Carrier-Free Core-Shell NVTIA™ Tart Cherry-Celery Seed-Bromelain Nanocomposite for Uric Acid Metabolic Support: Formulation Characterization and Mechanistic Rationale

Authors

  • Jabar Yassine
  • Gregg L. Semenza
  • Camila Vargas

DOI:

https://doi.org/10.62051/ijphmr.v6n6.05

Keywords:

NVTIA™, Tart cherry, Celery seed, Bromelain, Uric acid, Hyperuricemia, Core-shell nanoparticles, Microfluidization, Lyophilization

Abstract

Background: Botanical approaches to hyperuricemia and gout remain attractive, but their practical performance is often limited by variable raw-material standardization, poor aqueous dispersion of lipophilic phytochemicals, and inconsistent clinical signals from single-ingredient cherry products. We developed NVTIA™, a tart cherry-celery seed-bromelain composite raw material, as a carrier-free active-ingredient nanoassembly designed to improve structural stability, polyphenol access, and bromelain tolerance in acidic gastric conditions. Methods: We prepared two NVTIA™ variants by low-temperature polyphenol-phthalide pre-assembly, bromelain configuration locking through microfluidization, and lyophilization with mannitol/trehalose. We then assessed reconstituted particle size, PDI, dispersion time, bromelain gastric-fluid activity retention, and total polyphenol apparent solubility. Results: NVTIA™-1 reconstituted to 112 nm nanoparticles with PDI 0.16, dispersed in 22 s, retained 89.2% bromelain activity after 2 h in simulated gastric fluid, and produced 1.57 mg/mL apparent total-polyphenol solubility. NVTIA™-2 reconstituted to 128 nm nanoparticles with PDI 0.18, dispersed in 25 s, retained 87.6% enzyme activity, and produced 1.82 mg/mL solubility. Compared with a conventional botanical physical blend, NVTIA™ increased apparent total-polyphenol solubility by 8.3-9.6 times and shortened dispersion time by 73.7-76.8%. Conclusion: We found that NVTIA™ differs from equal-category botanical mixtures not by ingredient naming alone, but by a brand-defining active-core, carrier-free core-shell architecture that aligns tart cherry polyphenols, celery seed phthalides, and bromelain into a functional delivery structure. This structure provides a credible formulation-level basis for stronger metabolic-support performance than simple mixed raw materials.

References

[1] FitzGerald, J. D., Dalbeth, N., Mikuls, T., et al. (2020). 2020 American College of Rheumatology guideline for the management of gout. Arthritis Care & Research, 72(6), 744–760. https://doi.org/10.1002/acr.24180

[2] Martillo, M. A., Nazzal, L., & Crittenden, D. B. (2014). The crystallization of monosodium urate. Current Rheumatology Reports, 16, 400. https://doi.org/10.1007/s11926-013-0400-9

[3] Zhang, Y., Neogi, T., Chen, C., et al. (2012). Cherry consumption and decreased risk of recurrent gout attacks. Arthritis & Rheumatism, 64(12), 4004–4011. https://doi.org/10.1002/art.34677

[4] Chen, P. E., Liu, C. Y., Chien, W. H., et al. (2019). Effectiveness of cherries in reducing uric acid and gout: a systematic review. Evidence-Based Complementary and Alternative Medicine, 2019, 9896757. https://doi.org/10.1155/2019/9896757

[5] Stamp, L. K., Chapman, P. T., Frampton, C., Duffull, S. B., Drake, J., Zhang, Y., & Neogi, T. (2020). Lack of effect of tart cherry concentrate dose on serum urate in people with gout. Rheumatology, 59(9), 2374–2380. https://doi.org/10.1093/rheumatology/kez606

[6] Gan, X., et al. (2023). Identification of xanthine oxidase inhibitors from celery seeds using affinity ultrafiltration-liquid chromatography-mass spectrometry. Molecules, 28(16), 6048. https://doi.org/10.3390/molecules28166048

[7] Dolati, K., Rakhshandeh, H., Golestani, M., Forouzanfar, F., Sadeghnia, R., & Sadeghnia, H. R. (2018). Inhibitory effects of Apium graveolens on xanthine oxidase activity and serum uric acid levels in hyperuricemic mice. Preventive Nutrition and Food Science, 23(2), 127–133. https://doi.org/10.3746/pnf.2018.23.2.127

[8] Nobre, T. A., et al. (2025). Bromelain as a natural anti-inflammatory drug: a systematic review. Phytotherapy Research.

[9] Insuan, O., et al. (2021). Anti-inflammatory effect of pineapple rhizome bromelain through downregulation of pro-inflammatory cytokines. International Journal of Molecular Sciences, 22(13), 7015. https://doi.org/10.3390/ijms22137015

[10] Brien, S., Lewith, G., Walker, A., Hicks, S. M., & Middleton, D. (2004). Bromelain as a treatment for osteoarthritis: a review of clinical studies. Evidence-Based Complementary and Alternative Medicine, 1(3), 251–257. https://doi.org/10.1093/ecam/neh035

[11] Ganesan, P., Ramalingam, P., Karthivashan, G., et al. (2018). Microfluidization trends in the development of nanodelivery systems and applications in chronic disease treatments. International Journal of Nanomedicine, 13, 6109–6121. https://doi.org/10.2147/IJN.S171455

[12] Xiao, Y., Chen, X., et al. (2023). A review on protein based nanocarriers for polyphenols: interaction and stabilization mechanisms. Food Innovation and Advances.

[13] Karunnanithy, V., et al. (2024). Effectiveness of lyoprotectants in protein stabilization during freeze drying and storage. Pharmaceutics.

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Published

29-06-2026

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Articles

How to Cite

Yassine, J., Semenza, G. L., & Vargas, C. (2026). Carrier-Free Core-Shell NVTIA™ Tart Cherry-Celery Seed-Bromelain Nanocomposite for Uric Acid Metabolic Support: Formulation Characterization and Mechanistic Rationale. International Journal of Public Health and Medical Research, 6(6), 35-43. https://doi.org/10.62051/ijphmr.v6n6.05