Araştırma Makalesi
BibTex RIS Kaynak Göster
Yıl 2023, Cilt: 2 Sayı: 2, 53 - 58, 28.08.2023
https://doi.org/10.55971/EJLS.1320502

Öz

Proje Numarası

2005S039

Kaynakça

  • Scott LJJD. Selexipag: first global approval. Drugs. 2016;76:413-8. https://doi.org/10.1007/s40265-016-0549-4
  • Richter MJ, Gall H, Grimminger J, Grimminger F, Ghofrani H-A. Selexipag for the treatment of pulmonary arterial hypertension. Expert Opin Pharmacother. 2016;17(13):1825-34. https://doi.org/10.1080/14656566.2016.1215429
  • Xie S, Shi L, Chen J, Xu R-a, Ye X, Analysis B. Simultaneous quantification and pharmacokinetic investigation of selexipag and its main metabolite ACT-333679 in rat plasma by UPLC-MS/MS method. J Pharm Biomed Anal. 2020;190:113496. https://doi.org/10.1016/j.jpba.2020.113496
  • Gumustas M, Kurbanoglu S, Uslu B, Ozkan SA. UPLC versus HPLC on drug analysis: advantageous, applications and their validation parameters. J Chromatographia. 2013;76:1365-427. https://doi.org/10.1007/s10337-013-2477-8
  • Damireddy S, Pravalika K, Praveen M, Sathish G, Anusha M. Method development and validation of selexipag in its bulk and dosage form by rp-HPLC. J Int J Pharm Biol Sci. 2017;7:84. ISSN: 2230-7605
  • Youssef YM, Mahrouse MA, Mostafa E. Assessment of environmental impact of a novel stability-indicating RP-HPLC method and reported methods for the determination of selexipag in bulk and dosage form: A comparative study using different greenness assessment tools. Microchem J. 2023;185:108256. https://doi.org/10.1016/j.microc.2022.108256
  • Amara Babu NL, Koganti K, Palakeeti B, Srinivas KS, Rao KP. Development of an efficient stability-indicating LC–MS/MS method for the analysis of selexipag and characterization of its degradation products. Biomed. Chromatogr. 2021;35(10):e5178.
  • Bhadru B, Rao VV, Vidhyadhara S, Research. Development and validation of bioanalytical method for the quantitative estimation of selexipag in biological matrices using LC-MS/MS. J Pharm Sci. 2019;11(7):2722-7. ISSN:0975-1459
  • Gorumutchu GP, Ratnakaram NR. Oxidative coupling: A tranquil approach for determination of selexipag by visible spectrophotometry. Orient. J. Chem. 2018;34(6):3112. http://dx.doi.org/10.13005/ojc/340656
  • Ceylan B, Tırıs G, Tekkeli SEK, Önal C, Önal A. A novel HPLC method for selexipag in human plasma and application to a pharmacokinetic study. Research Square. 2022. https://doi.org/10.21203/rs.3.rs-1877128/v1
  • Prathyusha SM, Deepti CA, Naik RR, Technology. Development and validated of spectrophotometric methods for the determination of Selexipag (An anti-hypertensive agent). RJPT. 2020;13(3):1346-50. https://doi.org/10.5958/0974-360X.2020.00248.6

A new HPLC method for selexipag analysis in pharmaceutical formulation and bulk form

Yıl 2023, Cilt: 2 Sayı: 2, 53 - 58, 28.08.2023
https://doi.org/10.55971/EJLS.1320502

Öz

Selexipag is a new non-prostanoid prostacyclin receptor agonist used to treat pulmonary arterial hypertension. Selexipag is a long-acting IP receptor agonist with a shorter half-life than all other licensed drugs targeting the prostacyclin pathway, mostly administered intravenously or by subcutaneous infusion or inhalation. In this study, a new high performance liquid chromatography (HPLC) method was developed to analyze Selexipag in bulk and pharmaceutical formulations. The method used a column with Supelco Ascentis® Express (Sigma Aldrich, USA) model phenyl hexyl functional group (100×4.6 mm, ID, 2.7µm). Chromatographic separation was in isocratic elution mode, and the mobile phase mixture was acetonitrile containing 0.1% formic acid: water containing 0.1% formic acid (60:40, v/v) ratio. The method was linear in the concentration range of 15.7-117.6 µg/mL, and the LOD and LOQ were obtained as 2.4 and 3.1 µg/mL, respectively. Various method parameters have been tested according to the ICH Q2(R1) manual, and it is a method with high accuracy and precision. Therefore, the developed method is suitable for selexipag’s bulk and pharmaceutical formulation analysis.

Destekleyen Kurum

Anadolu University Scientific Research Projects Fund Commission

Proje Numarası

2005S039

Kaynakça

  • Scott LJJD. Selexipag: first global approval. Drugs. 2016;76:413-8. https://doi.org/10.1007/s40265-016-0549-4
  • Richter MJ, Gall H, Grimminger J, Grimminger F, Ghofrani H-A. Selexipag for the treatment of pulmonary arterial hypertension. Expert Opin Pharmacother. 2016;17(13):1825-34. https://doi.org/10.1080/14656566.2016.1215429
  • Xie S, Shi L, Chen J, Xu R-a, Ye X, Analysis B. Simultaneous quantification and pharmacokinetic investigation of selexipag and its main metabolite ACT-333679 in rat plasma by UPLC-MS/MS method. J Pharm Biomed Anal. 2020;190:113496. https://doi.org/10.1016/j.jpba.2020.113496
  • Gumustas M, Kurbanoglu S, Uslu B, Ozkan SA. UPLC versus HPLC on drug analysis: advantageous, applications and their validation parameters. J Chromatographia. 2013;76:1365-427. https://doi.org/10.1007/s10337-013-2477-8
  • Damireddy S, Pravalika K, Praveen M, Sathish G, Anusha M. Method development and validation of selexipag in its bulk and dosage form by rp-HPLC. J Int J Pharm Biol Sci. 2017;7:84. ISSN: 2230-7605
  • Youssef YM, Mahrouse MA, Mostafa E. Assessment of environmental impact of a novel stability-indicating RP-HPLC method and reported methods for the determination of selexipag in bulk and dosage form: A comparative study using different greenness assessment tools. Microchem J. 2023;185:108256. https://doi.org/10.1016/j.microc.2022.108256
  • Amara Babu NL, Koganti K, Palakeeti B, Srinivas KS, Rao KP. Development of an efficient stability-indicating LC–MS/MS method for the analysis of selexipag and characterization of its degradation products. Biomed. Chromatogr. 2021;35(10):e5178.
  • Bhadru B, Rao VV, Vidhyadhara S, Research. Development and validation of bioanalytical method for the quantitative estimation of selexipag in biological matrices using LC-MS/MS. J Pharm Sci. 2019;11(7):2722-7. ISSN:0975-1459
  • Gorumutchu GP, Ratnakaram NR. Oxidative coupling: A tranquil approach for determination of selexipag by visible spectrophotometry. Orient. J. Chem. 2018;34(6):3112. http://dx.doi.org/10.13005/ojc/340656
  • Ceylan B, Tırıs G, Tekkeli SEK, Önal C, Önal A. A novel HPLC method for selexipag in human plasma and application to a pharmacokinetic study. Research Square. 2022. https://doi.org/10.21203/rs.3.rs-1877128/v1
  • Prathyusha SM, Deepti CA, Naik RR, Technology. Development and validated of spectrophotometric methods for the determination of Selexipag (An anti-hypertensive agent). RJPT. 2020;13(3):1346-50. https://doi.org/10.5958/0974-360X.2020.00248.6
Toplam 11 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Eczacılık ve İlaç Bilimleri (Diğer)
Bölüm Research Articles
Yazarlar

Saniye Özcan 0000-0002-5492-0457

Egemen Güvenç Öğüt 0009-0007-6708-1166

Serkan Levent 0000-0003-3692-163X

Nafiz Öncü Can 0000-0003-0280-518X

Proje Numarası 2005S039
Yayımlanma Tarihi 28 Ağustos 2023
Gönderilme Tarihi 27 Haziran 2023
Yayımlandığı Sayı Yıl 2023 Cilt: 2 Sayı: 2

Kaynak Göster

Vancouver Özcan S, Öğüt EG, Levent S, Can NÖ. A new HPLC method for selexipag analysis in pharmaceutical formulation and bulk form. Eur J Life Sci. 2023;2(2):53-8.