Determination of proline in human plasma samples using the encapsulation of proline dehydrogenase enzyme in dendritic silica: a new platform for the enzymatic biosensing of amino acids
Determination of proline in human plasma samples using the encapsulation of proline dehydrogenase enzyme in dendritic silica: a new platform for the enzymatic biosensing of amino acids
نویسندگان: آرزو میرزایی آس , آرزو سعادتی , سودابه حسن پور , محمد حسن زاده محله , محمد رضا سیاهی شادباد , ابوالقاسم جویبان
کلمات کلیدی: Enzyme, encapsulation, silica nanoparticle, electrochemical biosensing, amino acids, genetic disorder.
نشریه: 0 , 36 , 11 , 2019
| نویسنده ثبت کننده مقاله |
محمد حسن زاده محله |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
مرکز تحقیقات آنالیز دارویی |
| کد مقاله |
69010 |
| عنوان فارسی مقاله |
Determination of proline in human plasma samples using the encapsulation of proline dehydrogenase enzyme in dendritic silica: a new platform for the enzymatic biosensing of amino acids |
| عنوان لاتین مقاله |
Determination of proline in human plasma samples using the encapsulation of proline dehydrogenase enzyme in dendritic silica: a new platform for the enzymatic biosensing of amino acids |
| ناشر |
6 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
بلی |
| عنوان نشریه (خارج از لیست فوق) |
Analytical Methods |
| نوع مقاله |
Original Article |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح یک – ISI - Web of Science |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
|
| An innovative electrochemical biosensor for the sensitive and specific detection of L-proline (L-Pro) in human plasma samples was prepared by the encapsulation of proline dehydrogenase on amine functionalized dendritic fibrous nano-silica KCC-1. Fibrous nano-silica KCC-1-NH2 with its high surface area showed great properties for the encapsulation of proline dehydrogenase. By combining KCC-1-NH2 with proline dehydrogenase and casting it onto a glassy carbon electrode surface, a biosensor for the determination of L-Pro was fabricated. The prepared enzyme biosensor selectively detects L-Pro at physiological pH. The results demonstrate that the catalytic oxidation of L-Pro is diffusion-controlled and irreversible. Using cyclic voltammetry, the oxidation peak current was shown to be compatible with a concentration range of L-Pro from 2.26 to 40 mM and a low limit of quantification was 2.26 mM under physiological-like conditions was obtained. The fabricated biosensor was employed for the determination of L-Pro in unprocessed human plasma samples. It is shown that the prepared enzyme biosensor provides a sensitive and rapid strategy for the detection of L-Pro in plasma samples. The current response of the electrocatalytic oxidation of L-Pro by the engineered biosensor was retained in analytical solution up to 60 °C. The employed approach resulted in superior resistance to temperature in comparison to the free enzyme. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| 197.pdf | 1398/06/29 | 4836622 | دانلود |