Evaluation of Safety and Efficacy of Welstone™️Drops in Experimentally-Induced Calcium Oxalate Urolithiasis in Rats

Authors

  • Poorva Tiwari Scientific & Medical Affairs Department; Dr. Willmar Schwabe India Pvt. Ltd.
  • Snigdha Suman Dalua Scientific & Medical Affairs Department; Dr. Willmar Schwabe India Pvt. Ltd.
  • Praveen Saxena Marketing Department; Dr. Willmar Schwabe India Pvt. Ltd.
  • Ramachandran Valavan Scientific, Medical & Regulatory Department; Dr. Willmar Schwabe India Pvt Ltd

DOI:

https://doi.org/10.48165/ahr.2026.11.3.2

Keywords:

Urolithiasis, WelstoneTM, ethylene glycol, ammonium chloride, calcium oxalate, renal function, homeopathy, Wistar rats

Abstract

Background Urolithiasis is a recurrent urinary disorder  characterized by crystal formation and deposition  within the urinary tract, with CaOx being the  predominant stone type. The present study evaluated  the safety and antiurolithiatic efficacy of three variants  of the homeopathic formulations, with the objective  of commercializing the most efficacious and safe  formulation under the brand name Welstone™️, in an  experimental model of urolithiasis. The safety and  efficacy of Welstone™️ compared with the controls  are presented in this paper. 

Materials & Methods Male Wistar rats were allocated into 12 groups (n =  6/group). Urolithiasis was induced using 0.75% v/v  ethylene glycol (EG) and 1% w/v ammonium chloride  (AC) in drinking water for the initial 7 days, followed  by 0.75% EG until Day 28. Three homeopathic  formulations were administered orally at low,  medium, and high dose levels in 9 different groups  from Day 8 to Day 28, while Cystone® (750 mg/kg)  served as the reference standard. Treatment effects  were assessed through body-weight changes, renal  biochemical and mineral parameters, absolute and  relative kidney weights, and renal histopathological  evaluation. 

Results EG + AC exposure impaired body-weight gain and  increased serum creatinine, urea, blood urea nitrogen,  uric acid, calcium, phosphorus, and kidney weight,  accompanied by marked renal histopathological  alterations. Treatment with Welstone™ at low,  medium, and high doses attenuated these changes  to varying degrees. Welstone™ at the high dose  showed the most consistent overall response, with  improvement in renal biochemical and mineral  parameters, body-weight gain, kidney weight, and  preservation of renal architecture, while the Low  and Medium doses also improved relative to the  disease-control group. The concordance between  biochemical improvement and histopathological  recovery supports the antiurolithiatic potential of  Welstone™ in this experimental model.

Conclusion Improvements in biochemical parameters and  kidney histoarchitecture suggest that Welstone™️  has antiurolithiatic potential in EG + AC-induced  experimental urolithiasis. Among the doses tested, the  high dose of Welstone™️ showed the most consistent  response, with effects comparable to the standard  treatment. Further studies are needed to elucidate  its mechanism of action through the assessment of  urinary lithogenic factors and quantitative calcium  oxalate (CaOx) crystal formation. 

 

References

Türk, C. (2020). EAU guidelines on urolithiasis. European Association of Urology, 28.

Pearle, M. S., Goldfarb, D. S., Assimos, D. G., Curhan, G., Denu-Ciocca, C. J., Matlaga, B. R., Monga, M., Penniston, K. L., Preminger, G. M., Türk, T. M., & White, J. R. (2014). Medical management of kidney stones: AUA guideline. The Journal of Urology, 192(2), 316–324.

Sorokin, I., Mamoulakis, C., Miyazawa, K., Rodgers, A., Talati, J., & Lotan, Y. (2017). Epidemiology of stone disease across the world. World Journal of Urology, 35(9), 1301–1320.

Khan, S. R., Pearle, M. S., Robertson, W. G., Gambaro, G., Canales, B. K., Doizi, S., Traxer, O., & Tiselius, H. G. (2016). Kidney stones. Nature Reviews Disease Primers, 2(1), 16008.

Khan, S. R. (2014). Reactive oxygen species, inflammation and CaOx nephrolithiasis. Translational Andrology and Urology, 3(3), 256.

Aggarwal, K. P., Narula, S., Kakkar, M., & Tandon, C. (2013). Nephrolithiasis: Molecular mechanism of renal stone formation and the critical role played by modulators. BioMed Research International, 2013, 292953.

Boericke, W. (2002). New manual of homoeopathic materia medica & repertory: With relationship of remedies (2nd re-augmented & revised ed., reprint ed.). B. Jain Publishers.

Clarke, J. H. (1992). Dictionary of practical materia medica (Reprint ed.). B. Jain Publishers.

Das, I., Gupta, S. K., Pandey, V. N., & Ansari, S. A. (2004). Inhibition and dissolution of CaOx crystals by Berberis vulgaris-Q and other metabolites. Journal of Crystal Growth, 267(3–4), 654–661.

Atmani, F., & Khan, S. R. (2000). Effects of an extract from Herniaria hirsuta on CaOx crystallization in vitro. BJU International, 85(6), 621–625.

Katsuma, S., Shiojima, S., Hirasawa, A., Takagaki, K., Kaminishi, Y., Koba, M., Hagidai, Y., Murai, M., Ohgi, T., Yano, J., & Tsujimoto, G. (2002). Global analysis of differentially expressed genes during progression of calcium oxalate nephrolithiasis. Biochemical and Biophysical Research Communications, 296(3), 544–552.

Partovi, N., Fatemi, S. J., & Ebadzadeh, M. R. (2024). Antiurolithiatic effects of Cassia fistula Linn. fruit extracts on ethylene glycol-induced nephrolithiasis in rats. Microscopy Research and Technique, 87(7), 1494–1506.

Yuan, S., Ibrahim, I. A., & Ren, R. (2023). Anti-urolithiatic activity of daidzin in ethylene glycol-induced urolithiasis in rats. Applied Biochemistry and Biotechnology, 195(2), 905–918.

Azimi, A., Eidi, A., Mortazavi, P., & Haeri Rohani, A. (2021). Protective effect of apigenin on ethylene glycol-induced urolithiasis via attenuating oxidative stress and inflammatory parameters in adult male Wistar rats. Life Sciences, 279, 119641. https://doi.org/10.1016/j.lfs.2021.119641

Das, I., Gupta, S. K., Pandey, V. N., & Ansari, S. A. (2004). Inhibition and dissolution of CaOx crystals by Berberis vulgaris-Q and other metabolites. Journal of Crystal Growth, 267(3–4), 654–661.

Jyothilakshmi, V., Thellamudhu, G., Kumar, A., Khurana, A., Nayak, D., & Kalaiselvi, P. (2013). Preliminary investigation on ultra high diluted B. vulgaris in experimental urolithiasis. Homeopathy, 102(3), 172–178.

Jarald, E. E., Kushwah, P., Edwin, S., Asghar, S., & Patni, S. A. (2011). Effect of Unex on ethylene glycol-induced urolithiasis in rats. Indian Journal of Pharmacology, 43(4), 466.

Shukla, A. B., Mandavia, D. R., Barvaliya, M. J., Baxi, S. N., & Tripathi, C. R. (2014). Evaluation of anti-urolithiatic effect of aqueous extract of Bryophyllum pinnatum (Lam.) leaves using ethylene glycol-induced renal calculi. Avicenna Journal of Phytomedicine, 4(3), 151.

Telang, R. (2021). An in vitro study of Hydrangea arborescens, homoeopathic preparation as an inhibitor of calcium oxalate crystallisation. Indian Journal of Research in Homoeopathy, 15(1), 24–30.

Kumar, R., Sahu, S. G., Das, A. K., Upadhyay, D., & Saroj, A. K. (2025). A case report on the homeopathic management of renal calculi with Pareira brava 3CH. International Journal of Homoeopathic Sciences, 9(4), 905–908. https://doi.org/10.33545/26164485.2025.v9.i4.N.2016

Gupta, D., & Dubey, P. K. (2020). Effect of ethanolic extracts of Tribulus terrestris, Phyllanthus niruri and combination on CaOx urolithiasis in rats. International Journal of Pharmacy & Life Sciences, 11(2), 6491.

Published

2026-09-17

How to Cite

Evaluation of Safety and Efficacy of Welstone™️Drops in Experimentally-Induced Calcium Oxalate Urolithiasis in Rats. (2026). Advancements in Homeopathic Research, 11(3), 20-29. https://doi.org/10.48165/ahr.2026.11.3.2