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Analytical developments of p-hydroxy prenylamine reference material for dope control research: Characterization and purity assessment.
Joseph, Athira; Kumar, Gangasani Jagadeesh; Pawar, Sachin Dattram; Hirlekar, Bhakti Umesh; Bharatam, Prasad V; Konda, Satyanand; Mudiam, Mohana Krishna Reddy; Murty, Upadhyayula Suryanarayana; Sahu, P L; Dubey, Sachin; Radhakrishnanand, P; Adye, Daya Raju; Borkar, Roshan M; Thirupathi, Choppari; Kumar, Pramod.
Afiliação
  • Joseph A; Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research (NIPER), SilaKatamur (Halugurisuk), P.O.: Changsari, Dist: Kamrup, Guwahati, Assam, 781101, India.
  • Kumar GJ; Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research (NIPER), SilaKatamur (Halugurisuk), P.O.: Changsari, Dist: Kamrup, Guwahati, Assam, 781101, India.
  • Pawar SD; Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), SilaKatamur (Halugurisuk), P.O.: Changsari, Dist: Kamrup, Guwahati, Assam, 781101, India.
  • Hirlekar BU; Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research (NIPER), SilaKatamur (Halugurisuk), P.O.: Changsari, Dist: Kamrup, Guwahati, Assam, 781101, India.
  • Bharatam PV; Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), SilaKatamur (Halugurisuk), P.O.: Changsari, Dist: Kamrup, Guwahati, Assam, 781101, India.
  • Konda S; Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), Sector 67, S.A.S. Nagar, Mohali, Punjab, 160062, India.
  • Mudiam MKR; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
  • Murty US; Analytical & Structural Chemistry Department, CSIR-Indian Institute of Chemical Technology, Uppal Road, Tarnaka, Hyderabad, Telangana, 500007, India.
  • Sahu PL; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
  • Dubey S; Analytical & Structural Chemistry Department, CSIR-Indian Institute of Chemical Technology, Uppal Road, Tarnaka, Hyderabad, Telangana, 500007, India.
  • Radhakrishnanand P; Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research (NIPER), SilaKatamur (Halugurisuk), P.O.: Changsari, Dist: Kamrup, Guwahati, Assam, 781101, India.
  • Adye DR; National Dope Testing Laboratory, J.L.N Stadium Complex, East Gate No. 10, Near MTNL Building, New Delhi, 110003, India.
  • Borkar RM; National Dope Testing Laboratory, J.L.N Stadium Complex, East Gate No. 10, Near MTNL Building, New Delhi, 110003, India.
  • Thirupathi C; Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research (NIPER), SilaKatamur (Halugurisuk), P.O.: Changsari, Dist: Kamrup, Guwahati, Assam, 781101, India.
  • Kumar P; Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research (NIPER), SilaKatamur (Halugurisuk), P.O.: Changsari, Dist: Kamrup, Guwahati, Assam, 781101, India.
Drug Test Anal ; 14(2): 224-232, 2022 Feb.
Article em En | MEDLINE | ID: mdl-34617411
ABSTRACT
Prenylamine was initially used for the treatment of angina pectoris and later on withdrawn from the market in 1988 due to cardiac arrhythmias concern. The major phase I metabolite of prenylamine is p-hydroxy prenylamine that has a chiral center in the structure. Even though p-hydroxy prenylamine was synthesized earlier, it lacked complete analytical developments for chiral high-performance liquid chromatography (HPLC) separation. However, p-hydroxy prenylamine reference material is not commercially available. The innovation of this manuscript is the development and validation of a chiral HPLC separation method and more extensive characterization of the reference material than previously reported method. Therefore, it was hypothesized to develop and validate normal phase HPLC method for p-hydroxy prenylamine reference material. p-Hydroxy prenylamine was synthesized in two batches and characterized successfully using 13 C NMR, 1 H NMR, high-resolution mass spectrometry (HRMS), Fourier transform infrared spectroscopy (FT-IR), and thermogravimetric analysis (TGA). A normal phase chiral HPLC method was developed to analyze the p-hydroxy prenylamine purity. Separation of the p-hydroxy prenylamine enantiomers were achieved using ultra-high-performance liquid chromatography (UHPLC) on a ChiralCel ODH column at wavelength of 220 nm. The developed method was validated in terms of its linearity, accuracy, precision, and robustness for purification, purity assessment, and stability studies. Proton and carbon peaks were confirmed by nuclear magnetic resonance (NMR) analysis. Functional groups were confirmed by FT-IR. Loss on drying was 0.3% and 0.6% for Batches 1 and 2, respectively. The purity of the developed reference material for Batches 1 and 2 was found to be 99.59% and 100%, respectively. Therefore, the synthesized batches of p-hydroxy prenylamine can be used in dope testing as reference material.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prenilamina Idioma: En Revista: Drug Test Anal Assunto da revista: FARMACOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prenilamina Idioma: En Revista: Drug Test Anal Assunto da revista: FARMACOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Índia