Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Validated HPTLC Method for Determination of Repaglinide in Bulk and Tablet Dosage Form


Affiliations
1 Department of Pharmaceutical Chemistry, J. L. Chaturvedi College of Pharmacy, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur-440016, Maharashtra, India
2 University Department of Pharmaceutical Sciences, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur- 440033, Maharashtra, India
3 Department of Pharmaceutical Chemistry, Sharad Pawar College of Pharmacy, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur-441110, Maharashtra, India
     

   Subscribe/Renew Journal


A simple, rapid, accurate and precise high performance thin layer chromatographic (HPTLC) method has been developed and validated for the estimation of the repaglinide as bulk and in tablet dosage form. The method employed TLC precoated silica gel 60 F254 aluminium plates as the stationary phase. The solvent system consisted of methanol: chloroform: toluene: triethylamine (5:3:2:0.1 v/v/v/v). The detection of spots was carried out densitometrically using a UV detector at 241 nm in absorbance mode. This system was found to give compact spot for repaglinide with (Rf value of 0.45 ± 0.08). The method was validated in terms of linearity, accuracy, precision, limit of detection, limit of quantification and specificity as per ICH guidelines. The calibration curve was found to be linear over the concentration range of 100-500 ng/spot for repaglinide with significantly high value of correlation coefficient (r2 > 0.99). The limits of detection and quantitation were found to be 20 ng/spot and 90 ng/spot, respectively for repaglinide. The % assay was found to be 99.14 ± 0.34(SD). Accuracy of the method was accessed by percentage recovery and mean % value was found to be 99.51±0.74. The proposed method was found to be accurate, precise, reproducible and specific and can be successfully applicable for the quality control analysis of repaglinide as in bulk drug and pharmaceutical formulations.

Keywords

Repaglinide, High-performance thin layer chromatography (HPTLC), Method Validation
Subscription Login to verify subscription
User
Notifications
Font Size


  • Rang HP, Dale MM, Ritter JM, Moore PK. Pharmacology. Edinburgh:Churchill Livingstone. 2003; 5th ed: pp. 310.
  • Budavari S. The Merck Index, In: An Encyclopedia of Chemicals, Drugs and Biologicals. Whitehouse Station, NJ: Merck and Co Inc. 2001; 13th ed: pp. 790.
  • Reynolds JEF. Martindale, The Complete Drug Reference. Pharmaceutical Press, London. 2002; 33rd ed: p. 334.
  • Goyal A, Singhvi I. Visible spectrophotometric methods for estimation of repaglinide in tablet formulation. Indian Journal Pharmaceutical Sciences. 5(3); 2006: 79-80.
  • Sharma S, Sharma MC. Simultaneous determination of repaglinide in pharmaceutical dosage form using indigo carmine. American-Eurasian Journal of Scientific Research. 6(1); 2011: 47-51.
  • Patel JR, Suhagia BN, Patel BH. Simultaneous specrophotometric estimation of metformin and Repaglinide in a synthetic mixture. Indian Journal Pharmaceutical Sciences. 69(6); 2007: 844-846.
  • Kaushal N, Jain S, Tiwary AK. Development of spectrofluorimetric and HPLC methods for In vitro analysis of repaglinide. Indian Journal Pharmaceutical Sciences. 72; 2010: 240-244.
  • Khalidi B, Shtaiwi M, Khatib H, Mohammad M, Bustanji Y. A Comparative Study of First-Derivative Spectrophotometry and Column High-Performance Liquid Chromatography Applied to the Determination of Repaglinide in Tablets and for Dissolution Testing. Journal of AOAC International. 91(3); 2008: 530-535.
  • Gandhimathi M, Renu TK. Determination of repaglinide in pharmaceutical formulation by HPLC with UV detection. Analytical Sciences. 19(12); 2003: 1675-1677.
  • Prameela RA, Bala SC, Archana N, Siva TP, Aruna B. Determination of repaglinide in pharmaceutical formulation by HPLC. Journal of Applied Sciences Research. 5(10); 2009: 1500-1504.
  • Sharma MC, Sharma S. Stability Indicating RP-HPLC Method for Determination and Validation of Repaglinide in Pharmaceutical Dosage Form. International Journal of ChemTech Research. 3(1); 2011: 210-216.
  • Ruzilawati AB, Wahab MSA, Imran A, Ismail Z, Gana SH. Method development and validation of repaglinide in human plasma by HPLC and its application in pharmacokinetic studies. Journal of Pharmaceutical and Biomedical Analysis. 43; 2007: 1831-1835.
  • International Conference on Harmonization Q2B, Validation of Analytical Procedures: Methodology, Geneva, 1996.
  • The United States Pharmacopoeia 24 and National Formulary 19, Asian edition. Rockville (MD): United States Pharmacopoeia convection, 2000: pp. 2149-52.

Abstract Views: 321

PDF Views: 2




  • Validated HPTLC Method for Determination of Repaglinide in Bulk and Tablet Dosage Form

Abstract Views: 321  |  PDF Views: 2

Authors

Seema M. Dhole
Department of Pharmaceutical Chemistry, J. L. Chaturvedi College of Pharmacy, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur-440016, Maharashtra, India
Pramod B. Khedekar
University Department of Pharmaceutical Sciences, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur- 440033, Maharashtra, India
Nikhil D. Amnerkar
Department of Pharmaceutical Chemistry, Sharad Pawar College of Pharmacy, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur-441110, Maharashtra, India

Abstract


A simple, rapid, accurate and precise high performance thin layer chromatographic (HPTLC) method has been developed and validated for the estimation of the repaglinide as bulk and in tablet dosage form. The method employed TLC precoated silica gel 60 F254 aluminium plates as the stationary phase. The solvent system consisted of methanol: chloroform: toluene: triethylamine (5:3:2:0.1 v/v/v/v). The detection of spots was carried out densitometrically using a UV detector at 241 nm in absorbance mode. This system was found to give compact spot for repaglinide with (Rf value of 0.45 ± 0.08). The method was validated in terms of linearity, accuracy, precision, limit of detection, limit of quantification and specificity as per ICH guidelines. The calibration curve was found to be linear over the concentration range of 100-500 ng/spot for repaglinide with significantly high value of correlation coefficient (r2 > 0.99). The limits of detection and quantitation were found to be 20 ng/spot and 90 ng/spot, respectively for repaglinide. The % assay was found to be 99.14 ± 0.34(SD). Accuracy of the method was accessed by percentage recovery and mean % value was found to be 99.51±0.74. The proposed method was found to be accurate, precise, reproducible and specific and can be successfully applicable for the quality control analysis of repaglinide as in bulk drug and pharmaceutical formulations.

Keywords


Repaglinide, High-performance thin layer chromatography (HPTLC), Method Validation

References