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Sustainable Spectrophotometric Quantification of Lansoprazole Through Mixed Hydrotropy Approach

Received: 30 August 2024     Accepted: 18 September 2024     Published: 18 November 2024
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Abstract

Solubility is the property of a substance to dissolve in or form a homogeneous mixture with another substance. One of the most common problems associated with making a solution is poor solubility. There are many drugs that are sparingly soluble or insoluble in water, and lansoprazole is one of them. Aqueous solubility of lansoprazole is 0.05 mg/ml at room temperature. The current study aims to improve lansoprazole solubility using a mixed hydrotropy method. The purpose of the mixed hydrotropic solubilization approach is to increase the solubility of weakly water-soluble drugs in hydrotropic agent blends. To avoid the use of organic solvents, the mixed hydrotropy idea may be a good option. In this current research attempt, a novel method for spectrophotometric estimation of lansoprazole using a mixed solvent blend (containing 10% SC and 20% SB) as the solvent was developed. By observing the absorbances of the drug's standard solutions, the calibration curve for lansoprazole was drawn. The absorbances were measured at 275 nm compared to the corresponding reagent blanks. The percent label claims were found to be very near to 100, showing that the proposed approach is accurate. The suggested method estimates percent recoveries to be near 100 with significantly low percentage deviation and standard error values. As a result, the proposed process is simple, safe, and precise, and it does not require the use of harmful chemical solvents.

Published in Science Journal of Analytical Chemistry (Volume 12, Issue 3)
DOI 10.11648/j.sjac.20241203.11
Page(s) 33-37
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

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Keywords

Lansoprazole, Spectrophotometer, Hydrotropic Agents, Mixed Hydrotropy, Sodium Benzoate

References
[1] Vikas P, Santosh T, Santosh B, Rupali S, Lalit G. (2010). Spectrophotometric estimation of cefprozil by using Different hydrotropic agents. International Journal of Pharmacy and Pharmaceutical Sciences, 2(1): 82–87.
[2] Swathi CH, Subrahmanyam C, Kedarnath SA, Puvvadir SB. (2011). Solubilization of mefenamic acid. International Journal of Pharmacy and Technology, 3: 3267–3276.
[3] Kumar UMR, Nandan J, Jhalak P, Mittal MK, Chand. (2011). New spectrophotometric estimation of naproxen tablet formulation employing mixed solvency concept (at 331 nm). International Journal of Pharmacy and Technology, 3(4): 3618–3623.
[4] Kumar UMR, Navneet J, Jitendra P, Mittal P, Ravikant. (2012). New spectrophotometric analysis of gatifloxacin tablets utilizing mixed solvency concept (at 288 nm). Der Pharmacia Lettre, 4(1): 1–4.
[5] Ruchi J, Nilesh J, Kumar MR, Kumar JS. (2013). Quantitative estimation of levofloxacin and ornidazole by uv spectrophotometer. A mixed hydrotropy solubilization approach. International Journal of Pharmaceutical Sciences and Research, 4(1): 3073–3079.
[6] El-Houssieny BM, El-Dein EZ, Hm EM. (2014). Enhancement of solubility of dexibuprofen applying mixed hydrotropic solubilization technique. Drug discoveries & therapeutics, 31(4): 178–184.
[7] Kumar MR, Jawade S, A F. (2015). Formulation development of aqueous injection of poorly soluble drug using mixed hydrotropic solubilization concept and its evaluation. International Journal of Pharmaceutical Sciences and Drug Research, 7(1): 8–12.
[8] Jyotsana M, Kiran P, Kamal D. (2015). Solubility enhancement studies on lurasidone hydrochloride using mixed hydrotropy. International journal of pharmaceutical investigation, 5(2): 114–120.
[9] Rajesh M, Kumar S, Akash P, Lovkush P, Tiwari SP. (2016). Solid as solvent: novel spectrophotometric analytical technique for quantitative analysis of tinidazole tablets using solids (eutectic liquid of phenol and metformin hydrochloride) as solubilizing agents (mixed solvency concept). The Pharma Innovation Journal, 5(3): 1–02.
[10] Sanjay J, Kumar RMR, Kumar N, Indrajeet S. (2017). Development and validation of simple UV spectrophotometric method of quantization of Nifedipine in solid dosage formulation using mixed solvency concept. World Journal of Pharmaceutical Research, 6(13): 1014–1021.
[11] Jain R, Jain N, Jain DK, Patel VK, Rajak H, Jain SK. (2017). Novel UV spectrophotometer methods for quantitative estimation of metronidazole and furazolidone using mixed hydrotropy solubilization. Arabian Journal of Chemistry, 10(2): 151–156.
[12] Sanjay J, Kumar RMR, Kumar N, Indrajeet S. (2017). New Spectrophotometric Estimation of Frusemide in the Tablets using mixed solvency concept Approach. International Journal of Current Advanced Research, 6(12): 8510–8513.
[13] Poonam S, Komal R, Ashvini R, Giridhar R, Shital P, Wagh R, et al. (2017). Development and validation of mixed hydrotropic solubilization method for spectrophotometric determination of Ornidazole in bulk drug and tablet. Journal of Pharmacy Research, 11(11): 1114–1119.
[14] Kumar MR, Rashmi D. (2017). Solid as solvent”- Novel spectrophotometric analytical technique for quantitative estimation of tinidazole in tablets using solids (eutectic liquid of phenol and lignocaine hydrochloride) as solubilizing agents (mixed solvency concept). Journal of Drug Delivery and Therapeutics, 7(3): 127–130.
[15] Kumar MR, Prakhar G, Himanshi G. Formulation development of a model dry injection for reconstitution of poorly water soluble drug ornidazole using mixed solvency concept and its evaluation. International Journal of Science and Research. 2018; 7(4): 408–414.
[16] Asmat, Raza SN, Khan NA. (2019). Hydrotropy: Novel Solubility Enhancement Technique: A Review. International Journal of Scientific progress and research, 10(3): 1025–1036.
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    Soni, K., Sharma, K. (2024). Sustainable Spectrophotometric Quantification of Lansoprazole Through Mixed Hydrotropy Approach. Science Journal of Analytical Chemistry, 12(3), 33-37. https://doi.org/10.11648/j.sjac.20241203.11

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    ACS Style

    Soni, K.; Sharma, K. Sustainable Spectrophotometric Quantification of Lansoprazole Through Mixed Hydrotropy Approach. Sci. J. Anal. Chem. 2024, 12(3), 33-37. doi: 10.11648/j.sjac.20241203.11

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    AMA Style

    Soni K, Sharma K. Sustainable Spectrophotometric Quantification of Lansoprazole Through Mixed Hydrotropy Approach. Sci J Anal Chem. 2024;12(3):33-37. doi: 10.11648/j.sjac.20241203.11

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  • @article{10.11648/j.sjac.20241203.11 ,
      author = {Ketan Soni and Kavita Sharma},
      title = {Sustainable Spectrophotometric Quantification of Lansoprazole Through Mixed Hydrotropy Approach
    },
      journal = {Science Journal of Analytical Chemistry},
      volume = {12},
      number = {3},
      pages = {33-37},
      doi = {10.11648/j.sjac.20241203.11 },
      url = {https://doi.org/10.11648/j.sjac.20241203.11 },
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.sjac.20241203.11 },
      abstract = {Solubility is the property of a substance to dissolve in or form a homogeneous mixture with another substance. One of the most common problems associated with making a solution is poor solubility. There are many drugs that are sparingly soluble or insoluble in water, and lansoprazole is one of them. Aqueous solubility of lansoprazole is 0.05 mg/ml at room temperature. The current study aims to improve lansoprazole solubility using a mixed hydrotropy method. The purpose of the mixed hydrotropic solubilization approach is to increase the solubility of weakly water-soluble drugs in hydrotropic agent blends. To avoid the use of organic solvents, the mixed hydrotropy idea may be a good option. In this current research attempt, a novel method for spectrophotometric estimation of lansoprazole using a mixed solvent blend (containing 10% SC and 20% SB) as the solvent was developed. By observing the absorbances of the drug's standard solutions, the calibration curve for lansoprazole was drawn. The absorbances were measured at 275 nm compared to the corresponding reagent blanks. The percent label claims were found to be very near to 100, showing that the proposed approach is accurate. The suggested method estimates percent recoveries to be near 100 with significantly low percentage deviation and standard error values. As a result, the proposed process is simple, safe, and precise, and it does not require the use of harmful chemical solvents.
    },
     year = {2024}
    }
    

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  • TY  - JOUR
    T1  - Sustainable Spectrophotometric Quantification of Lansoprazole Through Mixed Hydrotropy Approach
    
    AU  - Ketan Soni
    AU  - Kavita Sharma
    Y1  - 2024/11/18
    PY  - 2024
    N1  - https://doi.org/10.11648/j.sjac.20241203.11 
    DO  - 10.11648/j.sjac.20241203.11 
    T2  - Science Journal of Analytical Chemistry
    JF  - Science Journal of Analytical Chemistry
    JO  - Science Journal of Analytical Chemistry
    SP  - 33
    EP  - 37
    PB  - Science Publishing Group
    SN  - 2376-8053
    UR  - https://doi.org/10.11648/j.sjac.20241203.11 
    AB  - Solubility is the property of a substance to dissolve in or form a homogeneous mixture with another substance. One of the most common problems associated with making a solution is poor solubility. There are many drugs that are sparingly soluble or insoluble in water, and lansoprazole is one of them. Aqueous solubility of lansoprazole is 0.05 mg/ml at room temperature. The current study aims to improve lansoprazole solubility using a mixed hydrotropy method. The purpose of the mixed hydrotropic solubilization approach is to increase the solubility of weakly water-soluble drugs in hydrotropic agent blends. To avoid the use of organic solvents, the mixed hydrotropy idea may be a good option. In this current research attempt, a novel method for spectrophotometric estimation of lansoprazole using a mixed solvent blend (containing 10% SC and 20% SB) as the solvent was developed. By observing the absorbances of the drug's standard solutions, the calibration curve for lansoprazole was drawn. The absorbances were measured at 275 nm compared to the corresponding reagent blanks. The percent label claims were found to be very near to 100, showing that the proposed approach is accurate. The suggested method estimates percent recoveries to be near 100 with significantly low percentage deviation and standard error values. As a result, the proposed process is simple, safe, and precise, and it does not require the use of harmful chemical solvents.
    
    VL  - 12
    IS  - 3
    ER  - 

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