Saputra, Arya Ananda
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Synthesis and Characterization of Porous Polymer as a Support Matrix for Lipase Immobilization Erwanto, Erwanto; Saputra, Arya Ananda; Abimanyu, Muhammad Rakha
Hydrogen: Jurnal Kependidikan Kimia Vol. 13 No. 4 (2025): August 2025
Publisher : Universitas Pendidikan Mandalika

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33394/hjkk.v13i4.16864

Abstract

Immobilization of lipase on solid supports has become a promising approach to improve enzyme stability, activity, and reusability in various industrial processes. This study focuses on the development of a porous polymer, poly(glycidyl methacrylate-co-trimethylolpropane trimethacrylate) [Poly(GM-co-TT)], as a functional support for covalent lipase immobilization. The experimental procedure included three main stages. First, Poly(GM-co-TT) was synthesized via free radical polymerization using a ternary porogenic solvent system consisting of 1,4-butanediol, 1-propanol, and water in a 4:7:1 (v/v) ratio to obtain a porous structure. Second, lipase was immobilized covalently through the reaction between epoxy groups of the polymer and amino groups of the enzyme, using a 0.2 M KCl–NaOH buffer (pH 11) at a final enzyme concentration of 10 mg/mL, incubated at room temperature for 120 minutes. Third, characterization was performed using FTIR spectroscopy and scanning electron microscopy (SEM) to verify successful immobilization. FTIR analysis revealed the presence of ester (C=O), ether (C–O–C), and epoxide (C–O) groups in the polymer. Post-immobilization spectra showed reduced epoxy band intensity (~910 and 840 cm⁻¹) and the appearance of amide bands (~1640–1660 cm⁻¹), indicating covalent bonding between polymer and enzyme. SEM images confirmed a porous, globular, interconnected morphology with well-distributed pores, ideal for enzyme anchoring. The open and rough surface increases surface area, enhancing immobilization efficiency. The novelty of this study lies in employing Poly(GM-co-TT) as a porous polymer that preserves epoxy functionality while effectively supporting covalent lipase immobilization.
Synthesis AuNPs Using Moringa oleifera Extract and Potential Study as Colorimetric Microplastic Detection Thohir, Muhammad Bakhru; Setyaningrum, Dyah; Efendi, Meilisa Rusdiana Surya; Saputra, Arya Ananda; Nursaida, Marta Citra
Hydrogen: Jurnal Kependidikan Kimia Vol. 13 No. 3 (2025): June 2025
Publisher : Universitas Pendidikan Mandalika

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33394/hjkk.v13i3.16603

Abstract

Nanoparticles are multipurpose materials that have been utilized in the medical, energy, and environmental monitoring fields. The advantage of nanoparticles is that they have unique physicochemical properties such as surface area, optical activity, and surface modifiability. One of the important uses of nanoparticles is for environmental monitoring. This is because the surface of nanoparticles can be modified, and with their small size, they can reach analytes in difficult matrices. However, conventional synthesis methods of nanoparticles have been unsustainable. Therefore, the synthesis of AuNPs using bioreductors was considered urgent. The aim of this research was to determine the optimum conditions for the synthesis of AuNPs with Moringa oleifera (MO) as a bioreductor to obtain AuNPs-MO, to characterize the synthesized AuNPs-MO, and to study the application of AuNPs-MO for monitoring microplastic pollutants. This research was conducted through the stages of extraction, determination of optimum conditions, characterization, and literature study of the potential of AuNPs-MO as a detector. Determination of optimum conditions was carried out by applying variations in pH and precursor-reducing agent ratio. The optimal pH was found to be 6, and the optimal volume ratio was 15:5 (mL). Characterization of AuNPs-MO was conducted using FTIR and PSA. The FTIR spectra showed identical absorption patterns for AuNPs synthesized with bioreductants, and the particle size was found to be 61.15 nm. In addition, microplastics were detected using AuNPs both directly, through surface modification with proteins, and indirectly, with the assistance of acetone. From this series of experiments, satisfactory results were obtained.