Standard Addition Method for the Determination of 1 Pharmaceutical Residues in Drinking Water by Spe-

نویسندگان

  • Isabelle Soutrel
  • Marguerite Lemasle
  • Alain Laplanche
  • André Crocq
چکیده

21 The study of the occurrence and fate of pharmaceutical compounds in drinking or waste 22 water processes has become very popular in recent years. LC-MS/MS is a powerful 23 analytical tool often used to determine pharmaceutical residues at trace level in water. 24 However, many steps may disrupt the analytical procedure and bias the results. A list of 27 25 environmentally relevant molecules, including various therapeutic classes and 26 (cardiovascular, veterinary and human antibiotics, neuroleptics, non-steroidal anti-27 inflammatory drugs, hormones and other miscellaneous pharmaceutical compounds) was 28 selected. In this work, a method was developed using Ultra Performance Liquid 29 Chromatography coupled to tandem Mass Spectrometry (UPLC-MS/MS) and solid phase 30 extraction (SPE) to determine the concentration of the 27 targeted pharmaceutical 31 compounds at the nanogram per liter level. The matrix effect was evaluated from water 32 sampled at different treatment stages. Conventional methods with external calibration and 33 internal standard correction were compared to the standard addition method. An accurate 34 determination of pharmaceutical compounds in drinking water was obtained by the 35

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Standard addition method for the determination of pharmaceutical residues in drinking water by SPE-LC-MS/MS.

The study of the occurrence and fate of pharmaceutical compounds in drinking or waste water processes has become very popular in recent years. Liquid chromatography with tandem mass spectrometry is a powerful analytical tool often used to determine pharmaceutical residues at trace level in water. However, many steps may disrupt the analytical procedure and bias the results. A list of 27 environ...

متن کامل

Development a HPLC method for simultaneous determination of Azinphose methyl, Diazinon, Phosalone and Chlorpyrifos residues in fruit

A high-performance liquid chromatography with ultraviolet detection (HPLC/UV) methodwhich was used solid-phase extraction for cleanup, was developed for the determination ofAzinphos methyl ,Phosalone, Diazinon and Chlorpyrifos residues in fruits. A full factorialexperimental design was used for development of HPLC condition and evaluation of effect ofthree factors (pH of mobile phase, percent o...

متن کامل

Gabapentin Determination in Human Plasma and Capsule by Coupling of Solid Phase Extraction, Derivatization Reaction, and UV-Vis Spectrophotometry

Gabapentin is an anticonvulsant widely used in the treatment of epilepsy. No peculiar chromophore is available on the gabapentin moiety for direct analysis by absorption spectrophotometry. A sensitive spectrophotometric method for the determination of gabapentin in bulk, pharmaceutical formulations and human plasma has been developed. In this method, gabapentin directly derivatized with vanilli...

متن کامل

Gabapentin Determination in Human Plasma and Capsule by Coupling of Solid Phase Extraction, Derivatization Reaction, and UV-Vis Spectrophotometry

Gabapentin is an anticonvulsant widely used in the treatment of epilepsy. No peculiar chromophore is available on the gabapentin moiety for direct analysis by absorption spectrophotometry. A sensitive spectrophotometric method for the determination of gabapentin in bulk, pharmaceutical formulations and human plasma has been developed. In this method, gabapentin directly derivatized with vanilli...

متن کامل

Development and Validation of RP-HPLC-UV Method for Determination of Diclofenac Sodium Residues on Surfaces for Cleaning Validation

In recent years, cleaning validation has achieved a position of increasing in the pharmaceutical industry. It provides assurance to the cleaning procedure that ensures equipment is consistently cleaned from the product, detergent and microbial residues to an acceptable level to avoid cross-contamination and adulteration of drug product with other active ingredients. The aim of this study was to...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2013