Formulation and evaluation of solid lipid nano particle of Vaccinium Macrocarpon Extract and Its Antimicrobial Activity

Authors

  • Diksha Gurjar M. Pharma IV Sem (Pharmaceutics), Malhotra College of Pharmacy, Bhopal, M.P.
  • Brajesh Kumar Arjariya Professor & Head, Department of Pharmaceutics, Malhotra College of Pharmacy, Bhopal, M.P.
  • Sheenam Mansuri Associate Professor, Malhotra College of Pharmacy, Bhopal, M.P.

DOI:

https://doi.org/10.69968/ijisem.2026v5i2431-438

Keywords:

Solid Lipid Nanoparticles, Vaccinium Macrocarpon, Antimicrobial Activity, Solvent Evaporation Method, Phytochemical Screening, Zeta Potential

Abstract

A promising and adaptable drug delivery method that fills the gap between "polymeric nanoparticles" and "lipid emulsions" is solid lipid nanoparticles (SLNs). The goal of the current work was to formulate, optimize, and assess SLNs loaded with cranberry (Vaccinium macrocarpon) extract for increased antibacterial activity. Vaccinium macrocarpon, a member of the Ericaceae family, is renowned for its broad-spectrum antibacterial qualities, antioxidant potential, and high phenolic and flavonoid content. Methanol and petroleum ether were used as solvents in the soxhlet extraction process to create the extract. Flavonoids, alkaloids, tannins, glycosides, phenolic chemicals, triterpenoids, and steroids were all found in the methanolic extract, according to phytochemical screening. The results showed that the "total flavonoid content (TFC)" was 15.23 mg per gram equivalent of rutin and the total phenolic content (TPC) was 62.03 mg per gram equivalent of gallic acid. "Compritol" was used as the "lipid phase" and "sodium lauryl sulphate" as the "surfactant" in the solvent evaporation process utilized to create SLNs. Lipid and surfactant amounts were varied to create five formulations (F1–F5). Malvern Zetasizer's particle size study showed sizes ranging from 574.2 to 993.4 nm; formulation F3 had the smallest particle size, measuring 574.2 nm. The range of zeta potential readings was "-1.2 mV to 5.3 mV". The smooth surface and spherical shape were verified by scanning electron microscopy (SEM). The antimicrobial activity of optimized formulation "F3" against "Escherichia coli" was demonstrated by dose-dependent zones of inhibition measuring 7 mm, 10 mm, and 13 mm at 0.5, 1.0, and 1.5 mg/mL, respectfully. The F3 formulation remained stable for a three-month period with no appreciable changes in size of particles or zeta potential, according to stability assays conducted under accelerated settings. The findings show that SLNs loaded with Vaccinium macrocarpon extract are a stable and practical nanoformulation with strong antibacterial activity.

References

[1]. Mitchell, M. J., Billingsley, M. M., Haley, R. M., Wechsler, M. E., Peppas, N. A., & Langer, R. (2021). Engineering precision nanoparticles for drug delivery. Nature Reviews Drug Discovery, 20(2), 101–124.

[2]. Arias, L. S., Pessan, J. P., Vieira, A. P. M., Lima, T. M. T. D., Delbem, A. C. B., & Monteiro, D. R. (2018). Iron oxide nanoparticles for biomedical applications: A perspective on synthesis, drugs, antimicrobial activity, and toxicity. Antibiotics, 7(2), 46.

[3]. Lorente, C., Cabeza, L., Clares, B., Ortiz, R., Halbaut, L., Delgado, A. V., & Melguizo, C. (2018). Formulation and in vitro evaluation of magnetoliposomes as a potential nanotool in colorectal cancer therapy. Colloids and Surfaces B: Biointerfaces, 171, 553–565.

[4]. Gordillo-Galeano, A., & Mora-Huertas, C. E. (2018). Solid lipid nanoparticles and nanostructured lipid carriers: A review emphasizing on particle structure and drug release. European Journal of Pharmaceutics and Biopharmaceutics, 133, 285–308.

[5]. Kokate, C. K., Purohit, A. P., & Gokhale, S. B. (2000). Textbook of Pharmacognosy. Nirali Prakashan, 1–4.

[6]. Aldayel, T. S., Badran, M. M., Alomrani, A. H., AlFaris, N. A., Altamimi, J. Z., Alqahtani, A. S., & Orfali, R. (2023). Chitosan-coated solid lipid nanoparticles as an efficient avenue for boosted biological activities of Aloe perryi: Antioxidant, antibacterial, and anticancer potential. Molecules, 28(8), 3569.

[7]. Alshawwa, S. Z., Labib, G. S., Badr-Eldin, S. M., & Kassem, A. A. (2023). Solid lipid lyo-nanosuspension: A promising stabilized oral delivery system for the antihyperglycemic extract of Mistletoe Plicosepalus acacia. Saudi Pharmaceutical Journal.

[8]. Zabihi, M., Shafaei, M., Ramezani, V., Dara, T., & Mirzaie, F. (2023). Preparation of thymol nanoliposome and solid lipid nanoparticle and evaluation of their inhibitory effects on Leishmania major promastigotes. Advances in Pharmacology and Therapeutics Journal, 3(1), 49–60.

[9]. Nemati, S., Rahimi, H. M., Hesari, Z., Sharifdini, M., Jalilzadeh Aghdam, N., Mirjalali, H., & Zali, M. R. (2022). Formulation of Neem oil-loaded solid lipid nanoparticles and evaluation of its anti-Toxoplasma activity. BMC Complementary Medicine and Therapies, 22(1), 122.

[10]. Minocha, V., et al. (2022). Solid lipid nanoparticles of wheatgrass extract: Effect of chemical stabilizers and sonication time on entrapment efficiency. International Journal of Pharmaceutical Research.

[11]. Sanei-Dehkordi, A., Agholi, M., Shafiei, M., & Osanloo, M. (2022). Promising larvicidal efficacy of solid lipid nanoparticles containing Mentha longifolia L., Mentha pulegium L., and Zataria multiflora Boiss. essential oils against the main malaria vector, Anopheles stephensi Liston. Acta Parasitologica, 67(3), 1265–1272.

[12]. Haghighi, P., Ghaffari, S., Arbabi Bidgoli, S., Qomi, M., & Haghighat, S. (2018). Preparation, characterization and evaluation of Ginkgo biloba solid lipid nanoparticles. Nanomedicine Research Journal, 3(2), 71–78.

[13]. Sawant, P., Karekar, P., & Waghmare, K. (2020). Formulation and characterization of solid lipid nanoparticles containing ginger oil for enhancement of stability. International Journal of Pharmacy and Pharmaceutical Sciences, 12(6), 36–44.

[14]. Sabapati, M., Palei, N. N., CK, A. K., & Molakpogu, R. B. (2019). Solid lipid nanoparticles of Annona muricata fruit extract: formulation, optimization and in vitro cytotoxicity studies. Drug Development and Industrial Pharmacy, 45(4), 577–586.

[15]. Parthasarathy, S., Bin Azizi, J., Ramanathan, S., Ismail, S., Sasidharan, S., Said, M. I., et al. (2009). Evaluation of antioxidant and antibacterial activities of aqueous, methanolic and alkaloid extracts from Mitragyna speciosa (Rubiaceae Family) leaves. Molecules, 14, 3964–3974.

[16]. Rahman, Z., Zidan, A. S., & Khan, M. A. (2010). Non-destructive methods of characterization of risperidone solid lipid nanoparticles. European Journal of Pharmaceutics and Biopharmaceutics, 76(1), 127–137.

[17]. Penjuri, S. C. B., Ravouru, N., Damineni, S., Bns, S., & Poreddy, S. R. (2016). Formulation and evaluation of lansoprazole loaded Nanosponges. Turk. J. Pharm. Sci, 13(3), 304-310.

[18]. Mohammadi-Sichani, M., Karbasizadeh, V., Aghai, F., & Mofid, M. R. (2012). Effect of different extracts of Stevia rebaudiana leaves on Streptococcus mutans growth. J Med Plants Res, 6(32), 4731-19.

[19]. Manandhar, S., Luitel, S., & Dahal, R. K. (2019). In vitro antimicrobial activity of some medicinal plants against human pathogenic bacteria. Journal of tropical medicine, 2019.

[20]. Kumar, S., Trotta, F., & Rao, R. (2018). Encapsulation of babchi oil in cyclodextrin-based nanosponges: Physicochemical characterization, photodegradation, and in vitro cytotoxicity studies. Pharmaceutics.

Downloads

Published

13-06-2026

Issue

Section

Articles

How to Cite

[1]
Diksha Gurjar et al. 2026. Formulation and evaluation of solid lipid nano particle of Vaccinium Macrocarpon Extract and Its Antimicrobial Activity. International Journal of Innovations in Science, Engineering And Management. 5, 2 (Jun. 2026), 431–438. DOI:https://doi.org/10.69968/ijisem.2026v5i2431-438.