Research Article

Impact of Orange Peel Essential Oil Microcapsules (OPEOM) on Feed Utilisation, Performance, and Blood Biochemistry in Grower-Phase Sentul Chickens

Denny Rusmana1*, Heni Natalia Aritonang2,3, Eli Sahara4, Andi Mushawwir1

1Department of Animal Nutrition and Feed Technology, Faculty of Animal Science, Padjadjaran University, Jalan Ir. Soekarno Km. 21 Jatinangor, Sumedang 45363, West Java, Indonesia; 2Doctoral Programme, Faculty of Animal Science, Padjadjaran University, Jatinangor Campus Jl. Ir. Soekarno KM.21, Jatinangor-Sumedang 45363, Indonesia; 3Department of Animal Bioscience, Faculty of Food Security, Surabaya State University. Campus 3, Jl. Prof. Dr. Moestopo No. 4, Pacar Keling, Tambaksari District, Surabaya, East Java 60131, Indonesia; 4Animal Science, Faculty of Agriculture, Sriwijaya University, Jalan Palembang-Prabumulih, KM 32, Inderalaya, Ogan Ilir Regency, 30662, South Sumatra, Indonesia.

Received | September 27, 2025; Accepted | October 22, 2025; Published | December 03, 2025

*Correspondence | Denny Rusmana, Department of Animal Nutrition and Feed Technology, Faculty of Animal Science, Padjadjaran University, Jalan Ir. Soekarno Km. 21 Jatinangor, Sumedang 45363, West Java, Indonesia; Email: [email protected]

Citation | Rusmana D, Aritonang HN, Sahara E, Mushawwir A (2025). Impact of orange peel essential oil microcapsules (OPEOM) on feed utilisation, performance, and blood biochemistry in grower-phase sentul chickens. Adv. Anim. Vet. Sci., 13(12):2598-2606.

DOI | https://dx.doi.org/10.17582/journal.aavs/2025/13.12.2598.2606

ISSN (Online) | 2307-8316

Copyright: 2025 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

INTRODUCTION

The livestock industry’s focus on zero waste and products free from synthetic materials has increased interest in researching the potential of natural plant-based materials as feed additives. Previous studies have been quite interesting because compounds from these natural materials can trigger immunity, modulate metabolism, and improve performance (Kamil et al., 2020; Mousapour et al., 2020). Further research and application in local chickens is fundamental and has not been widely reported.

Plant-derived essential oils, such as orange-peel oil, have gained significant attention in animal nutrition studies because they contain diverse bioactive compounds like terpenes, terpenoids, and phenylpropene (Meligy et al., 2023). These compounds affect physiological and biochemical functions, boosting antioxidant defenses and promoting better growth in animal. Microencapsulation protects the volatile components of these oils from degradation in the digestive system (Mushawwir et al., 2021a), allowing for targeted and sustained release to maximize their effectiveness (Prachumchai et al., 2024).

Previous researchers have widely reported the application of essential oils to animals. For example, Mousapour et al. (2020) compared encapsulated and non-encapsulated essential oils. They reported that broiler performance appeared to be better with the encapsulation technique, while feed digestibility did not show an increase in the essential oil treatment group without encapsulation. Other studies have shown that unencapsulated garlic essential oil is ineffective due to polymer degradation before reaching the ileum. It inhibits glycogenolysis even at relatively high doses (Mushawwir et al., 2021a).

This method tackles issues related to essential oils’ instability, like oxidation and volatilization, helping to maintain their bioactivity and therapeutic effects. Microencapsulation techniques, such as polymer shells or carrier materials (Rahmania et al., 2022), significantly improve these active ingredients’ stability, bioavailability, and controlled release (Li et al., 2022), shielding them from harmful environmental factors during feed processing and digestion. This increased stability ensures a more reliable delivery of active compounds, leading to better animal physiological responses (Muhammad et al., 2023; Prachumchai et al., 2024; Mushawwir et al., 2023).

Research on essential oils, including those from oregano and cinnamon, has demonstrated their ability to replace antibiotic growth promoters, primarily due to their antimicrobial, antioxidant, anti-inflammatory, and analgesic properties (Chen et al., 2023). Although their application does not always yield satisfactory results (Li et al., 2022), even excessive doses can cause a decline in performance (Prachumchai et al., 2024). Adding phytogenic feed additives, particularly essential oils, has improved feed efficiency in broiler chickens by modulating lipid and protein intermediate metabolic signalling pathways, ultimately enhancing growth performance and meat characteristics (Dorantes-Iturbide et al., 2023). While the application of orange peel, often reported as orange peel powder, has been studied in livestock by Purwanti et al. (2024), the results showed no significant difference compared to the control group without orange peel powder. Meanwhile, Purwanti et al. (2024) applied it to ruminant. However, research reports on using essential oils from orange peel in poultry remain sporadic.

Phytogenic compounds from fruit peels have attracted much interest because they can improve ileum function, boost feed efficiency, and reduce environmental pollutants (Tanuwiria et al., 2023; Manin et al., 2024). Microencapsulation, particularly of citrus peel essential oils, offers an effective way to deliver these compounds specifically and enable sustained release in the digestive system, enhancing their benefits for animal metabolism and productivity. Such strategies are essential for sustainable livestock farming.

The strategic application of phytogenic microcapsules, such as this orange peel essential oil, is very important to study, as this technique is a new approach to improving the overall nutritional utilisation and health of animals. However, the specific mechanisms by which orange peel essential oil microcapsules affect nitrogen retention, energy metabolism, and growth hormone receptor expression in local chickens have not been extensively explored. It can be assumed that the administration of OPEOM can improve feed efficiency, stimulate metabolism, reduce oxidative stress, and enhance broiler performance.

MATERIALS AND METHODS

Animal samples, basal rations, and experimental design

Two-month-old Sentul chickens were used in this experiment. The chickens were randomly assigned to five treatment groups with four replicates. Each treatment group included forty chickens, with ten chickens per replicate. The chickens were housed in litter system cages measuring 2.5 meters each, equipped with feeding and drinking troughs. They were maintained for two months, with free access to feed and water. The temperature and humidity of the cage were recorded during the study, averaging 260C and 75%, respectively. The same applies to the temperature and humidity surrounding the experimental animal housing, which were 28 oC and 78%, respectively.

 

Table 1: Nutrient and metabolisable energy content of the basal diet used in the experimental study.

Description	Amount	Standard requirement
Metabolic energy (kcal/kg)	2918	Minimum 2850
Crude Protein (%)	18	17–18
Crude Fat (%)	8	Min. 3
Crude Fibre (%)	6	Max. 10
Calcium (%)	4.1	3.25–4.25
Phosphorus (%)	0.6	Minimum 0.55

 

All experimental chickens were fed a basal diet throughout the study. OPEOM was administered at different levels as follows: MC0: Basal Ration without OPEOM; MC1: Basal Ration + 100 mg of OPEOM; MC2: Basal Ration + 150 mg of OPEOM; MC3: Basal Ration + 200 mg of OPEOM; MC4: Basal Ration + 250 mg of OPEOM.

 

The basal feed used in this experiment consisted of a mixture of feed ingredients and their composition in the ration, namely corn (56%), rice bran (5%), soybean meal (11%), fish meal (10%), coconut meal (15%), bone meal (25%), and coconut oil (1%). The total nutrient content of the ration is shown in Table 1.

Preparation of OPEOM

Essential oil from orange peel has been separated using steam distillation. Fresh orange peel, cut into small pieces weighing 350 g, is placed in a flask heated to 80 oC. Water was added to half the volume of the orange peel.

Microcapsule production was carried out using a complex coacervation method with orange peel essential oil as the core, a gelatin-sodium alginate layer, cross-linked with glutaraldehyde, and a Tween 80 emulsifier based on a modified procedure by Julaeha et al. (2024). Essential oil was obtained by hydrodistillation. Gelatin (2.8 g) was stirred in distilled water using a magnetic stirrer at a temperature of 60±1°C.

Tween-80 (0.8 g) and 3.5 g of essential oil and 0.8 g of sodium alginate were added to 40 ml of distilled water and stirred again for 15 minutes at 60°C with a stirring speed of 600 rpm. Add 2.5% glacial acetic acid drop by drop until the pH reaches 3.75, then cool to 5–10°C. 1.25 mmol of glutaraldehyde was added to the previous solution at up to 35°C, stirring for 3–4 hours and cooling to room temperature. Filtration and washing using n-hexane were carried out at the final stage of this procedure, before drying.

The characterization of OPEOM, tested with a Particle Size Analyzer, showed an average particle size of 1.635 µm. Particle stability was measured with a Thermogravimetric Analyzer, showing a decrease in water mass and volatile compounds occurring at temperatures below 250°C, and the degradation process beginning at temperatures exceeding 420°C.

Blood sampling and sample analysis

Blood biochemistry testing used blood plasma samples from blood collected using 3 mL EDTA tubes. Blood was collected from the wing veins of each experimental chicken sample at 4 months of age. The blood samples were then centrifuged at 3500 rpm for 15 minutes. The clear yellowish upper portion was pipetted into plasma tubes and stored in a freezer at -70°C until the plasma was analysed. Spectrophotometry based on Biolabo and Randox analysis kits was used to determine the concentration of all blood biochemical parameters in this experiment. 100 µL of reagent (provided in the kit for each parameter) was pipetted into a cuvette containing 10 µL of plasma. Absorbance was measured at wavelengths of 450–550 nm.

Energy utilisation was determined using the force-feeding method, a paste inserted through the oesophagus using a syringe, based on the procedure described by Abun et al. (2023). Similarly, digestibility was determined using an internal indicator (lignin), based on a modified method described by Abun et al. (2022).

Data analysis

All data were collected using Microsoft Excel, and the tabulated data were analysed using analysis of variance (ANOVA) based on a completely randomised design to determine the effect of treatment with α = 0.05. Differences between treatments were determined using Duncan’s multiple range test.

RESULTS AND DISCUSSION

Feed utilisation

The results shown in Table 2 measure feed utilisation efficiency during the study with OPEOM administration to Sentul chickens in the grower phase.

 

Table 2: Effect of OPEOM on DDM, DOM, DCP, ME, MEn, and nitrogen retention.

OPEOM level	DOM (%)	DDM (%)	DCP (%)	Nitrogen retention (%)	MEn (kcal/kg)	ME (kcal/kg)
MC0	59.49a	48.68a	65.35a	67.27a	2439a	2306a
MC1	68.84b	65.87b	70.73b	71.52b	2601a	2576b
MC2	73.64c	68.92c	73.68c	75.57c	2773b	2605b
MC3	65.58d	64.28b	64.43ac	70.26d	2561a	2564b
MC4	50.37e	60.59d	63.25ac	66.94a	2342c	2398a

 

a,bDifferent superscript on the same row indicates significant differences (P < 0.05). DOM: digestibility of organic matter; DDM: digestibility of dry matter; DCP: digestibility of crude protein; MEn: metabolisable energy-nitrogen; ME: metabolisable energy.

 

The current study shows that the administration of OPEOM is highly effective for Sentul chickens in utilising their feed intake. The MC2 dosage level (150 mg) showed the best dosage level (P < 0.05) of all OPEOM dosage levels. Microencapsulation is very beneficial because this technique can improve the stability and targeted delivery of active and sensitive compounds, such as essential oils, in animal feed. This process protects bioactive ingredients from degradation during processing and passage through the digestive tract, ensuring controlled release at specific locations.

Previous studies, for instance, have demonstrated that liposomal encapsulation significantly enhances the delivery and bioavailability of essential oils, resulting in improved growth, easier digestion, and better regulation of gut microbiota in broiler chickens. Additionally, microencapsulation methods such as core-shell or microdroplet techniques are vital for preserving the bioactivity of these volatile substances, especially when subjected to high temperatures or mechanical stress during feed processing. The microencapsulation’s protective matrix ensures a slow release, minimizes active compound loss, and prevents adverse effects on feed intake.

Increases in DOM, DDM, DCP nitrogen retention, and ME at MC2 dosage levels demonstrate the ability of active compounds in essential oils to stimulate physiological and biochemical conditions in experimental chickens. Previous research results have also reported that microencapsulated essential oils significantly improve organic digestibility, as this formulation protects the active compounds from premature degradation, allowing them to provide optimal effects on digestive enzyme activity and nutrient absorption in the intestinal lumen. Regarding intestinal function, several studies have also reported (Aguiar et al., 2020; Mushawwir et al., 2021b) that it can effectively prevent pathogen proliferation and promote intestinal health. It has been shown that when microencapsulated, essential oil components, such as carvacrol and malondialdehyde (Rahmania et al., 2022; Meligy et al., 2023), have been proven to replace growth-promoting antibiotics by improving intestinal integrity and nutrient absorption. Other research results show that adding microencapsulated essential oils has increased nitrogen retention in poultry (Manin et al., 2024; Firmansyah et al, 2024; Aritonang et al., 2025).

Based on current research results (especially with MC1 and MC2 levels), the increase in ME can be stimulated by OPEOM’s ability to modulate the enzyme pathways involved in energy distribution, resulting in more efficient energy utilisation. Supported by research findings (Li et al., 2022), this enhanced energy metabolism can impact overall growth performance and animal productivity by optimising nutrient allocation for various physiological functions.

Performance

The active compounds in OPEOM appear to trigger growth and feed efficiency. Adding the MC2 level is the best dosage (P < 0.05) compared to the other levels. Figure 1 compares body weight and feed conversion during the study at 4 months of age.

Figure 1 shows the superior performance of experimental chickens at the MC2 level. The experimental chicken group at this dosage level achieved the highest average body weight (1473 g) and the best feed conversion efficiency (3.53). Essential oils in microcapsule form stimulate increased nutrient absorption, directly contributing to superior zootechnical performance metrics, such as weight gain and feed conversion. Previous research reports (Flees et al., 2020; Mushawwir et al., 2021b; 2023; Purwanti et al., 2024) indicate that this method outperforms the control group of chickens that did not receive essential oil supplements.

 

Additionally, the type and concentration of essential oils in the microcapsules significantly influence their biological activity, with specific compounds such as thymol and carvacrol exhibiting strong antimicrobial and anti-inflammatory properties (Mushawwir et al., 2021a; Meligy et al., 2023), which indirectly support growth performance. These active compounds can capture free radicals, thereby reducing fatty acid oxidation. This leads to decreased cell death, thereby improving and increasing the metabolic rate. Ultimately, cell proliferation and muscle mass increase. Similarly, when microencapsulated, combinations of active compounds in essential oils such as carvacrol, cinnamaldehyde, and oleoresin capsicum have shown increased weight gain and antioxidant status in broiler chickens (Adriani et al., 2015). This supports the idea that the protective matrix of microcapsules enhances the delivery of these bioactive compounds, maintaining their effectiveness throughout the digestive tract and optimising their systemic impact (Aguiar et al., 2020; Aritonang et al., 2025).

Growth hormone receptor (GHR) concentration also appears to be closely related (r = 0.92) to weight gain, with an influence proportion (R2) of 0.8534, indicating that GHR concentration can influence body weight (Figure 2).

Based on the regression analysis of the data collected in this study, the regression equation y= 255.39+178.26x was obtained. This mathematical model shows that every one ng/dL increase in GHR concentration causes a 178.26 g increase in body weight. The results of this study indicate that higher concentrations of GHR cause higher growth, or that there is a linear relationship between the two. This relationship suggests that increased expression of growth hormone receptors mediated by essential oil microcapsules may indicate a better endocrine response, which supports higher growth and metabolic efficiency. The reported research results (Meligy et al., 2023; Mushawwir et al., 2025) show that increased GHR optimises protein synthesis and nutrient partitioning towards muscle tissue accumulation and egg production (Nurfauziah et al., 2024). This enhanced anabolic signalling pathway can increase the systemic availability of insulin-like growth factor-1 (IGF-1), a key mediator of growth hormone action. IGF-1 promotes skeletal muscle development and overall growth (Amer et al., 2021).

 

Blood biochemistry

Table 3 presents plasma blood biochemistry concentrations as effects of OPEOM administration, including markers of free radical activity and biochemical profiles.

The OPEM levels were able to influence (P < 0.05) the free radical activity markers concentration and plasma metabolism in Sentul chickens. Overall, there was a decrease in free radical activity with the administration of OPEOM while simultaneously stimulating the physiological system in various tissues to regulate metabolism. Based on the results of the lowest average bilirubin level obtained in the MC2 treatment, which is 3.42 (P < 0.05), compared to the bilirubin concentration of Sentul chickens in the experimental group of essential oil microcapsule administration levels. The highest mean bilirubin level was obtained in the MC0 treatment, which was 4.25 (P < 0.05) compared to the other experimental levels. The same results were also observed with alkaline phosphatase. Conversely, the MDA level decreased dramatically with the administration of the MC2 level (0.04 mg/dL), which was lower (P < 0.05) than the MDA level in the other treatment groups.

The decrease in MDA levels with OPEOM administration in this study is strong evidence that the active compounds in OPEOM can inhibit the activity of free radicals in oxidising fatty acids. This ability also reduces the risk of inflammation and damage to liver cells, resulting in a decrease in the release of bilirubin and alkaline phosphatase from liver cells into the body’s fluid circulation system, especially blood plasma.

 

Table 3: Effect of OPEOM levels on plasma concentrations of free radical activity markers and metabolic markers in Sentul chickens.

Parameters	Level of OPEOM
	MC0	MC1	MC2	MC3	MC4	P value
Effect free radical activity (mg/dL)
Bilirubin	4.25a	3.98b	3.42c	3.66d	3.73d	0.003
Alkaline phosphatase	5.20a	5.07a	4.28b	4.62bc	4.59c	0.011
Malondialdehyde (MDA)	0.09a	0.08a	0.04b	0.05b	0.05b	0.003
Total Antioxidant	0.13a	0.22b	0.46c	0.43c	0.48c	0.017
Metabolic (mg/dL)
Albumin	4.21a	5.16b	5.89c	4.64d	4.66d	0.001
Uric Acid	3.68a	2.81b	2.06b	2.63c	2.72c	0.001
Total Protein	4.52a	7.63b	8.27c	7.46b	7.18b	0.002
Creatinine	2.85a	1.79b	1.63c	1.92d	2.01d	0.021
Creatinine Kinase	0.94a	0.63b	0.51c	0.71d	0.72d	0.032
Triglycerides (TAG)	72.94a	55.26b	50.73b	61.29c	63.68c	0.001
Non-esterified fatty acids (NEFA)	3.24a	4.25b	4.58c	3.96d	3.77ad	0.002
Glucose-6-phosphate	1.28a	2.37b	2.83c	2.33b	2.31b	0.004

 

a,bDifferent letters on the same row indicates significant differences (P<0.05).

 

Previous researchers have reported the strong antioxidant ability of orange peel essential oil, mainly due to its rich composition of d-limonene, β-myrcene, α-pinene, and linalool, which collectively contribute more than 94% of its total active compound content (Rahmania et al., 2022; Bortoluzzi et al., 2021). The high concentration of these monoterpenes and monoterpenoids contributes significantly to their antioxidant effectiveness (Purwanti et al., 2024), as these compounds can donate hydrogen atoms to neutralise free radicals, thereby inhibiting oxidative chain reactions, one effect of which is to reduce the oxidation product of fat, MDA (Chen et al., 2023; Mushawwir et al., 2021b; Flees et al., 2020).

This reduction of malondialdehyde (MDA) content is highly effective as a critical biomarker for assessing lipid peroxidation. This process is often accelerated in biological systems and food products due to the reaction of free radicals with fatty acids (Mushawwir et al., 2023, 2024; Meligy et al., 2923). Its presence indicates oxidative damage, particularly in omega-3 and omega-6 fatty acids. The damage caused by free radicals can be measured through various indicators, including conjugated dienes and 4-hydroxynonenal, with MDA as the primary determinant of lipid peroxidation (Li et al., 2022; Chen et al., 2023).

The decrease in malondialdehyde (MDA) levels observed in various previous studies, as well as the reported decrease in MDA in pears treated with encapsulated savoury essential oil, further support the potential of critical oil microencapsulation in reducing lipid peroxidation, thereby preventing liver tissue damage and avoiding the migration of bilirubin and alkaline phosphatase into the blood circulation system (Tanuwiria et al., 2023; Prachumchai et al., 2024). Specifically, malondialdehyde, a stable and abundant secondary lipid oxidation product with reactive carbonyl groups, is readily involved in nucleophilic reactions that alter the chemical behaviour of nucleic acids, lipoproteins, and peptides. Therefore, measuring the concentration of malondialdehyde provides direct insight into the level of lipid peroxidation and the cellular damage that follows. The concentration of this biomarker can indicate oxidative damage, as seen in fat peroxidation (Faramarzidozein et al., 2024; Aritonang et al., 2024). Low levels indicate decreased free radical activity, reducing bilirubin, alkaline phosphatase, ALT, and AST (Rahmania et al., 2022; Amer et al., 2021).

The inclusion of OPEOM in the feed to Sentul chickens effectively reduced free radical activity. However, the experimental group of chickens given the MC2 treatment also appeared to be generally able to regulate a more beneficial metabolism. The total protein expressed and circulating in the blood plasma was highest (P < 0.05) with the MC2 treatment (8.27 mg/dL) compared to the other experimental chicken groups. Similarly, the albumin level in MC2 (5.89) was higher (P < 0.05) than in the different groups. The same results were also seen with 6-phosphate glucose concentrations, which showed that the metabolic rate increased with the administration of MC2.

Adding OPEOM to the diet protects active compounds like those in orange peel essential oil from degradation and directs their delivery to the digestive tract, enhancing their ability to regulate metabolic pathways (Tanuwiria et al., 2022; Chen et al., 2023). The strategy allows for the sustained release of bioactive compounds, increasing their interaction with the host’s physiological systems (Aritonang et al., 2024,2025; Faramarzidozein et al., 2024) and influencing vital metabolic markers (Mushawwir et al., 2011; Li et al., 2022). It also stabilizes essential oils against environmental factors, ensuring their biological availability, which improves nutrient utilization and overall animal health.

An increase in Protein synthesis and albumin and a decrease in catabolism indicate improved nutrient utilisation (Mushawwir et al., 2021a; Prachumchai et al., 2024). This can be attributed to the protective benefits of microencapsulation, which shield active compounds during feed processing and digestion (Flees et al., 2020; Adriani et al., 2024a). These results ensure that the active components can optimally express their biological activity in the lower digestive tract, influencing protein synthesis and overall metabolic efficiency (Adriani et al., 2024; Abdelli et al., 2021).

On the other hand, lower TAG levels (50.73–63.68 mg/dL) (P < 0.05) observed with OPEOM administration compared to without it suggest that the active compounds can inhibit lipogenesis. This effect increases NEFA levels, serving as energy precursors for muscle tissue synthesis. Plasma triglyceride levels are a vital metabolic marker in chickens. Supplementing essential oils, especially from sources like orange peel, can influence lipid metabolism (Dudi et al., 2023; Muhammad et al., 2023). Studies indicate that these compounds may alter circulating triglyceride levels (Manin et al., 2024; Firmansyah et al., 2024), potentially affecting hepatic lipid synthesis or lipoprotein metabolism, key factors in determining plasma triglyceride levels (Meligy et al., 2023).

Other studies suggest that dietary essential oils can significantly alter triglyceride profiles (Kharazi et al., 2022; Mousapour et al., 2020; Mushawwir et al., 2025), leading to decreases associated with improved lipid utilization or reduced synthesis (Dorantes-Iturbide et al., 2022), which explains the increase in NEFA levels (Kamil et al., 2020; Flees et al., 2020; Kharazi et al., 2022). Conversely, some plant essential oil compounds may raise triglyceride levels in broiler chickens (Adriani et al., 2015; Bortoluzzi et al., 2021). These contrasting effects underline the complex regulation of lipid metabolism by external compounds, emphasizing the need for further research into how orange-peel essential oil microcapsules specifically impact these pathways.

CONCLUSION

The results of this study indicate that the administration of OPEOM at a level of 125 mg/kg (MC2) of feed has the best potential for improving the productivity of Sentul chickens, including feed utilisation, performance, reducing radical activity. This confirms that the active compounds in OPEOM at this level are most optimal in supporting the productivity of Sentul chickens. These results can also serve as a basis for further research on the potential of OPEOM in increasing egg production, the expression of economically valuable genes, and as a nutrigenomic agent.

ACKNOWLEDGEMENT

The authors express their appreciation and gratitude to the Ministry of Higher Education, Research, and Technology of the Republic of Indonesia for funding this research through a basic grant. The authors also thank all research teams and parties directly involved for their excellent cooperation and contributions during the planning and writing of this article.

NOVELTY STATEMENT

The use of essential oils from various types of plants has been widely applied and reported, although the results of essential oils from orange peel with encapsulation for poultry feed additive have not been widely reported. Furthermore, microencapsulation technology for orange peel essential oil in local chicken feed has not been reported. A more in-depth study of its potential as an antioxidant and metabolism regulator, as is the aim of this research, has not been reported previously.

AUTHOR’S CONTRIBUTION

All authors listed in this article have contributed equally, from planning, designing, and conducting the research to writing this article. All authors have played an equal role with their respective expertise and specialisation.

Ethical approval

The Animal Ethics Committee of the Research Licence Management Directorate, with certificate (No. 462/KEP.04/SK/01/2025), has evaluated, approved, and declared this in vivo study, with applications described in the research methods, to meet animal ethics requirements.

Generative AI and AI-assisted technology statement

All authors listed in this article declare with complete sincerity that the writing of this article did not utilise any AI software and technology.

Conflict of interest

All authors declare no conflict of interest regarding costs, data, or any other aspects related to this research with any party.

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Julaeha E, Puspita W R, Permadi N (2024). Optimization of Citrus aurantifolia peel extract encapsulation in alginate-gelatin hydrogel microbeads for antibacterial wound dressing applications. Carbohyd. Polym. Technol. Appl., 7(6): 100406. https://doi.org/10.1016/j.carpta.2023.100406

Kamil KA, Mushawwir A, Latipudin D, Rahmat D, Lobo R (2020). The effects of ginger volatile oil (GVO) on the metabolic profile of glycolytic pathway, free radical and antioxidant activities of heat-stressed Cihateup duck. Int. J. Adv. Sci. Engin. Inf. Tech., 10: 1228-1233. https://doi.org/10.18517/ijaseit.10.3.11117

Kharazi AY, Latipudin D, Suwarno N, Puspitasari T, Nuryanthi N, Mushawwir A (2022). Lipogenesis in Sentul chickens of starter phase inhibited by irradiated chitosan. IAP Conf. Proc., 1001(1): 1-7. https://doi.org/10.1088/1755-1315/1001/1/012021

Li J, Wu J, Yu L, Kong F, Zhang R, Sun J, Liao W, Li, Z, Shi J, Wang Y, Wei Y, Zhang K, Lei Z (2022). Oregano essential oils mediated intestinal microbiota and metabolites and improved growth performance and intestinal barrier function in sheep. Front. Immunol., 13(10): 484. https://doi.org/10.3389/fimmu.2022.908015

Manin F, Yusrizal M, Adriani L, Mushawwir A (2024). Effects of the combination of probiotic probio fmand phytobiotics on broiler meat’s performance, gut dysbiosis, and lipid profile. Adv. Anim. Vet. Sci., 12(11): 2110-2117. https://doi.org/10.17582/journal.aavs/2024/12.11.2110.2117

Meligy AMA, El-Hamid MIA, Yonis, AE, Elhaddad GY, Abdel-Raheem SM, El‐Ghareeb WR, Mohamed MHA, Ismail H, Ibrahim D (2023). Liposomal encapsulated oregano, cinnamon, and clove oils enhanced the performance, bacterial metabolites antioxidant potential, and intestinal microbiota of broiler chickens. Poult. Sci., 102(6): 102683. https://doi.org/10.1016/j.psj.2023.102683

Mousapour A, Salarmoini M, Afsharmanesh M, Ebrahimnejad H, Meimandipour A (2020). Efficacy of savory essential oil utilization in conventional and encapsulated forms on performance of broiler chickens. Braz. J. Poult. Sci., 22(4): 85-92. https://doi.org/10.1590/1806-9061-2020-1284

Muhammad LN, Purwanti S, Pakiding W, Marhamah, Nurhayu, Prahesti KI, Sirajuddin, SN, Mushawwir A (2023). Effect of combination of Indigofera zollingeriana, black soldier fly larvae, and turmeric on performance and histomorphological characteristics of native chicken at starter phase. J. Anim. Feed Res., 13(4): 279-285. https://doi.org/10.51227/ojafr.2023.42

Mushawwir A, Adriani L, Kamil KA (2011). Prediction models for olfactory metabolic and sows % RNAreticulocyt (RNArt) by measurement of atmospheric ammonia exposure and microclimate level. J. Indon. Trop. Anim. Agric., 36: 14-20. https://doi.org/10.14710/jitaa.36.1.14-20

Mushawwir A, Adriani L, Permana R, Sahara E (2025). Egg production and physiological assessment of sentul hens in temperate and lowland regions of West Java, Indonesia. Adv. Anim. Vet. Sci., 13(2): 413-420. https://doi.org/10.17582/journal.aavs/2025/13.2.413.420

Mushawwir A, Permana R, Darwis D, Puspitasari T (2024). The villi ileum growth of native quail fed by irradiated chitosan with glutathione from an early age in high temperature. IOP Conf. Ser. Earth Environ. Sci., 1292(1): 1-6. https://doi.org/10.1088/1755-1315/1292/1/012016

Mushawwir A, Permana R, Darwis D, Puspitasari T, Pangerteni DS, Nuryanthi N, Suwarno N (2021b). Enhancement of the liver histologic of broiler induced by irradiated chitosan (IC). AIP Conf. Proc., 2381: 020046. https://doi.org/10.1063/5.0066271

Mushawwir A, Permana R, Latipudin D, Suwarno D (2023). Flavonoids avoid the damage of ileal plaque-patches of heat-stressed cihateup ducks. IAP Conf. Proc., 2628: 140007-1-14007-6. https://doi.org/10.1063/5.0144095

Mushawwir A, Permana R, Latipudin D, Suwarno N (2021a). Organic Diallyl-n-Sulfide (Dn-S) inhibited the glycogenolysis pathway and heart failure of heat-stressed laying hens. IOP Conf. Ser. Earth Environ. Sci., 788: 012091. https://doi.org/10.1088/1755-1315/788/1/012091

Nurfauziah I, Adriani L, Ramadhan RF, Mushawwir A, Ishmayana S (2024). Bacteriocin activity of yogurt probiotics on increasing production of laying hens. Adv. Anim. Vet. Sci., 12(8): 1548-1555. https://doi.org/10.17582/journal.aavs/2024/12.8.1548.1555

Prachumchai R, Suriyapha C, Dagaew G, Sommai S, Matra, M, Phupaboon S, Phasuk Y, Wanapat M (2024). Microencapsulation of lemongrass and mangosteen peel as phytogenic compounds to gas kinetics, fermentation, degradability, methane production, and microbial population using in vitro gas technique. PLoS One, 19(6): https://doi.org/10.1371/journal.pone.0304282

Purwanti S, Pakiding W, Nadir M, Nurhayu, Prahesti KI, Sirajuddin SN, Syamsu JA, Mushawwir A (2024). Lipid regulation and cardiovascular biomarkers of native chickens fed a combination of maggot, Indigofera, and Turmeric. J. Anim. Health Prod., 12(2): 173-181. https://doi.org/10.17582/journal.jahp/2024/12.2.173.181

Rahmania H, Permana R, Latipudin D, Suwarno N, Puspitasari T, Nuryanthi N, Mushawwir A (2022). Enhancement of the liver status of Sentul chickens from the starter phase induced by irradiated chitosan. IAP Conf. Proc., 1001: 1-7. https://doi.org/10.1088/1755-1315/1001/1/012007

Tanuwiria UH, Mushawwir A, Zain M, Despal D (2023). Lipid regulation and growth on native ram lambs in the south coast of West Java, Indonesia, fed legume forages. Biodiversity, 24: 4183-4192. https://doi.org/10.13057/biodiv/d240763

Tanuwiria UH, Susilawati I, Tasripin D, Salman LB, Mushawwir A (2022). Evaluation of cardiovascular biomarkers and lipid regulation in lactation friesian holstein at different West Java, Indonesia altitudes. Hayati J. Biosci., 29: 428-434. https://doi.org/10.4308/hjb.29.4.428-434