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Estimation of purity of antimicrobial lead compound sulfonamide-anthranilate derivative methyl-ester-toluene-sulfonamide using LC to develop a new drug application.
Deshpande, Girish K; Akshinthala, Parameswari; Katari, Naresh Kumar; Deshmukh, Balasaheb; Kowtharapu, Leela Prasad; Battula, Sreenivas Rao; Gundla, Rambabu.
Afiliação
  • Deshpande GK; Department of Chemistry, GITAM School of Science, GITAM Deemed to Be University, Visakhapatnam, Andhra Pradesh, India.
  • Akshinthala P; Department of Science and Humanities, MLR Institute of Technology, Hyderabad, India.
  • Katari NK; Department of Chemistry, GITAM School of Science, GITAM Deemed to Be University, Hyderabad, Telangana, India.
  • Deshmukh B; Department of Chemistry, GITAM School of Science, GITAM Deemed to Be University, Visakhapatnam, Andhra Pradesh, India.
  • Kowtharapu LP; Department of Chemistry, GITAM School of Science, GITAM Deemed to Be University, Hyderabad, Telangana, India.
  • Battula SR; Department of Chemistry, GITAM School of Science, GITAM Deemed to Be University, Visakhapatnam, Andhra Pradesh, India.
  • Gundla R; Department of Chemistry, GITAM School of Science, GITAM Deemed to Be University, Hyderabad, Telangana, India.
Biomed Chromatogr ; 37(8): e5646, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37070159
ABSTRACT
The newly synthesized lead molecule methyl-ester-toluene-sulfonamide is the combined derivative of sulfonamide-anthranilate. It was estimated by gradient elution using 0.1% triethylamine in water with pH 2.0 as mobile phase A and the mixture of acetonitrile and tetrahydrofuran in the ratio of 97525 (v/v) as mobile phase B at a flow rate of 0.8 ml/min and 210 nm wavelength on an Agilent 1260 infinity series HPLC system equipped with a diode array detector. The column used was ACE 3 C18-PFP (250 × 4.6 mm, 3 µm i.d.) operating at 40°C. The gradient program was time (min)/% B 0.0/50, 3.0/50, 15.0/70, 25.0/90, 30.0/90, 31/50, and 38/50. The method is simple, accurate, rapid, and selective. The method was linear with a concentration range of 1.6-240 µg/ml. The accuracy data obtained were 98.5-100.5%. The method validation data and quality by design-based robustness study results indicate that the developed method is robust and fit for routine use in the quality control laboratory. Therefore, the ready availability of the method can be useful in pharmaceutical new drug development.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anti-Infecciosos Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anti-Infecciosos Idioma: En Ano de publicação: 2023 Tipo de documento: Article