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Phase solubility studies of poorly soluble drug molecules by using O -phosphorylated calixarenes as drug-solubilizing agents

Journal of Chemical and Engineering Data · Ocak 2012

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YÖKSİS Kayıtları
Phase Solubility Studies of Poorly Soluble Drug Molecules by Using Phosphorylated Calixarenes as Drug Solubilizing Agents
Journal of Chemical & Engineering Data · 2012 SCI-Expanded 10 atıf
Prof. Dr. ŞEREF ERTUL →
YÖKSİS ISSN Eşleşmesi

Bu dergide (ISSN eşleşmesi) kurumun 5 kaydı bulundu.

YÖKSİS Kayıtları — ISSN Eşleşmesi
Phase Solubility Studies of Poorly Soluble Drug Molecules by Using Phosphorylated Calixarenes as Drug Solubilizing Agents
2012 ISSN: 0021-9568 SCI-Expanded 10 atıf
Prof. Dr. ŞEREF ERTUL →
Transportation of Poorly Soluble Drug Molecules from the Organic Phase to the Aqueous Phase by Using Phosphorylated Calixarenes
2011 ISSN: 0021-9568 SCI-Expanded 12 atıf
Prof. Dr. ŞEREF ERTUL →
Magnetizing Calixarene: Azo Dye Removal from Aqueous Media by Fe3O4 Nanoparticles Fabricated with Carboxylic-Substituted Calix[4]arene
2018 ISSN: 0021-9568 SCI
Prof. Dr. MUSTAFA YILMAZ →
Thermodynamic and Kinetic Studies for Adsorption of Reactive Blue (RB-19) Dye Using Calix[4]arene-Based Adsorbent
2019 ISSN: 0021-9568 SCI-Expanded
Dr. Öğr. Üyesi FATİH DURMAZ →
Magnetizing Calixarene: Azo Dye Removal from Aqueous Media by Fe sub3/sub O sub4/sub Nanoparticles Fabricated with Carboxylic-Substituted Calix[4]arene/title
2017 ISSN: 0021-9568 SCI-Expanded Q3
Doç. Dr. MEHMET OĞUZ →

Makale Bilgileri

ISSN00219568
Yayın TarihiOcak 2012
Cilt / Sayfa57 · 233-239
Özet This study is the first report on the solubilizing effect of O-phosphorylated calix[n]arenes that form complexes with neutral molecules such as nifedipine, niclosamide, and furosemide by host-guest complexation. These complexation studies were carried out by using the phase solubility technique. From the obtained results, it was observed that the solubility of guest molecules such as nifedipine, niclosamide, and furosemide was significantly increased in the presence of host molecules tetrakis-O-(diethoxyphosphoryl)-p- tert-butylcalix[4]arene (1), tetrakis-O-(diethoxyphosphoryl)-calix[4]arene (2), bis-O-(diethoxyphosphoryl)-p-tert-butylcalix[4]arene (3), bis-O- (diethoxyphosphoryl)-calix[4]arene (4), and octakis-O-(diethoxyphosphoryl)-p- tert-butylcalix[8]arene (5). The increase in solubility of drugs by the calixarene host 1 to 5 was most probably due to inclusion complexation between drug molecules and cavities of the calixarene skeleton similar to drug-cyclodextrin complexes. © 2011 American Chemical Society.

Yazarlar (3)

1
Mevlüt Bayrakc
2
Seref Ertul
3
Mustafa Yilmaz

Kurumlar

Selçuk Üniversitesi
Selçuklu Turkey
University of Nigǧde
Konya Turkey
Scimago Dergi (ISSN Eşleşmesi)
Journal of Chemical and Engineering Data
Q2
SJR Skoru0,449
H-Index162
YayıncıAmerican Chemical Society
ÜlkeUnited States
Chemical Engineering (miscellaneous) (Q2)
Chemistry (miscellaneous) (Q2)
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