1. Introduction
Pineapple is a major economic crop both globally and in Thailand, generating substantial income for farmers and contributing significantly to national export revenues. In 2022, global production reached 28.99 million tons, with Thailand contributing 1.714 million tons (5.91% of global output), establishing the country as a leading canned pineapple exporter, with export values of USD 460.51 million and a total export value of USD 683.22 million [
1]. Thailand allocates 70–80% of its pineapple production to processing factories for export, while the remaining 20–30% is used for domestic consumption. Cultivation is concentrated in western and eastern regions, producing 1,075,537 tons from 294,262 rai in 2024, with average yields of 3655 kg/rai and factory prices of THB 11.88 per kilogram [
2]. This extensive processing industry generates substantial organic waste, including peels, pomace, cores, and crown, representing approximately 40–60% of the fruit’s weight. Based on significant production volume and the economic importance of pineapple processing in Thailand, both environmental benefits and additional revenue streams are yielded when this waste is upcycled into value-added products, whereby circular economy principles are supported, and processor disposal costs are concurrently reduced.
The circular economy concept transforms the linear economic model—which focuses on producing goods for disposal after consumption—into a sustainable approach that emphasizes the efficient reuse and recycling of agro-industrial waste [
3]. This circular economy model for agro-industrial waste aligns with Sustainable Development Goal (SDG) 12, which aims to ensure sustainable consumption and production patterns [
4].
The valorization of pineapple processing waste for various applications has recently gained increasing attention [
5]. The chemical composition of this waste shows that it is a source of polysaccharides, including cellulose and pectin. The technological functions of these extracted components include the enhancement of texture due to rich dietary fiber contents, which improves the structural integrity of food products. Moreover, pineapple dietary fibers are effective in reducing fat content and improving the overall consistency of beef sausages [
6].
Dried pomace powder has been supplemented into flour prior to producing cookies, resulting in increased dietary fiber [
7]. The extraction of pectin from fruit and vegetable by-products to replace fat in yogurt has been reported [
8]. Pectin extracted from banana peels was used as a fat replacer in muffins [
9]. Moreover, low-methoxyl pectin from pineapple peel was successfully used to produce a hydrogel for use as a fat replacer in beef patties [
10]. This type of pectin has also been reported to improve the quality of low-fat yogurt [
11].
Pectin recovery from pineapple peel is typically performed using microwave-assisted extraction, which effectively mitigates the shortcomings of conventional methods. Furthermore, the simultaneous enhancement of extraction yields and the quality improvement of the resulting pectin are facilitated [
12]. Thus, the extraction of low-methoxyl pectin from pineapple waste to produce a fat replacer for sausages is possible. This approach represents a strategy for upcycling pineapple waste to produce reduced-fat sausages as a healthier meat product.
Besides pectin, cellulose has been isolated from pineapple by-products and successfully modified by attaching carboxymethyl moieties to form carboxymethyl cellulose (CMC) [
13]. This CMC has been used to produce edible films via combinations with gelatin. These gelatin composite films exhibited antioxidant activity and modified material properties [
14]. However, the use of these films as edible casings for sausages has not been reported. Evaluating the potential of these films as casings for reduced-fat sausages represents a promising area. This would strengthen the approach for upcycling pineapple industry waste while enabling the meat and fishery industries to produce healthier products.
Therefore, this study aimed to (1) update waste generation estimates from the pineapple industry in Thailand; (2) demonstrate waste upcycling by extracting pectin to produce fat-replacing hydrogels crosslinked by natural calcium from fish bone powder; and (3) evaluate the feasibility of using an edible film made with gelatin/carboxymethyl cellulose films, synthesized from pineapple waste cellulose, as casings for reduced-fat sausages during cold storage.
2. Materials and Methods
2.1. Materials
Data regarding pineapple production from 2015 to 2024 were obtained from the Office of Agricultural Economics, Ministry of Agriculture and Cooperatives, Thailand.
Pineapple samples were sourced from a local farmer at Ban Mor, Srichiang Mai, Nong Khai, Thailand, with geographical coordinates of “17.956839, 102.589471”. The whole fruit was separated into peel, core, and flesh after removing the crown. The peel was washed with tap water and vacuum dried at 60 °C until a constant weight was achieved. Soy protein isolates (approximately 90% purity) were provided by Shandong Yuwang Ecological Food Industry Co., Ltd. (Dezhou, China). Commercial pectin (HSA310, low-methoxyl medium-reactivity calcium pectin E440) was obtained from Dangshan Haisheng Pectin Co., Ltd., (Suzhou, China).
2.2. Estimation of Pineapple Waste
The estimation of pineapple waste generation was based on 75% of the annual production, which is supplied to processing factories, according to the Office of Agricultural Economics of Thailand report for 2015–2024. Finally, the amounts of each waste constituent were determined based on our review [
15], with peel and core accounting for an average of 35.5% and 14.7% of the fruit’s weight, respectively.
2.3. Utilization of Pectin from Pineapple Waste to Produce Reduced-Fat Sausage
2.3.1. Extraction of Pectin from Pineapple Waste
Pectin was extracted using a previously developed method [
16]. A 5 g sample was mixed with citric acid (adjusted to pH 1.5) at a raw-material-to-solvent ratio of 1:30. Extraction was performed via microwave treatment at 300 W for 5, 7, and 10 min, followed by cooling in a cold bath for 15 min. The extract was filtered through filter paper prior to 30 min of centrifugation at 10,000×
g. The clear fraction was mixed with 500 mL of 95% ethanol and allowed to precipitate overnight in a cold room. The precipitated pectin was washed with 70% ethanol and recovered via centrifugation at 10,000×
g for 5 min. The final precipitate was vacuum-dried at 60 °C for 1 h to produce the fat replacer.
2.3.2. Production of Fat Replacer with Extracted Pectin
The fat replacer preparation followed a previously published method [
10]. Pectin extracted from pineapple peel was mixed with commercial pectin at a 1:3 ratio to obtain mixed pectin. This mixed pectin sample was classified as low-methoxyl pectin as the degree of methylation was lower than 50%. This mixture was then combined with soy protein isolates (1.0%) before heating at 90 °C for 30 min. Fish bone powder (0.5%) from catfish was then added to release available calcium ions in order to induce the gelation of low-methoxyl pectin, while heating continued for 5 min. After cooling, the resulting hydrogel was used as a fat replacer (FR) in sausage formulations.
2.3.3. Production of Reduced-Fat Sausage
Sausage production followed the method of Hemung et al. [
17]. The recipe ratio consisted of minced fish, corn oil, salt, and ice maintained at 60%, 20%, 0.5%, and 19.5%, respectively. Fat was reduced from the original recipe by substituting FR at 25% to facilitate quality comparisons. Minced fish, salt, and a quarter of the total ice were chopped for 30 s using a handheld food mixer (Bowl Rest™ mixer, Hamilton Beach, Glen Allen, VA, USA). The remaining ice was then added, and the mixture was chopped for an additional minute. Corn oil was then incorporated, and chopping continued for one more minute to form a batter with a temperature below 16 °C. This batter was stuffed into edible casings measuring 1.30 cm in diameter and hand-tied with a cotton rope at approximately 3 cm intervals. The sausages were incubated at 40 °C for 15 min, followed by cooking at 80 °C for an additional 15 min. The cooked samples were then cooled in ice water for 15 min. After cooling in a cold room overnight, the edible casings were removed before evaluating their characteristics.
2.3.4. Characterization of Reduced-Fat Sausage
Water-Holding Capacity (WHC)
Cubic samples (1.0 g) were prepared and wrapped in filter paper (3 layers); then, they were placed in centrifuge tubes. The samples were centrifuged at 2000×
g for 30 min at ambient temperature. The sample’s weight was recorded before (W
i) and after (W
f) centrifugation. WHC was calculated as the percentage of weight remaining after centrifugation using Equation (1). The mean and standard deviation were calculated according to 3 replicates:
Texture Profile Analysis
Sausage texture was analyzed following a previously published method [
18]. Sausage samples were cut into 1 cm cubes and compressed twice using a cylindrical aluminum probe with a texture analyzer (TA XT Plus, Godalming, UK). Cubes were compressed to half their original height at a 5 mm/s probe speed. Average texture parameters, including hardness, springiness, adhesiveness, cohesiveness, gumminess, and chewiness, were calculated according to 5 replicates.
Chemical Composition
The chemical composition of sausages was evaluated following standard procedures with slight adjustments [
19]. Moisture content was assessed by drying the samples in an oven at 105 °C for over 12 h. Crude fat was measured using Soxhlet extraction with petroleum ether as the solvent. The total ash content was determined via dry ashing in a muffle furnace at approximately 550 °C for more than 6 h. Protein levels were quantified using the Kjeldahl method, and crude dietary fibers were evaluated according to AOAC [
19]. All composition values were reported as averaged standard deviations from 3 replicates. Total carbohydrate content was calculated by subtracting all other compositions from a hundred.
2.4. Application of Cellulose from Pineapple Waste to Produce Edible Film
2.4.1. Extraction of Cellulose from Pineapple Waste
Pineapple waste was soaked in water for 8 h before drying under the same conditions as those for pectin extraction. Dried samples were stored under dry conditions until used. The cellulose was extracted according to a previously published method [
20]. The procedure involved heating dried pineapple waste powder with 0.5 M NaOH at a 1:60 ratio for 3 h. The slurry obtained from this treatment was then filtered, and the cellulose was washed with cold water. The obtained cellulose was vacuum-dried at 60 °C for 1 h prior to carboxymethyl cellulose synthesis.
2.4.2. Synthesis of CMC and Film Formation with Gelatin
The CMC from pineapple core was synthesized according to Seubsunthorn et al. [
11], and it was used to produce composite films with gelatin. This was compared with films made from commercial cellulose according to Seubsunthorn et al. [
14]. Cellulose from pineapple waste (5.0 g) was mixed with 30.0% NaOH (50 mL) and isopropyl alcohol (150 mL). The mixture was stirred at 30 °C for 30 min before adding monochloroacetic acid (6 g). Thereafter, the mixture was continually stirred for 90 min prior to incubating at 55 °C for 3 h. The incubated mixture was filtered through Whatman
® No. 1 filter paper (Marlow, UK). The retentate was washed by mixing with 70.0% (
v/
v) ethanol (50 mL) and stirred for 5 min (adjusted pH to 7.00) before filtering through the filter paper. This washing step was repeated 4 more times. Then, the final retentate was dried overnight at 55 °C and used as CMC powder. The abbreviations CCMC and PCMC are used to denote commercial and pineapple waste CMC, respectively.
2.4.3. Storage Stability of Reduced-Fat Sausage Wrapped in Gelatin/CMC Film
The CCMC and PCMC were used to wrap the reduced-fat sausage, and they were kept at 4 °C for 5 days. Changes in quality were monitored as detailed in the following subsections.
Changes in Color Values
The color value of the sausages was measured using a Hunter colorimeter (Color reader, CR-10, Minolta, Osaka, Japan). The results were reported using Hunter L, a, and b scales, representing lightness, redness, and yellowness, respectively. Average values and standard errors were obtained from 5 measurements.
Changes in pH
The sausage’s pH was measured using a pH meter (PH850-BS Portable, Shanghai, China) following Janardhanan et al. [
21] at room temperature. The pH meter was calibrated with standard buffer solutions at pH 4, 7, and 10 before measurement. A solid probe was inserted directly into the samples for each measurement. The reported pH values represent the average of 5 measurements.
Changes in Microbial Indices
The total viable count (TVC) is a measurement that estimates the total amount of living microorganisms in a sample. The TVC was determined using the spread plate method with a focus on aerobic bacteria, which normally deteriorate a sausage’s quality. In summary, a 25 g sausage sample was aseptically homogenized with 225 mL of normal saline (0.9% NaCl) in a stomacher (Model 400 Seward, London, UK) for 2 min. Then, a serial dilution was prepared using a normal saline solution. Then, a 0.1 mL sample mixture was spread on the plate count agar (PCA) prior to incubation at 37 °C for 24 h. The results were reported as log CFU/g from 3 replications. The number of
Staphylococcus aureus was quantified according to the analysis method in the Bacteriological Analytical Manual Online (BAM). The quantification of
Clostridium perfringens was carried out according to the analysis method in the Bacteriological Analytical Manual Online (BAM). The quantity of
Salmonella spp. was determined according to the ISO 6579-1: 2017 standard reference method [
22]. In addition,
Escherichia coli was quantified according to the analysis method from the Food and Drug Administration [
23].
Changes in TBARS
Lipid oxidation in sausages was assessed using the TBARS method [
24]. Patty samples (2.00 g) were combined with 3 mL of the TBA solution; then, 17 mL of the TCA mixture was added. The mixture was boiled for 30 min and cooled to room temperature, and 5 mL of the clear upper layer was transferred to a 50 mL centrifuge tube containing 5 mL of chloroform. After centrifugation at 200×
g for 5 min, 3 mL of the upper liquid was decanted, mixed with 3 mL of petroleum ether, vortexed, and centrifuged again at 200×
g for 10 min. The absorbance of the lower layer was measured at 532 nm using a UV/VIS spectrometer (PG Instruments Model T70 Plus, PG Instruments Limited, Louth, UK). The TBARS results were expressed as mg malondialdehyde (MDA)/kg sample, averaged from 3 replications.
DPPH Radical Scavenging Ability
Antioxidant activities were determined using the DPPH assay. Antioxidants were extracted from the samples by immersing them in 3 mL of methanol for 48 h. Subsequently, 0.5 mL of the extract was mixed with 1.5 mL of ethyl acetate, followed by the addition of 1.5 mL of a DPPH solution. The mixture was then incubated in the dark for 30 min, and absorbance was measured at 515 nm (A sample) using a spectrophotometer (PG Instruments Model T70 Plus, PG Instruments Limited, Louth, UK). A control was prepared under the same conditions without the sample extract. The DPPH radical scavenging activity was calculated according to Equation (2). The average values were calculated from 3 replicates:
2.5. Statistical Analysis
The data were presented as mean ± SD. IBM SPSS statistical software (Version 28.0, IBM, Armonk, NY, USA) was used for data analysis. One-way analysis of variance (ANOVA) and F-tests were employed to determine statistical differences at a confidence level of 95%.
4. Conclusions
Thailand, a key global canned pineapple exporter, generates significant annual processing waste (peels and cores), averaging approximately 600,000 metric tons (MT) over the past decade. Analyzing these constituents is essential for successful resource recovery and the promotion of sustainability. Pineapple waste could be a source of pectin, and quick extractions could be performed using the microwave-assisted method. The resultant pectin can be used to produce hydrogels as fat replacers in meat products. The application of this fat replacer in sausages not only reduces fat content without compromising desirable properties but also improves technological and textural properties. In addition, cellulose could also be extracted from pineapple waste, and its derivative, carboxymethyl cellulose, serves as an alternative material to composite with gelatin for forming edible films with superior antioxidative properties compared to those made from commercial cellulose. This film demonstrated suitability as an edible casing for reduced-fat sausages. Therefore, the upcycling approach results in maximized efficiency in these sectors and promotes the meat and fishery industries through the development of healthier food products.