09 mm (1:4), and 11.83 ± 0.08 mm (4:1), respectively. Among the herbal-coated samples, SaC exhibited the highest activity of 23.67 ± 2.84 mm against E. coli
Embargo
Kinetic study of in vitro release of curcumin from chitosan biopolymer and the evaluation of biological efficacy
(Elsevier B.V., 2024-09) Wijayawardana, S; Thambiliyagodage, C; Jayanetti, M
Sustained release of curcumin from the polymeric carrier system chitosan, a natural biopolymer material derived from chitin originated from natural shrimp shell waste, was studied. Six kinetic models, zero order, first order, Korsmeyer–Peppas (KP), Peppas – Sahlin (PS), Higuchi, and Hixson–Crowell, were applied to study the drug release kinetics. The release mechanism of the drug from the curcumin-chitosan composite was evaluated by changing the pH, ionic strength of the release media, and drug concentration. KP and PS models were selected among the studied models to investigate the drug release mechanism from the chitosan biopolymer based on the R2 values (R2 > 0.99). The model constants m in the PS model and n in the KP model stand for the case II relaxation and Fickian diffusion contribution, respectively. The n being < 0.43 in the KP model suggests that the Fickian diffusion governs the drug release. Furthermore, there is a noticeable difference between the values obtained for model parameters m and n in the PS and KP models, indicating that Case II relaxation and Fickian diffusion play crucial roles in the curcumin release mechanism from chitosan. Polymer relaxation has been proven to play a predominant role in releasing curcumin from the composite at lower ionic strengths and higher pH values. Anti-inflammatory activity was tested using the egg-albumin denaturation assay, and the diphenyl-2-picrylhydrazyl assay was carried out to determine the antioxidant activity of the composite. The composite material showed IC50 values of 0.29 mg/ mL and 1.08 mg/ mL for anti-inflammatory and anti-oxidant activities, respectively. The drug composite has shown antibacterial activity against Pseudomonas aeruginosa, Klebsiella pneumoniae, and Staphylococcus aureus, which are highly effective against S.aureus. The resulting inhibition zones for S.aureus were 13.34 ± 0.34 mm, 16.34 ± 0.60 mm, and 13.34 ± 0.73 mm for 5, 10, and 20 mg/ml concentrations, respectively. The drug composite’s minimum inhibitory concentration/ minimum bactericidal concentration ratio for S.aureus, K. pneumoniae, and P.aeruginosa was greater than 4, suggesting that they cause bacteriostatic effects.
Open Access
The photocatalytic and antibacterial activity of graphene oxide coupled CoOx /MnOx nanocomposites
(Elsevier B.V., 2025-02) Liyanaarachchi, H; Thambiliyagodage, C; Jayanetti, M; Ekanayake, G; Wijayawardana, S; Samarakoon, U
CoOx and MnOx metal oxide composites were fabricated via co-precipitation varying the Co:Mn (CM) weight ratio as 4:1, 2:1, 1:1, 1:2 and 1:4, and they hydrothermally coupled with 30 wt% of graphene oxide (GO). XRD analysis revealed the presence of Co3O4 and CoO, and Mn2O3 and Mn3O4 phases in pure CoOx and MnOx metal oxides, respectively. The irregularly shaped metal oxide nanocomposites comprised Co3O4, Mn2O3 and Mn3O4 phases and were immobilized on GO. The band gap values of the composites varied in the range of 1.86 – 2.22 eV. The highest photocatalytic activity with a rate constant of 3.5 × 10−3 min−1 was obtained with CMG (1:4). The total removal of MB increased by 55.8 % when CM (1:4) were coupled with GO. The rate of photocatalysis was dramatically increased in the presence of S2O82- and was decreased in the presence of EDTA and isopropyl alcohol. The effect of catalyst dosage was determined by varying the weight to 25, 50, 75, and 100 mg, and the dye concentration was varied in the range of 25, 50, 75 and 100 mg/L. The presence of Pb2+ and Rhodamine B decreased the photocatalytic activity, while it remained the same in the presence of Cl- and PO43- as co-pollutants. The photocatalytic activity of CMG (1:4) was reduced to 72 % upon using the catalyst for five cycles. All the synthesized nanocomposites exhibited greater sensitivity to the Gram-positive strain than the Gram-negative strains.