کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
599009 1454259 2016 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Studies on the interaction between promethazine and human serum albumin in the presence of flavonoids by spectroscopic and molecular modeling techniques
ترجمه فارسی عنوان
مطالعات بر روی تعامل پرومتازین و آلبومین سرم انسان در حضور فلاونوئیدها با تکنیک های مدل سازی اسپکتروسکوپی و مولکولی
کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی شیمی کلوئیدی و سطحی
چکیده انگلیسی


• The binding characterizations of PMT binding to HSA were investigated.
• The influences of flavonoids on HSA–PMT interaction were investigated.
• The fluorescence, absorption, CD spectra and molecular modeling were used.
• This work may be helpful to illustrate food-drugs interactions.

Fluorescence, absorption, time-correlated single photon counting (TCSPC), and circular dichroism (CD) spectroscopic techniques as well as molecular modeling methods were used to study the binding characterization of promethazine (PMT) to human serum albumin (HSA) and the influence of flavonoids, rutin and baicalin, on their affinity. The results indicated that the fluorescence quenching mechanism of HSA by PMT is a static quenching due to the formation of complex. The reaction was spontaneous and mainly mediated by hydrogen bonds and hydrophobic interactions. The binding distance between the tryptophan residue of HSA and PMT is less than 8 nm, which indicated that the energy transfer from the tryptophan residue of HSA to PMT occurred. The binding site of PMT on HSA was located in sites I and the presence of PMT can cause the conformational changes of HSA. There was the competitive binding to HSA between PMT and flavonoids because of the overlap of binding sites in HSA. The flavonoids could decrease the association constant and increase the binding distance. In addition, their synergistic effect can further change the conformation of HSA. The decrease in the affinities of PMT binding to HSA in the presence of flavonoids may lead to the increase of free drug in blood, which would affect the transportation or disposition of drug and evoke an adverse or toxic effect. Hence, rationalising dosage and diet regimens should be taken into account in clinical application of PMT.

Binding of promethazine (PMT) and its competitive binding with flavonoids to the site I of human serum albumin (HSA)Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Colloids and Surfaces B: Biointerfaces - Volume 145, 1 September 2016, Pages 820–829
نویسندگان
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