Abstract
Amid growing concerns about antibiotic resistance in livestock systems, there is a global shift toward identifying plant-based alternatives to conventional synthetic feed additives. This study explored the physicochemical characteristics of raw Napier grass (Pennisetum purpureum) and assessed its viability as a low-cost, functional feed additive for colored broiler chicken diets. Comprehensive characterization was conducted on the raw grass, revealing structural features and functional groups characteristic of bioactive, fibrous biomass. A subsequent feeding trial was conducted with 216 Sasso broiler chicks divided among six dietary regimens: a negative control (basal diet), a positive control (100 mg/kg oxytetracycline), and four supplementation levels of P. purpureum grass meal (1.25 to 5.00 g/kg). The highest supplementation level (5.00 g/kg) significantly enhanced growth performance (p < 0.05), reducing feed conversion ratio (FCR) while maintaining low feed intake. Economic analyses demonstrated that this treatment yielded the greatest profitability, exhibiting superior net profit margin, break-even efficiency, and margin of safety. These findings indicated P. purpureum as a promising phytogenic feed additive with dual benefits of enhancing production efficiency and promoting sustainable poultry farming.
Download PDF
Full Article
Dual Role of Pennisetum purpureum as a Phytogenic Feed Additive: Enhancing Growth and Profitability in Antibiotic-Free Broiler Production
Alvin Lim Teik Zheng,a Kelly Kai Seng Wong
,b Yee Lyn Ong
,c Jacqueline Lease
,d Yoshito Andou
,d Faez Firdaus Abdullah Jess
,e and Eric Lim Teik Chung
,c,*
Amid growing concerns about antibiotic resistance in livestock systems, there is a global shift toward identifying plant-based alternatives to conventional synthetic feed additives. This study explored the physicochemical characteristics of raw Napier grass (Pennisetum purpureum) and assessed its viability as a low-cost, functional feed additive for colored broiler chicken diets. Comprehensive characterization was conducted on the raw grass, revealing structural features and functional groups characteristic of bioactive, fibrous biomass. A subsequent feeding trial was conducted with 216 Sasso broiler chicks divided among six dietary regimens: a negative control (basal diet), a positive control (100 mg/kg oxytetracycline), and four supplementation levels of P. purpureum grass meal (1.25 to 5.00 g/kg). The highest supplementation level (5.00 g/kg) significantly enhanced growth performance (p < 0.05), reducing feed conversion ratio (FCR) while maintaining low feed intake. Economic analyses demonstrated that this treatment yielded the greatest profitability, exhibiting superior net profit margin, break-even efficiency, and margin of safety. These findings indicated P. purpureum as a promising phytogenic feed additive with dual benefits of enhancing production efficiency and promoting sustainable poultry farming.
DOI: 10.15376/biores.20.4.8654-8673
Keywords: Pennisetum purpureum; Phytogenic feed additive; Broiler performance; Physicochemical characterization; Antibiotic alternative; Cost-benefit analysis
Contact information: a: Institute of Ecoscience Borneo, Universiti Putra Malaysia Bintulu Campus, Bintulu 97008, Sarawak, Malaysia; b: Department of Agribusiness and Bioresource Economics, Faculty of Agriculture, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia; c: Department of Animal Science, Faculty of Agriculture, Universiti Putra Malaysia, 43400; d: Graduate School of Life Sciences and Systems Engineering, Kyushu Institute of Technology, Fukuoka 808-0196, Japan; e: Department of Veterinary Clinical Studies, Faculty of Veterinary Medicine, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia; *Corresponding author: ericlim@upm.edu.my
GRAPHICAL ABSTRACT
INTRODUCTION
The intensive use of antibiotics in animal agriculture particularly in poultry has long been a subject of concern due to its contribution to the global surge in antimicrobial resistance. Antibiotics are traditionally administered not only for therapeutic purposes but also as prophylactic agents and growth promoters. However, this non-therapeutic application, especially in sub-therapeutic doses, has contributed to the emergence of antibiotic-resistant pathogens, posing a serious threat to both animal and public health (Selaledi et al. 2020). In response, there has been a growing research emphasis on phytogenic feed additives or natural bioactive compounds derived from plants that offer antimicrobial, antioxidant, and growth-promoting properties. Despite considerable exploration into herbal extracts and essential oils, the potential of whole plant-based feed materials, particularly leaf and grass meals, remains under-investigated (Alghirani et al. 2021, 2022).
Napier grass (Pennisetum purpureum), a fast-growing tropical forage crop, is widely cultivated in tropical and subtropical regions. Traditionally used as ruminant fodder, it is characterized by high biomass yield, adaptability to marginal soils, and notable agronomic value (Negawo et al. 2017; Islam et al. 2023). Nutritionally, P. purpureum is rich in crude protein, fiber, and an array of secondary metabolites including flavonoids, saponins, tannins, and alkaloids compounds known for their functional roles in modulating gut health, immunity, and metabolic efficiency in livestock (Cao et al. 2012; Ng et al. 2020). Additionally, flavonoids have demonstrated estrogenic and antioxidant activities that may positively influence lipid metabolism and disease resistance in poultry (Seomoon and Jang 2022; Tan et al. 2022).
Although P. purpureum is extensively recognized as a high-yield forage grass with diverse applications in ruminant nutrition, its potential use in poultry feed formulations remains largely unexplored. Unlike ruminants, poultry possess a relatively short and simple digestive tract, which limits their ability to ferment and extract nutrients from high-fiber forages. Consequently, the inclusion of grass-based materials in poultry diets must be carefully controlled, as excessive crude fiber (>5%) can impair nutrient digestibility and growth performance (Jha and Mishra 2021). However, at low inclusion levels, grass-derived bioactives and functional fibers may provide prebiotic and gut-modulating effects without compromising digestibility, supporting their potential as phytogenic additives in broiler nutrition (Alghirani et al. 2022). Recent studies have indicated that the young leaves and tender shoots of P. purpureum are abundant in dietary protein, essential minerals, vitamins, and antioxidant compounds. Notably, its extracts have demonstrated antifungal activity, which has been primarily attributed to the presence of phenolic compounds (Ng et al. 2020). A phytochemical analysis indicated that sun-dried young shoots have comparatively high concentrations of flavonoids (0.021%), followed by glycosides (0.008%) and saponins (0.002%) (Jack et al. 2020). Flavonoids, in particular, are known to exert estrogenic and antioxidant effects in animals, with reported benefits including improved lipid metabolism (Negasa 2024). When incorporated into broiler diets, these bioactive compounds have been associated with enhanced immune responses, increased immune organ indices, and elevated humoral immunity against infectious agents such as Newcastle disease and Avian influenza virus (Sugiharto et al. 2019).
The application of P. purpureum in poultry nutrition has not been systematically evaluated, and there has been a lack of studies characterizing its raw physicochemical profile in the context of monogastric animal diets. The current study addresses this gap by (i) providing a comprehensive physicochemical characterization of untreated P. purpureum using FTIR, XRD, TGA, and SEM techniques; and (ii) investigating the impact of graded supplementation levels of P. purpureum grass meal on the growth performance and economic viability of colored-broiler (Sasso) chicken production. It is hypothesized that the bioactive and fibrous components of P. purpureum can serve as a functional and sustainable feed additive that enhances broiler performance while improving production economics. The results from this investigation aim to contribute to the growing body of evidence supporting phytogenic alternatives in antibiotic-free poultry systems.
EXPERIMENTAL
Materials
Unless otherwise specified, all chemicals and reagents used in this study were of analytical grade and applied without further purification.
Planting and Harvesting of P. purpureum Grass
P. purpureum grass was grown at Farm 15, Department of Animal Science, Universiti Putra Malaysia. At four weeks of growth, the plants were harvested, weighed, and dried in a hot-air oven at 60 °C for 72 h or until a constant weight was attained. The dried material was then milled using a mechanical grinder and stored in airtight containers to preserve its integrity for further analyses.
Nutritional Composition, Phytochemical and Antioxidant Activity Analyses
The proximate composition of P. purpureum grass meal, including dry matter (DM), crude protein (CP), crude fibre (CF), ether extract (EE), and ash content, was determined in accordance with the Official Methods of Analysis by AOAC International as shown in Table 1. Quantification of key phytochemicals such as saponins, tannins, flavonoids, and alkaloids was carried out using a modified protocol (Osuntokun 2014). Antioxidant activity was assessed using the DPPH (2,2-diphenyl-1-picrylhydrazyl) radical scavenging assay following the method described previously with appropriate modifications (Jack et al. 2020).
Table 1. Proximate Composition, Phytochemical constituents, and Antioxidant Capacity of P. purpureum Grass Meal
Physicochemical Characterizations
To determine the structural and thermal characteristics of P. purpureum, the following analytical techniques were employed. Surface morphology was examined using a JEOL JSM-6000 microscope operated at 15 kV. Prior to imaging, samples were sputter-coated with carbon to improve conductivity and resolution.
Crystallinity was analyzed using a Rigaku diffractometer with Cu K-α radiation (λ = 1.5406 Å), operated at 40 kV and 15 mA, with a scanning rate of 10°/min across a 2θ range of 5° to 70°. Spectral FTIR analysis was performed using a Nicolet iS5 spectrometer to identify functional groups characteristic of plant biomass. Thermal stability was assessed using an EXSTAR TG/DTA7000 system under a nitrogen atmosphere, with a heating rate of 10 °C/min from 30 to 600 °C.
Broiler Chickens Feeding Trial
The study was evaluated and endorsed by the Universiti Putra Malaysia Institutional Animal Care and Use Committee (IACUC; Approval ID: UPM/IACUC/AUP-R047/2022). Two hundred and sixteen one‐day‐old Sasso broiler chicks were sourced from a licensed hatchery, individually weighed, and then randomly assigned to six dietary treatment groups (36 birds per treatment), with each treatment subdivided into six replicates of six birds. Birds were housed in stainless steel tiered cages (113 cm × 82 cm × 45 cm) in an open-sided facility under standard management conditions, with ad libitum access to feed and water (Chung et al. 2020, 2021). All birds received standard vaccinations: intraocular vaccination against Infectious Bronchitis (IB) and Newcastle Disease (ND) on day 7, and eye-drop vaccination for Infectious Bursal Disease (IBD) on day 14. Environmental parameters were recorded with a mean temperature of 30.9 °C and relative humidity of 71.24%. All broilers received standard vaccinations via intraocular route on day 7, and IBD by eye drop on day 14 under trial conditions of 30.9 °C and 71.2% humidity. The broiler chickens were fed with commercial starter and finisher diets formulated mainly from crumbled soybean meal and maize, administered from day 0 to 28 and day 29 to 56, respectively. For the negative control group (Treatment 1), antibiotic-free commercial feed was provided. In contrast, Treatment 2 (positive control) received commercial feed supplemented with 100 mg/kg of oxytetracycline (Alhendi et al. 2000; Alghirani et al. 2022). Treatments 3 through 6 were offered the same basal diet without antibiotics but incorporated with P. purpureum grass meal at incremental inclusion levels of 1.25, 2.50, 3.75, and 5.00 g/kg, respectively. It is important to note that P. purpureum grass meal was supplemented into the basal diet for treatments T3 to T6, rather than replacing any portion of the existing ingredients such as corn or soybean meal. This approach ensured that the basal nutritional composition (energy and protein content) remained constant across treatments, thereby isolating the effects of P. purpureum supplementation on growth performance and economic outcomes. Table 2a outlines the composition of the basal starter and finisher feeds, while Table 2b summarizes the nutrient profiles of each treatment group. Body weight (BW) and feed intake (FI) were recorded per replicate to calculate BW gain (BWG), total feed intake (TFI), and feed conversion ratio (FCR = TFI / BWG).
Table 2a. Composition of the Basal Diets for Starter and Finisher Phases from Day 1 to Day 28 and Day 29 to Day 56 Respectively
Table 2b. Nutrient Profiles of Broiler Diets Formulated with Graded Supplementation Levels of P. purpureum Grass Meal
Statistical Analysis
All data were analyzed using RStudio version 4.1.3. A one-way analysis of variance (ANOVA) was performed based on a completely randomized design. Tukey’s Honest Significant Difference (HSD) test was used for post-hoc comparisons, with significance set at p < 0.05. Mortality rates were analyzed using the Chi-square test.
Cost and Benefit Analysis
A comprehensive economic evaluation was conducted to assess the cost-effectiveness and financial viability of P. purpureum grass meal supplementation in broiler production. The analysis considered both fixed and variable costs, as well as profitability metrics across all treatment groups. Fixed costs, including labor and electricity, were standardized at RM 558.97 for each treatment, as they remained constant regardless of feed formulation or output. Variable costs, which included expenditures for chicks, feed, water, antibiotics (for T2 only), and P. purpureum grass meal (for T3–T6), varied based on the supplementation level and treatment type. The following financial indicators were computed including total cost (RM), total revenue (RM), total profit (RM), average cost per bird (RM), average revenue per bird (RM), average profit per bird (RM), net profit margin (%), break-even point (birds), margin of safety (birds) and margin of safety (%), as previously reported (Seng et al. 2025).
Total Cost (RM) = Fixed Cost + Variable Cost (1)
Total Revenue (RM) = Number of live birds ×
Final body weight per bird (kg) × Market price (RM 18/kg) (2)
Total Profit (RM) = Total Revenue – Total Cost (3)
Average Cost per Bird (RM) = Total Cost / Number of birds sold (4)
Average Revenue per Bird (RM) = Total Revenue / Number of birds sold (5)
Average Profit per Bird (RM) = Average Revenue – Average Cost (6)
Net Profit Margin (%) = (Total Profit / Total Revenue) × 100 (7)
Break-even Point (birds) = Total Fixed Cost /
(Selling Price per Bird – Variable Cost per Bird) (8)
Margin of Safety (birds) = Actual birds sold – Break-even birds (9)
Margin of Safety (%) = (Margin of Safety / Actual birds sold) × 100 (10)
These metrics were applied to each treatment group to determine relative cost efficiency and financial resilience. A lower break-even threshold and higher margin of safety reflect improved cost control and the ability to withstand market or operational fluctuations. Treatments that resulted in positive profit margins with lower average costs and higher per-bird returns were considered economically superior. All economic data were processed using Microsoft Excel and validated through manual cross-checking for accuracy. All data were analyzed using RStudio version 4.1.3. A one-way analysis of variance (ANOVA) was performed based on a completely randomized design. Tukey’s Honest Significant Difference (HSD) test was used for post-hoc comparisons, with significance set at p < 0.05. Mortality rates were analyzed using the Chi-square test.
RESULTS AND DISCUSSION
Physicochemical Characterization
The surface morphology of ground P. purpureum was examined using SEM to assess its structural features. Prior to imaging, samples were carbon-coated using a vacuum sputter coater to improve electrical conductivity and image resolution. At low magnification (100×), the SEM micrographs shown in Fig. 1(a) revealed irregularly shaped agglomerates distributed across the surface.
Fig. 1. SEM micrographs of the P. purpureum grass under (a) 100x magnification and (b) 500x magnification
This was indicative of a heterogeneous and porous matrix (Wang et al. 2008). At higher magnification (500×) shown in Fig. 1(b), fibrous-like particles and aggregated structures were more pronounced, suggesting a complex network of cellulose, hemicellulose, and lignin commonly found in lignocellulosic biomass (Bajpai 2016, 2022). The average particle size was estimated at 28 μm, ranging from 40 to 110 μm, confirming that the grinding process yielded sufficiently small particles for feed incorporation without requiring chemical pretreatment.
FTIR spectroscopy was carried out to identify the functional groups present in P. purpureum. The resulting FTIR spectrum depicted in Fig. 2(a) exhibited characteristic absorbance bands typical of plant biomass.
Fig. 2. (a) XRD spectra, (b) TGA thermogram, (c) and XRD spectra of P. purpureum grass
A broad peak centered at 3372 cm⁻¹ was attributed to O–H stretching vibrations, primarily arising from hydroxyl groups in cellulose, hemicellulose, and lignin, as well as from adsorbed water molecules (Soliman et al. 2016; Cichosz and Masek 2020; Baker and Oguntoye 2023; Talik et al. 2023). Distinct symmetric and asymmetric C–H stretching vibrations appeared at 2850 cm⁻¹ and 2916 cm⁻¹, indicating the presence of aliphatic hydrocarbons. Peaks at 1055 cm⁻¹, 1161 cm⁻¹, and 1311 cm⁻¹ were assigned to C–O stretching and C–H bending modes within the cellulose structure (Rana et al. 2018). A shoulder at 1739 cm⁻¹ corresponded to C=O stretching in ester linkages, likely originating from lipid membranes and cell wall pectins (Wu et al. 2020). A notable absorption peak at 1641 cm⁻¹ corresponded to C=C stretching vibrations of aromatic rings, indicative of phenolic compounds within the plant matrix.
Thermogravimetric analysis (TGA) was used to assess the thermal decomposition profile of P. purpureum under a nitrogen atmosphere depicted in Fig. 2(b). An initial weight loss below 100 °C was attributed to moisture evaporation and the volatilization of light compounds (Zheng et al. 2021; Jeffrey et al. 2024). The major degradation phase occurred between 250 and 321 °C, corresponding to the breakdown of hemicellulose and cellulose, and accounted for approximately 45% of the total weight loss (Gu et al. 2021). A continued decline in weight between 322 and 600 °C was linked to the decomposition of lignin and more thermally stable macromolecules. These results indicate that P. purpureum contains approximately 70% volatile matter, highlighting its potential for thermochemical conversion into bio-crude and other energy-dense products, as supported by previous findings (Toor et al. 2022).
XRD analysis was performed to assess the crystallographic properties and degree of structural order in the P. purpureum grass meal as shown in Fig. 2(c). The resulting diffractogram exhibited distinct peaks centered at approximately 16° and 22° (2θ), which are indicative of the cellulose I polymorph specifically representing the (110) and (200) crystallographic planes, respectively (French 2022; Salem et al. 2023). These peaks confirm the presence of semi-crystalline cellulose, a major component of lignocellulosic biomass. The sharpness and intensity of these peaks reflect the partial ordering of the cellulose chains within the plant matrix, which plays a critical role in determining mechanical strength, enzymatic accessibility, and digestibility in animal feed applications. In addition to the characteristic cellulose reflections, several minor yet well-defined peaks were detected between 28° and 60° (2θ). These are likely attributable to crystalline impurities or trace amounts of inorganic constituents such as metal oxides or mineral residues, which may be naturally incorporated into the biomass from the soil during plant growth (Alves et al. 2022). These smaller peaks can also be attributed to additional crystalline regions of cellulose (Sofla et al. 2016; Soltani et al. 2024). Their presence could influence the mineral profile and bioavailability of micronutrients when the biomass is used as a feed ingredient. Overall, the XRD results affirm that P. purpureum possesses a heterogeneous fibrous structure with moderate crystallinity, which may influence both its physicochemical behavior and nutritional utility in poultry feed formulations. These findings align with crystallographic data reported for P. purpureum grass reported previously (Luengnaruemitchai and Anupapwisetkul 2020).
Growth Performance
Table 3 illustrates the impact of P. purpureum grass meal supplementation on the growth performance metrics of Sasso broiler chickens.
Table 3. Impact of P. purpureum Grass Meal Supplementation on Growth Performance Parameters in Sasso Broiler Chickens
Table 4. Total Production Costs, Income, & Net Returns for Sasso Broilers Fed Varying Levels of P. purpureum Grass Meal
Key performance indicators including final body weight (BW), body weight gain (BWG), feed intake (FI), and feed conversion ratio (FCR) were used to assess treatment efficacy. While final BW and BWG did not differ significantly among the treatment groups (p > 0.05), notable differences were observed in FI (p = 0.037) and FCR (p < 0.001), suggesting that dietary modifications influenced feed efficiency more than overall weight gain. Among the groups, Treatment 6 (T6), which included 5.00 g/kg of P. purpureum grass meal, yielded the most favorable FCR (1.82 ± 0.00), significantly outperforming both the negative control (T1) and lower supplementation treatments (T3 to T5). Remarkably, this improved efficiency occurred despite T6 having the lowest total feed intake, indicating that birds on this diet utilized their feed more effectively to support growth. This observation suggests that P. purpureum supplementation, particularly at higher supplementation levels, may confer functional benefits beyond basic nutrition. It is important to note that the FCR values observed in this study (1.82 to 2.14) were higher than typical values for fast-growing commercial broilers (1.5 to 1.7), reflecting differences in genotype (slow-growing Sasso birds), housing (open-sided tropical facility), and production conditions. These contextual factors should be considered when comparing our results to intensive commercial systems.
Several phytochemical constituents identified in P. purpureum, particularly flavonoids, saponins, and tannins, are known to exert bioactive effects that could contribute to enhanced gut health, nutrient digestibility, and metabolic regulation. Flavonoids, for example, have been shown to stimulate digestive enzyme secretion, reduce oxidative stress, and modulate gut microbiota composition, thereby improving nutrient absorption and energy utilization (Rahimi et al. 2011; Kuralkar and Kuralkar 2021). The reduction in feed intake observed in T6 could be partially attributed to increased nutrient density or satiety signaling induced by the presence of these compounds, while the improved FCR indicated the physiological efficiency with which nutrients were converted into body mass.
Although P. purpureum contains a relatively high crude fiber content, its supplementation at up to 5 g/kg did not raise the total dietary fiber beyond the tolerable limit for broilers (≤5% CF). The improved feed conversion ratio and body weight gain observed at this inclusion level may be partly explained by the action of bioactive compounds, such as flavonoids and saponins, which are known to enhance gut morphology, stimulate digestive enzyme secretion, and improve nutrient absorption. However, it is acknowledged that digestibility was not directly evaluated in this trial, which limits mechanistic interpretation. Future work should incorporate ileal digestibility and gut histological assessments to validate these findings.
Moreover, the enhanced feed efficiency observed in the absence of antibiotic growth promoters (as in T6) supports the potential of P. purpureum as a viable phytogenic alternative. Notably, while the positive control group (T2) also showed good FCR (1.93 ± 0.01), it was still inferior to T6, reinforcing the comparative efficacy of the grass meal supplement. These results align with existing literature on the use of phytobiotic additives in poultry diets, which report similar improvements in feed efficiency and health status under antibiotic-free conditions (Ong et al. 2024). Mortality rates were low across all treatments and did not differ significantly (p = 0.416), indicating that the supplementation of P. purpureum did not compromise animal welfare or survivability. Collectively, the findings from this trial suggest that 5.00 g/kg of P. purpureum grass meal is an optimal supplementation level that enhances feed efficiency without adversely affecting feed intake or survival, offering a promising natural alternative to in-feed antibiotics in sustainable poultry production systems.
Cost and Benefit Analysis
The cost of production was calculated based on the summation of the variable cost and fixed cost (Table 4). The fixed cost (RM 558.97) remained constant across all six treatments, indicating that the cost for electricity and labor used across all treatments will stay constant regardless of the poultry production levels. Among the six treatments, the proportion of fixed costs to total costs was around 53%, indicating the importance of fixed costs in firm production, particularly for firms with low output. Furthermore, variable costs among treatments ranged from RM 491.06 to RM 523.94, according to Table 4. T4 had the lowest variable costs and T1 had the highest variable costs. In terms of variable costs, T1 had the highest total cost of production (RM 1,082.91), while T4 had the lowest total cost of production (RM 1,050.03). Producing output with a lower cost per unit implies that the rational producer has an economy of scale to produce more output with the least amount of waste in the production chain. Table 5 shows that T2 was the most cost-effective of the five treatments, with the lowest average variable cost, average fixed cost, and average total cost. T3 and T4, on the other hand, had the highest average cost (cost inefficiency), at RM 31.61 and RM 30.88 per bird, respectively. T5 and T6, which produced a chicken at an average cost of RM 30.43 and RM30.26 per bird, respectively, were moderately cost-effective.
It is important to note that while the unit price of chicks, feed, and water remained constant across treatments, the total cost per treatment varied due to differences in mortality-adjusted live bird counts (affecting chick costs), as well as actual recorded consumption of feed and water in each group. This approach ensures that the economic analysis reflects real-world production dynamics rather than theoretical uniform costs. Electricity and labor were treated as fixed costs, as they were independent of consumption patterns.
Comparing the overall cost performance among the six treatments, T2 with antibiotics had the lowest average cost relative to other treatments, but the cost difference was not significant. According to Azabo et al. (2022), the use of antibiotics will help to reduce the cost of production in broiler production. However, reducing antibiotic use in broiler farming can lead to higher production costs due to increased mortality rates and additional management expenses (Azabo et al. 2022). This supports the idea that the average cost of production for T2 is lower than other treatments. However, the average cost of Treatment 6 was almost the same as T2 if it substituted the conventional feed without antibiotics with 5 grams of grass treatment. Furthermore, compared to the final weight gained by each chicken, T6 (1.75 kg per bird) was even higher than T2 (1.69 kg per bird).
The revenue ranged from RM1,003.68 to RM 1,102.5, with T6 asserting its dominance by yielding the most revenue and T4 yielding the least (Table 4). The four treatments with the loss were T1, T3, T4, and T5. On the other hand, this indicates that only T2 and T6 generated a positive profit and that the total revenue exceeded the total cost. T6, for example, generated a higher revenue and profit of RM 1,102.50 and RM 43.50, respectively. This substantial return demonstrates that T6 had effective cost management and a healthy return on investment (higher profit margin of 4.96%). T6 can generate the highest returns of about RM 31.50 per bird, or a net profit of about RM 1.24 per bird. When it comes to profitability, treatments ranged from a loss of RM 52.86 (T3) to a substantial profit of RM 43.50 (T6). This disparity highlights the critical role of revenue generation and cost management strategies in determining profitability. Furthermore, profit margins range from -5.17% (T3) to 3.95% (T6), emphasizing T6’s continued superiority in terms of profitability and efficiency.
As a rational investor with good decision-making, the main objective must aim for higher profit with minimum costs of production (Dahan and Srinivasan 2011). As a result, comparing revenue and profit (financial accounting information) across treatments is critical for providing additional evidence to support the best treatment investment decision (Ball et al. 2003; Al-Sehali and Spear 2004). T6 continued to produce the highest revenue per bird among treatments based on the estimated average revenue. This substantial return demonstrates that T6 exhibited effective cost management (efficient) and a healthy return on investment (profitability).
Table 5 displays the estimated break-even points for the six treatments, which ranged from 33 to 39 birds, as well as the margins of safety, which ranged from -10.45% to 7.22%. Treatments with lower break-even points, such as T6 with 33 birds, were more efficient in covering costs and achieving profitability, allowing for a greater margin of safety against losses. At the same time, T6 had a significantly positive margin of safety, i.e., 7.22%, indicating that it could cover costs and withstand market fluctuations better than other treatments.
Break-even analysis is an important cost-and-benefit analysis indicator that identifies the point at which total revenue equals total costs, thereby explaining the minimum number of sales required to avoid losses. Treatments with lower break-even points are more efficient in terms of covering costs and generating profits, i.e., T6. Furthermore, margins of safety are important too in determining the amount of output or sales that can fall before a business reaches its break-even point or becomes unprofitable. Higher positive margins of safety imply a larger buffer against losses and greater resilience to market fluctuations (Fatmawatie 2021). Overall, the current T6 produces more birds (35 birds) than the break-even units (33 birds) as well as shows the highest percentage of margins of safety among other treatments. This indicates that T6 was more profitable and more cost-efficient than other treatments.
Table 5. Summary of Economic Performance Indicators for Sasso Broilers Fed Diets with Incremental Levels of P. purpureum Grass Meal Supplementation
Future research should elucidate the mechanisms by which P. purpureum bioactives interact with the gut microbiome, immune pathways, and nutrient transport systems in monogastric animals, and evaluate performance under commercial-scale production.
CONCLUSIONS
- Physicochemical characterization (SEM, FTIR, TGA, XRD) confirmed that P. purpureum grass is a heterogeneous lignocellulosic material composed of semi-crystalline cellulose, amorphous hemicellulose and lignin, and rich in bioactive functional groups (hydroxyl, carbonyl, aliphatic chains).
- The biochemical complexity of P. purpureum suggests inherent health-promoting properties when incorporated into animal feed.
- Broiler supplementation at 5.00 g/kg significantly improved feed conversion efficiency, reduced total feed intake, and enhanced body weight gain without the use of synthetic antibiotics.
- Unchanged mortality rates across treatments confirm the safety of P. purpureum supplementation at the tested inclusion level.
- Economic analysis identified Treatment 6 (5 g/kg) as the most profitable strategy, delivering the highest revenue, net profit margin, and margin of safety with a low break-even threshold.
- While this study demonstrated growth and economic benefits, a key limitation is the absence of direct assessments of digestibility, immune response, antioxidant status, and gut microbiota, which should be prioritized in future research; additionally, exploring enzymatic (e.g., peroxidase, laccase) or fungal pretreatment of P. purpureum could improve its digestibility and enhance the bioavailability of its phytogenic compounds for poultry.
ACKNOWLEDGMENTS
The project was funded by the Geran Putra – Geran Putra Berimpak (GP-GPB), Universiti Putra Malaysia (Grant no: 9713700). The authors confirm that there are no additional funders. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors acknowledged the anonymous reviewers for comments to improve the quality of this work.
REFERENCES CITED
Alghirani, M. M., Chung, E. L. T., Kassim, N. A., Ong, Y. L., Jesse, F. F. A., Sazili, A. Q., and Loh, T. C. (2022). “Effect of Brachiaria decumbens as a novel supplementation on the production performance of broiler chickens,” Tropical Animal Health and Production 54(6), article 386. DOI: 10.1007/s11250-022-03384-4
Alghirani, M. M., Chung, E. L. T., Sabri, D. S. M., Tahir, M. N. J. M., Kassim, N. A., Kamalludin, M. H., Nayan, N., Jesse, F. F. A., Sazili, A. Q., and Loh, T. C. (2021). “Can Yucca schidigera be used to enhance the growth performance, nutrient digestibility, gut histomorphology, cecal microflora, carcass characteristic, and meat quality of commercial broilers raised under tropical conditions?,” Animals 11(8), article 2276. DOI: 10.3390/ani11082276
Al-Sehali, M., and Spear, N. (2004). “The decision relevance and timeliness of accounting earnings in Saudi Arabia,” The International Journal of Accounting 39(2), 197-217. DOI: 10.1016/j.intacc.2004.02.004
Alhendi, A. B., Homeida, A., and Gaili, E. (2000). “Drug residues in broiler chickens fed with antibiotics in ration,” Veterinary Archives 70(4), 199-205.
Alves, Z., Ferreira, N. M., Figueiredo, G., Mendo, S., Nunes, C., and Ferreira, P. (2022). “Electrically conductive and antimicrobial agro-food waste biochar functionalized with zinc oxide particles,” International Journal of Molecular Sciences 23(14), article 8022. DOI: 10.3390/ijms23148022
Azabo, R. R., George, J. I., Mshana, S. E., Matee, M. I., and Kimera, S. I. (2022). “Farm costs and benefits of antimicrobial use reduction on broiler farms in Dar es Salaam, Tanzania,” Frontiers in Antibiotics 1, 1011929. DOI: 10.3389/frabi.2022.1011929
Bajpai, P. (2016). “Structure of lignocellulosic biomass,” in: Pretreatment of Lignocellulosic Biomass for Biofuel Production, Springer, Singapore, pp. 7-12. DOI: 10.1007/978-981-10-0687-6_2
Bajpai, P. (2022). “Physical and chemical characteristics of lignocellulosic biomass,” in: Lignocellulosic Biomass in Biotechnology, Elsevier, Amsterdam, pp.11-24. DOI: 10.1016/B978-0-12-821889-1.00001-1
Baker, M. T., and Oguntoye, O. S. (2023). “Physical and spectroscopic characterization of the microcrystalline cellulose derivatives from corn cob and Daniella oliveri wastes,” Journal of the Turkish Chemical Society Section A: Chemistry 10(1), 31-38. DOI: 10.18596/jotcsa.1107627
Ball, R., Robin, A., and Wu, J. S. (2003). “Incentives versus standards: Properties of accounting income in four East Asian countries,” Journal of Accounting and Economics 36(1-3), 235-270. DOI: 10.1016/j.jacceco.2003.10.003
Cao, F. L., Zhang, X. H., Yu, W. W., Zhao, L. G., and Wang, T. (2012). “Effect of feeding fermented Ginkgo biloba leaves on growth performance, meat quality, and lipid metabolism in broilers,” Poultry Science 91(5), 1210-1221. DOI: 10.3382/ps.2011-01886
Chung, E. L. T., Alghirani, M. M., Kamalludin, M. H., Nayan, N., Jesse, F. F. A., Wei, O. T. A., Stephen, M. A. F. M. H., Reduan, M. F. H., and Loh, T. C. (2021). “Do different vaccination regimes affect the growth performance, immune status, carcase characteristics and meat quality of broilers?,” British Poultry Science 62(1), 32-37. DOI: 10.1080/00071668.2020.1817327
Chung, E. L. T., Nayan, N., Kamalludin, M. H., Alghirani, M. M., Jesse, F. F. A., Kassim, N. A., Azizi, A., Reduan, M. F. H., and Loh, T. C. (2020). “The effects of alkaline water and rainwater on the production and health performance of commercial broilers under tropical conditions,” The Thai Journal of Veterinary Medicine 50(1), 65-73. DOI: 10.56808/2985-1130.3076
Cichosz, S., and Masek, A. (2020). “IR study on cellulose with the varied moisture contents: Insight into the supramolecular structure,” Materials 13(20), article 4573. DOI: 10.3390/ma13204573
Dahan, E., and Srinivasan, V. (2011). “The impact of unit cost reductions on gross profit: Increasing or decreasing returns?,” IIMB Management Review 23(3), 131-139. DOI: 10.1016/j.iimb.2011.06.004
Fatmawatie, N. (2021). “Implementation of break event point analysis and margin of safety in profit planning,” Idarotuna : Journal of Administrative Science 2(2), 132-146. DOI: 10.54471/idarotuna.v2i2.20
French, A. (2022). “How crystalline is my cellulose specimen? Probing the limits of X-ray diffraction,” BioResources 17(4), 5557-5561. DOI: 10.15376/17.4.5557-5561
Gu, X., Fu, X., and Chen, S. (2021). “Hydrothermal liquefaction conversion of lignocelluloses with enhanced fungal pretreatment,” Industrial Crops and Products 162, article 113268. DOI: 10.1016/j.indcrop.2021.113268
Islam, M. R., Garcia, S. C., Sarker, N. R., Islam, Md. A., and Clark, C. E. F. (2023). “Napier grass (Pennisetum purpureum Schum) management strategies for dairy and meat production in the tropics and subtropics: Yield and nutritive value,” Frontiers in Plant Science 14, article 1269976. DOI: 10.3389/fpls.2023.1269976
Jack, I. R., Clark, P. D., and Ndukwe, G. I. (2020). “Evaluation of phytochemical, antimicrobial and antioxidant capacities of Pennisetum purpureum (Schumach) extracts,” Chemical Science International Journal 1-14. DOI: 10.9734/CSJI/2020/v29i430170
Jeffrey, K. B., Zheng, A. L. T., Hii, T. T., Seng, K. W. K., Chung, E. L. T., Lease, J., and Andou, Y. (2024). “Sustainable dye wastewater treatment: Utilizing duckweed-derived adsorbents for efficient methylene blue removal,” Biomass Conversion and Biorefinery 15, 19157-19173. DOI: 10.1007/s13399-024-06432-1
Jha, R., and Mishra, P. (2021). “Dietary fiber in poultry nutrition and their effects on nutrient utilization, performance, gut health, and on the environment: A review,” Journal of Animal Science and Biotechnology 12, article 51. DOI: 10.1186/s40104-021-00576-0
Kuralkar, P., and Kuralkar, S. V. (2021). “Role of herbal products in animal production – An updated review,” Journal of Ethnopharmacology 278, article 114246. DOI: 10.1016/j.jep.2021.114246
Luengnaruemitchai, A., and Anupapwisetkul, C. (2020). “Surface morphology and cellulose structure of Napier grass pretreated with the ionic liquid 1-ethyl-3-methylimidazolium acetate combined with either water or dimethyl sulfoxide as a co-solvent under microwave irradiation,” Biomass Conversion and Biorefinery 10(2), 435-446. DOI: 10.1007/s13399-019-00422-4
Negasa, J. G. (2024). “Dietary plant flavonoid supplementation for poultry as a potent scavenger of hydroxyl radicals and antioxidants: A review,” PeerJ Organic Chemistry 6, article e9. DOI: 10.7717/peerj-ochem.9
Negawo, A., Teshome, A., Kumar, A., Hanson, J., and Jones, C. (2017). “Opportunities for Napier grass (Pennisetum purpureum) improvement using molecular genetics,” Agronomy 7(2), article 28. DOI: 10.3390/agronomy7020028
Ng, K. S., Mohd Zin, Z., MohdMaidin, N., Mamat, H., Juhari, N. H., and Zainol, M. K. (2020). “High-performance liquid chromatography (HPLC) analysis for flavonoids profiling of Napier grass herbal tea,” Food Research 5(1), 65-71. DOI: 10.26656/fr.2017.5(1).311
Ong, Y. L., Chung, E. L. T., Nayan, N., Tan, N. P., Jesse, F. F. A., and Sazili, A. Q. (2024). “Ascertaining the effects of grass and leaf meals on the gut health and blood indices of broiler chickens – A systematic review,” Poultry Science Journal 12(1), article 1980. DOI: 10.22069/psj.2024.21707.1980
Osuntokun, O. (2014). “Comparative study of phytochemical and proximate analysis of seven Nigerian medicinal plants,” Annual Review of Biomedical Sciences 1, 67-85.
Rahimi, S., Zadeh, Z. T., Torshizi, M. A. K., Omidbaigi, R., and Rokni, H. (2011). “Effect of the three herbal extracts on growth performance, immune system, blood factors and intestinal selected bacterial population in broiler chickens,” Journal of Agricultural Science and Technology 13(4).
Rana, R., Herz, K., Bruelheide, H., Dietz, S., Haider, S., Jandt, U., and Pena, R. (2018). “Leaf attenuated total reflection fourier transform infrared (ATR-FTIR) biochemical profile of grassland plant species related to land-use intensity,” Ecological Indicators 84, 803-810. DOI: 10.1016/j.ecolind.2017.09.047
Salem, K. S., Kasera, N. K., Rahman, Md. A., Jameel, H., Habibi, Y., Eichhorn, S. J., French, A. D., Pal, L., and Lucia, L. A. (2023). “Comparison and assessment of methods for cellulose crystallinity determination,” Chemical Society Reviews 52(18), 6417-6446. DOI: 10.1039/D2CS00569G
Selaledi, L. A., Mohammed Hassan, Z., Manyelo, T. G., and Mabelebele, M. (2020). “The current status of the alternative use to antibiotics in poultry production: An African perspective,” Antibiotics 9(9), article 594. DOI: 10.3390/antibiotics9090594
Seng, K. W. K., Zheng, A. L. T., Ong, Y. L., Lease, J., Andou, Y., Jesse, F. F. A., Dunshea, F. R., and Chung, E. L. T. (2025). “Physicochemical properties and cost-benefit of supplementing signal grass (Brachiaria decumbens) in Sasso broilers production,” BioResources 20(2), 3176-3194. DOI: 10.15376/biores.20.2.3176-3194
Seomoon, K.-M., and Jang, I.-S. (2022). “Application of plant flavonoids as natural antioxidants in poultry production,” Korean Journal of Poultry Science 49(4), 211-220. DOI: 10.5536/KJPS.2022.49.4.211
Sofla, M. R. K., Brown, R. J., Tsuzuki, T., and Rainey, T. J. (2016). “A comparison of cellulose nanocrystals and cellulose nanofibres extracted from bagasse using acid and ball milling methods,” Advances in Natural Sciences: Nanoscience and Nanotechnology 7(3), article 035004. DOI: 10.1088/2043-6262/7/3/035004
Soliman, A. M., Elwy, H. M., Thiemann, T., Majedi, Y., Labata, F. T., and Al-Rawashdeh, N. A. F. (2016). “Removal of Pb(II) ions from aqueous solutions by sulphuric acid-treated palm tree leaves,” Journal of the Taiwan Institute of Chemical Engineers 58, 264-273. DOI: 10.1016/j.jtice.2015.05.035
Soltani, M., Farhadi, A., Rajabi, S., Homayouni‐Tabrizi, M., Hussein, F. S., and Mohammadian, N. (2024). “Folic acid-modified nanocrystalline cellulose for enhanced delivery and anti-cancer effects of crocin,” Scientific Reports 14(1), article 13985. DOI: 10.1038/s41598-024-64758-2
Sugiharto, S., Yudiarti, T., Isroli, I., Widiastuti, E., Wahyuni, H. I., and Sartono, T. A. (2019). “Recent advances in the incorporation of leaf meals in broiler diets,” Livestock Research for Rural Development 31(7).
Talik, P., Moskal, P., Kucharska, M., Proniewicz, L. M., and Wesełucha-Birczyńska, A. (2023). “Raman spectroscopy investigations of hydrated hydroxypropyl cellulose mixtures with low-soluble salicylic acid: Molecular interactions and the water-binding structure,” Journal of Molecular Structure 1294, article 136452. DOI: 10.1016/j.molstruc.2023.136452
Tan, Z., Halter, B., Liu, D., Gilbert, E. R., and Cline, M. A. (2022). “Dietary flavonoids as modulators of lipid metabolism in poultry,” Frontiers in Physiology 13, article 863860. DOI: 10.3389/fphys.2022.863860
Toor, S. S., Shah, A. A., Sharma, K., Seehar, T. H., Pedersen, T. H., and Rosendahl, L. A. (2022). “Bio-crude production from protein-extracted grass residue through hydrothermal liquefaction,” Energies 15(1), article 364. DOI: 10.3390/en15010364
Wang, C., Ma, D., and Bao, X. (2008). “Transformation of biomass into porous graphitic carbon nanostructures by microwave irradiation,” The Journal of Physical Chemistry C 112(45), 17596-17602. DOI: 10.1021/jp805113y
Wu, X., Hao, Y., Riaz, M., and Jiang, C. (2020). “Changes in leaf structure and chemical compositions investigated by FTIR are correlated with different low potassium adaptation of two cotton genotypes,” Agronomy 10(4), article 479. DOI: 10.3390/agronomy10040479
Zheng, A. L. T., Boonyuen, S., Ohno, T., and Andou, Y. (2021). “Accessing effects of aliphatic dicarboxylic acid towards the physical and chemical changes in low temperature hydrothermally reduced graphene hydrogel,” Journal of Porous Materials 28(4), 1291-1300. DOI: 10.1007/s10934-021-01072-6
Article submitted: May 29, 2025; Peer review completed: July 26, 2025; Revised version received and accepted: August 1, 2025; Published: August 11, 2025.
DOI: 10.15376/biores.20.4.8654-8673