Formulation of Nanoencapsulated Pigeon Pea (Cajanus cajan L. (Huth.)) Extract as an Antidiabetic Agent

Authors

  • Rifkarosita Putri Ginaris Program Studi Sarjana Farmasi, Sekolah Tinggi Ilmu Kesehatan Tujuh Belas, Indonesia
  • Anggi Aryadi Program Studi Sarjana Keperawatan, Sekolah Tinggi Ilmu Kesehatan Tujuh Belas, Indonesia
  • Nadya Afifa Program Studi Sarjana Farmasi, Sekolah Tinggi Ilmu Kesehatan Tujuh Belas, Indonesia
  • Arief Kusuma Wardani Departemen Farmasi, Fakultas Ilmu Kesehatan, Universitas Muhammadiyah Magelang, Indonesia
  • Lyna L. Indrayati Fakultas Pertanian, Universitas Tidar, Indonesia
  • Blegoh Iwan Santoso Program Studi Diploma Tiga, Politeknik Unggulan Kalimantan, Indonesia

DOI:

https://doi.org/10.54445/pharmademica.v5i2.126

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15

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2

Keywords:

α-glucosidase , antidiabetic , flavonoid, cajanus cajan , nanoencapsulation

Abstract

Pigeon pea (Cajanus cajan L. (Huth.)) contains flavonoids that exhibit potential antidiabetic activity through the inhibition of the α-glucosidase enzyme. The main limitation in the application of flavonoid compounds is their low solubility and stability. Nanoencapsulation using chitosan–TPP via a simple ionic gelation method can enhance the stability and bioactivity of active compounds. This study aimed to develop a nanoencapsulation formulation of pigeon pea extract and to evaluate its physical characteristics, stability, and α-glucosidase inhibitory activity. The research was conducted using variations in nanoencapsulation extract concentrations: F1 (0.2%), F2 (0.4%), and F3 (1%). Physical characterization included particle size, polydispersity index (PDI), and zeta potential, along with a freeze–thaw stability test for five cycles. Antidiabetic activity was assessed by measuring α-glucosidase inhibition and determining the IC₅₀ value. Data were analyzed using one-way ANOVA followed by Tukey’s post hoc test (p < 0.05). The results showed that particle size decreased from 290.40 nm (F1) to 198.30 nm (F3), with polydispersity index values below 0.3 for F2 and F3. The zeta potential ranged from −28.10 to −36.10 mV. F3 demonstrated the highest stability and the strongest antidiabetic activity with an IC₅₀ value of 68 ppm (p < 0.05).

In conclusion, the nanoencapsulation formulation of pigeon pea extract produced small-sized, stable particles with effective α-glucosidase inhibitory activity. The optimal formulation was F3, which shows potential for further development as a natural-based antidiabetic nanoencapsulation system.

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Published

14-03-2026

How to Cite

Ginaris, R. P. ., Aryadi, A. ., Afifa, N. ., Wardani, A. K. ., Indrayati, L. L. ., & Santoso, B. I. . (2026). Formulation of Nanoencapsulated Pigeon Pea (Cajanus cajan L. (Huth.)) Extract as an Antidiabetic Agent. PHARMADEMICA : Jurnal Kefarmasian Dan Gizi, 5(2), 157–169. https://doi.org/10.54445/pharmademica.v5i2.126