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RP-HPLC method development, validation and pharmacokinetic applicability in preclinical evaluation of rhein treated with novel diacerein eutectics.
Patel, Rajeshri D; Raval, Mihir K; Pethani, Trupesh M; Waghela, Bhargav N; Shukla, Riddhi H; Buch, Prakruti R; Vadalia, Jigna M; Sharma, Tejas P; Airao, Vishal A.
Afiliação
  • Patel RD; School of Pharmaceutical Sciences, Atmiya University, Rajkot, Gujarat, India.
  • Raval MK; Department of Pharmaceutical Sciences, Sardar Patel University, Vallabh Vidyanagar, Gujarat, India.
  • Pethani TM; Department of Pharmaceutical Sciences, Saurashtra University, Rajkot, Gujarat, India.
  • Waghela BN; Department of Microbiology, Atmiya University, Rajkot, Gujarat, India.
  • Shukla RH; School of Pharmaceutical Sciences, Atmiya University, Rajkot, Gujarat, India.
  • Buch PR; Department of Pharmaceutical Sciences, Saurashtra University, Rajkot, Gujarat, India.
  • Vadalia JM; Graduate School of Pharmacy, Gujarat Technological University, Gandhinagar, Gujarat, India.
  • Sharma TP; Department of Pharmaceutical Sciences, Saurashtra University, Rajkot, Gujarat, India.
  • Airao VA; Department of Pharmaceutical Sciences, Saurashtra University, Rajkot, Gujarat, India.
Biomed Chromatogr ; 36(11): e5465, 2022 Nov.
Article em En | MEDLINE | ID: mdl-35904137
ABSTRACT
The current study represents a bioanalytical method for the estimation of rhein (Rh, an active metabolite of diacerein, DIA) in rats treated with novel DIA eutectics to investigate the pharmacokinetics of DIA. A simple protein precipitation technique was used to extract Rh and the internal standard (IS), p-aminobenzoic acid, injected into a Phenomenex Gemini C18 column. The separation was achieved by a gradient elution comprising ammonium acetate (10 mm; pH 3.0) and acetonitrile in an 18 min run time at a flow rate of 0.8 ml/min with retention times of 11.8 min (Rh) and 5.9 min (IS). The results revealed that the proposed method is linear over a range of 200-20,000 ng/ml (r2 > 0.9988) of Rh and is precise and accurate. The method was fully validated as per the US Food and Drug Administration guidelines and a pharmacokinetic study in rats was performed for Rh following oral administration of the pure DIA and newly developed eutectics. Therefore, the present method could be used to estimate DIA to illustrate a comparative pharmacokinetic analysis. This can also be applied to its related multicomponent formulations for future studies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácido 4-Aminobenzoico Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácido 4-Aminobenzoico Idioma: En Ano de publicação: 2022 Tipo de documento: Article