Analysis of a Urinary Biomarker Hydroxyproline for Clinical Assessment in Osteoporosis Patients
- سال انتشار: 1400
- محل انتشار: مجله تحقیقات شیمی تجزیه و تجزیه زیستی، دوره: 8، شماره: 4
- کد COI اختصاصی: JR_ANALCH-8-4_005
- زبان مقاله: انگلیسی
- تعداد مشاهده: 131
نویسندگان
Dept. of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education and ResearchShivarathreeshwara Nagar, MYSURU-۵۷۰ ۰۱۵, India.
Dept. of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education and ResearchShivarathreeshwara Nagar, MYSURU-۵۷۰ ۰۱۵, India
Dept. of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education and ResearchShivarathreeshwara Nagar, MYSURU-۵۷۰ ۰۱۵, India.
Dept. of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education and ResearchShivarathreeshwara Nagar, MYSURU-۵۷۰ ۰۱۵, India
Indegene Private Limited, Bengaluru, Karnataka, India
Department of Orthopedics, JSS Medical College & Hospital, JSS Academy of Higher Education & Research, Mysuru-۵۷۰۰۱۵, India.
چکیده
The various degradation products derived from bone collagen are pyridinoline, deoxypyridinoline, N- telopeptides, and hydroxyproline are excreted in the urine. Among that hydroxyproline is an important biomarker used to correlate the osteoporosis condition. A simple method of reversed phased ultra-fast liquid chromatography (RP UFLC) with a PDA detector. Hydroxyproline a UV inactive molecule is derivatized with Fluorenyl methyl chloroformate (FMOC) to form a UV active adduct. FMOC- Hydroxyproline adduct and Chlorthalidone as an internal standard were spiked to healthy adult urine and processed through strata Phenomenex C۱۸ cartridges. Extracts from cartridges were collected and analysed on Phenomenex C۱۸ column (۲۵۰mm ×۴.۶mm i.d., ۵µm particle size) as a stationary phase. The mobile phase was composed of acetonitrile and diethylamine (DEA) buffer pH ۹.۰ in the ratio ۵۰:۵۰v/v at a flow rate of ۰.۸ ml/min. Elutes were analyzed using a PDA detector at a detection wavelength of ۲۶۵nm. The proposed method was validated as per US-FDA Guidance. In this study, the chromatographic peaks of hydroxyproline and chlorthalidone show better resolution with a retention time of ۲.۵ and ۶.۴ min respectively. Hydroxyproline shows excellent linearity with ۰.۹۹۹۴ of the correlation coefficient (R۲). The newly developed and validated bioanalytical method established is conveniently used for the clinical assessment of hydroxyproline in biological fluids & is used to quantify the biomarker concentration (hydroxyproline) in a urine sample and correlate to disease condition (osteoporosis).کلیدواژه ها
Hydroxyproline, Fluorenyl methyl chloroformate (FMOC), RP-UFLC, Bioanalytical methodاطلاعات بیشتر در مورد COI
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