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Application of stability-indicating HPTLC method for quantitative determination of metadoxine in pharmaceutical dosage form.
Farmaco. 2005 Apr; 60(4):351-60.F

Abstract

A sensitive, selective, precise and stability-indicating high-performance thin-layer chromatographic method for analysis of metadoxine both as a bulk drug and in formulations was developed and validated. The method employed TLC aluminium plates precoated with silica gel 60F-254 as the stationary phase. The solvent system consisted of acetone-chloroform-methanol-ammonia (7.0:4.0:3.0:1.2, v/v/v/v). Densitometric analysis of metadoxine was carried out in the absorbance mode at 315 nm. This system was found to give compact spots for metadoxine (Rf value of 0.45+/-0.02, for six replicates). Metadoxine was subjected to acid, alkali and neutral hydrolysis, oxidation, dry and wet heat treatment and photo and UV degradation. The drug undergoes degradation under all stress conditions. Also, the degraded products were well resolved from the pure drug with significantly different Rf values. The method was validated for linearity, precision, robustness, LOD, LOQ, specificity and accuracy. Linearity was found to be in the range of 100-1500 ng/spot with significantly high value of correlation coefficient r2=0.9997+/-1.02. The linear regression analysis data for the calibration plots showed good linear relationship with r2=0.9999+/-0.58 in the working concentration range of 200-700 ng/spot. The mean value of slope and intercept were 0.11+/-0.04 and 18.73+/-1.89, respectively. The limits of detection and quantitation were 50 and 100 ng/spot, respectively. Statistical analysis proves that the method is repeatable and specific for the estimation of the said drug. As the method could effectively separate the drug from its degradation products, it can be employed as a stability-indicating one. Moreover, the proposed HPTLC method was utilized to investigate the kinetics of acid and base degradation process. Arrhenius plot was constructed and activation energy was calculated respectively for acid and base degradation process.

Authors+Show Affiliations

Department of Quality Assurance Techniques, Bharati Vidyapeeth Deemed University, Poona College of Pharmacy, Erandwane, Pune 411038, Maharashtra State, India.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Validation Study

Language

eng

PubMed ID

15848212

Citation

Kaul, Neeraj, et al. "Application of Stability-indicating HPTLC Method for Quantitative Determination of Metadoxine in Pharmaceutical Dosage Form." Farmaco (Societa Chimica Italiana : 1989), vol. 60, no. 4, 2005, pp. 351-60.
Kaul N, Agrawal H, Patil B, et al. Application of stability-indicating HPTLC method for quantitative determination of metadoxine in pharmaceutical dosage form. Farmaco. 2005;60(4):351-60.
Kaul, N., Agrawal, H., Patil, B., Kakad, A., & Dhaneshwar, S. R. (2005). Application of stability-indicating HPTLC method for quantitative determination of metadoxine in pharmaceutical dosage form. Farmaco (Societa Chimica Italiana : 1989), 60(4), 351-60.
Kaul N, et al. Application of Stability-indicating HPTLC Method for Quantitative Determination of Metadoxine in Pharmaceutical Dosage Form. Farmaco. 2005;60(4):351-60. PubMed PMID: 15848212.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Application of stability-indicating HPTLC method for quantitative determination of metadoxine in pharmaceutical dosage form. AU - Kaul,Neeraj, AU - Agrawal,Himani, AU - Patil,Bharat, AU - Kakad,Abhijit, AU - Dhaneshwar,S R, PY - 2003/07/27/received PY - 2005/01/03/revised PY - 2005/01/03/accepted PY - 2005/4/26/pubmed PY - 2005/9/13/medline PY - 2005/4/26/entrez SP - 351 EP - 60 JF - Farmaco (Societa chimica italiana : 1989) JO - Farmaco VL - 60 IS - 4 N2 - A sensitive, selective, precise and stability-indicating high-performance thin-layer chromatographic method for analysis of metadoxine both as a bulk drug and in formulations was developed and validated. The method employed TLC aluminium plates precoated with silica gel 60F-254 as the stationary phase. The solvent system consisted of acetone-chloroform-methanol-ammonia (7.0:4.0:3.0:1.2, v/v/v/v). Densitometric analysis of metadoxine was carried out in the absorbance mode at 315 nm. This system was found to give compact spots for metadoxine (Rf value of 0.45+/-0.02, for six replicates). Metadoxine was subjected to acid, alkali and neutral hydrolysis, oxidation, dry and wet heat treatment and photo and UV degradation. The drug undergoes degradation under all stress conditions. Also, the degraded products were well resolved from the pure drug with significantly different Rf values. The method was validated for linearity, precision, robustness, LOD, LOQ, specificity and accuracy. Linearity was found to be in the range of 100-1500 ng/spot with significantly high value of correlation coefficient r2=0.9997+/-1.02. The linear regression analysis data for the calibration plots showed good linear relationship with r2=0.9999+/-0.58 in the working concentration range of 200-700 ng/spot. The mean value of slope and intercept were 0.11+/-0.04 and 18.73+/-1.89, respectively. The limits of detection and quantitation were 50 and 100 ng/spot, respectively. Statistical analysis proves that the method is repeatable and specific for the estimation of the said drug. As the method could effectively separate the drug from its degradation products, it can be employed as a stability-indicating one. Moreover, the proposed HPTLC method was utilized to investigate the kinetics of acid and base degradation process. Arrhenius plot was constructed and activation energy was calculated respectively for acid and base degradation process. SN - 0014-827X UR - https://www.unboundmedicine.com/medline/citation/15848212/Application_of_stability_indicating_HPTLC_method_for_quantitative_determination_of_metadoxine_in_pharmaceutical_dosage_form_ DB - PRIME DP - Unbound Medicine ER -