Rambutan seeds are by-products generated from fruit-processing factories; the leftover seeds are buried in landfills, generating methane emissions. This work aimed to extract polysaccharides (POLS) from rambutan seeds by using subcritical water extraction (SWE). The effects of defatting pretreatment and operating parameters in SWE were investigated using a Box–Behnken design. The results show that defatting pretreatment significantly enriched the POLS yield, while it had no significant effect on the total sugar content. Using the desirability approach, the suitable feedstock for SWE was defatted rambutan seeds. The maximum desirability of 0.86 was found at a temperature range of 145–150 °C, an extraction time of 15 min, and a liquid–solid ratio of 10:1. The POLS yield and total sugar content were in the range of 52.33–55.63 g/100 g feedstock and 83.37–87.45 g/100 g POLS, respectively. The extracted POLS had an equivalent molecular weight of 413.70 kDa that could be used as an extender in plant-based products. In conclusion, the defatting pretreatment of rambutan seeds not only improved the POLS yield obtained via SWE but also generated additional lipids that could be utilized as an unconventional source of specialty fat.

Rambutan seeds (RS) are industrial waste often generated in the canned fruit industry. The aim of this study was to extract polysaccharides from defatted rambutan seeds or crude polysaccharides (POLS-DRSs) with subcritical water. Defatted seed powder (DRS) was extracted by hot-water extraction (HWE) at 100 °C as a reference condition. Subcritical water extraction (SWE) was performed at 120–140 °C and an initial pressure of 2 MPa. A sample-to-water ratio of 1:10 (w/w) and an extraction time of 15–60 min were used for both methods. The results show that gravimetric extraction yields of 53.01 g/100 g DRS and 7.71–41.70 g/100 g DRS were obtained from HWE and SWE, respectively. Additionally, HWE provided a total sugar content of 30.75 g/100 g POLS-DRSs, while SWE generated a total sugar content in the range of 27.00–49.76 g/100 POLS-DRSs. The antioxidant activities of POLS-DRSs were measured with a 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assay. An amount of 40 mg of POLS-DRSs obtained at 120 °C after 60 min provided the highest DPPH activity of 82.93% inhibition. The POLS-DRSs were suitable for growing microorganisms because they had a high sugar content and a low total phenolic content. A prebiotic activity assay will be carried out in future studies.