Square wave voltammetric determination of valproic acid in pharmaceuticalPreparations

The electrochemical behavior of valproic acid (VAL) was investigated using square wave voltammetry, cyclicvoltammetry, and sampled direct current polarography and a new square wave voltammetric method was developed fordetermination of VAL in pharmaceutical preparations. VAL showed two reduction peaks at about {0.2 V and {0.8 V vs.Ag/AgCl 3 M KCl with a hanging mercury drop electrode in 0.05 M pH 3.3 Britton{Robinson (BR) buffer. These peakswere named peak I and peak II, respectively. The types of limiting current of both peaks were determined as diffusioncontrolled based on cyclic voltammetry studies. A linear calibration graph was obtained in the range 1.46104{1.0103M. The limit of detection (LOD) and limit of quanti cation (LOQ) were 1.09104M (21.05g/mL) and1.10104M (144.20g/mL), respectively. Recovery studies for the accuracy of the method were performed byadding known amounts of VAL and it was found to be 109.674.85%. The proposed method was successfully appliedto pharmaceutical products on the market.

Yazar Acar, Ebru Türköz
Onar, Atiye Nur
Yayın Türü Article
Tek Biçim Adres https://hdl.handle.net/20.500.11831/5357
Konu Başlıkları Mühendislik
Kimya
Koleksiyonlar Araştırma Çıktıları | Ön Baskı | WoS | Scopus | TR-Dizin | PubMed
04- TR-Dizin İndeksli Yayınlar Koleksiyonu
Dergi Adı Turkish Journal of Chemistry
Cild 40
Dergi Sayısı 1
Sayfalar 106 - 116
Yayın Tarihi 2016
Eser Adı
[dc.title]
Square wave voltammetric determination of valproic acid in pharmaceuticalPreparations
Yazar
[dc.contributor.author]
Acar, Ebru Türköz
Yazar
[dc.contributor.author]
Onar, Atiye Nur
Yayın Türü
[dc.type]
article
Özet
[dc.description.abstract]
The electrochemical behavior of valproic acid (VAL) was investigated using square wave voltammetry, cyclicvoltammetry, and sampled direct current polarography and a new square wave voltammetric method was developed fordetermination of VAL in pharmaceutical preparations. VAL showed two reduction peaks at about {0.2 V and {0.8 V vs.Ag/AgCl 3 M KCl with a hanging mercury drop electrode in 0.05 M pH 3.3 Britton{Robinson (BR) buffer. These peakswere named peak I and peak II, respectively. The types of limiting current of both peaks were determined as diffusioncontrolled based on cyclic voltammetry studies. A linear calibration graph was obtained in the range 1.46104{1.0103M. The limit of detection (LOD) and limit of quanti cation (LOQ) were 1.09104M (21.05g/mL) and1.10104M (144.20g/mL), respectively. Recovery studies for the accuracy of the method were performed byadding known amounts of VAL and it was found to be 109.674.85%. The proposed method was successfully appliedto pharmaceutical products on the market.
Kayıt Giriş Tarihi
[dc.date.accessioned]
2020-03-18
Yayın Tarihi
[dc.date.issued]
2016
Açık Erişim Tarihi
[dc.date.available]
2020-03-18
Dil
[dc.language.iso]
eng
Konu Başlıkları
[dc.subject]
Mühendislik
Konu Başlıkları
[dc.subject]
Kimya
Haklar
[dc.rights]
info:eu-repo/semantics/openAccess
ISSN
[dc.identifier.issn]
1300-0527
ISSN
[dc.identifier.issn]
1303-6130
Yayının ilk sayfa sayısı
[dc.identifier.startpage]
106
Yayının son sayfa sayısı
[dc.identifier.endpage]
116
Dergi Adı
[dc.relation.journal]
Turkish Journal of Chemistry
Dergi Sayısı
[dc.identifier.issue]
1
Cild
[dc.identifier.volume]
40
Tek Biçim Adres
[dc.identifier.uri]
http://www.trdizin.gov.tr/publication/paper/detail/TWpVMk1EVTBOQT09
Tek Biçim Adres
[dc.identifier.uri]
https://hdl.handle.net/20.500.11831/5357
Görüntülenme Sayısı ( Şehir )
Görüntülenme Sayısı ( Ülke )
Görüntülenme Sayısı ( Zaman Dağılımı )
Görüntülenme
7
20.03.2023 tarihinden bu yana
İndirme
1
20.03.2023 tarihinden bu yana
Son Erişim Tarihi
29 Eylül 2023 03:16
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Tıklayınız
method respectively studies pharmaceutical voltammetry current square proposed detection 46104{1 obtained quanti successfully calibration linear appliedto products cyclic market 09104M cation amounts byadding performed accuracy 20g/mL) 10104M 05g/mL) Recovery diffusioncontrolled reduction showed preparations fordetermination developed
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