Modification Of Starch Research Articles

Pulsed Light Technology: Is it Sustainable?

Abstract Pulsed light is a non-thermal method that was initially researched for microbial inactivation using high-power, broad-spectrum light pulses, with the UV-C light portion being the most lethal. This method was introduced to the Western hemisphere with the Hiramoto US patent in 1984 and was developed by PurePulse Technologies. It obtained the FDA approval for food use in 1996 and has been under continuous study and testing by academic institutions since 1998. It is linked to sustainable development goals 2, 3, 6, and 12, but its relation to goal 13 is particularly important, although hindered by lack of data. While numerous applications beyond microbial inactivation have been developed, only two are currently used industrially, namely, the decontamination of food contact surfaces for packaging and the enhancement of vitamin D concentration in edible fungi. Other potential applications include enzyme inactivation, phytochemical synthesis, water pollutant degradation, protein allergen inactivation, mycotoxin inactivation, modification of functional properties of proteins, and starch modification. The main advantage of pulsed light is its rapid effects although it is limited to surfaces and transparent liquids. Further refinement of dosimetry should facilitate the easier scaling up of laboratory results to more industrial applications. Information © The Author 2024

Enzymatic biocatalysis processes on the semicrystalline and morphological order of native cassava starches (Manihot esculenta)

Enzymatic biocatalysis has emerged as a green technology in starch modification with divergent results at the morphological level depending on the origin of the starch source. Therefore, various enzymatic biocatalysts were implemented to evaluate their effect on the morphological and semi-crystalline characteristics of native cassava starches. The degree of affinity of the biocatalysts and the conversion rate on native cassava starches were determined by kinetic parameters such as the Michaelis-Menten constant, whose results revealed the following order of affinity from highest to lowest: α-amylase, amyloglucosidase, pullulanase, and β-amylase. In addition, greater biocatalytic activity of α-amylase and β-amylase was evidenced on the amorphous zones of the polymer associated with the decrease in the amylose content and a significant increase in the degree of relative crystallinity. According to morphological analyses and XDR, the action of amyloglucosidase promoted exo-erosion phenomena and the appearance of lacerations on the granular surface of starch with the consequent decrease in the semicrystalline order. The pullulanase caused slightly eroded fragmented granules with greater biocatalytic activity on the crystalline lamellae, associated with a significant increase in the apparent amylose content. FTIR analysis in the 1,200-900 cm-1 region, corresponding to the starch fingerprint, allowed us to detect notable changes in the degree of molecular order after the enzymatic attack; this result was consistent with the degree of relative crystallinity estimated by X-ray diffraction. Likewise, the results allowed us to notice significant changes in the semi-crystalline order and morphological characteristics during the modification with α-amylase (AAM) and amyloglucosidase (AMG) associated with their greater affinity and preferential action on the amorphous structures located on the granular surface of native cassava starch.

Research on electron beam irradiation in the multiscale structure of starch and its related applications: A review.

Electron beam irradiation (EBI), as a typical "green" emerging technology, can effectively alter the functional properties of starch by influencing its microstructure. This alteration enables starch to meet the current demands of consumers and the market for "health food." This paper reviews studies on modifying various starches using EBI and describes the changes in microstructure, physicochemical properties, and functional properties induced by this method. Additionally, the effects of EBI on starch-containing food products are discussed, along with issues to be addressed and research gaps in the synergistic treatment of modified starch. It is noted that the source, irradiation dose, and irradiation time all influence the effectiveness of starch modification. Given the characteristics of EBI technology, integrating physical, chemical, and biological modification methods can optimize the modification process and enhance efficiency. This technology can potentially diversify modified starch varieties and expand their applications. Furthermore, there remains significant research potential in producing modified starch using EBI technology and applying it to the food industry.

Modifikasi Biofoam Berbasis Pati Singkong dengan Serat Eceng Gondok dan Variasi Konsentrasi Plasticizer

Biofoam is a plant-based alternative packaging. The biofoam was prepared by using the extrusion method and baking process. This research aims to determine the lowest ratio of PVA and glycerol in absorbing water and testing the mechanical properties of biofoam (tensile strength, biodegradation test and FTIR analysis. The best biofoam composition in absorbing water was obtained at a ratio of PVA: glycerol 8%. The results of biofoam characteristics obtained by the water absorption test were 9.76%, maximum bending strength was 9.20 MPa and biofoam can be degraded 100% on day 15. The results of FTIR analysis showed the presence of absorption spectra at wave numbers 3410,15 cm-1, which is a typical region of O-H functional groups (strong and broad) carbohydrates and polyphenols. Modification of starch with fiber and plasticizer in research improves the physicochemical characteristics of biofoam in terms of increasing water absorption and biofoam biodegradation. In contrast, in terms of mechanical properties, the bending strength of biofoam requires further research referring to the characteristics of biofoam mechanical properties toward SNI standards.

Exploring the potential of browntop millet (Urochloa ramosa) starch: Physicochemical, morphological, thermal and rheological properties across four cultivars

This comprehensive research explores the starch isolated from four browntop millet cultivars to determine physicochemical, thermal, morphological, powder flow, pasting, and rheological properties. Significant variations (p ≤ 0.05) were observed among the cultivars. Aerated bulk density (ABD) and Tapped bulk density (TBD) values ranged from 0.476 g/mL (BTM4) to 0.591 g/mL (BTM1), and 0.591 g/mL (BTM1) to 0.476 g/mL (BTM4). Amylose content varied from 22.55% (BTM4) to 25.86% (BTM3), influencing gelling strength and film-forming properties. Water absorption capacity ranged from 1.78 g/g to 1.92 g/g, while oil absorption capacity varied from 2.20 g/g to 2.47 g/g. DSC analysis showed gelatinization temperatures (Tp, and Tc) ranging from 85.44–91.61 °C, and 147.08–154.21 °C, respectively. X-ray diffraction (XRD) patterns revealed A-type crystalline patterns, with relative crystallinity ranging from 22.66% (BTM3) to 27.81% (BTM2). Pasting properties exhibited variations among cultivars, with peak viscosity ranging from 2480 c P to 3119 cP, and pasting temperature from 77.50 °C to 82.35 °C. Rheological analysis indicated shear-thinning behavior. The findings offer insights into the diverse properties of browntop millet starch, contributing to its potential applications in various industries and potentially guiding future studies on browntop millet starch modifications and novel utilization.

Recent Advances in Physical Processing Techniques to Enhance the Resistant Starch Content in Foods: A Review.

The physical modification of starch to produce resistant starch (RS) is a viable strategy for the glycemic index (GI) lowering of foods and functionality improvement in starchy food products. RS cannot be digested in the small intestine but can be fermented in the colon to produce short-chain fatty acids rather than being broken down by human digestive enzymes into glucose. This provides major health advantages, like better blood sugar regulation, weight control, and a lower chance of chronic illnesses. This article provides a concise review of the recent developments in physical starch modification techniques, including annealing, extrusion, high-pressure processing, radiation, and heat-moisture treatment. Specifically, the focus of this paper is on the alteration of the crystalline structure of starch caused by the heat-moisture treatment and annealing and its impact on the resistance of starch to enzymatic hydrolysis, as well as the granular structure and molecular arrangement of starch caused by extrusion and high-pressure processing, and the depolymerization and crosslinking that results from radiation. The impacts of these alterations on starch's textural qualities, stability, and shelf life are also examined. This review demonstrates how physically modified resistant starch can be used as a flexible food ingredient with both functional and health benefits. These methods are economically and ecologically sustainable since they successfully raise the RS content and improve its functional characteristics without the need for chemical reagents. The thorough analysis of these methods and how they affect the structural characteristics and health advantages of RS emphasizes the material's potential as an essential component in the creation of functional foods that satisfy contemporary dietary and health requirements.

Transglutaminase and protease: How starch granule-associated protein modification affects starch retrogradation

This study investigated the effects of transglutaminase (TG) and protease on starch granule-associated proteins and their impact on starch properties, especially retrogradation. TG incorporated storage protein onto the starch surface, while protease removed starch-granule associated proteins from it. Neither treatment altered the basic structural characteristics of starch such as its crystallinity or thermal properties, but could significantly affect swelling power, amylose leaching, and retrogradation. TG-treated wheat starch (WST) showed reduced swelling power (11.50) and amylose leaching (28.92 mg/g) compared with the control wheat starch (WSC) at 11.95 and 30.53 mg/g, respectively, suggesting a more stable structure. Conversely, protease-treated starch (WSP) exhibited increased swelling power at 12.47 and amylose leaching at 33.17 mg/g, suggesting a disintegration of starch granules. Both WSC and WST showed the same degree of retrogradation at the equilibrium state (a) at 0.06, whereas WSP, with a higher degree at 0.08, promoted retrogradation. The rate constant (k) for WST was lower (1.41 d−1) than that for WSC (2.37 d−1), indicating that TG treatment effectively inhibited retrogradation. These findings illustrated the distinct mechanisms through which TG and protease modify starch properties by acting on starch granule-associated proteins. This also highlighted the potential of TG and protease to control starch modifications for specific applications.

Energy-size relationship and starch modification in planetary ball milling of quinoa

The effects of speed (250–450 rpm) and time (10–50 min) on milling energy (E), particle size distribution (PSD), crystallinity degree (CD), damaged starch (DS), microstructure, hydration and pasting properties of flours obtained in a planetary ball mill (PBM) were investigated. As increasing milling severity quinoa flours showed polydispersed PSD (peaks at 417, 40 and 2 μm) with a shift towards smaller size and greater dispersion (Span: 3.0–5.2) as well as particles with rounded edges and polished surfaces (SEM images). The relationship E − D50 were satisfactorily predicted by the Walker's equation. The hydration tests as function of temperature and milling conditions revealed a complex flour behavior due to differences in PSD, composition, and DS content. The increasing milling energy caused a decrease in peak viscosity (PV), trough viscosity (TV) and final viscosity (FV) of up to 36%, 29%, and 25%, respectively. Significant correlations between flour attributes were found (DS-CD, r = −0.83, p < 0.01; PV-D50, r = 0.92, p < 0.01; TV-D50, r = 0.94, p < 0.01; FV-D50, r = 0.90, p < 0.01) denoted the increase of starch degradation as milling severity rises. These results can be used to improve the manufacture and the selection criteria of quinoa flour with specific functional attributes.

Effect of microwave irradiation and conventional heating on high pressure modified white finger millet starch hydrogel properties

High pressure modified (200 MPa and 400 MPa for 10 min) white finger millet starch hydrogels were prepared with three starch concentrations (12 %, 15 % and 18 % (w/v)), by conventional heat treatment (75 °C for 12 min) and microwave treatment (50 s at 900 W, surface temperature 75 °C). The prepared hydrogels were compared to native white finger starch hydrogels for understanding the effect of modification as well as the gel synthesis method. Effect of the storage period on physical stability was evaluated for ten days by evaluating weight loss, water activity, and color. The whiteness index of the prepared hydrogel intensified during the storage period, and water activity was reduced (0.99–0.976). While stored at 4 °C, the hydrogel weight decreased due to moisture migration. The results emphasize that treatment conditions, starch modification, and concentration significantly affected water absorption. The maximum gel strength was identified for conventional heat-induced 400 MPa high-pressure modified hydrogel stored for ten days. 1H NMR relaxation time showed microwave-induced gel synthesis had a shorter relaxation time. The gel microstructure helped to correlate the swelling and gel strength increment in the modified gel sample, as it had a higher wall thickness and a smaller pore size than heat-induced hydrogels. These findings help to conclude high pressure modified white finger millet starch hydrogel synthesised by microwave irradiation can be alternative to conventional heat gelatinisation method.

Combined effects of high hydrostatic pressure and pulsed electric fields on quinoa starch: Analysis of microstructure, morphology, thermal, and pasting properties

The aim of this study was to evaluate the impact of non-thermal methods, using high hydrostatic pressure (HHP) and pulsed electric field (PEF), on the dual modification of quinoa starch and to analyze the microstructural, morphological, thermal, pasting, and texture properties. Starch was treated with HHP at 400 MPa for 10 min, while PEF was applied using voltages of 10 and 30 kV cm−1 for a total time of 90s. The modification techniques were effective in breaking down amylose molecules and amylopectin branches, where for the dual treatment, higher values of DP6–12 were found. The average diameter and gelatinization temperatures were elevated after HHP, thus forming clusters that require more energy for paste formation. The use of 30 kV cm−1 and 400 MPa (HP30) in starch facilitates the creation of new food products with better texture, stability and nutritional value, making them suitable for use in food emulsions and the cosmetics industry.

Advancements in Pulse Starches: Exploring Non-Thermal Modification Methods.

The surge in the global demand for plant-based proteins has catapulted pulse protein into the spotlight. To ensure economic viability and sustainable production, it is crucial to utilize pulse starch, a by-product of plant protein fractionation. Despite the increasing interest in pulse starches, there is a notable gap in knowledge regarding their modifications and applications compared to cereal and tuber starches. Non-thermal techniques such as electron beam radiation, static high pressure, microfluidization, and cold plasma are emerging as innovative methods for starch modification. These techniques offer significant advantages, including enhanced safety, environmental sustainability, and the development of unique functional properties unattainable through conventional methods. However, challenges such as equipment availability, high costs, and energy consumption hinder their widespread adoption. In light of the growing emphasis on "clean and green labelling" and effective "waste management" in food production, evaluating non-thermal techniques for pulse starch modification is critical. This review aims to thoroughly assess these non-thermal techniques and their combinations, offering valuable insights for researchers and the food industry. By maximizing the potential of pulse starches in innovative food applications, it provides a comprehensive guide for effective non-thermal methods that add value and align with sustainable practices.

Modified starch as a component of environmentally friendly polymer adsorbents − from synthesis and characterization to potential application in the removal of toxic C.I. Basic Yellow 2 dye

Increasing global degradation of the aquatic environment is forcing the search for new and low-cost adsorbents of reduced toxicity, derived from natural and renewable sources. To meet these expectations, a new approach to adsorbent fabrication was developed.The study aimed to synthesize, characterize, and apply environmentally friendly adsorbents based on poly(ethylene glycol dimethacrylate-co-vinyl acetate) (EGDMA-VA) with unmodified/modified starch (St). The first step proposed a new mechanochemical method of starch modification using thiourea (T) and potassium dihydrogen phosphate (P). Then, the functionalized starch was used to obtain polymeric microspheres. The final step involves their application for the removal of toxic C.I. Basic Yellow 2 (BY2) dye. The pristine materials and adsorbents were characterized by ATR/FT-IR and XPS, DSC, SEM/EDX, porous structure, particle size distribution, tendency to swell, and pHpzc.Adsorption batch studies of BY2 as a function of time (1–60 min), initial dye concentration (1–25 mg/L, pH=8.3), temperature (298–328 K), and competing electrolyte (5–15 g/L Na2SO4) and surfactant (0.1–0.5 g/L CTAB) presence were carried out. The kinetic studies were analyzed using pseudo-first order, pseudo-second order, and intraparticle diffusion models. The equilibrium studies revealed that the Freundlich isotherm model (kF=5.62–6.56 mg1-1/n L1/n) described BY2-adsorbents systems rather than Langmuir, Temkin or Dubinin-Radushkevich. Thermodynamic parameters (ΔG°, ΔH°, and ΔS°) pointed to the exothermic nature of adsorption and its spontaneousness. Importantly, the starch-modified microspheres were regenerated, too.

Gadung (Dioscorea hispida) tuber starch modified by freeze moisture treatment and heat moisture treatment: a study of functional, pasting, and physicochemical properties

ABSTRACT Gadung starch has limitations in several functional properties and thermal stability. Modifying starch through temperature treatments such as Freeze Moisture Treatment (FMT) and Heat Moisture Treatment (HMT) potentially improves these weaknesses. This research aimed to determine the effects of FMT and HMT on the functional, pasting, and physicochemical properties of gadung starch. This study consisted of a variety of treatments, namely native starch, FMT, HMT 100°C, HMT 110°C, FMT + HMT 100°C, and FMT + HMT 110°C. The results showed that FMT and HMT treatments significantly affected the functional, pasting, and physicochemical properties of gadung starch. The combination modification treatment of FMT + HMT 110°C increased swelling volume by 1.44 times, and water absorption capacity increased by 1.37 times. This was confirmed by the formation of porous and amorphous starch granules. Modified starch also had the best heat stability, as indicated by a low breakdown viscosity of 31.00 ± 9.90 cP. FMT+HMT110°C modified treatment was the best treatment because it had more pores, cracks, and higher swelling volume. The starch crystallinity index of modified starch decreased from 35.75 to 31.58 and changed the crystallinity type from B-type to A-type. The starch modification did not cause changes in functional groups but reduced crystallinity as indicated by the smaller ratio of the bands at 1045/1022 and the higher ratio at 1022/995 from FTIR spectra. Thus, FMT and HMT could effectively improve the characteristics of gadung starch by forming heat-stable amorphous starch.

Starch phosphorylation—A needle in a haystack

Phosphoesterification is the only naturally occurring covalent starch modification identified to date, and it has a major impact on overall starch metabolism. The incorporation of phosphate groups mediated by dikinases [α-glucan, water dikinase (GWD), EC 2.7.9.4; phosphoglucan, water dikinase (PWD), EC 2.7.9.5] massively alters the starch granule properties; however, previous studies did not determine whether the starch-related dikinases bind the phosphate to the glucosyl units within the amylopectin molecules in a specific pattern or randomly. In order to answer this challenging question, a number of approaches were initially pursued until a protocol could be established that enabled a massive step forward in the in vitro analysis of phosphorylated glucan chains obtained from starch. For this purpose, phosphorylation by GWD was investigated, including the final state of phosphorylation i.e., the state of substrate saturation when GWD lacks further free hydroxyl groups at OH-C6 for the catalysis of monophosphate esters. Since the separated phosphorylated glucan chains were required for the analysis, isoamylase digestion was performed to cleave the α-1,6-glycosidic bonds and to allow for the removal of the huge number of existing neutral chains by means of anion exchange chromatography. Via Matrix-Assisted Laser Desorption/Ionization–Time of Flight (MALDI-TOF) MS and MALDI-MS/MS, the phosphorylated α-glucan chains were analysed, and the position of the phosphate group within the chain in relation to the reducing end was determined. Here, we demonstrate a protocol that enables the analysis of phosphorylated oligosaccharides, even in small quantities.

Ultrasonication: An Efficient Alternative for the Physical Modification of Starches, Flours and Grains.

Ultrasonic (USC) treatments have been applied to starches, flours and grains to modify their physicochemical properties and improve their industrial applicability. The extent of the modification caused by USC treatment depends on the treatment conditions and the natural characteristics of the treated matter. Cavitation leads to structural damage and fragmentation and partial depolymerization of starch components. The amorphous regions are more susceptible to being disrupted by ultrasonication, while the crystalline regions require extended USC exposure to be affected. The increased surface area in USC-treated samples has a higher interaction with water, resulting in modification of the swelling power, solubility, apparent viscosity, pasting properties and gel rheological and textural properties. Starch digestibility has been reported to be modified by ultrasonication to different extents depending on the power applied. The most important treatment variables leading to more pronounced modifications in USC treatments are the botanical origin of the treated matter, USC power, time, concentration and temperature. The interaction between these factors also has a significant impact on the damage caused by the treatment. The molecular rearrangement and destruction of starch structures occur simultaneously during the USC treatment and the final properties of the modified matrix will depend on the array of treatment parameters. This review summarizes the known effects of ultrasonic treatments in modifying starches, flours and grains.

Diseminasi Teknologi Tepat Guna Pengembangan Produk Olahan Sagu untuk Peningkatan Ekonomi UMKM di Kabupaten Manokwari - Papua Barat

Sago utilization in Papua has not been maximized due to the limited knowledge and abilities of local communities. This technology dissemination activity aims to increase the utilization of local Papuan resources as a substitute for wheat, by applying the equipment and processing methods that have been developed. The method used is tool dissemination and training on sago starch modification and the manufacture of various processed products in the development of business units. Prototype technology disseminated in the form of starch acidification equipment and drying equipment with UV irradiation. The trial results showed that the capacity of the acidification tool produced was 50 kg of wet sago starch (50% moisture content) with an acidification process duration of 3 days. Meanwhile, the capacity of the dryer is 25 kg of wet sago starch (50% moisture content) with a drying time of ± 20 hours. The use of disseminated tools can reduce material contact with contaminant sources resulting in better product quality.

In situ starch and water modification using atmospheric plasma: Structure, functionality and in vitro digestibility

Starch modification has become necessary to develop functional foods. Sustainable technologies like plasma-activated water (PAW) have been combined with hydrothermal treatments; however, the scaling-up process is challenging. Therefore, a simultaneous treatment of starch and water in a plasma reactor and a 24 h soaking of starch-water after the treatment were compared. The effect of the treatments on the structural, functional, and digestibility properties of starches (normal (NS), waxy (WS), and high amylose (HAS)) with different amylose/amylopectin content was assessed. The results show that simultaneous treatment mainly affected the water properties. Nevertheless, the contact time (24 h) after treatment between starch and water promoted the alteration of amylose chains, branching amylopectin molecules and hydrated crystals of HAS, increasing its rapidly (RDS) and slowly (SDS) digestible starch content. Meanwhile, in NS, the contact time favored the high re-engagement of amylose-amylopectin chains inside starch granules, significantly improving the resistant starch (RS) fraction from 31 % to 75 %.

Modification of pea starch using ternary mixtures of natural crosslinking agents: Vanillin-chitosan-betaine and vanillin-gelatin-betaine

Different methods of starch modification have been proposed to broaden its application. In this study, the effects of ternary mixtures of natural crosslinking agents: chitosan-betaine-vanillin and gelatin-betaine-vanillin on the properties of pea starch were explored. These combinations of substances were selected because they have complementary crosslinking mechanisms. The effects of the ternary crosslinker mixtures on the gelatinization, mechanical properties, thermal stability, and microstructure of pea starch were compared. Both combinations of crosslinkers enhanced the gelatinization viscosity, viscoelasticity, gel hardness, and thermal stability of the pea starch, by an amount that depended on the ratio of the different components in the ternary mixtures. In all cases, the crystal structure of the starch granules disappeared after gelatinization. The modified starch had a more compact and uniform microstructure than the non-modified version, especially when it was crosslinked by vanillin, gelatin, and betaine. The improvement in the gelation properties of the starch were primarily attributed to hydrogen bonding, electrostatic attraction, and Schiff base crosslinking of the various components present. Gelatin enhanced the gel strength more than chitosan, which was probably because of greater hydrogen bonding. Our findings suggest that the properties of starch can be enhanced by adding ternary mixtures of natural crosslinkers.

Structural characterization and in vitro digestibility of rice starch processed with the combination of ultra‐high pressure homogenization, debranching, and temperature‐cycled crystallization

AbstractThis study examined the structural characterization and in vitro digestibility of rice starch processed with the combination of ultra‐high pressure homogenization (UHPH), debranching, and temperature‐cycled crystallization under various pressures (0–160 MPa). After UHPH treatment, the degree of branching (DB) of processed starches (0.65%–2.03%) was lower than that of the native rice starch (NS, 2.96%). Assessment of chain length distribution suggested that the considerable amylose was produced after treatments. Processed starches exhibited an irregular fragmented structure, and the crystalline structure was transformed from A‐type (native rice starch) into B + V‐type (processed starches). Moreover, the relative crystallinity (RC) and the absorbance ratio of 1047/1022 cm−1 (R1047/1022) of processed starches decreased from NS (RC, 22.99%; R1047/1022, 0.79) to 13.47%–18.21% (RC) and 0.51–0.78 (R1047/1022), respectively. Iodine binding curves revealed that processed starches possessed the higher degree of polymerization (DP). Furthermore, the contents of slowly digestible starch (SDS) and resistant starch (RS) increased in all processed starches, and the RS content of starch treated under 160 MPa (35.33%) was notably greater than that of native starch (9.37%). These results suggested that the UHPH can be used as a pretreatment strategy to reduce the digestibility of starch products.Practical applicationsUHPH pretreatment disrupts starch molecular chains to produce the large amounts of short linear amylose. Debranching followed by temperature‐cycled crystallization can increase the content of resistant starch (RS), yielding a raw material suitable for boosting the health of the digestive system and overall health. Therefore, UHPH pretreatment has a high application value in the field of starch modification.

Oxidation-induced starch molecular degradation: A comprehensive kinetic investigation using NaClO/NaBr/TEMPO system

Starch degradation often coincides with its chemical modification, and understanding how chemical modification influences starch degradation is vital for determining the properties of the resultant modified products. This work investigates the effect of oxidation on starch molecular degradation, examining factors such as oxidation degree, reaction kinetics, and degradation patterns during 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-mediated starch oxidation under varying conditions, including reaction time, pH, temperature, and concentrations of NaBr, TEMPO, and NaClO. Results emphasize that extended reaction durations primarily lead to β-elimination, causing α-1,4 linkage cleavages. pH 8.5 favored non-selective oxidation, while pH 11 enhanced β-elimination, both slowing the reaction rate and severely damaging starch chains (Mw of 8.8 × 105 g/mol and 7.2 × 105 g/mol, respectively). Elevated temperature from 0 to 30 °C significantly expedited both selective and non-selective oxidation, dramatically reducing molecular mass to 8.1 × 105 g/mol. Increasing concentrations of NaBr and TEMPO boost the reaction rate with minimal impact on molecular mass. Meanwhile, increasing NaClO concentration from 0.2 to 2.2 mmol/g-starch not only affects the reaction rate but also reinforces β-elimination, enhancing molecular degradation. This study is insightful for starch modification to achieve desired oxidation levels and chain lengths by controlling reaction conditions, offering potential advancements in oxidized starch-based materials like nano micelles.